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Ito JT, Alves LHV, Oliveira LDM, Xavier RF, Carvalho-Pinto RM, Tibério IDFLC, Sato MN, Carvalho CRF, Lopes FDTQDS. Effect of exercise training on modulating the TH17/TREG imbalance in individuals with severe COPD: A randomized controlled trial. Pulmonology 2025; 31:2441069. [PMID: 39764722 DOI: 10.1080/25310429.2024.2441069] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/29/2023] [Accepted: 11/13/2024] [Indexed: 01/11/2025] Open
Abstract
BACKGROUND Chronic obstructive pulmonary disease (COPD) induces an imbalance in T helper (Th) 17/regulatory T (Treg) cells that contributes to of the dysregulation of inflammation. Exercise training can modulate the immune response in healthy subjects. OBJECTIVE We aimed to evaluate the effects of exercise training on Th17/Treg responses and the differentiation of Treg phenotypes in individuals with COPD. METHODS This randomized controlled trial included 50 individuals with severe or very severe COPD who were allocated to the Exercise or Control groups. The Exercise group underwent eight weeks of aerobic and muscle strength training, whereas the Control group received usual care. The primary outcome was the change in the phenotypic characteristics of Tregs and Th17 profile differentiation in systemic inflammation. RESULTS Exercise training increased the frequency of total and activated Tregs and decreased the frequency of Th17 cells in between-group comparisons. Additionally, Th17/Treg responses were moderately correlated with improvements in the six-minute walking test, muscle strength of the upper and lower limbs, and daily life physical activity levels. CONCLUSION Exercise training improved functional exercise capacity, muscle strength, and physical fitness, which was associated with a decrease in the Th17 inflammatory response and an increase in Treg cell phenotypes immunosuppressive activity.
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Affiliation(s)
- Juliana Tiyaki Ito
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Luan Henrique Vasconcelos Alves
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Luana de Mendonça Oliveira
- Laboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, Tropical Medicine Institute of Sao Paulo, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | | | - Regina Maria Carvalho-Pinto
- Pulmonary Division, Heart Institute (InCor), Clinics Hospital, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | | | - Maria Notomi Sato
- Laboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, Tropical Medicine Institute of Sao Paulo, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Celso R F Carvalho
- Department of Physical Therapy, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
| | - Fernanda Degobbi Tenorio Quirino Dos Santos Lopes
- Laboratory of Experimental Therapeutics, LIM-20, Department of Clinical Medicine, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
- Thoracic Surgery Research Laboratory (LIM-61), Division of Thoracic Surgery, Heart Institute (InCor), Clinics Hospital, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
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Pini L, Giordani J, Levi G, Guerini M, Piva S, Peli E, Violini M, Piras S, El Masri Y, Pini A, Visca D, Assanelli D, Muiesan ML, Latronico N, Tantucci C, on behalf of the LOTO Investigators Working Group. Long-term alveolar-capillary diffusion impairments after severe SARS-CoV-2 pneumonia. Ann Med 2025; 57:2483383. [PMID: 40152750 PMCID: PMC11956098 DOI: 10.1080/07853890.2025.2483383] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/29/2024] [Revised: 03/06/2025] [Accepted: 03/10/2025] [Indexed: 03/29/2025] Open
Abstract
BACKGROUND Persistent respiratory symptoms and impaired gas exchange are common in patients recovering from COVID-19 pneumonia. The Lung Diffusing Capacity for Carbon Monoxide (DLCO) and Carbon Monoxide Transfer Coefficient (KCO) do not adequately distinguish alveolar membrane dysfunction from vascular abnormalities. This study aimed to characterize persistent diffusion impairment in post-ICU patients with prior SARS-CoV-2 pneumonia and reduced DLCO. METHODS After hospital discharge, patients underwent spirometry, DLCO measurement, and a 6-minute walking test every six months. If DLCO remained impaired at 18-24 months, a combined Lung Diffusing Capacity for Nitric Oxide (DLNO) and DLCO assessment was performed to differentiate alveolar-capillary membrane (DmCO) and pulmonary capillary blood volume (Vc) alterations. RESULTS Among 20 patients with persistent DLCO reduction, 3 had an obstructive ventilatory pattern, 6 had restriction, and 12 had low KCO. In restrictive cases, KCO was reduced but remained within normal limits without compensation. The DLNO/DLCO ratio exceeded 113.5% predicted in all patients. DmCO was impaired in 7 patients, while Vc was reduced in 16. CONCLUSION Both DLCO determinants were affected, with vascular impairment predominating. Vc reduction was present in most patients, with mean values below the lower limit of normality, whereas DmCO was less affected and often normal. The elevated DLNO/DLCO ratio suggests that persistent DLCO reduction is primarily driven by prolonged pulmonary capillary circulation dysfunction rather than alveolar membrane alterations, highlighting the vascular component as the primary site of long-term impairment.
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Affiliation(s)
- Laura Pini
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
- Respiratory Physiopathology Unit, ASST – Spedali Civili di Brescia, Brescia, Italy
| | - Jordan Giordani
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
| | - Guido Levi
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
- Pulmonology Department, ASST – Spedali Civili di Brescia, Brescia, Italy
| | - Michele Guerini
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
| | - Simone Piva
- Department of Anesthesia, Critical Care and Emergency, ASST Spedali Civili University Hospital, Brescia, Italy
- Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy
| | - Elena Peli
- Department of Anesthesia, Critical Care and Emergency, ASST Spedali Civili University Hospital, Brescia, Italy
| | - Manuela Violini
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
| | - Stefano Piras
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
| | - Yehia El Masri
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
| | - Alessandro Pini
- Department of Emergency, Anaesthesiological and Resuscitation Sciences, University Cattolica Sacro Cuore, Rome, Italy
| | - Dina Visca
- Department of Medicine and Surgery, University of Insubria, Varese, Italy
- Department of Medicine and Cardiopulmonary Rehabilitation, Istituti Clinici Scientifici Maugeri IRCCS, Tradate, Italy
| | - Deodato Assanelli
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
- Internal Medicine Unit, ASST Spedali Civili di Brescia, Brescia, Italy
| | - Maria Lorenza Muiesan
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
- Internal Medicine Unit, ASST Spedali Civili di Brescia, Brescia, Italy
| | - Nicola Latronico
- Department of Anesthesia, Critical Care and Emergency, ASST Spedali Civili University Hospital, Brescia, Italy
- Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy
| | - Claudio Tantucci
- Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy
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3
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Shingai K, Ikeuchi T, Rassam P, Kozu R, Ichiki K, Jimi T, Kawano T, Kato K, Tsuda T. Development of a new ambulatory oxygen delivery method combining continuous oxygen flow and demand oxygen delivery system: A prospective, single-blind, randomized crossover trial. Respir Med 2025; 243:108140. [PMID: 40345260 DOI: 10.1016/j.rmed.2025.108140] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/29/2025] [Revised: 04/19/2025] [Accepted: 05/03/2025] [Indexed: 05/11/2025]
Abstract
BACKGROUND AND OBJECTIVE Although demand oxygen delivery system (DODS) prolongs ambulatory oxygen supply, the efficacy of preventing hypoxemia is likely to be lower than continuous oxygen flow (CF). We developed a new oxygen delivery method combining CF and DODS (CF + DODS). This study aimed in comparing the efficacy between conventional oxygen delivery methods and a new method during walking in patients with COPD. METHODS We conducted three-treatment crossover study. Stable COPD patients performed three 6-min walk tests (6MWT) with different oxygen delivery methods in random order with CF, DODS, and CF + DODS. RESULTS Twenty-six COPD patients were included in the study. The linear mixed model on SpO2 revealed significant main effects of oxygen conditions (P < 0.001) and exercise time (P < 0.001), however no significant interaction (P = 0.537). In the post-hoc analysis, SpO2 in DODS was significantly lower than in CF and CF + DODS throughout the 6MWT. CF and CF + DODS showed no significant differences in SpO2 at any exercise timepoint. There were no significant differences among each oxygen delivery method in walking distance and dyspnea before and after 6MWT. DODS utilized significantly less oxygen than CF and CF + DODS, and CF + DODS consumed significantly less oxygen than CF during 6MWT. CONCLUSION CF + DODS enables a longer duration of oxygen supply, while preventing hypoxemia to the same degree as CF. These findings suggest that CF + DODS promotes outdoor activities in daily living while preventing hypoxemia in patients with COPD. TRIAL REGISTRATION This study was registered in the UMIN Clinical Trials Registry (UMIN00005299).
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Affiliation(s)
- Kazuya Shingai
- Pulmonary Rehabilitation Center, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan; Clinical Research Institute, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan; Department of Physical Therapy Science, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1, Sakamoto, Nagasaki, 852-8520, Japan.
| | - Tomoyuki Ikeuchi
- Pulmonary Rehabilitation Center, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan; Department of Physical Therapy Science, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1, Sakamoto, Nagasaki, 852-8520, Japan.
| | - Peter Rassam
- Department of Physical Therapy, University of Toronto, 160-500, University Avenue, Toronto, Ontario, MG5 1V7, Canada.
| | - Ryo Kozu
- Department of Physical Therapy Science, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1, Sakamoto, Nagasaki, 852-8520, Japan.
| | - Katsuyuki Ichiki
- Department of Respiratory Medicine, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan.
| | - Takeo Jimi
- Department of Respiratory Medicine, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan.
| | - Tetsuya Kawano
- Department of Respiratory Medicine, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan.
| | - Kaori Kato
- Department of Respiratory Medicine, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan.
| | - Tohru Tsuda
- Department of Respiratory Medicine, Kirigaoka Tsuda Hospital, 3-9-20, Kirigaoka, Kokurakita, Kitakyusyu, Fukuoka, 802-0052, Japan.
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Kaminsky DA, Rowell J, Menson K, Hodgdon K, Devine D, Garrow OJ, Raymond C, Prehoda E, Morrison T, Irvin CG. Longitudinal assessment of lung function in patients following COVID-19. Respir Med 2025; 243:108130. [PMID: 40311850 DOI: 10.1016/j.rmed.2025.108130] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 12/09/2024] [Revised: 04/15/2025] [Accepted: 04/25/2025] [Indexed: 05/03/2025]
Abstract
BACKGROUND While effects of COVID-19 on lung function are commonly described in those with severe illness, less is known about those with less severe illness, and most studies do not extend beyond 6 months following initial presentation. RESEARCH QUESTION What are the effects of COVID-19 on lung function in a cohort of participants that included those with more severe and less severe disease over a 1 year period from time of enrollment? STUDY DESIGN We enrolled 52 participants who included those with more severe (had been hospitalized) and less severe (not hospitalized) illness and measured spirometry, lung volumes, diffusing capacity, oscillometry, maximal muscle pressures, inspiratory drive, exercise capacity, and symptom and quality of life surveys at presentation, and repeated the measurements 6 and 12 months later. RESULTS While participants who had been hospitalized had consistently lower lung function in all measures, all values were within normal reference ranges. The pattern of lung function change suggested a predominant restrictive physiologic defect with reduced exercise capacity. Over 1 year, there was no significant improvement in lung function. Similar findings were seen when participants were stratified by whether they had shortness of breath at presentation. INTERPRETATION In our cohort of participants with both more severe and less severe disease, there were only minor differences in lung function associated with severe illness or whether participants had shortness of breath. COVID-19 resulted in subtle changes related to physiologic restriction, but overall lung function remained in the normal range with little change over time, suggesting that other factors besides lung function contribute to shortness of breath in participants following COVID-19.
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Affiliation(s)
- David A Kaminsky
- Pulmonary and Critical Care, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA; Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA; University of Vermont Larner College of Medicine, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA.
| | - Jamie Rowell
- Internal Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Burlington, VT, 05401, USA.
| | - Katherine Menson
- Pulmonary and Critical Care, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA; Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA; University of Vermont Larner College of Medicine, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA.
| | - Kevin Hodgdon
- Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA.
| | - Derek Devine
- Biomedical Statistics, 360 South Park Drive, Colchester, 05446, Burlington, VT, USA.
| | - Olivia J Garrow
- Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA.
| | - Cory Raymond
- Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA.
| | - Elise Prehoda
- University of Vermont Larner College of Medicine, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA.
| | - Tessalyn Morrison
- Internal Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Burlington, VT, 05401, USA.
| | - Charles G Irvin
- Pulmonary and Critical Care, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA; Vermont Lung Center, 792 College Parkway, Suite 305, Colchester, VT, 05446, USA; University of Vermont Larner College of Medicine, Given D208, 89 Beaumont Avenue, Burlington, VT, 05405, USA.
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5
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Li J, Wang M, Xie Y, Li S, Yu X, Li F, Xue H, Li Z, Zhang N, Liu G, Zhang W, Miao Q, Sun Z, Ge Z, Ma Z, Cai H, Sun Z, Zhang H, Wang Y. A Randomized, Double-Blinded, Placebo-Controlled Study of the Use of Traditional Chinese Medicine for Treating Patients With Mild/Moderate Chronic Obstructive Pulmonary Disease. J Evid Based Med 2025; 18:e70023. [PMID: 40207428 DOI: 10.1111/jebm.70023] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 04/11/2025]
Abstract
AIM Chronic obstructive pulmonary disease (COPD) is a critical disease, with lung function closely linked to disease severity. This study aimed to evaluate the clinical efficacy of treatments for stable COPD in patients with pulmonary function Grades I and II. PATIENTS AND METHODS We conducted a multicenter, randomized, double-blind, placebo-controlled trial (registration number: NCT01486186). A total of 502 patients were randomly assigned to an experimental group (n = 251, treated with Bufei, Bufei Jianpi, and Bufei Yishen granules based on traditional Chinese medicine [TCM] syndromes) and a control group (n = 251, treated with a Chinese medicine-based placebo). Acute exacerbations (AEs), lung function, clinical symptoms, 6-min walking distance (6MWD), and dyspnea were assessed over 12 months of treatment and 12 months of follow-up. RESULTS A total of 432 patients, including 214 and 218 patients in the experimental and control groups, respectively, completed the trial. The early treatment group had fewer AEs (p < 0.05), better clinical symptom scores (p < 0.05), longer 6MWD (p < 0.05), and better Modified Medical Research Council (mMRC) scores than the control group (p < 0.05). No significant differences were found in forced vital capacity (FVC) and forced expiratory volume in first second (FEV1%) between the two groups, but there was a significant difference in FEV1 and the annual rate of FEV1 decline between the groups over 2 years (p < 0.05). CONCLUSION Treatment with TCM for stable COPD significantly reduced AEs, increased the 6MWD, and alleviated dyspnea in patients with pulmonary function Grades I and II. FEV1 was improved, and the slower FEV1 decline indicates a potential benefit in mitigating disease progression.
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Affiliation(s)
- Jiansheng Li
- Co-Construction Collaborative Innovation Center for Chinese Medicine and Respiratory Diseases, Henan and Education Ministry of China, Zhengzhou, China
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
| | - Minghang Wang
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
| | - Yang Xie
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
| | - Suyun Li
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
| | - Xueqing Yu
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
| | - Fengsen Li
- Department of Respiratory Medicine, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, China
| | - Hanrong Xue
- Department of Respiratory, The Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine, Nanchang, China
| | - Zegeng Li
- The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China
| | - Nianzhi Zhang
- Department of Respiratory, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei, China
| | - Guiying Liu
- Department of Respiratory, The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China
| | - Wei Zhang
- Department of Respiratory, Shanghai Shuguang Hospital Affiliated With Shanghai University of Traditional Chinese Medicine, Shanghai, China
| | - Qing Miao
- Department of Respiratory, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China
| | - ZiKai Sun
- The Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China
| | - Zhenghang Ge
- Department of Respiratory, The Second Hospital of Guiyang University of Traditional Chinese Medicine, Guiyang, China
| | - Zhanping Ma
- Department of Respiratory Diseases, Shanxi Provincial Hospital of Traditional Chinese Medicine, Xian, China
| | - Hongyan Cai
- Jilin Province Academy of Traditional Chinese Medicine, Changchun, China
| | - Zhijia Sun
- The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China
| | - Hailong Zhang
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
| | - Yanfang Wang
- Henan Key Laboratory of Chinese Medicine for Respiratory Disease, Henan University of Chinese Medicine, Zhengzhou, China
- Department of Respiratory Diseases, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China
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Oke D, Gulec MG, Yalcinkaya EY, Taskiran OO. Does mild COVID-19 in healthcare workers affect functional capacity and work performance in short term? Work 2025; 81:2598-2606. [PMID: 40421562 DOI: 10.1177/10519815241311189] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/28/2025] Open
Abstract
BackgroundDisproportionately increased workload is one of the main reasons affecting work performance. Healthcare workers who got infected by COVID-19 were further affected mentally and physically which had an impact on their work performance.ObjectiveIn this study, we aimed to show whether work performance is affected even in people with mild Covid 19 disease or whether it is a part of Post-Acute COVID-19 Syndrome (PACS).MethodsThirty healthcare workers in a tertiary hospital had COVID-19 one month ago and gender and age matched 30 healthy workers without a history of COVID-19 (control group) was enrolled between January 2021 and March 2021. Work performance was assessed on a 7-point Likert scale. Participants performed 1-min sit-to-stand test (1MSTS), 5 times sit-to-stand test (5TSTS), and 6-min walk test (6MWT).ResultsAll participants in the COVID-19 group had a mild (non-hospitalized) form of the disease. 23 patients had ongoing symptoms 4-7 weeks after the initial symptoms of COVID-19 (fatigue/malaise (n = 9), myalgia/arthralgia (n = 7), cough (n = 7), loss of smell/taste (n = 5), headache (n = 5), dyspnea (n = 4), and diarrhea (n = 1). The increase in systolic blood pressure after 6MWT was higher in the COVID group (p = 0.018).ConclusionThe functional status and work performance in healthcare workers with COVID-19 infection were negatively affected in the first month even if the disease severity was mild. It is important to prevent both acute and long-term physical and mental complications of the disease and to ensure that these strategies improve the functional status and work performance of healthcare professionals.
