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World J Cardiol. Dec 26, 2025; 17(12): 113820
Published online Dec 26, 2025. doi: 10.4330/wjc.v17.i12.113820
Efficacy of ivabradine in heart rate reduction after cardiac transplantation: Systematic review and meta-analysis
Faizan Ahmed, Ramsha Ali, Faseeh Haider, Haider Hussain Shah, Kanza Farhan, Kainat Jahangir, Madiha Kiyani, Muhammad Saad Khan, Zaima Afzaal, Shayan Iqbal Khan, Muhammad Abdullah Nizam, Muhammad Usman, Najam Gohar, Mushood Ahmed, Tehmasp Rehman Mirza, Yasar Sattar, Amro Taha, Jesus Almendral, Fawaz Alenezi
Faizan Ahmed, Jesus Almendral, Department of Medicine, Jersey Shore University Medical Center, Neptune, NJ 27710, United States
Ramsha Ali, Department of Medicine, Peoples University of Medical and Health Sciences, Nawabshah 67450, Sindh, Pakistan
Faseeh Haider, Department of Medicine, Allama Iqbal Medical College, Lahore 54000, Punjab, Pakistan
Haider Hussain Shah, Department of Medicine, Bayhealth Hospital, Kent Campus, Dover, DE 19901, United States
Kanza Farhan, Department of Medicine, Sindh Medical College, Jinnah Sindh Medical University, Karachi 75510, Sindh, Pakistan
Kainat Jahangir, Department of Medicine, Dow Medical College, Karachi 74200, Sindh, Pakistan
Madiha Kiyani, Department of Medicine, Medstar Georgetown University Baltimore Program, Baltimore, MD 21237, United States
Muhammad Saad Khan, Department of Medicine, Jinnah Sindh Medical University, Karachi 75510, Sindh, Pakistan
Zaima Afzaal, Muhammad Usman, Najam Gohar, Department of Medicine, Ameer-Ud-Din Medical College, Lahore 54000, Punjab, Pakistan
Shayan Iqbal Khan, Department of Medicine, Jefferson Torresdale Hospital, Philadelphia, PA 19114, United States
Muhammad Abdullah Nizam, Department of Internal Medicine, Trinity Health Livonia Hospital, Michigan City, MI 43202, United States
Mushood Ahmed, Department of Internal Medicine, Rawalpindi Medical University, Rawalpindi 74200, Pakistan
Tehmasp Rehman Mirza, Department of Medicine, Shalamar Medical and Dental College, Lahore 54000, Punjab, Pakistan
Yasar Sattar, Department of Cardiology, West Virginia University, Morgantown, WV 26534, United States
Amro Taha, Department of Internal Medicine, Weiss Memorial Hospital, Chicago, IL 60614, United States
Fawaz Alenezi, Department of Medicine, Duke University School of Medicine, Durham, NC 27710, United States
Author contributions: Ahmed F, Ali R, and Haider F were responsible for conceptualization; Ahmed F and Gohar N were responsible for writing (original draft); Farhan K, Jahangir K, Kiyani M, Khan MS, Afzaal Z, Khan SI, Nizam MA, Usman M, and Gohar N were responsible for data curation and formal analysis; Farhan K, Jahangir K, Kiyani M, Khan MS, and Gohar N were responsible for methodology and investigation; Shah HH, Usman M, Ahmed M, Mirza TR, Sattar Y, Almendral J, Taha A, and Alenezi F were responsible for writing (review and editing); Ali R, Sattar Y, and Almendral J were responsible for supervision, project administration and resources; all authors have read and approved the final manuscript.
Conflict-of-interest statement: The authors have no financial conflicts of interest to declare.
PRISMA 2009 Checklist statement: The authors have read the PRISMA 2009 Checklist, and the manuscript was prepared and revised according to the PRISMA 2009 Checklist.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Muhammad Usman, Researcher, Department of Medicine, Ameer-Ud-Din Medical College, 6 Birdwood Road, Jinnah Town, Lahore 54000, Punjab, Pakistan. deustchusman23@gmail.com
Received: September 4, 2025
Revised: September 26, 2025
Accepted: October 28, 2025
Published online: December 26, 2025
Processing time: 111 Days and 17.1 Hours
Abstract
BACKGROUND

Persistent sinus tachycardia affects up to 40% of patients after heart transplantation and is linked with graft dysfunction, impaired diastolic filling, and increased morbidity. Conventional rate-limiting therapies such as beta-blockers and calcium channel blockers are quite often contraindicated due to risks of bradyarrhythmia or hypotension. Ivabradine, a selective I(f) channel inhibitor, reduces heart rate (HR) without negative inotropic or hypotensive effects.

AIM

To evaluate the efficacy and safety of ivabradine in heart transplant recipients.

METHODS

A comprehensive search of PubMed, EMBASE, Scopus, Cochrane Library, and Google Scholar was conducted from inception to April 15, 2025. Eligible studies evaluated ivabradine in heart transplant recipient vs placebo or metoprolol, reporting HR, mortality, left ventricular mass (LVM), or safety. Data were independently extracted by two reviewers, and quality was assessed. Review Manager 5.4 performed pooled analyses using random-effects models. Mean differences (MD) or standardized MD (SMD) were calculated for continuous outcomes, and risk ratios for dichotomous outcomes.

RESULTS

Of 415 records identified, four studies comprising 264 patients (126 ivabradine, 138 control) met the inclusion criteria. Ivabradine significantly reduced resting HR compared with controls (MD = -11.06 beats per minute; 95%CI: -19.50 to -2.62; P < 0.00001; I2 = 93%). Sensitivity analysis demonstrated consistent findings (SMD = -6.74; 95%CI: -9.23 to -4.24; I2 = 0%). No significant difference in all-cause mortality was observed (MD = 0.52; 95%CI: 0.17-1.64; P = 0.27; I2 = 85%). Pooled analysis of LVM revealed no significant effect of ivabradine (MD = -3.57 g; 95%CI: -29.21 to 22.08; P = 0.79; I2 = 73%), with sensitivity analysis confirming neutrality. Adverse events were rare and mostly comparable between groups.

CONCLUSION

Ivabradine reduces HR effectively in heart transplant recipients without added adverse outcomes, supporting its use as safe and well-tolerated alternative when conventional agents are unsuitable. Despite potential clinical benefit, small sample size and heterogeneity the need for larger randomized trials to confirm long-term outcomes and establish ivabradine’s role in post-transplant care.

Keywords: Ivabradine; Heart transplant; Heart rate; Meta-analysis; Tachycardia; Decision making

Core Tip: Persistent sinus tachycardia after heart transplantation is linked to graft dysfunction and poor outcomes, yet beta-blockers are often limited by hypotension or bradyarrhythmia. Ivabradine, a selective inhibitor of funny current, lowers heart rate (HR) without negative inotropic or hypotensive effects. Our systematic review and meta-analysis of four studies (264 patients) found ivabradine significantly reduced resting HR and was well tolerated in transplant patients, underscoring its role as a promising therapeutic option for rate control when conventional treatments are unsuitable.