Induction therapy in heart transplantation: A systematic review and network meta‐analysis for developing evidence‐based recommendations

Author:

Kugathasan Lakshmi1,Rayner Daniel G2,Wang Sabrina Mianchen3,Rodenas‐Alesina Eduardo1,Orchanian‐Cheff Ani4,Stehlik Josef5ORCID,Gustafsson Finn6,Greig Douglas7,McDonald Michael1,Bertolotti Alejandro Mario8,Demas‐Clarke Penny4,Kozuszko Stella1,Guyatt Gordon2,Foroutan Farid12ORCID,Alba Ana Carolina1ORCID

Affiliation:

1. Ted Rogers Centre for Heart Research University Health Network Toronto Ontario Canada

2. Department of Health Research Methods Evidence, and Impact, McMaster Hamilton Ontario Canada

3. Faculty of Medicine University of Toronto Toronto Ontario Canada

4. Toronto General Hospital University Health Network Toronto Canada

5. Department of Medicine Division of Cardiovascular Medicine University of Utah School of Medicine Salt Lake City Utah USA

6. Rigshospitalet ‐ Copenhagen University Hospital Copenhagen Denmark

7. Pontificia Universidad Católica de Chile Santiago Chile

8. Cardiothoracic Surgery Department Favaloro Foundation University hospital Buenos Aires Argentina

Abstract

AbstractIntroductionInduction therapy (IT) utility in heart transplantation (HT) remains contested. Commissioned by a clinical‐practice guidelines panel to evaluate the effectiveness and safety of IT in adult HT patients, we conducted this systematic review and network meta‐analysis (NMA).MethodsWe searched for studies from January 2000 to October 2022, reporting on the use of any IT agent in adult HT patients. Based on patient‐important outcomes, we performed frequentist NMAs separately for RCTs and observational studies with adjusted analyses, and assessed the certainty of evidence using the GRADE framework.ResultsFrom 5156 publications identified, we included 7 RCTs and 12 observational studies, and report on two contemporarily‐used IT agents—basiliximab and rATG. The RCTs provide only very low certainty evidence and was uninformative of the effect of the two agents versus no IT or one another. With low certainty in the evidence from observational studies, basiliximab may increase 30‐day (OR 1.13; 95% CI 1.06–1.20) and 1‐year (OR 1.11; 95% CI 1.02–1.22) mortality compared to no IT. With low certainty from observational studies, rATG may decrease 5‐year cardiac allograft vasculopathy (OR .82; 95% CI .74–.90) compared to no IT, as well as 30‐day (OR .85; 95% CI .80–.92), 1‐year (OR .87; 95% CI .79–.96), and overall (HR .84; 95% CI .76–.93) mortality compared to basiliximab.ConclusionWith low and very low certainty in the synthetized evidence, these NMAs suggest possible superiority of rATG compared to basiliximab, but do not provide compelling evidence for the routine use of these agents in HT recipients.

Publisher

Wiley

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