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Affiliation(s)
- Deniz Oke
- Department of Physical Medicine and Rehabilitation, Gaziosmanpasa Training and Research Hospital, Istanbul, Turkey
| | - Meryem Guneser Gulec
- Department of Physical Medicine and Rehabilitation, Gaziosmanpasa Training and Research Hospital, Istanbul, Turkey
| | - Ebru Yilmaz Yalcinkaya
- Department of Physical Medicine and Rehabilitation, Gaziosmanpasa Training and Research Hospital, Istanbul, Turkey
| | - Ozden Ozyemisci Taskiran
- Department of Physical Medicine and Rehabilitation, Koc University School of Medicine, Istanbul, Turkey
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Nissen A, Gerbek T, Fogelstrøm K, Schmidt-Andersen P, Sørensen K, Mackey AL, Fridh MK, Müller K. Cardiorespiratory Fitness, Physical Performance and Metabolic Syndrome in Adult Survivors of Paediatric Haematopoietic Stem Cell Transplantation. Pediatr Blood Cancer 2025; 72:e31684. [PMID: 40159658 DOI: 10.1002/pbc.31684] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/13/2024] [Revised: 03/10/2025] [Accepted: 03/11/2025] [Indexed: 04/02/2025]
Abstract
BACKGROUND We examined cardiorespiratory fitness and physical performance in long-term survivors of paediatric haematopoietic stem cell transplantation (HSCT) and explored how these are associated with the presence of metabolic syndrome (MetS). PROCEDURE We included 90 survivors of paediatric HSCT (median age, 30.3 years; range, 19.6-53.0; median follow-up time, 20.2 years) and 32 healthy controls. Cardiorespiratory fitness was evaluated by cardiopulmonary exercise tests, and physical performance was assessed through sit-to-stand, handgrip strength, timed-up-and-go, walking pace and six-minute walk tests. We assessed for components of MetS (blood pressure, waist circumference, plasma lipids, and glucose). For comparison of physical capacity between survivors and controls and survivors with or without the presence of MetS, a multiple linear regression analysis corrected for age and sex was applied. RESULTS Survivors demonstrated lower cardiorespiratory fitness compared with controls (mean ± SD VO2 peak 29.3 ± 7.0 mL/kg/min vs. 44.3 ± 6.8 mL/kg/min, p < 0.0001) and impairment in all physical performance outcomes, where the most prominent differences compared with controls were seen in the sit-to-stand test (33% reduction). Twenty-eight percent of survivors fulfilled the criteria for MetS. The presence of MetS associated with lower VO2 peak (p = 0.03), poorer outcomes in the six-minute walk test (p = 0.02), walking pace (p = 0.03) and the timed-up-and-go test (p = 0.003). CONCLUSIONS Young adult survivors of paediatric HSCT are at risk of markedly reduced physical capacity compared with age- and sex-matched controls, and the high incidence of MetS observed among survivors was associated with this impairment. Overall, these data underline the importance of monitoring physical capacity in survivors of paediatric HSCT.
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Affiliation(s)
- Anne Nissen
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Tina Gerbek
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Kathrine Fogelstrøm
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Peter Schmidt-Andersen
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
- Department of Occupational Therapy and Physiotherapy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Kaspar Sørensen
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Abigail Louise Mackey
- Institute of Sports Medicine Copenhagen, Department of Orthopaedic Surgery, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Copenhagen, Denmark
- Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
| | - Martin Kaj Fridh
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
| | - Klaus Müller
- Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
- Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
- Institute for Inflammation Research, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
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8
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Webber T, Macdonald C, Tameris M, Tredoux N, Bierman A, Gutschmidt A, Tönsing S, Hiemstra A, Noor F, Snyders C, Richardson T, Fransman B, Allwood B, Hatherill M, Kleynhans L, Loxton AG, Walzl G, Chegou N, du Plessis N, Shaw JA, Malherbe ST. Immune, metabolic, anatomical, and functional features of people after successful tuberculosis treatment: an exploratory analysis. Sci Rep 2025; 15:18392. [PMID: 40419526 DOI: 10.1038/s41598-025-01656-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/07/2025] [Accepted: 05/07/2025] [Indexed: 05/28/2025] Open
Abstract
We explored the underlying mechanisms that may drive post-tuberculosis (TB) lung disease, a multifactorial, heterogenous, and prevalent disease. Extensive clinical phenotyping through fluorine-18 Fluorodeoxyglucose (FDG) positron emission tomography (PET)-computed tomography (CT) scans, pulmonary function testing, and symptom and quality of life questionnaires, was performed on a cohort of 48 adults who completed TB treatment within 6 months prior. Immunological characteristics of paired blood- and bronchoalveolar lavage fluid (BALF)-derived immune cells were assessed by multiplex bead-based immunoassay, ELISA and flow cytometry. There was agreement between measures of inflammation on PET, the severity of anatomical abnormalities on CT, and pulmonary function testing. However, of these, only PET was associated with exercise tolerance and symptom scores. Measures of radiologic extent (total glycolytic activity and SUVmax on PET, and segments involved on CT) also correlated with proteins detected in blood that implicate type 1 (IFN-γ, TNFα, IL-12) and type 2 (IL-4, IL-33) responses, ongoing remodelling of lung tissue (MMPs), airways and vasculature (VEGF), as well as subsets of activated CD8+ and CD4+ T-cells. The radiologic extent of structural post-TB lung involvement is associated with a range of impaired lung function measures and immunological dysregulation. Our findings suggest that obstructive and restrictive lung pathology due to pulmonary TB do not occur in opposition but rather point towards a mixed pathology in most TB survivors.
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Affiliation(s)
- Tariq Webber
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Candice Macdonald
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Michele Tameris
- South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa
| | - Nicolette Tredoux
- South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa
| | - Anandi Bierman
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Andrea Gutschmidt
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Susanne Tönsing
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Andriëtte Hiemstra
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Firdows Noor
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Candice Snyders
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Tracy Richardson
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Bernadine Fransman
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Brian Allwood
- Division of Pulmonology, Department of Medicine, Stellenbosch University and Tygerberg Hospital, Cape Town, South Africa
| | - Mark Hatherill
- South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa
| | - Leanie Kleynhans
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
- Mater Research Institute, The University of Queensland, Translational Research Institute, Brisbane, QLD, Australia
| | - André G Loxton
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Gerhard Walzl
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Novel Chegou
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Nelita du Plessis
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Jane A Shaw
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa
| | - Stephanus T Malherbe
- South African Medical Research Council Centre for Tuberculosis Research, Biomedical Research Institute, Division of Immunology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
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9
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Halacli B, Guven G, Kaya EK, Yildirim M, Kilic S, Ayyildiz Cinar S, Gul O, Ortac Ersoy E, Herridge M, Topeli A. Post-intensive care syndrome in critically-ill COVID-19 survivors followed for one-year. Chronic Illn 2025:17423953251333171. [PMID: 40400387 DOI: 10.1177/17423953251333171] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 05/23/2025]
Abstract
ObjectiveTo document the occurrence of post-intensive care syndrome (PICS) in intensive care unit (ICU) survivors with coronavirus disease-2019 (COVID-19) up to one year.MethodsRetrospective observational study at a university hospital post-ICU outpatient clinic. Patients were followed up in-person at 1 month, 3 months, 6 months and one-year after hospital discharge. Cognitive, physical and psychological domains of PICS were evaluated. PICS was defined as at least one dysfunction in the assessment tools in each domain.ResultsSixty-four patients were evaluated during the study period. Median age was 62.5 (55.0-71.0). Fifty-eight percent of them were male. Median APACHE II and admission SOFA scores were 13 (10-16) and 3 (3-4), respectively. Sixty-four, 54, 44, 20 patients were evaluated during the 1 -month, 3-month, 6-month and one-year visits. 94% of patients had PICS at the 1st visit and this declined to 75% in one-year. The ratio of patients who fulfilled all PICS domains were 15%, 10%, 13% and 13%, respectively at 4 follow-up visits. Physical impairment was the most commonly observed dysfunction during all visits.DiscussionThis study showed that at least one domain of PICS persisted in 75% of patients at one-year in COVID-19 ICU survivors.
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Affiliation(s)
- Burcin Halacli
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Goksel Guven
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Esat Kivanc Kaya
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Mehmet Yildirim
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Selman Kilic
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Sinem Ayyildiz Cinar
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Ozgul Gul
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Ebru Ortac Ersoy
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
| | - Margaret Herridge
- Critical Care Medicine, Toronto General Hospital, University Health Network, Toronto, Canada
| | - Arzu Topeli
- Department of Internal Medicine, Division of Intensive Care Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye
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10
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Haynes JM. Year in Review: Pulmonary Function Testing. Respir Care 2025. [PMID: 40398965 DOI: 10.1089/respcare.13066] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/23/2025]
Abstract
Pulmonary function testing dates back to the 19th century, and the most commonly performed tests pre-date the use of computers. Despite its long and rich history, much is still unknown about how to best perform, interpret, and apply pulmonary function tests. This year-in-review article will discuss recently published papers covering important topics including the performance of lung volume testing, the definition and severity grading of air flow obstruction, the clinical utility of bronchodilator responsiveness, and the use of race-neutral reference equations.
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Affiliation(s)
- Jeffrey M Haynes
- Mr. Haynes is affiliated with Pulmonary Function Laboratory, Elliot Health System, Manchester, New Hampshire, USA
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11
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Barbosa MM, Correia NS, Moreira NN, Pereira DM, do Amaral PD, Mesquita R, Dal Corso S, de Oliveira MR, Furlanetto KC. Cutoff points of simple, rapid, and low-cost functional tests to reflect functional exercise capacity as assessed by the six-minute walk test in the elderly. A multicenter study. Geriatr Nurs 2025:103344. [PMID: 40393813 DOI: 10.1016/j.gerinurse.2025.04.017] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/27/2024] [Revised: 03/30/2025] [Accepted: 04/28/2025] [Indexed: 05/22/2025]
Abstract
INTRODUCTION The 6-Minute Walk Test (6MWT) is recommended for assessing the functional exercise capacity of the elderly. It was hypothesized that faster functional tests could identify low exercise capacity in this population. OBJECTIVE To investigate which simple functional test are associated with the performance in the 6MWT of fully functional adults above 60 years of age and to determine the cutoff points that discriminate the worst functional capacity. METHODS The Sit-to-stand test, usual and maximum gait speed, usual and maximum Timed-up-and-go test and the 6MWT were performed. RESULTS A total of 113 elderly people aged 67(64-73) years were analyzed. The ROC curve identified the cutoff point of each functional test, which discriminated the worst exercise capacity. The area under the curve were satisfatory (0.549 CONCLUSION Cutoff points of simple functional tests can be used to identify elderly people with low exercise capacity.
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Affiliation(s)
- Marcelo Moreira Barbosa
- Stricto Sensu Graduate Program in Physical Exercise in Health Promotion, University Pitágoras Unopar, Londrina, Paraná, Brazil
| | - Natielly Soares Correia
- Stricto Sensu Graduate Program in Rehabilitation Sciences, University Pitágoras Unopar, Londrina, Paraná, Brazil
| | - Natalia Neves Moreira
- Stricto Sensu Graduate Program in Rehabilitation Sciences, University Pitágoras Unopar, Londrina, Paraná, Brazil
| | - Daniel Martins Pereira
- Department of Physiotherapy, University for the Development of the State and the Pantanal Region, (UNIDERP), Campo Grande, Brazil
| | - Pereira Daniel do Amaral
- Graduate Program in Rehabilitation Sciences, University Nove de Julho (UNINOVE), São Paulo, Brazil
| | - Rafael Mesquita
- Masters Program in Physiotherapy and Functioning, Federal University of Ceara (UFC), Fortaleza, Brazil
| | - Simone Dal Corso
- Graduate Program in Rehabilitation Sciences, University Nove de Julho (UNINOVE), São Paulo, Brazil
| | - Márcio Rogério de Oliveira
- Stricto Sensu Graduate Program in Physical Exercise in Health Promotion, University Pitágoras Unopar, Londrina, Paraná, Brazil
| | - Karina Couto Furlanetto
- Stricto Sensu Graduate Program in Physical Exercise in Health Promotion, University Pitágoras Unopar, Londrina, Paraná, Brazil; Stricto Sensu Graduate Program in Rehabilitation Sciences, University Pitágoras Unopar, Londrina, Paraná, Brazil.
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12
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Ünlü B, Yıldız Özer A, Özmen İ, Polat MG. The effectiveness of dual-task exercises in individuals with chronic obstructive pulmonary disease: a study protocol for a randomized controlled trial. Trials 2025; 26:164. [PMID: 40390096 PMCID: PMC12090634 DOI: 10.1186/s13063-025-08854-2] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/25/2024] [Accepted: 04/27/2025] [Indexed: 05/21/2025] Open
Abstract
BACKGROUND Central nervous system dysfunction is an extrapulmonary complication of chronic obstructive pulmonary disease (COPD), and brain function, particularly frontal lobe function, has been shown to deteriorate. It has also been reported that the time taken to complete a functional test involving a cognitive task is prolonged in patients with COPD. The aim of this study is to evaluate the effect of dual-task performance on motor and cognitive function in COPD and to determine the effect of dual-task exercises delivered in a pulmonary rehabilitation program on cardiopulmonary and musculoskeletal parameters. METHODS COPD patients who are admitted to pulmonary rehabilitation, meet the inclusion criteria, and volunteer to participate will be randomly divided into the pulmonary rehabilitation group (control group) and dual-task exercise group. The Dual Task Exercise Group will continue the established rehabilitation programs. During the walking and balance exercises in the program, they will also do cognitive exercises, which are different from those in the pulmonary rehabilitation control group. The COPD Assessment Questionnaire will be applied, and dyspnea assessment will be done with the Modified Medical Research Council Dyspnea Scale. Mini-Mental State Examination and Frontal Assessment Battery will be used to assess cognitive status. Mini-BESTest: Balance Evaluation Systems Test will be used to assess balance. Functional balance and mobility assessment will be performed with the Timed Up and Go Test and the 10-m Walk Test. The tests will be applied twice, as a single task (normal walking) and a dual task (walking and cognitive task). The 6-min walk test will be used to assess functional capacity. Quality of life will be assessed using the St. George Respiratory Questionnaire. Results of pulmonary function tests performed at routine check-ups will be obtained. Assessments will be repeated at the end of the 8-week exercise program. DISCUSSION Extrapulmonary clinical problems may affect the treatment process in COPD. Studies examining the effect of cognitive dysfunction evaluated dual-task performance in COPD and compared it with healthy controls. Despite the differences in the results, it emphasized that the effects of adding dual-task training to pulmonary rehabilitation should be investigated. Our study may contribute to the literature at this point. TRIAL REGISTRATION ClinicalTrials.gov ID: NCT05930158 (Date: 14.06.2023).
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Affiliation(s)
- Begüm Ünlü
- Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Marmara University, Istanbul, Türkiye.
| | - Aysel Yıldız Özer
- Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Marmara University, Istanbul, Türkiye
| | - İpek Özmen
- Department of Chest Diseases, Hamidiye Faculty of Medicine, University of Health Sciences, Süreyyapaşa Chest Diseases Thoracic Surgery Training and Research Hospital, Istanbul, Türkiye
| | - Mine Gülden Polat
- Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Marmara University, Istanbul, Türkiye
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13
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Jebaraj P, Paul B, Isaac R, Reddy SR, Kumar R, Vikas B, Das D, Norrie J, Weller D, Pinnock H, RESPIRE Collaboration. Optimising participation in a pulmonary rehabilitation programme for people living with chronic respiratory diseases in rural India: a feasibility study. J Glob Health 2025; 15:04143. [PMID: 40340958 PMCID: PMC12063193 DOI: 10.7189/jogh.15.04143] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/10/2025] Open
Abstract
Background Pulmonary rehabilitation (PR) plays a vital role in managing chronic obstructive pulmonary disease and other chronic respiratory diseases (CRDs). However, implementation of this multidisciplinary approach in resource-poor settings may not be sufficient because of referrers' uncertainty regarding the effectiveness of PR, inconvenient timing, travel issues, patients' lack of motivation, and poor family support. The aim was to test the feasibility of a peer-led, professionally assisted community-based PR programme for CRD patients in a rural, low literacy setting. Methods We conducted a single-centre, pre-post feasibility study. Participants with a confirmed diagnosis of CRD were recruited and treatment was optimised. After completing baseline assessments, the participants underwent eight weeks of PR training (16 sessions) in six groups at five local facilities led by peers selected by the participants and assisted by professionals. Exercise capacity was assessed with 6-Minute Walk Test. Other outcomes were: International Physical Activity Questionnaire; Hospital Anxiety and Depression Scale; London Chest Activity of Daily Living scale. Upper and lower limb strength were assessed using a handheld dynamometer and cycle ergometer, respectively. Descriptive analysis was performed, and pre-and post-outcomes were compared using parametric tests. Results Thirty participants (20 chronic obstructive pulmonary disease and 10 asthma; 15 female; median age 57.5 years) completed baseline and endline assessments. Seventy percent completed at least 12/16 sessions. After eight weeks of training, the 6-Minute Walk Test had improved from 263.3 (standard deviation (SD) = 72.3) to 319.6 (SD = 84.7) metres (P < 0.001) with significant improvement in modified Medical Research Council (P = 0.022), London Chest Activity of Daily Living scale (P < 0.001) and dominant handgrip strength (P < 0.001) but no significant change in physical activity (P = 0.791). Conclusions The community-based PR led by peer volunteers and supported by professionals proved to be feasible in our low-resource setting and was associated with improved exercise tolerance and other outcomes. Registration The study was registered at the Clinical Trials Registry - India (CTRI/2020/09/027818).
