Rizza G, Glynou K, Eletskaya M. Impact of hepatitis B immunoglobulin mode of administration on treatment experiences of patients after liver transplantation: Results from an online survey. World J Transplant 2024; 14(3): 90949 [PMID: 39295979 DOI: 10.5500/wjt.v14.i3.90949]
Corresponding Author of This Article
Masha Eletskaya, MSc, Director, Lumanity Insight (Cello Health Insight), Great Suffolk Yard, 2nd Floor, 131 Great Suffolk Street, London SE1 1PP, United Kingdom. masha.eletskaya@lumanity.com
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Transplantation
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Observational Study
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Sep 18, 2024 (publication date) through Mar 11, 2026
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Publication Name
World Journal of Transplantation
ISSN
2220-3230
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
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Rizza G, Glynou K, Eletskaya M. Impact of hepatitis B immunoglobulin mode of administration on treatment experiences of patients after liver transplantation: Results from an online survey. World J Transplant 2024; 14(3): 90949 [PMID: 39295979 DOI: 10.5500/wjt.v14.i3.90949]
World J Transplant. Sep 18, 2024; 14(3): 90949 Published online Sep 18, 2024. doi: 10.5500/wjt.v14.i3.90949
Impact of hepatitis B immunoglobulin mode of administration on treatment experiences of patients after liver transplantation: Results from an online survey
Giorgia Rizza, Kyriaki Glynou, Masha Eletskaya
Giorgia Rizza, General Surgery and Liver Transplant Center, S. Giovanni Battista Hospital, Turin I-10126, Italy
Kyriaki Glynou, Medical Affairs, Biotest AG, Dreieich 63303, Germany
Masha Eletskaya, Lumanity Insight (Cello Health Insight), London SE1 1PP, United Kingdom
Author contributions: Glynou K and Eletskaya M designed the study; Eletskaya M contributed to the study conduct, data acquisition, analysis, and interpretation of results; Rizza G, Glynou K, and Eletskaya M drafted the manuscript; and all authors have read and approved the final manuscript.
Institutional review board statement: This study was conducted within the BHBIA guidelines following the code of conduct of the European Pharmaceutical Market Research Association, European Society for Opinion and Marketing Research, and the Market Research Society. Ethics committee review was not sought for this online patient survey research. In addition, the reporting of the study followed guidance provided by the Consolidated Criteria for Reporting Qualitative Studies. The study conduct adhered with the provisions of the European Union’s General Data Protection Regulation with regard to data protection.
Informed consent statement: Informed consent was obtained electronically from all individual participants included in the study. Participants’ rights and privacy were protected at all times throughout the study. Participants were granted the right to withdraw from the study at any time during the study conduct and to withhold information as they saw fit. All information/data that could identify respondents to third parties was kept strictly confidential; all respondents remained anonymous as their answers were reported in aggregate with the answers of all other participants.
Conflict-of-interest statement: Glynou K is an employee of Biotest AG. Eletskaya M is an employee of Lumanity (previously Cello Health Insight); the study was conducted under a contract with Biotest AG. Rizza G received consulting fees under a contract with Biotest AG. The authors have no non-financial competing interests to declare.
Data sharing statement: An anonymous version of the datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
STROBE statement: The authors have read the STROBE Statement-checklist of items, and the manuscript was prepared and revised according to the STROBE Statement-checklist of items.
Corresponding author: Masha Eletskaya, MSc, Director, Lumanity Insight (Cello Health Insight), Great Suffolk Yard, 2nd Floor, 131 Great Suffolk Street, London SE1 1PP, United Kingdom. masha.eletskaya@lumanity.com
Received: December 18, 2023 Revised: May 2, 2024 Accepted: June 7, 2024 Published online: September 18, 2024 Processing time: 225 Days and 21 Hours
Core Tip
Core Tip: Hepatitis B immunoglobulin (HBIG) combined with a potent nucleos(t)ide analog is recommended in patients undergoing liver transplantation for hepatitis B virus-associated disease. A survey was conducted to determine patients’ thoughts about three forms of HBIG treatment administration - subcutaneous (SC), intramuscular, and intravenous. Regarding current treatment, SC HBIG had the least negative impact on emotional well-being and social life, was most convenient, easiest to administer and least painful. Considering hypothetical HBIG products, SC was preferred over intramuscular and intravenous for ease of administration, convenience, and pain. For these patients, the most important considerations were ease of use, frequency, duration, and side effects.