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Affiliation(s)
- Paul Jebaraj
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
| | - Biswajit Paul
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
| | - Rita Isaac
- Karkinos Healthcare Private limited, Ernakulam, India
| | - Shadrack Ravindra Reddy
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
| | - Rakesh Kumar
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
| | - Bochu Vikas
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
| | - Deepa Das
- Bangalore Baptist Hospital, Bangalore, India
| | - John Norrie
- Usher Institute, The University of Edinburgh, Edinburgh, UK
| | - David Weller
- Usher Institute, The University of Edinburgh, Edinburgh, UK
| | - Hilary Pinnock
- Usher Institute, The University of Edinburgh, Edinburgh, UK
| | - RESPIRE Collaboration
- Christian Medical College, Vellore, Rural Unit for Health and Social Affairs Department, Vellore, India
- Karkinos Healthcare Private limited, Ernakulam, India
- Bangalore Baptist Hospital, Bangalore, India
- Usher Institute, The University of Edinburgh, Edinburgh, UK
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Baldi BG, das Posses Bridi G, Heiden GI, Salge JM, Queiroz DS, Ribeiro Carvalho CR, de Carvalho CRF. Mechanisms of exercise limitation and pulmonary rehabilitation in patients with cystic lung diseases. Expert Rev Respir Med 2025:1-15. [PMID: 40314321 DOI: 10.1080/17476348.2025.2501277] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/19/2025] [Revised: 04/12/2025] [Accepted: 04/29/2025] [Indexed: 05/03/2025]
Abstract
INTRODUCTION The main diffuse cystic lung diseases (DCLD) include lymphangioleiomyomatosis (LAM), pulmonary Langerhans cell histiocytosis (PLCH), Birt-Hogg-Dubé syndrome, and lymphocytic interstitial pneumonia. Exercise limitation is frequent and secondary to multiple mechanisms in DCLD. Some studies addressed mechanisms for exercise limitation, field tests, and pulmonary rehabilitation (PR) in DCLD. AREAS COVERED This review aims to present the main mechanisms that determine exercise limitation, the responses of patients in field tests, and the details regarding the safety and efficacy of PR in DCLD, with emphasis on LAM and PLCH. A search on the issue was performed in the MEDLINE and SciELO databases between 27 November 2024 and 20 February 2025. Manuscripts were reviewed and important topics were included in this review. EXPERT OPINION Reduced exercise capacity is common and multifactorial, including ventilatory, cardiocirculatory, and peripheral limitations, pulmonary hypertension (PH), and impaired gas exchange in LAM and PLCH. Variables from field tests are correlated with pulmonary function tests, and PR is safe and beneficial in LAM. Further studies are necessary to evaluate exercise in other DCLDs, the impact of other therapeutic modalities on DH, hypoxemia, and exercise-induced PH in LAM and PLCH, and the safety and benefits of PR mostly in PLCH.
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Affiliation(s)
- Bruno Guedes Baldi
- Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil
- Hospital do Coração, São Paulo, Brazil
| | - Guilherme das Posses Bridi
- Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil
- Núcleo de Pulmão e Torax, AC Camargo Cancer Center, São Paulo, Brazil
| | - Gláucia Itamaro Heiden
- Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil
| | - João Marcos Salge
- Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil
| | - Douglas Silva Queiroz
- Departamento de Fisioterapia, Faculdade de Medicina, Universidade de Sao Paulo, São Paulo, Brazil
- Hospital Israelita Albert Einstein, São Paulo, Brazil
| | - Carlos Roberto Ribeiro Carvalho
- Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil
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15
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Levett DZH, Grocott MPW. Prehabilitation: Impact on Postoperative Outcomes. Int Anesthesiol Clin 2025:00004311-990000000-00094. [PMID: 40323728 DOI: 10.1097/aia.0000000000000481] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/07/2025]
Affiliation(s)
- Denny Z H Levett
- Perioperative and Critical Care Theme, NIHR Southampton Biomedical Research Centre, University Hospital Southampton/University of Southampton, Southampton, UK
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Lee AL, Clark IN, Lewis A. Harnessing music therapy and music medicine in chronic respiratory disease management. Expert Rev Respir Med 2025:1-17. [PMID: 40310448 DOI: 10.1080/17476348.2025.2501279] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/09/2025] [Revised: 04/23/2025] [Accepted: 04/29/2025] [Indexed: 05/02/2025]
Abstract
INTRODUCTION Treatment options for those living with chronic respiratory disease include non-pharmacological therapies to maximize outcomes. However, some individuals are limited by their symptoms, which inhibit their ability to benefit to an equivalent or expected level. Both music therapy and music medicine are therapeutic approaches which could address these limitations. AREAS COVERED This perspective reviews the clinical effects of music therapy and music medicine in chronic respiratory diseases. This considers active music therapy methods of re-creating (group singing), improvisation (instrument playing), receptive music listening and music medicine, with a specific focus at rest and during exercise. EXPERT COMMENTARY The precise role of music therapy or music medicine as an adjunct to exercise testing or structured exercise programs for people with chronic respiratory disease is unclear. Choice of music (for background or individual use for this purpose) requires input from participants and would benefit from music therapists to guide selection. While preliminary findings of group singing and instrument playing highlight some efficacy, their role in comparison to pulmonary rehabilitation requires further clarification. At present, these music therapy and music medicine approaches can be considered as adjunct therapies which may assist in managing symptoms and improving wellbeing alongside existing management strategies.
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Affiliation(s)
- Annemarie Louise Lee
- Department of Physiotherapy, School of Primary and Allied Health Care, Monash University, Frankston, Australia
- Institute for Breathing and Sleep, Austin Health, Heidelberg, Australia
| | - Imogen Nicola Clark
- Melbourne Conservatorium of Music, Faculty of Fine Arts and Music, University of Melbourne, Southbank, Victoria, Australia
| | - Adam Lewis
- School of Health Science, University of Southampton, Southampton, UK
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Miyata Y, Tanaka A, Goto Y, Ebato T, Suganuma H, Nojo M, Mikuni H, Uno T, Uchida Y, Jinno M, Ohta S, Homma T, Watanabe Y, Kusumoto S, Sagara H. One-minute sit-to-stand test to detect gas exchange capacity during exercise stress in patients with idiopathic or progressive pulmonary fibrosis: A randomized, crossover trial. Respir Investig 2025; 63:241-246. [PMID: 39938407 DOI: 10.1016/j.resinv.2025.01.008] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/26/2024] [Revised: 01/06/2025] [Accepted: 01/30/2025] [Indexed: 02/14/2025]
Abstract
BACKGROUND The 6-min walk test (6MWT), used to monitor disease progression or exacerbation in interstitial lung disease, faces challenges such as requiring a 30-m walking path and difficulty assessing patients with gait disturbance. The 1-min sit-to-stand test (1STST) offers a convenient alternative, potentially addressing these issues. Despite its advantages, the effectiveness of the 1STST in patients with idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF) still needs to be explored. We assessed 1STST's ability to detect exercise-induced desaturation in a randomized, crossover trial involving patients with IPF or PPF. METHODS Participants were divided into group A (6MWT to 1STST) and B (1STST to 6MWT), with a 30-min rest period between the tests. The primary endpoint was the difference in nadir oxygen saturation (SpO2) between the groups throughout the study. Secondary endpoints included the percentage of participants with a nadir SpO₂ <88% during the tests, a decline of ≥4% in SpO2, and the variation in Borg scores post-tests. RESULTS Twenty-three participants (91.3% male; mean age ± standard deviation: 77.2 ± 7.4 years) diagnosed with IPF and PPF were enrolled in this study. The difference in nadir SpO2 between the 1STST and 6MWT was 1.14% (95% confidence interval: -0.18, 2.48), with the 95% confidence intervals falling within the predefined equivalence range. No significant differences were observed in the secondary endpoints. CONCLUSIONS The results suggest that the 1STST is as effective as the 6MWT in detecting desaturation in patients with IPF and PPF. TRIAL REGISTRATION This study was registered on the website of the Japan Registry of Clinical Trials (jRCT1032230037; URL: https://jrct.niph.go.jp/).
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Affiliation(s)
- Yoshito Miyata
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan.
| | - Akihiko Tanaka
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Yuiko Goto
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Takaya Ebato
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Hiromitsu Suganuma
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Makoto Nojo
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Hatsuko Mikuni
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Tomoki Uno
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Yoshitaka Uchida
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Megumi Jinno
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Shin Ohta
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Tetsuya Homma
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Yoshio Watanabe
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Sojiro Kusumoto
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
| | - Hironori Sagara
- Department of Internal Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan
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18
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Marshall EM, Filiex A, Schulte M, Logie KM, Gin J, Horrigan M, Dowman L, Churchward TJ, Khor YH. Performance Comparison of Oximetry Devices During 6-Minute Walk Tests. Respir Care 2025; 70:492-501. [PMID: 40192549 DOI: 10.1089/respcare.12259] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 05/06/2025]
Abstract
Background: Pulse oximetry is a common technique used to measure SpO2, with increasing numbers of portable devices of different designs and technical specifications. This study examined accuracy of commercial and medical-grade portable oximetry devices (BioBeat wristwatch, Nonin WristOx2 3150, and Heart Sure A320) in measuring SpO2 compared with the reference standard (Masimo Rad-5) during 6-min walk tests (6MWTs). Methods: This prospective study included 50 subjects, with 10 recruited for each of the five target groups, including COPD, interstitial lung disease, pulmonary hypertension, oxygen therapy users, and other cardiac/respiratory diseases. All subjects underwent 6MWT using the reference standard and the three test oximetry devices. Accuracy was measured by comparing mean nadir SpO2. Subjects were asked to rate their preference for different oximetry devices at test completion. Results: In contrast to the Masimo, the Nonin had lower nadir and mean SpO2 (P ≤ .001 for both), with higher measurements for the BioBeat (P < .001 for both) and no differences for the Heart Sure (P = .18 for nadir SpO2, P = .96 for mean SpO2). Time spent at SpO2 ≤ 88 was higher for the Nonin (70%, P < .001) but lower for the Heart Sure (58%, P < .001), compared with the Masimo (64%). There were no significant differences observed in peak heart rate measurements between the Masimo with the Nonin and BioBeat (P < .05 for both), with lower measurements using the Heart Sure (P < .001). The BioBeat was most preferable amongst subjects (n = 31), with all test oximeters having high patient satisfaction (mean \7-point Likert scale scores of 6-7). Conclusion: The Heart Sure A320 and Nonin Wrist-Ox2 3150 had comparable performance in detecting nadir SpO2 within a mean difference of 3% in comparison with the Masimo Rad-5, with potential use for remote monitoring.
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Affiliation(s)
- Emma M Marshall
- Ms. Marshall, Dr. Dowman, Mr. Churchward, and Dr. Khor are affiliated with Institute of Breathing and Sleep, Victoria, Australia
- Ms. Marshall, Mr. Schulte, Ms. Logie, Mr. Churchward, and Dr. Khor are affiliated with Department of Respiratory and Sleep Medicine, Austin Health, Victoria, Australia
| | - Angeline Filiex
- Ms. Filiex, Drs. Dowman, and Khor are affiliated with Respiratory Research@Alfred, Monash University, Victoria, Australia
| | - Max Schulte
- Ms. Marshall, Mr. Schulte, Ms. Logie, Mr. Churchward, and Dr. Khor are affiliated with Department of Respiratory and Sleep Medicine, Austin Health, Victoria, Australia
| | - Karla M Logie
- Ms. Marshall, Mr. Schulte, Ms. Logie, Mr. Churchward, and Dr. Khor are affiliated with Department of Respiratory and Sleep Medicine, Austin Health, Victoria, Australia
| | - Julian Gin
- Dr. Gin, Dr. Horrigan are affiliated with Department of Cardiology, Austin Health, Melbourne, Victoria, Australia
| | - Mark Horrigan
- Dr. Gin, Dr. Horrigan are affiliated with Department of Cardiology, Austin Health, Melbourne, Victoria, Australia
| | - Leona Dowman
- Ms. Marshall, Dr. Dowman, Mr. Churchward, and Dr. Khor are affiliated with Institute of Breathing and Sleep, Victoria, Australia
- Ms. Filiex, Drs. Dowman, and Khor are affiliated with Respiratory Research@Alfred, Monash University, Victoria, Australia
- Dr. Dowman is affiliated with Department of Physiotherapy, Austin Health, Melbourne, Australia
| | - Thomas J Churchward
- Ms. Marshall, Dr. Dowman, Mr. Churchward, and Dr. Khor are affiliated with Institute of Breathing and Sleep, Victoria, Australia
- Ms. Marshall, Mr. Schulte, Ms. Logie, Mr. Churchward, and Dr. Khor are affiliated with Department of Respiratory and Sleep Medicine, Austin Health, Victoria, Australia
| | - Yet H Khor
- Ms. Marshall, Dr. Dowman, Mr. Churchward, and Dr. Khor are affiliated with Institute of Breathing and Sleep, Victoria, Australia
- Ms. Marshall, Mr. Schulte, Ms. Logie, Mr. Churchward, and Dr. Khor are affiliated with Department of Respiratory and Sleep Medicine, Austin Health, Victoria, Australia
- Ms. Filiex, Drs. Dowman, and Khor are affiliated with Respiratory Research@Alfred, Monash University, Victoria, Australia
- Dr. Khor us affiliated with Department of Medicine, University of Melbourne, Victoria, Australia
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19
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Lofuta Olenga Vuvu P, Klass M, Pauwen N, Kipula AM, van de Borne P, van Muylem A, Perez‐Bogerd S, Deboeck G. Effects of chronic exposure to biomass pollutants on cardiorespiratory responses and the occurrence of exercise-induced bronchoconstriction in healthy men. Physiol Rep 2025; 13:e70368. [PMID: 40346027 PMCID: PMC12064335 DOI: 10.14814/phy2.70368] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/07/2025] [Revised: 04/21/2025] [Accepted: 04/27/2025] [Indexed: 05/11/2025] Open
Abstract
Exposure to charcoal biomass (CB) pollutants affects the cardiorespiratory system. We assessed cardiopulmonary responses (CPR) to exercise in charcoal producers (CPs) compared to farmers and evaluated the prevalence of exercise-induced bronchoconstriction (EIB). Forty-five CPs and 36 farmers, healthy males aged 23-39, completed a 15-m Incremental Shuttle Walk and Run Test (15-m ISWRT). Air quality index (AQI) and CO intoxication were measured, CPR was assessed through heart rate (HR), blood pressures (SBP, DBP), and spirometry at rest, peak exercise, and during recovery at 5 and 15 min. Aerobic capacity (VO2 max) was estimated from the distance covered during the 15-m ISWRT, and EIB was defined as a >10% decrease in FEV1 from baseline values. AQI was worse in charcoal workplaces, and CPs had higher CO intoxication than farmers (p < 0.0001). Both groups reached maximal exercise %HRmax: 84 (82-89) versus 84 (80-89), p = 0.37 and showed similar predicted VO2 max 36.2 (31.1-43.1) versus 38.9 (32.2-43.7) mL/kg/min, p = 0.60. However, after ISWRT, CPs had lower FEV1 than farmers (2.9 ± 0.6 vs. 3.3 ± 0.6 L, p < 0.003) and slower recovery. EIB prevalence was higher in CPs (60.0% vs. 27.8%, p = 0.006). Chronic exposure to CB increases EIB in healthy CPs, suggesting heightened airway hyperreactivity.
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Affiliation(s)
- Pierre Lofuta Olenga Vuvu
- Cardiopulmonary Rehabilitation Unit, Physical Medicine and Rehabilitation Department, University Clinics of KinshasaUniversity of KinshasaKinshasaDemocratic Republic of the Congo
- Research Unit in Rehabilitation Sciences, Faculty of Human Movement SciencesUniversité Libre de BruxellesBrusselsBelgium
| | - Malgorzata Klass
- Research Unit in Biometry and Exercise Nutrition, Faculty of Human Movement SciencesUniversité Libre de BruxellesBrusselsBelgium
| | - Nathalie Pauwen
- Cardiopulmonary Exercise Laboratory, Faculty of Human Movement SciencesUniversité Libre de BruxellesBrusselsBelgium
| | - Augustin Mboko Kipula
- Cardiopulmonary Rehabilitation Unit, Physical Medicine and Rehabilitation Department, University Clinics of KinshasaUniversity of KinshasaKinshasaDemocratic Republic of the Congo
| | - Philippe van de Borne
- Cardiology Department, Erasme University HospitalUniversité Libre de BruxellesBrusselsBelgium
| | - Alain van Muylem
- Pulmonology Department, Erasme University HospitalUniversité Libre de BruxellesBrusselsBelgium
- Epidemiology and Biostatistics Unit, Public Health SchoolUniversité Libre de BruxellesBrusselsBelgium
| | - Silvia Perez‐Bogerd
- Pulmonology Department, Erasme University HospitalUniversité Libre de BruxellesBrusselsBelgium
| | - Gael Deboeck
- Research Unit in Rehabilitation Sciences, Faculty of Human Movement SciencesUniversité Libre de BruxellesBrusselsBelgium
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20
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Kim MJ, Yang J, Song JW. Polymyxin B-hemoperfusion in patients with acute exacerbation of idiopathic pulmonary fibrosis: a single-center prospective pilot study. Korean J Intern Med 2025; 40:458-467. [PMID: 40360222 PMCID: PMC12081109 DOI: 10.3904/kjim.2024.244] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/13/2024] [Revised: 09/17/2024] [Accepted: 10/07/2024] [Indexed: 05/15/2025] Open
Abstract
BACKGROUND/AIMS Patients with acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) typically have a poor prognosis; however, no effective treatment is available. In recent years, several retrospective studies have suggested the clinical benefits of direct hemoperfusion with a polymyxin B-immobilized fiber column (PMX-DHP) in patients with AE-IPF. Herein, we aimed to investigate the efficacy and safety of PMX-DHP treatment in patients with AE-IPF. METHODS Patients diagnosed with AE-IPF (n = 10) with a partial pressure of oxygen to fraction of inspiratory oxygen ratio (P/F ratio) > 100 were prospectively enrolled at a single center. PMX-DHP was performed twice for 6 hours (at 24-h intervals) at a flow rate of 80-100 mL/min, and steroid pulse therapy was concurrently administered (500 mg of methylprednisolone for 3 d). RESULTS The mean patient age was 67 years, and 80.0% were male. During the follow-up (median, 42.5 d; interquartile range, 16.0-174.0 d), seven (70.0%) patients died (including two who underwent transplantation); the in-hospital mortality rate was 70%, while the 30- and 90-day mortality rates were 50.0% and 70.0%, respectively. After 48 hours of PMX-DHP treatment, the P/F ratio improved (mean, 160.0 vs. 229.0; p = 0.054) and C-reactive protein level decreased (mean, 8.3 mg/dL vs. 3.5 mg/dL; p = 0.012). During hospitalization, no PMX-DHP-associated adverse events were observed. CONCLUSION Our results suggest that PMX-DHP treatment may be useful at improving oxygenation and reducing inflammation in patients with AE-IPF with acceptable safety profiles, however without affecting their prognosis.
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Affiliation(s)
- Min Jee Kim
- Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
| | - Jiyoul Yang
- Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
| | - Jin Woo Song
- Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
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21
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Thangakunam B, Isaac B, Sekar R, Abhilash KPP, Nellimootil MV, Paul H, Christopher DJ. Forty-steps desaturation test does not have prognostic value in COVID-19 due to omicron variant. Lung India 2025; 42:270-272. [PMID: 40296406 PMCID: PMC12097660 DOI: 10.4103/lungindia.lungindia_7_25] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Download PDF] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/06/2025] [Accepted: 01/21/2025] [Indexed: 04/30/2025] Open
Affiliation(s)
- Balamugesh Thangakunam
- Department of Pulmonary Medicine, Christian Medical College, Vellore, Tamil Nadu, India E-mail:
| | - Barney Isaac
- Department of Pulmonary Medicine, Christian Medical College, Vellore, Tamil Nadu, India E-mail:
| | - Rajasekar Sekar
- Department of Pulmonary Medicine, Christian Medical College, Vellore, Tamil Nadu, India E-mail:
| | | | | | - Hema Paul
- Department of Hospital Infection Control, Christian Medical College, Vellore, Tamil Nadu, India.
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Radovanovic D, Signorello JC, Fuccia G, Lazzaroni G, Danzo F, Guandalini GM, Massaro F, Tursi F, Santus P. Impact of L-arginine and liposomal vitamin C supplementation on quality of life and daily life activities in patients with COPD: a randomized, multicenter, single blind, placebo-controlled trial (ILDA study). Eur J Intern Med 2025:S0953-6205(25)00180-3. [PMID: 40316462 DOI: 10.1016/j.ejim.2025.04.039] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/15/2025] [Revised: 03/28/2025] [Accepted: 04/28/2025] [Indexed: 05/04/2025]
Abstract
OBJECTIVE Chronic Obstructive Pulmonary Disease (COPD) patients experience limitations in activities of daily living (ADL) despite optimal inhaled treatment. L-arginine depletion is associated with poor exercise performance. Our aim was to assess whether oral L-arginine supplementation improves dyspnea and ADL in COPD patients. DESIGN AND METHODS Randomized, multicenter, single blind, placebo-controlled study (NCT05412160). Stable COPD patients received L-arginine (1.66 g) plus liposomal vitamin C (500 mg) twice daily or placebo for 4 weeks. At baseline (T0) and after treatment (T1) lung function, six minutes walking test (6MWT), dyspnea and ADL perfomance, evaluated through: COPD assessment test (CAT), self-administered chronic respiratory questionnaire (CRQ-SA), Clinical COPD Questionnaire 24 h and 7 days (CCQ) and London Chest Activity of Daily Living Scale (LCADL) -were assessed. The primary endpoint was CRQ score change compared with placebo. RESULTS 150 patients were enrolled (67 % males, median FEV1 57 %predicted), with 76 receiving L-arginine. Baseline characteristics and questionnaire scores were balanced between arms. At T1, L-arginine patients demonstrated significant improvements compared to placebo in CRQ total score (median (IQR) 3.5 (0.0;6.75); P = 0.006), CRQ dyspnea domain (3.0 (0.0;6.0); P < 0.001); LCADL total score (-1.0 (-3.0;0.0); P = 0.005); LCADL housework (-1.0 (-3.0;0.0); P < 0.001) and LCADL free time (0.0 (-1.0;0.0); P = 0.003). More L-arginine patients reached the minimal clinically important difference (MCID) in CRQ dyspnea and total LCADL. Baseline CRQ dyspnea<20 (OR (95 %CI): 4.296 (2.051-8.999); P < 0.001) and a LCADL score<27 (7.126 (2.729-18.609); P < 0.001) predicted MCID response. CONCLUSION Oral supplementation with L-arginine added to inhaled therapy appears to improve dyspnea and ADL in COPD.
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Affiliation(s)
- Dejan Radovanovic
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy; Coordinated Research Center on Respiratory Failure, University of Milan, Milano, Italy
| | - Juan Camilo Signorello
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy
| | - Giuseppe Fuccia
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy
| | - Giada Lazzaroni
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy
| | - Fiammetta Danzo
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy
| | | | - Federica Massaro
- Cardiac and Pneumological Rehabilitation Medicine, Codogno Hospital, Lodi, Italy
| | - Francesco Tursi
- Cardiac and Pneumological Rehabilitation Medicine, Codogno Hospital, Lodi, Italy
| | - Pierachille Santus
- Department of Biomedical and Clinical Sciences (DIBIC), Università degli Studi di Milano, Division of Respiratory Diseases, Ospedale L. Sacco, ASST Fatebenefratelli-Sacco, Milano, Italy; Coordinated Research Center on Respiratory Failure, University of Milan, Milano, Italy.
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23
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Furukawa Y, Miyamoto A, Asai K, Tsutsumi M, Hirai K, Ueda T, Toyokura E, Nishimura M, Sato K, Yamada K, Watanabe T, Kawaguchi T. Respiratory Muscle Strength as a Predictor of Exacerbations in Patients With Chronic Obstructive Pulmonary Disease. Respirology 2025; 30:408-416. [PMID: 40009650 PMCID: PMC12060743 DOI: 10.1111/resp.70003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/18/2024] [Revised: 11/13/2024] [Accepted: 01/21/2025] [Indexed: 02/28/2025]
Abstract
BACKGROUND AND OBJECTIVE Chronic obstructive pulmonary disease (COPD) is closely related to skeletal muscle dysfunction, and the evaluation of respiratory muscle function has recently been recommended. We aimed to investigate the effects of respiratory muscle dysfunction on clinical outcomes. METHODS We retrospectively reviewed the medical records of patients with COPD whose respiratory muscle strength was measured between June 2015 and December 2021. We then analysed the effects of respiratory muscle strength on moderate-to-severe exacerbations after adjusting for confounding factors, including sex, age, forced expiratory volume in 1-s percent predicted, hand grip strength, and skeletal muscle mass index. We also compared the temporal relationship between respiratory and systemic skeletal muscle dysfunctions. RESULTS Respiratory muscle weakness (RMW) was observed in 48.1% (100) of the 208 patients. Low percent predicted maximal inspiratory pressure was an independent risk factor for moderate-to-severe exacerbations within 1 year in the Cox regression analysis (adjusted hazard ratio per 1 standard deviation increase, 0.521; 95% confidence interval, 0.317-0.856). Approximately half of the patients already exhibited RMW at the mild systemic skeletal muscle dysfunction, while those with sarcopenia had higher RMW rates. More patients with RMW experienced progressive systemic skeletal muscle dysfunction within 1 year compared to those without RMW. CONCLUSION Lower respiratory muscle strength is associated with an increased risk of exacerbation. Respiratory muscle function could serve as a marker of disease status and early prognosis in COPD.
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Affiliation(s)
- Yuichiro Furukawa
- Department of Respiratory Medicine, Graduate School of MedicineOsaka City UniversityOsakaJapan
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Atsushi Miyamoto
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Kazuhisa Asai
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Masaya Tsutsumi
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Kaho Hirai
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Takahiro Ueda
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Erika Toyokura
- Department of Respiratory Medicine, Graduate School of MedicineOsaka City UniversityOsakaJapan
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Misako Nishimura
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Kanako Sato
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Kazuhiro Yamada
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Tetsuya Watanabe
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
| | - Tomoya Kawaguchi
- Department of Respiratory Medicine, Graduate School of MedicineOsaka Metropolitan UniversityOsakaJapan
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Castro-Piñero J, Marín-Jiménez N, Perez-Bey A, Jiménez-Iglesias J, Grao-Cruces A, Alvarez-Gallardo IC, Cuenca-García M. Criterion-related validity and reliability of the 6-minute walk test in adults according to sex, age and physical activity level: The ADULT-FIT project. J Sports Sci 2025; 43:943-955. [PMID: 40148739 DOI: 10.1080/02640414.2025.2481361] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/19/2024] [Accepted: 03/12/2025] [Indexed: 03/29/2025]
Abstract
This study aimed to analyse the criterion-related validity and reliability of the 6-minute walk test (6MWT) to assess cardiorespiratory fitness in the adult population, according to sex, age and physical activity level. Sociodemographic and anthropometric measurements, a treadmill maximal test, and the 6MWT were performed on 410 adults aged 18-64 years. Measured VO2max was associated with the total distance in the 6MWT and estimated VO2max by Burr's and Manttari's equations (R2 = 0.35, 0.61 and 0.61, respectively, all p < 0.01; SEE = 6.564-5.089 ml* kg-1 * min-1, %SEE = 11.80-15.30). The stepwise linear regression analysis showed that the total distance in the 6MWT, sex, age, physical activity level and body fat mass (%) explained 75% variance of measured VO2max (SEE = 4.203 ml* kg-1 * min-1, %SEE = 9.78, p < 0.001). The systematic error in the total distance in the 6MWT was 0.87-m (p < 0.001). The ICC showed excellent agreement (0.99, p < 0.001), with low error values and most of the MCD95 close to 0.
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Affiliation(s)
- José Castro-Piñero
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
| | - Nuria Marín-Jiménez
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
| | - Alejandro Perez-Bey
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
| | - José Jiménez-Iglesias
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
- Sport Science Department Cádiz C.F., Cádiz, Spain
| | - Alberto Grao-Cruces
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
| | - Inmaculada C Alvarez-Gallardo
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
| | - Magdalena Cuenca-García
- GALENO Research Group, Department of Physical Education, Faculty of Education Sciences, University of Cadiz, Puerto Real, Spain
- Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, Spain
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25
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Unigarro-Martinez MF, Munevar-Velandia A, Aristizabal-Duque R, Rodriguez-Martinez CE. The Applicability of Existing Reference Equations for the 6-Minute Walk Test in Healthy Children and Adolescents Living in a City at a High Altitude. Pediatr Pulmonol 2025; 60:e71145. [PMID: 40432303 DOI: 10.1002/ppul.71145] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/27/2024] [Revised: 04/12/2025] [Accepted: 05/18/2025] [Indexed: 05/29/2025]
Abstract
OBJECTIVES This study aimed to evaluate the applicability of existing 6MWT reference equations to healthy children and adolescents living in a high-altitude city. METHODS Healthy children aged 5 to 15 years attending two non-randomly selected schools in Bogotá were invited to participate in the study. All participants performed the 6MWT according to the European Respiratory Society/American Thoracic Society technical standards. To identify the model or set of 6MWT equations that best predicted individually measured 6MWT values in our population, we identified the narrowest limits of agreement (LOA) (mean difference between measured and predicted values ± 1.96 SD) after constructing Bland-Altman plots. We performed separate analyzes based on sex and onset of puberty, which was assumed to occur at 12 years of age for girls and 13 years of age for boys. RESULTS 105 children and adolescents (61 girls, 58.1%) with a mean age of 10.04 years (±2.21), ranging from 6 to 15 years, were evaluated. We determined that equations derived from two different studies conducted in Brazil, de Assis, and Oliveira 6MWT equations provided the narrowest LOA in the Bland-Altman plots for the individually-measured 6MWT values for all study participants, except for the older female participants who obtained narrower LOA with the Ulrich equations. CONCLUSION For the mean walked distance of the 6MWT, we have provided information on the 6MWT predictive equations that may be most appropriate for use in healthy children living in Bogota, Colombia, a city at 2640 m altitude.
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Affiliation(s)
| | | | | | - Carlos E Rodriguez-Martinez
- Department of Pediatric Pulmonology, School of Medicine, Universidad El Bosque, Bogota, Colombia
- Department of Pediatrics, School of Medicine, Universidad Nacional de Colombia, Bogota, Colombia
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26
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Mendes MA, Janssen DJ, Marques A. Palliative care education as an integrated component of pulmonary rehabilitation: A real-world mixed-methods feasibility study. Respir Med 2025; 241:108034. [PMID: 40086640 DOI: 10.1016/j.rmed.2025.108034] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 10/01/2024] [Revised: 03/02/2025] [Accepted: 03/08/2025] [Indexed: 03/16/2025]
Abstract
AIM To explore the feasibility of integrating palliative care education in pulmonary rehabilitation (PR). METHODS A mixed-methods feasibility study was conducted in people with chronic respiratory diseases enrolled in 12-weeks outpatient hospital-based PR. A session about palliative care was integrated in the education content. Feasibility was assessed by attendance to the palliative care session, feasibility and acceptability of outcome assessment, acceptability of the intervention and undesirable effects. After PR, two focus groups were carried out. Descriptive and inductive thematic analyses were performed. RESULTS Out of 44 individuals referred to PR, 14 were excluded, six declined to participate and two were referred to another rehabilitation programme. Twenty-two people with chronic respiratory diseases started PR, however, six had discontinued the programme at the time of the palliative care session. Attendance to this session was 81 % (n = 13/16; 11 chronic obstructive pulmonary disease, 1 severe asthma and 1 interstitial lung disease; 77 % men, 65 ± 9 years-old, FEV1 41 ± 21 % of predicted). Outcome assessment was completed in 77 % (n = 10/13) of participants and lasted approximately 90 minutes. Three themes were identified from the focus groups: daily living with a chronic respiratory disease, meaningful care and demystifying misconceptions. Participants found the intervention and outcome assessment acceptable. An improvement in knowledge and change of attitude towards palliative care was considered a major effect of the palliative care session. No undesirable effects were reported. DISCUSSION Integrating an education session about palliative care in PR is feasible, meaningful for people with chronic respiratory diseases, and has no undesirable effects. A randomised controlled study is being prepared to strengthen these results.
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Affiliation(s)
- M Aurora Mendes
- Pulmonology, Unidade Local de Saúde da Região de Aveiro (ULSRA), Aveiro, Portugal; Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA), University of Aveiro, Aveiro, Portugal; Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal; Department of Health Services Research, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands
| | - Daisy Ja Janssen
- Department of Health Services Research, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands; Department of Family Medicine, Care and Public Health Research Institute, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands; Department of Research & Development, Ciro, Horn, the Netherlands
| | - Alda Marques
- Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA), University of Aveiro, Aveiro, Portugal; Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal.
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Daynes E, Evans RA, Greening NJ, Bishop NC, Yates T, Lozano-Rojas D, Ntotsis K, Richardson M, Baldwin MM, Hamrouni M, Hume E, McAuley H, Mills G, Megaritis D, Roberts M, Bolton CE, Chalmers JD, Chalder T, Docherty AB, Elneima O, Harrison EM, Harris VC, Ho LP, Horsley A, Houchen-Wolloff L, Leavy OC, Marks M, Poinasamy K, Quint JK, Raman B, Saunders RM, Shikotra A, Singapuri A, Sereno M, Terry S, Wain LV, Man WDC, Echevarria C, Vogiatzis I, Brightling C, Singh SJ, PHOSP-COVID Study Collaborative Group. Post-Hospitalisation COVID-19 Rehabilitation (PHOSP-R): a randomised controlled trial of exercise-based rehabilitation. Eur Respir J 2025; 65:2402152. [PMID: 39978856 PMCID: PMC12095904 DOI: 10.1183/13993003.02152-2024] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/11/2024] [Accepted: 01/13/2025] [Indexed: 02/22/2025]
Abstract
OBJECTIVE Post-COVID syndrome involves prolonged symptoms with multisystem and functional impairment lasting ≥12 weeks after acute coronavirus disease 2019 (COVID-19). We aimed to determine the efficacy of exercise-based rehabilitation interventions, either face-to-face or remote, compared to usual care in individuals experiencing post-COVID syndrome following a hospitalisation with acute COVID-19. DESIGN This single-blind randomised controlled trial compared two exercise-based rehabilitation interventions (face-to-face or remote) to usual care in participants with post-COVID syndrome following a hospitalisation. The interventions were either a face-to-face or remote 8-week programme of individually prescribed exercise and education. The primary outcome was the change in Incremental Shuttle Walking Test (ISWT) following 8 weeks of intervention (either face-to-face or remote) compared to usual care. Other secondary outcomes were measured including health-related quality of life (HRQoL), and exploratory outcomes included lymphocyte immunotyping. RESULTS 181 participants (55% male, mean±sd age 59±12 years, length of hospital stay 12±19 days) were randomised. There was an improvement in the ISWT distance following face-to-face rehabilitation (mean 52 m, 95% CI 19-85 m; p=0.002) and remote rehabilitation (mean 34 m, 95% CI 1-66 m; p=0.047) compared to usual care alone. There were no differences between groups for HRQoL self-reported symptoms. Analysis of immune markers revealed significant increases in naïve and memory CD8+ T-cells following face-to-face rehabilitation versus usual care alone (p<0.001, n=31). CONCLUSION Exercise-based rehabilitation improved short-term exercise capacity in post-COVID syndrome following an acute hospitalisation and showed potential for beneficial immunomodulatory effects.
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Affiliation(s)
- Enya Daynes
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Rachael A Evans
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Neil J Greening
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Nicolette C Bishop
- National Centre for Sport and Exercise Medicine, School of Sport, Exercise and Health Sciences, Loughborough University, Loughborough, UK
| | - Thomas Yates
- NIHR Leicester Biomedical Research Centre - Diabetes, Leicester, UK
- Diabetes Research Centre, College of Life Sciences, University of Leicester, Leicester, UK
| | - Daniel Lozano-Rojas
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Kimon Ntotsis
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Matthew Richardson
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Molly M Baldwin
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Malik Hamrouni
- Diabetes Research Centre, College of Life Sciences, University of Leicester, Leicester, UK
| | - Emily Hume
- Department of Sport, Exercise and Rehabilitation, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK
| | - Hamish McAuley
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - George Mills
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Dimitrios Megaritis
- Department of Sport, Exercise and Rehabilitation, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK
| | - Matthew Roberts
- Diabetes Research Centre, College of Life Sciences, University of Leicester, Leicester, UK
| | - Charlotte E Bolton
- Centre for Respiratory Research, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK
- NIHR Nottingham Biomedical Research Centre, Nottingham, UK
| | - James D Chalmers
- University of Dundee, Ninewells Hospital and Medical School, Dundee, UK
| | - Trudie Chalder
- Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK
| | - Annemarie B Docherty
- Centre for Medical Informatics, The Usher Institute, University of Edinburgh, Edinburgh, UK
| | - Omer Elneima
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | | | - Victoria C Harris
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Ling P Ho
- MRC Human Immunology Unit, University of Oxford, Oxford, UK
- NIHR Oxford Biomedical Research Centre, Oxford, UK
| | - Alex Horsley
- Manchester University NHS Foundation Trust, Manchester, UK
| | - Linzy Houchen-Wolloff
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Olivia C Leavy
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Population Health Sciences, University of Leicester, Leicester, UK
| | - Michael Marks
- Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, UK
- Hospital for Tropical Diseases, University College London Hospital, London, UK
| | | | | | - Betty Raman
- Radcliffe Department of Medicine, University of Oxford, Oxford, UK
- Oxford University Hospitals NHS Foundation Trust, Oxford, UK
| | - Ruth M Saunders
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Aarti Shikotra
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Amisha Singapuri
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Marco Sereno
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Sarah Terry
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
| | - Louise V Wain
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Population Health Sciences, University of Leicester, Leicester, UK
| | - William D-C Man
- Harefield Respiratory Research Group, Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK
- National Heart and Lung Institute, Imperial College, London, UK
- King's Centre for Lung Health, Faculty of Life Sciences and Medicine, King's College London, London, UK
| | - Carlos Echevarria
- The Newcastle upon Tyne Hospitals NHS Foundation Trust, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK
| | - Ioannis Vogiatzis
- Department of Sport, Exercise and Rehabilitation, Faculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, UK
| | - Christopher Brightling
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
| | - Sally J Singh
- The Institute for Lung Health, NIHR Leicester Biomedical Research Centre, University Hospitals of Leicester, Leicester, UK
- Department of Respiratory Sciences, University of Leicester, Leicester, UK
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Beaumont M. The Relevance of Normative Values for the 6-Minute Walk Test in Patients With COPD: A Clinical and Scientific Requirement. Arch Bronconeumol 2025:S0300-2896(25)00147-4. [PMID: 40393852 DOI: 10.1016/j.arbres.2025.04.011] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/15/2025] [Accepted: 04/23/2025] [Indexed: 05/22/2025]
Affiliation(s)
- Marc Beaumont
- Univ Brest, Inserm, CHRU Brest, UMR 1304 (GETBO), Rue Camille Desmoulins, 29200 Brest, France; Pulmonary Rehabilitation Unit, Morlaix Hospital Centre, Kersaint Gilly, 29600 Morlaix, France.
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29
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Murta MS, Duarte RLM, Waetge D, Gozal D, Cardoso AP, Mello FCQ. Exercise-induced oxyhemoglobin desaturation is an independent risk factor for sustained nocturnal hypoxemia in adults with precapillary pulmonary hypertension: A cross-sectional study. Heart Lung 2025; 73:26-32. [PMID: 40273807 DOI: 10.1016/j.hrtlng.2025.04.021] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/25/2025] [Revised: 03/11/2025] [Accepted: 04/02/2025] [Indexed: 04/26/2025]
Abstract
BACKGROUND Nocturnal hypoxemia (NH) negatively impacts the prognosis of several chronic cardiopulmonary diseases. OBJECTIVES To assess the risk factors associated with sustained NH in adults with precapillary pulmonary hypertension (pPH). METHODS This cross-sectional study was performed between June 2021 and June 2024. Outpatients with a hemodynamic diagnosis of pPH (Groups 1 and 4) were consecutively recruited. Sustained NH was defined as ≥ 30 % of the percentage of time spent with oxygen saturation (SpO2) <90 % during a home sleep apnea test (HSAT). Clinical, laboratory, hemodynamic, echocardiographic, functional, and exercise-related variables were collected blindly regarding the HSAT data. We considered a difference in SpO2 [resting - final] (Δ SpO2) ≥ 3 % as indicative of exercise-induced oxyhemoglobin desaturation (EID) by the six-minute walk test. Multiple logistic regression analysis was used to identify possible predictive factors for the occurrence of NH. RESULTS Fifty-two pPH adults were included (71.2 % were females). Thirty-one patients (59.6 %) were classified as having NH. In the univariate logistic regression analysis, four parameters were identified as risk factors for the presence of NH: mean pulmonary artery pressure (p = 0.023), right atrial mean pressure (p = 0.037), systolic pulmonary arterial pressure (p = 0.042) and EID (p = 0.003). However, only EID was an independent predictor for detecting NH with an adjusted odds ratio of 10.590 (95 % confidence interval: 1.095-102.420); p = 0.042. CONCLUSIONS EID is an easily implementable risk factor for prolonged NH, suggesting that adults with pPH who experience EID have a high probability of also experiencing NH.
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Affiliation(s)
- Marcia S Murta
- Instituto de Doenças do Tórax - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
| | - Ricardo L M Duarte
- Instituto de Doenças do Tórax - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
| | - Daniel Waetge
- Instituto de Doenças do Tórax - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
| | - David Gozal
- Department of Pediatrics, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV, USA
| | - Alexandre P Cardoso
- Instituto de Doenças do Tórax - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
| | - Fernanda C Q Mello
- Instituto de Doenças do Tórax - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
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30
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Marçalo R, Rodrigues G, Pinheiro M, Neto S, Marques SL, Simão P, Martins V, Andrade L, Mendes MA, Santos M, Afreixo V, Marques A, Moura G. Functional impairment in COPD can be predicted using genomic-derived data. Thorax 2025; 80:283-290. [PMID: 39880613 DOI: 10.1136/thorax-2024-222142] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/01/2024] [Accepted: 01/13/2025] [Indexed: 01/31/2025]
Abstract
OBJECTIVE Reduced functional capacity and muscle weakness are two major contributors to functional impairment in chronic obstructive pulmonary disease (COPD). The underlying causes of functional impairment are poorly understood and, therefore, we sought to investigate the contribution of genetic factors. METHODS We conducted a cross-sectional analysis of sociodemographic, clinical and genetic information of people with COPD. Hierarchical clustering based on functional capacity (6-minute walk test and 1-minute sit-to-stand test) and muscle strength (quadriceps isometric muscle strength and handgrip muscle strength) was performed. A genome-wide association study (GWAS) was performed using cluster assignment as phenotype. Polygenic risk scores (PRSs) were calculated for each variable. Genomic-derived data was used to construct a model to predict functional impairment. RESULTS Two clusters were identified among 245 individuals. Cluster 1 (n=104) was composed of younger, less symptomatic patients, with preserved functional capacity and muscle strength, whereas cluster 2 (n=141) included those older, more symptomatic, with reduced functional capacity and muscle weakness. GWAS identified two polymorphisms suggestively associated with functional impairment, mapped to xanthine dehydrogenase. Cluster 2 was enriched in individuals with risk alleles for rs1991541 and rs10524730, and lower PRSs for functional capacity and muscle strength. A prediction model using genomic-derived data was constructed (n=159) and tested (n=37), yielding an area under the curve of 0.87 (0.76-0.99). CONCLUSION Genetic factors are significantly associated with functional impairment in COPD. The incorporation of genetic information, particularly PRSs, into a predictive model offers a promising avenue for timely identifying individuals at greater risk of functional decline, potentially facilitating personalised and preventive interventions. Further studies on independent external cohorts are needed to validate our model.
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Affiliation(s)
- Rui Marçalo
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
- Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA) and Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal
- Department of Pulmonary Diseases, University Medical Center Groningen, University of Groningen, Groningen, Netherlands
| | - Guilherme Rodrigues
- Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA) and Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal
| | - Miguel Pinheiro
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
| | - Sonya Neto
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
| | - Sofia L Marques
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
| | - Paula Simão
- Pulmonology Department, Unidade Local de Saúde de Matosinhos EPE, Lavra matosinhos, Porto, Portugal
| | - Vitória Martins
- Pulmonology Department, Hospital Distrital Figueira Foz, Figueira da Foz, Figueira da Foz, Portugal
| | - Lília Andrade
- Department of Pulmonology, Hospital Center of Baixo Vouga, Aveiro, Portugal
| | - Maria Aurora Mendes
- Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA) and Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal
- Centro Hospitalar Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Porto, Portugal
| | - Manuel Santos
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
- Multidisciplinary Institute of Ageing, MIA-Portugal, University of Coimbra, Coimbra, Portugal
| | - Vera Afreixo
- Center for Research and Development in Mathematics and Applications, University of Aveiro, Aveiro, Portugal
- Department of Mathematics, University of Aveiro, Aveiro, Portugal
| | - Alda Marques
- Respiratory Research and Rehabilitation Laboratory (Lab3R), School of Health Sciences (ESSUA) and Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal
| | - Gabriela Moura
- Genome Medicine Laboratory, Institute of Biomedicine (iBiMED), Department of Medical Sciences, University of Aveiro, Aveiro, Portugal
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31
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Bergaoui J, Latiri I, MRAD S, Chaouch H, Amous S, Ben Abdallah J, Ernez Hajri S, Ben Saad H. Assessment of sub-maximal aerobic capacity in North African patients with chronic hepatitis B: a pilot case-control study. F1000Res 2025; 14:98. [PMID: 40291469 PMCID: PMC12022957 DOI: 10.12688/f1000research.160390.1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Accepted: 03/28/2025] [Indexed: 04/30/2025] Open
Abstract
Background Studies assessing sub-maximal aerobic capacity in non-cirrhotic chronic hepatitis B (CHB) patients are scarce. This study aimed to evaluate sub-maximal aerobic capacity in CHB patients compared to apparently healthy participants (control-group (CG)). Methods A 6-min walk test (6MWT) was performed. The 6-min walk distance (6MWD) was recorded, along with heart-rate (HR), oxy-hemoglobin saturation (SpO 2), blood-pressure, and dyspnea ( ie ; visual analogue scale) at rest (Rest) and at the end (End) of the 6MWT. Additionally, the 6-min walk work (6MWW), and estimated cardiorespiratory and muscular chain age were calculated. Signs of physical intolerance were determined including abnormal 6MWD ( ie ; 6MWD < lower limit of normal), chronotropic insufficiency (ie ; HREnd < 60% of maximal predicted HR (MPHR)), high dyspnea ( ie ; dyspneaEnd > 5), and desaturation ( ie ; drop in SpO 2 > 5 points). Results Compared to the CG (n=28), the CHB-group (n=26) exhibited significantly lower 6MWD by 61 meters (8%), lower 6MWW by 10%, and lower HR End by 21% (when expressed in bpm) and 17% (when expressed in %MPHR). The CHB-group, compared to the CG, included higher percentages of participants with chronotropic insufficiency and abnormal 6MWD (23.08% vs. 3.57%, and 34.61% vs. 3.57%, respectively). The CHB-group was 8.1 and 14.3 times more likely to have chronotropic insufficiency and abnormal 6MWD than the CG, respectively. CHB accelerated the aging of the cardiorespiratory and muscular chain by 11 years. Conclusion Non-cirrhotic CHB may contribute to reduced submaximal aerobic capacity and acceleration of cardiorespiratory and muscular chain aging.
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Affiliation(s)
- Jihene Bergaoui
- Hospital Farhat HACHED, Research laboratory “Heart Failure, LR12SP09, Universite de Sousse Faculte de Medecine de Sousse, Sousse, Sousse, 4000, Tunisia
| | - Imed Latiri
- Hospital Farhat HACHED, Research laboratory “Heart Failure, LR12SP09, Universite de Sousse Faculte de Medecine de Sousse, Sousse, Sousse, 4000, Tunisia
| | - Sawssen MRAD
- Biochemistry Research Laboratory (LR18ES47), Farhat Hached University Hospital of Sousse, Sousse, Sousse, 4000, Tunisia
| | - Houda Chaouch
- Department of Infectious Diseases, Viral Hepatitis Research Unit (UR12SP35), Farhat Hached University Hospital of Sousse, Sousse, Sousse, 4000, Tunisia
| | - Salma Amous
- Biochemistry Research Laboratory (LR18ES47), Farhat Hached University Hospital of Sousse, Sousse, Sousse, 4000, Tunisia
| | - Jihene Ben Abdallah
- Biochemistry Research Laboratory (LR18ES47), Farhat Hached University Hospital of Sousse, Sousse, Sousse, 4000, Tunisia
| | - Samia Ernez Hajri
- Hospital Farhat HACHED, Research laboratory “Heart Failure, LR12SP09, Universite de Sousse Faculte de Medecine de Sousse, Sousse, Sousse, 4000, Tunisia
| | - Helmi Ben Saad
- Hospital Farhat HACHED, Research laboratory “Heart Failure, LR12SP09, Universite de Sousse Faculte de Medecine de Sousse, Sousse, Sousse, 4000, Tunisia
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Conti PBM, Ribeiro MÂGO, Gomez CCS, Souza AP, Borgli DSP, Sakano E, Pascoa MA, Severino SD, Castilho T, Marson FAL, Ribeiro JD. Pulmonary and functional hallmarks after SARS-CoV-2 infection across three WHO severity level-groups: an observational study. Front Med (Lausanne) 2025; 12:1561387. [PMID: 40259977 PMCID: PMC12010923 DOI: 10.3389/fmed.2025.1561387] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/15/2025] [Accepted: 03/10/2025] [Indexed: 04/23/2025] Open
Abstract
Background The manifestations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection range from flu-like symptoms to severe lung disease. The consequences of this inflammatory process impact overall function, which can be detected through both short- to long-term assessments. This study aimed to assess the pulmonary functional and structural characteristics of post-SARS-CoV-2 infection in patients with mild/moderate, severe, and critical clinical presentations. Methods An observational, analytical, and cross-sectional study was conducted between 2020 and 2022, including participants with a confirmed diagnosis of coronavirus disease (COVID)-19, with mild/moderate (G1), severe (G2), and critical (G3) clinical presentations, all evaluated at least 3 months after acute infection. Spirometry, impulse oscillometry, fractional exhaled nitric oxide (FeNO), chest computed tomography, the 6-min walk test (6MWT), hand grip strength, maximum inspiratory pressure, and maximum expiratory pressure were assessed. Results We enrolled 210 participants aged 18-70 years, 32.6% of whom were male, with older age observed in G3. The participants were grouped as follows: G1 (42.3%), G2 (25.7%), and G3 (31.9%). Percentage of predicted X5 differed between G1 and G2, being higher in G1. The percentage of predicted forced vital capacity (FVC) according to the Global Lung Function Initiative and its z-score were higher in G1. The FVC by Pereira was lower in G3 compared to G1. The percentage of predicted forced expiratory volume in 1 s (FEV1) by Pereira was also lower in G3. The Tiffeneau (FEV1/FVC) index was different among groups, increasing with disease severity. The percentage of predicted forced expiratory flow rate at 25-75% (FEF25-75%) of the FVC and FeNO were both higher in G2 than G1. Chest computed tomography revealed the presence of interstitial abnormalities, associated with disease severity. The respiratory muscle strength evaluation showed an association between higher maximum expiratory pressure values in G3 compared to G1, but no association with maximum inspiratory pressure was observed. The 6MWT distance covered decreased with increasing severity, with a lower percentage of predicted values in G3 compared to G1. The right-hand grip strength was also lower in G3 compared to G1. Conclusion Alterations in pulmonary and functional markers were observed in post-COVID-19 evaluations, increasing with disease severity, as seen in G2 and G3. These findings highlight the complexity of post-COVID-19 functional assessments, given the long-term pulmonary sequelae and the consequent impairment of functional capacity.
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Affiliation(s)
| | | | | | - Aline Priscila Souza
- Department of Pediatrics, School of Medical Sciences, University of Campinas, Campinas, Brazil
| | | | - Eulália Sakano
- Department of Ophthalmology-Otorhinolaryngology, School of Medical Sciences, University of Campinas, Campinas, Brazil
| | - Mauro Alexandre Pascoa
- Department of Pediatrics, School of Medical Sciences, University of Campinas, Campinas, Brazil
| | - Silvana Dalge Severino
- Department of Pediatrics, School of Medical Sciences, University of Campinas, Campinas, Brazil
| | - Tayná Castilho
- Department of Pediatrics, School of Medical Sciences, University of Campinas, Campinas, Brazil
| | - Fernando Augusto Lima Marson
- LunGuardian Research Group, Epidemiology of Respiratory and Infectious Diseases, Postgraduate Program in Health Sciences, São Francisco University, Bragança Paulista, Brazil
- Laboratory of Molecular Biology and Genetics, Postgraduate Program in Health Sciences, São Francisco University, Bragança Paulista, Brazil
- Laboratory of Clinical Microbiology and Genetics, Postgraduate Program in Health Sciences, São Francisco University, Bragança Paulista, Brazil
| | - José Dirceu Ribeiro
- Department of Pediatrics, School of Medical Sciences, University of Campinas, Campinas, Brazil
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33
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Giménez-Esparza C, Relucio MÁ, Nanwani-Nanwani KL, Añón JM. Impact of patient safety on outcomes. From prevention to the treatment of post-intensive care syndrome. Med Intensiva 2025; 49:224-236. [PMID: 38664154 DOI: 10.1016/j.medine.2024.04.008] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/15/2023] [Accepted: 03/11/2024] [Indexed: 04/05/2025]
Abstract
Survivors of critical illness may present physical, psychological, or cognitive symptoms after hospital discharge, encompassed within what is known as post-intensive care syndrome. These alterations result from both the critical illness itself and the medical interventions surrounding it. For its prevention, the implementation of the ABCDEF bundle (Assess/treat pain, Breathing/awakening trials, Choice of sedatives, Delirium reduction, Early mobility and exercise, Family) has been proposed, along with additional strategies grouped under the acronym GHIRN (Good communication, Handout materials, Redefined ICU architectural design, Respirator, Nutrition). In addition to these preventive measures during the ICU stay, high-risk patients should be identified for subsequent follow-up through multidisciplinary teams coordinated by Intensive Care Medicine Departments.
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Affiliation(s)
| | | | | | - José Manuel Añón
- Servicio de Medicina Intensiva, Hospital Universitario La Paz, IdiPAZ, Madrid, Spain; CIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain.
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Vinas F, Goussault H, Boyer L, Bussac GR, Jabot L, Gibiot Q, Bonnefoy V, Brochard MA, Goro S, Jung C, Monnet I, Chouaïd C, Maitre B, Auliac JB. Evaluation of teleguided high-intensity exercise rehabilitation at home before lung-cancer surgery (PREPACHIR Study). Lung Cancer 2025; 202:108480. [PMID: 40058139 DOI: 10.1016/j.lungcan.2025.108480] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/21/2024] [Revised: 02/22/2025] [Accepted: 03/01/2025] [Indexed: 04/07/2025]
Abstract
INTRODUCTION Preoperative rehabilitation lowers the surgical morbidity-mortality risk of patients with non-small cell lung cancer (NSCLC). This study evaluated the feasibility of a preoperative-rehabilitation program consisting of high-intensity exercises, at home, teleguided by physical trained sports coach. METHODS This monocenter study included patients diagnosed with resectable NSCLC, scheduled segmentectomy or lobectomy, and FEV1 < 80 % and/or DLCO < 80 %. The main exclusion criteria were neoadjuvant chemotherapy, contraindication for high-intensity physical activity, poor understanding of connected-watch use, without a smartphone and cognitive or psychiatric disorder(s).The program combines 1-hour daily high-intensity training at home, teleguided, associated with non-supervised activity advice, with tracing via an internet-connected watch. T. Program-efficacy evaluation was based on the number of patients completing the entire program, mean increase of the maximum oxygen uptake (VO2 max) and postoperative complications assessed with the Clavien-Dindo classification. RESULTS Among the 76 patients eligible for surgery during the inclusion period, 29 (38 %) satisfied inclusion criteria and 24 (83 %) accomplished at least 7 days of training for a mean ± standard deviation of 17.8 ± 9 sessions; 44 % also executed non-scheduled supplementary sessions; 96 % used the internet-connected watch. VO2 max increased significantly from 19.3 ± 3.1 to 20.4 ± 3.5 ml/kg/min (p = 0.04). Postoperatively, 9/25 (36 %) experienced a grade 1-3 adverse event, without grade 4/5. CONCLUSION Preoperative rehabilitation with teleguided, high-intensity exercises at home is feasible and significantly increased VO2 max. Prospective, randomized studies are needed to evaluate the benefit compared to current care practices.
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Affiliation(s)
- Florent Vinas
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Hélène Goussault
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Laurent Boyer
- Physiology Department, Hôpital Henri-Mondor, APHP, 51, avenue du Maréchal de Lattre de Tassigny, 94010 Créteil Cedex, France
| | - Gaëlle Rousseau Bussac
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Laurence Jabot
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Quentin Gibiot
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Valentine Bonnefoy
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | | | - Seydou Goro
- Centre de Recherche Clinique, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Camille Jung
- Centre de Recherche Clinique, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Isabelle Monnet
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Christos Chouaïd
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France.
| | - Bernard Maitre
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
| | - Jean-Bernard Auliac
- Pneumology Department, Centre Hospitalier Intercommunal CHI Créteil, 40, avenue de Verdun, 94010 Créteil Cedex, France
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Reeves JM, Marouvo J, Chan A, Thomas N, Spencer LM. High-Flow Oxygen Therapy to Support Inpatient Pulmonary Rehabilitation During Very Severe Hepatopulmonary Syndrome Recovery Post Liver Transplant: A Case Report. Clin Case Rep 2025; 13:e70472. [PMID: 40264732 PMCID: PMC12012242 DOI: 10.1002/ccr3.70472] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/25/2025] [Revised: 03/28/2025] [Accepted: 04/07/2025] [Indexed: 04/24/2025] Open
Abstract
This case study reports the novel use of inpatient pulmonary rehabilitation (PR) with near-maximal high-flow oxygen therapy in a patient recovering from very severe hepatopulmonary syndrome (HPS) following liver transplantation. HPS is a rare condition where advanced liver disease alters lung microvasculature through intrapulmonary vascular dilatation (IPVD) and angiogenesis. Platypnoea-orthodeoxia (postural dyspnoea with concurrent blood oxygen desaturation) is characteristic of HPS due to redirection of blood flow to the basal lung where IPVDs are more prominent, secondary to gravity. Currently, the only definitive treatment is liver transplantation, which allows normalization of oxygenation over an extended period, typically within 1 year. Pulmonary rehabilitation is an effective intervention for improving dyspnoea, health-related quality of life (HRQoL), and exercise capacity in people with chronic respiratory disease. Despite this, little is known of the effect PR has on individuals recovering from HPS post liver transplant. The aim is to describe an inpatient PR program for a patient recovering from HPS. This case study describes a 27-year-old male with "very severe" HPS who undertook inpatient PR 5 months posttransplant. The patient completed an 8-week program of twice-weekly PR supported by high-flow oxygen therapy (fraction of inspired oxygen of 90%). He performed aerobic and resistance exercises for the upper and lower limbs in recumbent, seated, and standing positions. The patient improved in exercise capacity on the 1-min sit-to-stand test (+4 repetitions), lower limb strength on the 5-repetition sit-to-stand test (-3.4 s) and in HRQoL outcomes assessed. Following rehabilitation, the patient still had a high burden of respiratory symptoms and required continuous high-flow oxygen therapy. This case study demonstrates that inpatient PR, modified for HPS-associated platypnoea-orthodeoxia and supported by high-flow oxygen therapy, is safe and effective and therefore feasible for other HPS patients.
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Affiliation(s)
- Jack M. Reeves
- Graduate School of Health, Faculty of HealthUniversity of Technology SydneySydneyNew South WalesAustralia
- Physiotherapy DepartmentRoyal Prince Alfred HospitalSydneyNew South WalesAustralia
| | - Jessica Marouvo
- Physiotherapy DepartmentRoyal Prince Alfred HospitalSydneyNew South WalesAustralia
| | - Aveline Chan
- Physiotherapy DepartmentRoyal Prince Alfred HospitalSydneyNew South WalesAustralia
| | - Nicholas Thomas
- Physiotherapy DepartmentRoyal Prince Alfred HospitalSydneyNew South WalesAustralia
| | - Lissa M. Spencer
- Physiotherapy DepartmentRoyal Prince Alfred HospitalSydneyNew South WalesAustralia
- Sydney School of Health Sciences, Faculty of Medicine and HealthThe University of SydneySydneyNew South WalesAustralia
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Hong C, Zhou D, Chen H, Wu X, Guo W, Cui J, Guan W, Zhong N, Lin J. Pulmonary Artery Stent Implantation for Fibrosing Mediastinitis: Our Clinical Experience. Pulm Circ 2025; 15:e70076. [PMID: 40308630 PMCID: PMC12040597 DOI: 10.1002/pul2.70076] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/15/2024] [Revised: 02/21/2025] [Accepted: 03/31/2025] [Indexed: 05/02/2025] Open
Abstract
Fibrosing mediastinitis (FM) can block pulmonary vessels and airways, hindering treatment efficacy. Pulmonary artery (PA) stenting might provide a solution in such cases. This study involved 30 patients who had 49 PA stenting procedures for FM. Data on baseline characteristics, CT pulmonary angiography images, stent patency, and hemodynamics were collected. Patients with FM often had a history of chronic obstructive pulmonary disease (15/30), tuberculosis (12/30), and pneumoconiosis (11/30). Patients exhibited typical symptoms such as dyspnea, exercise intolerance, and cough. FM appeared as multiple bilateral shadows with enlarged hilar and mediastinal lymph nodes. Our study found that the PA involvement alone was predominantly in the left and right lower basilar trunk, with the left lower pulmonary arteries (LLPA) involved in 80% of cases and the right lower pulmonary arteries (RLPA) in 100%. Moreover, over 2/3 of patients showed involvement of both PA and pulmonary vein (PV), mainly in the bilateral upper lung lobes, then in the right middle lobe and left lingual lobe. After PA stent implantation, patients showed enhanced tricuspid annular plane systolic excursion (20.6 vs. 18.5, p < 0.001) and reduced right atrial diameter (35.5 vs. 37.3, p = 0.042), along with significant gains in 6-min walk distance (465.2 vs. 392.7, p = 0.002) and improved World Health Organization functional class (p < 0.001). Hemodynamic parameters improved after PA stent placement with significant reductions in systolic pulmonary artery pressure (PAP) (51.1 vs. 64.2, p < 0.001), mean PAP (28.4 vs. 35.2, p < 0.001), pulmonary vascular resistance (4.7 vs. 5.9, p = 0.004), and stent gradient (11.2 vs. 33.4, p < 0.001), along with increased patency (84.8% vs. 28%, p < 0.001), and fractional flow reserve (0.84 vs. 0.44, p < 0.001). Over a median follow-up of 331 days (range 45-980), no significant stent stenosis occurred (p = 0.287). Mild adverse events like cough and mild hemoptysis were noted during the procedure. Secondary intervention was needed for 5 of 49 stents. PA stents placement, especially the LLPA and RLPA, improved pulmonary vascular patency, hemodynamics, and symptoms.
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Affiliation(s)
- Cheng Hong
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Daibing Zhou
- Department of Pulmonary and Critical Care MedicineHuashan Hospital, Fudan UniversityShanghaiChina
| | - Haiming Chen
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Xiaofeng Wu
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Wenliang Guo
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Jiangyu Cui
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Weijie Guan
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Nanshan Zhong
- National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, State Key Laboratory of Respiratory DiseaseFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
| | - Jielong Lin
- Department of RadiologyFirst Affiliated Hospital of Guangzhou Medical UniversityGuangzhouChina
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Cox NS, McDonald C, Burge AT, Hill CJ, Bondarenko J, Holland AE. Comparison of Clinically Meaningful Improvements After Center-Based and Home-Based Telerehabilitation in People With COPD. Chest 2025; 167:1003-1011. [PMID: 39522594 DOI: 10.1016/j.chest.2024.11.001] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/30/2024] [Revised: 10/30/2024] [Accepted: 11/01/2024] [Indexed: 11/16/2024] Open
Abstract
BACKGROUND Response to pulmonary rehabilitation is not equal for all participants and may vary across health outcomes for any one individual. Alternative methods of pulmonary rehabilitation delivery, for example, telerehabilitation, may improve program access, but also could affect response to rehabilitation. RESEARCH QUESTION What is the rate of clinical response to home-based telerehabilitation compared with center-based pulmonary rehabilitation, and are any participant baseline characteristics associated with pulmonary rehabilitation response relative to the model of delivery? STUDY DESIGN AND METHODS In this secondary analysis of 2 randomized controlled trials, participants were categorized as responders or nonresponders according to achievement of the minimal important difference (MID) for each outcome of interest at end rehabilitation and after the 12-month follow-up (change from baseline). Outcomes of interest were functional exercise capacity (6-minute walk distance; MID, 30 m), health-related quality of life (chronic respiratory disease questionnaire: MID, 2.5, 2, 3.5, and 2 points for the dyspnea, fatigue, emotion, and mastery domains, respectively; CRQ total score MID, 10 points); and symptoms (modified Medical Research Council: MID, -1 point). RESULTS Two hundred sixty-six individuals with COPD were included in the analysis. The proportion of responders was not different between center-based pulmonary rehabilitation and home-based telerehabilitation at either end rehabilitation or 12-month follow-up for any outcome (range, 39%-62%). In a binary logistic regression analysis, baseline outcome values, but not participant demographic characteristics, were associated most commonly with responder status. The relative risk of program noncompletion in the center-based group was nearly 4 times greater than for telerehabilitation (center-based pulmonary rehabilitation: n = 79 [58%] vs home-based telerehabilitation: n = 116 [90%]; relative risk, 3.89; 95% CI, 2.28-6.63). INTERPRETATION In this study, responder status to pulmonary rehabilitation was not different between center-based and home-based telerehabilitation. The ability to identify patient characteristics that confer greater potential for rehabilitation response or better suitability for a particular model of rehabilitation remains a challenge.
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Affiliation(s)
- Narelle S Cox
- Respiratory Research@Alfred, School of Translational Medicine, Monash University, Melbourne, VIC, Australia; Institute for Breathing and Sleep, Melbourne, VIC, Australia.
| | - Christine McDonald
- Institute for Breathing and Sleep, Melbourne, VIC, Australia; Department of Respiratory and Sleep Medicine, Melbourne, VIC, Australia; Faculty of Medicine, University of Melbourne, Melbourne, VIC, Australia
| | - Angela T Burge
- Respiratory Research@Alfred, School of Translational Medicine, Monash University, Melbourne, VIC, Australia; Institute for Breathing and Sleep, Melbourne, VIC, Australia; Department of Physiotherapy, Alfred Health, Melbourne, VIC, Australia
| | - Catherine J Hill
- Institute for Breathing and Sleep, Melbourne, VIC, Australia; Department of Physiotherapy, Austin Health, Melbourne, VIC, Australia
| | - Janet Bondarenko
- Respiratory Research@Alfred, School of Translational Medicine, Monash University, Melbourne, VIC, Australia; Department of Physiotherapy, Alfred Health, Melbourne, VIC, Australia
| | - Anne E Holland
- Respiratory Research@Alfred, School of Translational Medicine, Monash University, Melbourne, VIC, Australia; Institute for Breathing and Sleep, Melbourne, VIC, Australia; Department of Physiotherapy, Alfred Health, Melbourne, VIC, Australia
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Tanhan A, Ozer AY, Timurtas E, Batirel A, Polat MG. Is asynchronous telerehabilitation equal to synchronous telerehabilitation in COVID-19 survivors with classes 4-6? J Telemed Telecare 2025; 31:347-358. [PMID: 37545432 DOI: 10.1177/1357633x231189761] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 08/08/2023]
Abstract
IntroductionThe first aim of this study was to compare synchronous and asynchronous telerehabilitation programs in COVID-19 survivors with classes 4-6 and determine the more appropriate telerehabilitation approach.MethodsThirty-six COVID-19 survivors with class 4-6 severity were randomly divided into two groups. Telerehabilitation programs were an 8-week exercise program that comprised pulmonary, aerobic, and strengthening exercises. Patients were assessed at the baseline, post-treatment, and follow-up for the incremental shuttle walk test (ISWT), short physical performance battery (SPPB), health-related quality of life (HRQoL) and hospital anxiety and depression scale (HADS)ResultsThe overall mean age of the study population was 54.06 (SD 10.50), and 15 (46.8%) were male. There were no significant differences between the two groups in any of the demographics and clinical characteristics at the baseline (p > 0.05), except for physical function (p < 0.05). There was a significant improvement in exercise capacity (p < 0.001) and lower extremity function (p < 0.01) within both groups in the short term and long term. There was a significant improvement in some subparameters of quality of life in both groups. As the synchronous group's short-term and long-term psychological status improved significantly, the asynchronous group's short-term psychological status improved significantly (p < 0.05). Telerehabilitation programs had similar effects, and only synchronous telerehabilitation outperformed asynchronous telerehabilitation in terms of physical function, role-emotional, and long-term anxiety.DiscussionAsynchronous telerehabilitation was as effective as synchronous telerehabilitation in developing clinical and functional parameters when properly planned and implemented.
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Affiliation(s)
- Abdurrahman Tanhan
- Health Sciences Faculty, Department of Physiotherapy and Rehabilitation, Bitlis Eren University, Bitlis, Turkey
- Health Sciences Faculty, Department of Physiotherapy and Rehabilitation, Marmara University, Istanbul, Turkey
| | - Aysel Yildiz Ozer
- Health Sciences Faculty, Department of Physiotherapy and Rehabilitation, Marmara University, Istanbul, Turkey
| | - Eren Timurtas
- Health Sciences Faculty, Department of Physiotherapy and Rehabilitation, Marmara University, Istanbul, Turkey
| | - Ayse Batirel
- University of Health Sciences, Kartal Dr Lutfi Kirdar City Hospital, Infectious Diseases and Clinical Microbiology, Istanbul, Turkey
| | - Mine Gulden Polat
- Health Sciences Faculty, Department of Physiotherapy and Rehabilitation, Marmara University, Istanbul, Turkey
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Hartman M, Dosbaba F, Batalik L, Vlazna D, Plutinsky M, Brat K, Costa RC, Lima AS, Cahalin LP, Formiga MF. Home-Based Inspiratory Muscle Training as Stand-Alone Therapy in COPD: A Randomized Sham-Controlled Trial Assessing Novel and Established Training Methods. COPD 2025; 22:2487473. [PMID: 40195869 DOI: 10.1080/15412555.2025.2487473] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/26/2025] [Revised: 03/25/2025] [Accepted: 03/27/2025] [Indexed: 04/09/2025]
Abstract
This randomized controlled trial evaluated the effectiveness of two home-based, stand-alone inspiratory muscle training (IMT) modalities - inspiratory flow-resistive loading with biofeedback (IRFL) and mechanical threshold loading (MTL) - compared to a sham MTL group for improving inspiratory muscle performance and functional exercise capacity in COPD patients. Thirty-six COPD patients trained at home for 8 weeks under remote monitoring. Primary outcomes included inspiratory muscle performance assessed via the Test of Incremental Respiratory Endurance (TIRE), functional exercise capacity, lung function, and other COPD-related measures. Both the TIRE IRFL and MTL groups showed significant improvements in inspiratory muscle strength compared to the sham MTL group (p < 0.05). Additionally, the IRFL with biofeedback group demonstrated significant gains in inspiratory muscle work capacity and 6MWT distance compared to both the MTL and sham groups (p < 0.05). No adverse events were reported, and adherence to training protocols was high across all groups. This study supports home-based IMT as a feasible, effective stand-alone intervention for COPD patients, particularly for those who face barriers in accessing traditional pulmonary rehabilitation programs. TIRE IFRL showed superior benefits in enhancing inspiratory muscle function and overall functional exercise capacity compared to fixed-load IMT.
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Affiliation(s)
- Martin Hartman
- Department of Rehabilitation and Sports Medicine, 2nd Faculty of Medicine, Charles University, University Hospital Motol, Prague, Czech Republic
| | - Filip Dosbaba
- Department of Physiotherapy and Rehabilitation, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- Department of Rehabilitation, University Hospital Brno, Brno, Czech Republic
- Rehabilitation Clinic, Faculty of Medicine, Masaryk University, Brno, Czech Republic
| | - Ladislav Batalik
- Department of Physiotherapy and Rehabilitation, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- Department of Rehabilitation, University Hospital Brno, Brno, Czech Republic
- Rehabilitation Clinic, Faculty of Medicine, Masaryk University, Brno, Czech Republic
| | - Daniela Vlazna
- Department of Physiotherapy and Rehabilitation, Faculty of Medicine, Masaryk University, Brno, Czech Republic
- Department of Rehabilitation, University Hospital Brno, Brno, Czech Republic
| | - Marek Plutinsky
- Department of Respiratory Diseases, University Hospital Brno, Brno, Czech Republic
- Faculty of Medicine, Masaryk University, Brno, Czech Republic
| | - Kristian Brat
- Department of Respiratory Diseases, University Hospital Brno, Brno, Czech Republic
- Faculty of Medicine, Masaryk University, Brno, Czech Republic
| | - Roberta Catunda Costa
- Programa de Pós-Graduação em Fisioterapia e Funcionalidade, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, Brazil
| | - Artur Solon Lima
- Programa de Pós-Graduação em Fisioterapia e Funcionalidade, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, Brazil
| | - Lawrence P Cahalin
- Department of Physical Therapy, University of Miami Miller School of Medicine, Coral Gables, Florida, USA
| | - Magno F Formiga
- Programa de Pós-Graduação em Fisioterapia e Funcionalidade, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, Brazil
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Zamboti CL, Bertin LD, Krinski GG, Silva H, Pimpão HA, Gois E, Pitta F, Camillo CA. Timed "up and go" to identify physically inactive individuals with interstitial lung disease. J Bras Pneumol 2025; 51:e20240248. [PMID: 40172411 PMCID: PMC12097730 DOI: 10.36416/1806-3756/e20240248] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/25/2024] [Accepted: 12/09/2024] [Indexed: 04/04/2025] Open
Abstract
OBJECTIVE To investigate the relationship between the timed "up and go" (TUG) test and physical activity in daily life (PADL) in patients with interstitial lung disease (ILD) and propose a cutoff point to identify physically inactive individuals. METHODS Participants performed the TUG test at a usual pace (TUGusual) and at a fast pace (TUGfast). Exercise capacity was assessed by the six-minute walk test, lung function was assessed by whole-body plethysmography, quadriceps strength was assessed by maximal voluntary isometric contraction, and PADL was assessed by an activity monitor worn for six consecutive days. PADL variables included number of steps/day, time spent/day in activities of different intensities, and time spent/day in different postures. A ROC curve was plotted to identify physically inactive individuals on the basis of daily steps (5,000 steps/day) and moderate to vigorous physical activity (MVPA; 30 min/day). RESULTS Fifty-three ILD patients (26 women, with a mean age of 60 ± 11 years) were included in the study. TUGusual and TUGfast correlated moderately with the number of steps/day and time spent/day in light physical activity and MVPA (-0.60 < r < -0.41; p < 0.05 for all). ROC curves for TUGusual showed that the cutoffs of ≥ 9.25 s and ≥ 7.9 s can identify physically inactive individuals on the basis of 5,000 steps/day (AUC: 0.73; sensitivity, 76%; specificity, 70%) and 30 min/day of MVPA (AUC: 0.85; sensitivity, 90%; specificity, 75%). Participants who performed worse on TUGusual (i.e., ≥ 9.25 s) showed lower peripheral muscle strength, exercise capacity, and PADL. CONCLUSIONS Performance on TUGusual and TUGfast correlates moderately with PADL in patients with ILD. A TUGusual performance ≥ 9.25 s appears to be able to identify physically inactive individuals in this population.
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Affiliation(s)
- Camile Ludovico Zamboti
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Fisioterapia, Faculdade de Ciências e Tecnologia, Universidade Estadual Paulista - UNESP - Presidente Prudente (SP) Brasil
| | - Larissa Dragonetti Bertin
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Ciências da Reabilitação, Universidade Pitágoras - UNOPAR - Londrina (PR) Brasil
| | - Gabriela Garcia Krinski
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Ciências da Reabilitação, Universidade Pitágoras - UNOPAR - Londrina (PR) Brasil
| | - Humberto Silva
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
| | - Heloise Angélico Pimpão
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Ciências da Reabilitação, Universidade Pitágoras - UNOPAR - Londrina (PR) Brasil
- . Departamento de Clínica Cirúrgica da Universidade Estadual de Londrina, Londrina (PR) Brasil
| | - Emanuel Gois
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Clínica Cirúrgica da Universidade Estadual de Londrina, Londrina (PR) Brasil
| | - Fabio Pitta
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
| | - Carlos Augusto Camillo
- . Departamento de Fisioterapia, Laboratório de Pesquisa em Fisioterapia Respiratória - LFIP - Universidade Estadual de Londrina, Londrina (PR) Brasil
- . Departamento de Fisioterapia, Faculdade de Ciências e Tecnologia, Universidade Estadual Paulista - UNESP - Presidente Prudente (SP) Brasil
- . Departamento de Ciências da Reabilitação, Universidade Pitágoras - UNOPAR - Londrina (PR) Brasil
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Wang P, Wang J, Ge L, Gao B, Wang S, Jiang S. Automatically titrating oxygen system versus constant flow oxygen system during exercise in patients with COPD: a systematic review and meta-analysis. BMC Pulm Med 2025; 25:140. [PMID: 40155894 PMCID: PMC11951597 DOI: 10.1186/s12890-025-03594-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/30/2024] [Accepted: 03/11/2025] [Indexed: 04/01/2025] Open
Abstract
BACKGROUND Hypoxemia is a common symptom among patients with chronic obstructive pulmonary disease (COPD). The constant flow oxygen system (CFOS) is often insufficient to correct this symptom. The automatically titrating oxygen system (ATOS), a new oxygen therapy mode, remains undetermined in its ability to improve exercise performance more effectively than CFOS in COPD patients. The main objective of this meta-analysis was to explore this issue. METHODS We conducted a thorough search of randomized controlled trials (RCTs) in PubMed, Embase, Web of Science (from inception to 1 November 2024). Study selection, data extraction, and risk of bias assessment were performed independently by two authors. Data synthesis was conducted using Stata software (Version 17.0). The Grading of Recommendations, Assessment, Development and Evaluation (GRADE) system was utilized to rate evidence quality. RESULTS Five eligible studies (n = 120) were included. Compared to CFOS, ATOS was more effective in extending the distance (MD = 180.28 m, 95%CI:133.03 to 227.52) and duration (MD = 237.63 s, 95%CI: 181.18 to 294.07) of endurance shuttle walking test (ESWT). Besides, ATOS could better prolong the percentage time of sustaining targeted SpO2 (92%-96%) (MD = 29.43%,95%CI:21.15 to 37.71) and relieve dyspnea at isotime (MD = -1.65, 95%CI -3.19 to -0.11) during ESWT. DISCUSSION ATOS may have more advantages in improving exercise tolerance, sustaining targeted SpO2, and ameliorating dyspnea during exercise in COPD patients. CLINICAL TRIAL REGISTRATION The review was registered with PROSPERO (The website is https://www.crd.york.ac.uk/prosp ero/, and the ID is CRD 42024574955) and we didn't make a protocol.
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Affiliation(s)
- Peijian Wang
- Department of Rehabilitation Medicine, China-Japan Friendship Hospital, 2 Yinghuayuan East St. Hepingli, Chaoyang District, Beijing, 100029, China
| | - Jing Wang
- Department of Radiotherapy, Xuzhou Central Hospital, Xuzhou, JiangSu Province, China
| | - Lijun Ge
- Department of Rehabilitation Medicine, China-Japan Friendship Hospital, 2 Yinghuayuan East St. Hepingli, Chaoyang District, Beijing, 100029, China
| | - Beiyao Gao
- Department of Rehabilitation Medicine, China-Japan Friendship Hospital, 2 Yinghuayuan East St. Hepingli, Chaoyang District, Beijing, 100029, China
| | - Siyuan Wang
- Department of Rehabilitation Medicine, China-Japan Friendship Hospital, 2 Yinghuayuan East St. Hepingli, Chaoyang District, Beijing, 100029, China.
| | - Shan Jiang
- Department of Rehabilitation Medicine, China-Japan Friendship Hospital, 2 Yinghuayuan East St. Hepingli, Chaoyang District, Beijing, 100029, China.
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Giovanelli L, Bernardelli G, Facchetti S, Malacarne M, Vandoni M, Carnevale Pellino V, Zuccotti G, Calcaterra V, Lucini D. Metabolic improvement after exercise training in children with obesity: Possible role of the six-minute walking test. PLoS One 2025; 20:e0320209. [PMID: 40153416 PMCID: PMC11952257 DOI: 10.1371/journal.pone.0320209] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/05/2024] [Accepted: 02/16/2025] [Indexed: 03/30/2025] Open
Abstract
The aims of this study are to evaluate the effectiveness of an online supervised training program in modulating lipid and glucose metabolism in children with obesity and to investigate the possible role of the 6-minute walking test (6MWT) as a predictor of metabolic improvement. A total of 35 Caucasian children with obesity (aged 8-13) were enrolled in the study and tested before (T0) and after (T1) a 12-week online supervised exercise training protocol: cardiovascular fitness (by means of 6MWT), metabolic biochemical profile, lifestyle (with ad hoc questionnaires focusing on physical activity, nutrition, sedentariness, sleep hours and quality, health perception) and Cardiac Autonomic Regulation (CAR) were assessed. Spearman correlations between the variations in the studied outcomes were explored. After intervention, the distance covered during 6MWT significantly increased (p < 0.001), and nutrition quality improved slightly but significantly (p = 0.03). The improvement in the 6MWT performance was shown to be significantly correlatee with the reduction of insulin levels (r = -0.455; p = 0.02), HOMA-IR Index (r = -0.452; p = 0.02), total cholesterol values (r = -0.549; p = 0.004) and Atherogenic Index of Plasma (AIP) (r = 0.422; p = 0.04). Moreover, there was a significant correlation between the improvement in 6MWT and health perception (r = 0.578; p = 0.002). We observed that the improvement in the 6MWT performance correlates with better metabolic profile after exercise training in children with obesity suggesting the goodness of this simple test on unveil changes in pathogenetic processes underlying obesity.
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Affiliation(s)
| | - Giuseppina Bernardelli
- IRCCS Istituto Auxologico Italiano, Exercise Medicine Unit, Milan, Italy
- DISCCO Department, University of Milan, Milan, Italy
| | | | | | - Matteo Vandoni
- Laboratory of Adapted Motor Activity (LAMA), Department of Public Health, Experimental Medicine and Forensic Science, University of Pavia, Pavia, Italy
| | | | - Gianvincenzo Zuccotti
- Department of Biomedical and Clinical Science, University of Milan, Milano, Italy
- Pediatric Department, Buzzi Children’s Hospital, Milano, Italy
| | - Valeria Calcaterra
- Pediatric Department, Buzzi Children’s Hospital, Milano, Italy
- Pediatric and Adolescent Unit, Department of Internal Medicine, University of Pavia, Pavia, Italy
| | - Daniela Lucini
- BIOMETRA Department, University of Milan, Milan, Italy
- IRCCS Istituto Auxologico Italiano, Exercise Medicine Unit, Milan, Italy
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Zou H, Chen X, Zhang J, Wu X, Wu S, Lin C, Zhu Y, Wu L. Breaking barriers: novel reference equations for the six-minute walk distance and work in obese Chinese adults. JOURNAL OF HEALTH, POPULATION, AND NUTRITION 2025; 44:91. [PMID: 40155996 PMCID: PMC11954308 DOI: 10.1186/s41043-025-00832-3] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 01/22/2025] [Accepted: 03/13/2025] [Indexed: 04/01/2025]
Abstract
BACKGROUND The six-minute walk test (6MWT) is a key tool for assessing fitness in obese individuals, but existing reference equations for the six-minute walk distance (6MWD) are limited and overlook the six-minute walk work (6MWW), in turn limiting the clinical applicability of the test. This study aims to establish new 6MWD and 6MWW equations to improve our understanding of functional capacity in obese Chinese adults. METHODS A cross-sectional study was conducted at Wenzhou People's Hospital from July 2021 to June 2023. Obese Chinese adults (BMI > 30 kg/m²), aged 18-69 years, completed the 6MWT following the ATS/ERS guidelines. Stepwise multiple regression was used to create sex-specific reference equations for the 6MWD and 6MWW. RESULTS A total of 309 obese Chinese adults participated in this study, achieving a mean 6MWD of 550.7 ± 45.85 m and a mean 6MWW of 46149.9 ± 6403.58 kg·m. Sex-specific equations for the 6MWD and 6MWW explained a significant portion of the variance in the values (34-61%). CONCLUSION The proposed reference equations for the 6MWD and 6MWW increase the accuracy and applicability of functional capacity assessment tests, outperforming existing reference equations. The inclusion of the 6MWW provides a relatively novel metric that integrates metabolic workload and mechanical efficiency, offering unique insights into the functional performance of obese individuals and allowing tailored health interventions.
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Affiliation(s)
- He Zou
- Department of Cardiology, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Xiaoshu Chen
- Department of Cardiology, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Jia Zhang
- Department of Medical Inspection, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Xinlei Wu
- Department of Cardiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325000, China
| | - Senxiang Wu
- Department of Neurology, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Cong Lin
- Department of Cardiology, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Yuan Zhu
- Department of Nephrology, Wenzhou Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou People's Hospital, Wenzhou, Zhejiang, China
| | - Lianpin Wu
- Department of Cardiology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325000, China.
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Smith-Turchyn J, Sabiston CM, Edward H, Richardson J, Nayiga BK, Page A, Brooks D, Mukherjee SD. Implementing physical activity for individuals with cancer during treatment: protocol for the IMPACT implementation-effectiveness trial. BMJ Open 2025; 15:e101013. [PMID: 40148001 PMCID: PMC11956335 DOI: 10.1136/bmjopen-2025-101013] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/20/2025] [Accepted: 03/14/2025] [Indexed: 03/29/2025] Open
Abstract
INTRODUCTION The prevalence of cancer in Canada is growing, leading to multiple lasting side effects in survivors. The physical and psychosocial benefits of regular physical activity (PA) during and after treatment for individuals with cancer are well established, however, not well implemented in a clinical setting. The overall aim of this project is to build on previous work and conduct a multicentred randomised controlled trial (RCT) and evaluate the effectiveness of a novel implementation strategy using PA and self-management versus usual care during cancer treatment. METHODS AND ANALYSIS Study design: a hybrid implementation-effectiveness RCT will occur at five cancer centres across Ontario, Canada. Participants: eligible participants include adults with a cancer diagnosis (any type or stage) who are receiving treatment and cleared for exercise by their oncology care team. Intervention: participants (n=129) will be randomised to one of three groups: (1) institution-based exercise and self-management (SM) (eight in-person sessions of aerobic exercise and eight SM modules), (2) SM alone (SM only: eight virtual modules) or (3) usual care (no intervention). Outcomes: the Reach, Effectiveness, Adoption, Implementation and Maintenance framework will assess implementation outcomes. The primary effectiveness outcome is self-report PA level postintervention. Data analysis: outcomes will be measured at four time points (baseline, postintervention, 6- and 12-month follow-up). Descriptive statistics will be used to present implementation outcomes. An analysis of covariance will assess change between groups over time. ETHICS AND DISSEMINATION Findings from this trial will build on previous work and inform the way PA services are provided within cancer institutions across Ontario, Canada, and inform decision-making on how to incorporate exercise evidence into real-world clinical practice in cancer care. The Hamilton Integrated Research Ethics Board (ID: 7673 & 17454) has approved this study. Results will be disseminated using a combination of peer-reviewed publications, conference presentations and community organisation presentations. Participants will contribute to dissemination by sharing 'participant perspectives', highlighting their experience in the project and thoughts on the implementation strategies used. TRIAL REGISTRATION NUMBER The study is registered on clinicaltrials.gov (ID: NCT06323707).
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Affiliation(s)
- Jenna Smith-Turchyn
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | | | - Holly Edward
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | - Julie Richardson
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | - Brenda K Nayiga
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | - Alicia Page
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | - Dina Brooks
- School of Rehabilitation Science, McMaster University, Hamilton, Ontario, Canada
| | - Som D Mukherjee
- Department of Oncology, McMaster University, Hamilton, Ontario, Canada
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Büsching G, Schmid JP. 6-Minute Walk Test: Exploring Factors Influencing Perceived Intensity in Older Patients Undergoing Cardiac Rehabilitation-A Qualitative Study. Healthcare (Basel) 2025; 13:735. [PMID: 40218033 PMCID: PMC11988596 DOI: 10.3390/healthcare13070735] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/16/2025] [Revised: 03/09/2025] [Accepted: 03/18/2025] [Indexed: 04/14/2025] Open
Abstract
Background/Objectives: In cardiac rehabilitation, the 6-minute walk test (6-MWT) is a standard assessment of initial evaluation. It measures walking distance as a surrogate of submaximal physical performance. Thereby, a subjective rating of perceived exertion, assessed by the Borg Scale, plays an important role. It has been observed that patients with coronary heart disease often rate themselves lower than the person supervising the test. Since this discrepancy might lead to inadequate exercise prescription, this study aims to explore reasons for low self-rating. Methods: In a qualitative study, influencing factors for low self-rating were collected from patients using interviews and questionnaires and from a focus group of physiotherapists. The evaluation was based on the grounded theory. Results: Self-image after retirement emerged as the central factor, as it shaped patients' behavior during the 6-MWT and their subsequent self-assessment. Additionally, five different categories of causal conditions were detected from ten patients and five therapists: fears, physical limitations, test instruction, testing conditions, and therapists' expectations. Conclusions: Patients with coronary heart disease had poor self-perception of exercise intensity and limited understanding of the meaning of the Borg Scale and the 6-MWT. Physiotherapists should place greater emphasis on patients' perceived exertion to be able to effectively tailor exercise prescription and, therefore, improve attainment of cardiac rehabilitation goals and long-term adherence.
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Affiliation(s)
- Gilbert Büsching
- Medical Therapeutic Departement, Klinik Barmelweid AG, 5017 Barmelweid, Switzerland
- Barmelweid Academy, Klinik Barmelweid AG, 5017 Barmelweid, Switzerland;
| | - Jean-Paul Schmid
- Barmelweid Academy, Klinik Barmelweid AG, 5017 Barmelweid, Switzerland;
- Department Internal Medicine, Klinik Gais AG, 9056 Gais, Switzerland
- Cardiovascular Prevention and Rehabilitation Unit, University Hospital (Inselspital), University of Bern, 3010 Bern, Switzerland
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46
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Liu F, Jones AYM, Tsang RCC, Yam TTT, Tsang WWN. Effects of inspiratory muscle training on respiratory function, diaphragmatic thickness, balance control, exercise capacity and quality of life in people after stroke: A randomized controlled trial protocol. PLoS One 2025; 20:e0319899. [PMID: 40131895 PMCID: PMC11936291 DOI: 10.1371/journal.pone.0319899] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/16/2024] [Accepted: 02/02/2025] [Indexed: 03/27/2025] Open
Abstract
BACKGROUND Stroke is associated with diaphragmatic weakness and impaired respiratory function as well as balance impairment. The role of inspiratory muscle training (IMT) on improvement of respiratory muscle strength in people after stroke has been reported. However, the training intensity associated with optimal diaphragm recruitment and the relationship between the effect of IMT and other functions in this population remains uncertain. PURPOSE This randomized controlled trial (RCT) aims to explore the effects of a 4-week IMT program with training intensity at 50% maximum inspiratory pressure (MIP) (previously shown to be associated with maximal diaphragm contraction), on respiratory function, balance control, exercise capacity and quality of life (QOL) in people after stroke. METHODS This is a patient- and assessor-blinded RCT. Eligible participants will be randomly allocated to the targeted-IMT group (with 50% MIP as the training intensity) or sham-IMT group (with 10% MIP as the training intensity). Both groups will also receive the same standardised hospital-based physical-rehabilitation protocol. All interventions will be implemented 5 days/week for 4 weeks. The primary outcome is the change of diaphragmatic thickness. Secondary outcomes are spirometry respiratory function, balance control, exercise capacity and QOL. Assessment will be conducted at baseline, post-intervention, and at 12th week follow-up. Data will be primarily analysed using repeated-measures ANOVA α=0.05. DISCUSSION Results of this study will primarily inform the effect of IMT on lung function, balance control, exercise capacity and QOL in addition to physical rehabilitation, further the interplay between the change in diaphragm thickness, balance and QOL will be analysed in detail.
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Affiliation(s)
- Fang Liu
- Department of Physiotherapy, School of Nursing and Health Sciences, Hong Kong Metropolitan University, Hong Kong, China
- Department of Rehabilitation, Shenzhen Second People’s Hospital, The First Affiliated Hospital of Shenzhen University Health Science Centre, Shenzhen, China
| | - Alice Y. M. Jones
- School of Health and Rehabilitation Sciences, The University of Queensland, Brisbane, Queensland, Australia
| | - Raymond C. C. Tsang
- Department of Rehabilitation Sciences, The Hong Kong Polytechnic University, Hong Kong, China
| | - Timothy T. T. Yam
- Department of Physiotherapy, School of Nursing and Health Sciences, Hong Kong Metropolitan University, Hong Kong, China
| | - William W. N. Tsang
- Department of Physiotherapy, School of Nursing and Health Sciences, Hong Kong Metropolitan University, Hong Kong, China
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Denehy L, Abo S, Swain C, Short CE, Kiss N, Khot A, Wong E, Purtill D, O'Donnell C, Klaic M, Granger CL, Tew M, Spelman T, Cavalheri V, Edbrooke L. Rehabilitation after bone marrow transplant compared with usual care to improve patient outcomes (REBOOT): protocol for a randomised controlled trial. BMC Cancer 2025; 25:532. [PMID: 40122792 PMCID: PMC11931774 DOI: 10.1186/s12885-025-13898-3] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/22/2024] [Accepted: 03/10/2025] [Indexed: 03/25/2025] Open
Abstract
BACKGROUND Haematological cancer affects more than 1.3 million people around the world annually and accounted for almost 800,000 deaths globally in 2020. The number of patients with these cancers undergoing bone marrow transplant is increasing. Of note, this intensive treatment is associated with complex and multifactorial side effects, often impacting nutritional status, physical functioning and overall health-related quality of life. The primary aim of this study is to investigate the effectiveness of an eight-week multidisciplinary rehabilitation intervention compared with usual care on the physical function domain of the European Organisation for the Research and Treatment of Cancer quality of life questionnaire (EORTC QLQ-C30 version 3) in patients with haematological cancer following bone marrow transplant. METHODS This is a multisite, pragmatic two-arm parallel-group, randomised controlled trial (RCT) with stratified randomisation, powered for superiority, recruiting 170 participants at 30 days following either allogeneic or autologous bone marrow transplant (ACTRN12622001071718). Recruitment sites include three Australian university affiliated teaching hospitals. Participants are eligible if aged ≥ 18 years, treated for haematological cancer with allogeneic or autologous bone marrow transplant and can walk independently. The intervention group will receive eight weeks of twice weekly telehealth-based exercise classes, an initial and follow up dietetics consult, post exercise protein supplements, and a home-based physical activity program, all with embedded behaviour change strategies. The primary outcome is patient reported physical function measured using the EORTC QLQ-C30 version 3. Secondary outcomes include other domains of the EORTC QLQ-C30, fatigue, physical function, physical activity levels, frailty, body composition, sarcopenia and nutrition assessment. We will also undertake a health economic analysis alongside the trial and a process evaluation exploring intervention fidelity, causal mechanisms as well as contextual influences through qualitative enquiry. DISCUSSION The REBOOT trial will add RCT-evidence from a rigorously conducted, statistically powered multi-site trial to existing limited knowledge on the effects of multi-disciplinary rehabilitation for people with haematological cancer. If effectiveness is supported, then implementation of rehabilitation into care pathways for people having bone marrow transplant can be considered. TRIAL REGISTRATION ACTRN12622001071718 prospectively registered 03/08/2022, last updated 08/03/2024.
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Affiliation(s)
- Linda Denehy
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia.
- Department of Health Services Research, Peter Maccallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
- Department of Oncology, Sir Peter Maccallum, University of Melbourne, Parkville, VIC, 3010, Australia.
| | - Shaza Abo
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
- Department of Physiotherapy, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia
| | - Christopher Swain
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
| | - Camille E Short
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
- Melbourne Centre for Behaviour Change, The University of Melbourne, 800 Swanston St, Melbourne, VIC, 3053, Australia
| | - Nicole Kiss
- Institute for Physical Activity and Nutrition, Deakin University, Burwood, VIC, 3125, Australia
| | - Amit Khot
- Department of Oncology, Sir Peter Maccallum, University of Melbourne, Parkville, VIC, 3010, Australia
- Clinical Haematology, Peter Maccallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia
| | - Eric Wong
- Clinical Haematology Austin Health, 145 Studley Road, Heidelberg, VIC, 3084, Australia
| | - Duncan Purtill
- Department of Haematology, Fiona Stanley Hospital, Perth, WA, Australia
- Department of Haematology, Pathwest Laboratory Medicine, Perth, WA, Australia
| | - Clare O'Donnell
- Department of Physiotherapy, Austin Hospital, 145 Studley Road, Heidelberg, VIC, 3084, Australia
| | - Marlena Klaic
- Melbourne School of Health Sciences, the University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
| | - Catherine L Granger
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
| | - Michelle Tew
- Melbourne Health Economics, Centre for Health Policy, Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, 3010, Australia
| | - Tim Spelman
- Department of Health Services Research, Peter Maccallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia
| | - Vinicius Cavalheri
- Faculty of Health Sciences, Curtin School of Allied Health, Curtin University, GPO Box U1987, Perth, WA, 6845, Australia
- Allied Health, South Metropolitan Health Service, 11 Robin Warren Drive, Murdoch, WA, 6150, Australia
| | - Lara Edbrooke
- Department of Physiotherapy, The University of Melbourne, 161 Barry Street, Parkville, VIC, 3010, Australia
- Department of Health Services Research, Peter Maccallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia
- Department of Oncology, Sir Peter Maccallum, University of Melbourne, Parkville, VIC, 3010, Australia
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Crooks MG, Wright C, Hart S, Allgar V, English A, Swan F, Dyson J, Richardson G, Twiddy M, Cohen J, Simpson A, Huang C, Sykes DL, Johnson M. Complex breathlessness intervention in idiopathic pulmonary fibrosis (BREEZE-IPF): a feasibility, wait-list design randomised controlled trial. BMJ Open Respir Res 2025; 12:e002327. [PMID: 40121019 PMCID: PMC11931949 DOI: 10.1136/bmjresp-2024-002327] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/19/2024] [Accepted: 12/05/2024] [Indexed: 03/25/2025] Open
Abstract
INTRODUCTION Breathlessness is common and impairs the quality of life of people with idiopathic pulmonary fibrosis (IPF) and non-IPF fibrotic interstitial lung diseases (ILD). We report the findings of a multicentre, fast-track (wait-list), mixed-methods, randomised controlled, feasibility study of a complex breathlessness intervention in breathless IPF and non-IPF fibrotic ILD patients. METHODS Breathless IPF and non-IPF fibrotic ILD patients were randomised to receive the intervention within 1 week (fast-track) or after 8 weeks (wait-list). The intervention comprised two face-to-face and one telephone appointment during a 3-week period covering breathing control, handheld fan-use, pacing and breathlessness management techniques, and techniques to manage anxiety. Feasibility and clinical outcomes were assessed to inform progression to, and optimal design for, a definitive trial. A qualitative substudy explored barriers and facilitators to trial and intervention delivery. RESULTS 47 patients (M:F 38:9, mean (SD) age 73.9 (7.2)) were randomised with a recruitment rate of 2.5 participants per month across three sites. The adjusted mean differences (95% CI) for key clinical outcomes at 4 weeks post randomisation were as follows: Chronic Respiratory Questionnaire breathlessness mastery domain (0.45 (-0.07, 0.97)); and numerical rating scales for 'worst' (-0.93 (-1.95, 0.10)), 'best' (-0.19 (-1.38, 1.00)), 'distress caused by' (-1.84 (-3.29, -0.39)) and 'ability to cope with' (0.71 (-0.57, 1.99)) breathlessness within the past 24 hours. The qualitative substudy confirmed intervention acceptability and informed feasibility and acceptability of study outcome measures. CONCLUSION A definitive trial of a complex breathlessness intervention in patients with IPF and non-IPF fibrotic ILD is feasible with preliminary data supporting intervention effectiveness. TRIAL REGISTRATION NUMBER ISRCTN13784514.
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Affiliation(s)
- Michael George Crooks
- Respiratory Research Group, Hull York Medical School, Cottingham, East Yorkshire, UK
- Hull University Teaching Hospitals NHS Trust, Hull, UK
| | - Caroline Wright
- Respiratory Research Group, Hull York Medical School, Cottingham, East Yorkshire, UK
- Hull University Teaching Hospitals NHS Trust, Hull, UK
| | - Simon Hart
- Respiratory Research Group, Hull York Medical School, Cottingham, East Yorkshire, UK
- Hull University Teaching Hospitals NHS Trust, Hull, UK
| | | | | | | | | | | | | | | | | | | | - Dominic L Sykes
- Respiratory Research Group, Hull York Medical School, Cottingham, East Yorkshire, UK
- Hull University Teaching Hospitals NHS Trust, Hull, UK
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Abo S, Denehy L. Reproducibility of Clinically Meaningful Change in Physical Capacity Tested by Online 6-Minute Walk Test. J Clin Oncol 2025:JCO2500023. [PMID: 40117524 DOI: 10.1200/jco-25-00023] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/04/2025] [Accepted: 02/18/2025] [Indexed: 03/23/2025] Open
Affiliation(s)
- Shaza Abo
- Shaza Abo, PhD, BPhysio, Department of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australia, Department of Physiotherapy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia; and Linda Denehy, PhD, FAHMS, BAppSc(Physio), Department of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australia, Department of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia, Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia
| | - Linda Denehy
- Shaza Abo, PhD, BPhysio, Department of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australia, Department of Physiotherapy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia; and Linda Denehy, PhD, FAHMS, BAppSc(Physio), Department of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australia, Department of Health Services Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia, Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia
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50
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Hamada Y, Gibson PG, Clark VL, Lewthwaite H, Fricker M, Thomas D, McDonald VM. Dysfunctional Breathing and Depression Are Core Extrapulmonary and Behavior/Risk Factor Traits in Type 2-High Severe Asthma. THE JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. IN PRACTICE 2025:S2213-2198(25)00267-3. [PMID: 40120804 DOI: 10.1016/j.jaip.2025.03.017] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/09/2024] [Revised: 02/24/2025] [Accepted: 03/12/2025] [Indexed: 03/25/2025]
Abstract
BACKGROUND Obesity and smoking are core treatable traits (TTs) in type 2 (T2)-low asthma, contributing to its pathophysiology. In contrast, core extrapulmonary and behavior/risk factor traits remain unclear in T2-high asthma. OBJECTIVE This study aimed to identify core extrapulmonary and behavior/risk factor traits for T2-high asthma. METHODS A cross-sectional study was conducted on 187 people (aged ≥18 years) with severe asthma who completed a multidimensional assessment. T2-high asthma was defined as blood eosinophils ≥150 cells/μL and/or fractional exhaled nitric oxide ≥20 ppb. Core TTs in T2-high asthma were identified among 9 extrapulmonary traits and 4 behavior/risk factor traits, using network analysis and dominance analysis for the Asthma Control Questionnaire scores, the Asthma Quality of Life Questionnaire scores, exacerbation frequency, and lung function. Associations between the identified core TTs and biomarkers were examined in participants with T2-high asthma. RESULTS Of 187 participants, 151 (80.7%) had T2-high severe asthma. Dysfunctional breathing and depression had higher values of node strength than other TTs, contributing most to worse asthma symptoms, poorer quality of life, and frequent exacerbations in T2-high asthma. These conditions in T2-high asthma were associated with elevated systemic inflammation, including blood neutrophils, neutrophil-lymphocyte ratio, and serum high-sensitivity C-reactive protein, independent of obesity, oral corticosteroid dose, and anxiety. CONCLUSIONS Core extrapulmonary and behavior/risk factor traits in T2-high severe asthma were dysfunctional breathing and depression, contributing to worse asthma outcomes, suggesting that core TTs may differ between asthma inflammatory phenotypes. Elevated systemic inflammation may help in recognizing the presence of dysfunctional breathing and depression in T2-high severe asthma.
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Affiliation(s)
- Yuto Hamada
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia; Clinical Research Center for Allergy and Rheumatology, NHO Sagamihara National Hospital, Sagamihara, Japan.
| | - Peter G Gibson
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, NSW, Australia
| | - Vanessa L Clark
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia; School of Nursing and Midwifery, College of Health, Medicine and Wellbeing, the University of Newcastle, Newcastle, NSW, Australia
| | - Hayley Lewthwaite
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia
| | - Michael Fricker
- Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia
| | - Dennis Thomas
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia
| | - Vanessa M McDonald
- Center of Excellence in Treatable Traits, College of Health, Medicine and Wellbeing, the University of Newcastle, New Lambton Heights, NSW, Australia; Asthma and Breathing Research Program, Hunter Medical Research Institute, New Lambton Heights, NSW, Australia; Department of Respiratory and Sleep Medicine, John Hunter Hospital, New Lambton Heights, NSW, Australia; School of Nursing and Midwifery, College of Health, Medicine and Wellbeing, the University of Newcastle, Newcastle, NSW, Australia
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