Primary heart dysfunction is greater with combined heart and lung compared with isolated heart procurement.

combined heart and lungs heart transplantation lung procurement multiple organ procurement primary graft dysfunction

Journal

The Journal of thoracic and cardiovascular surgery
ISSN: 1097-685X
Titre abrégé: J Thorac Cardiovasc Surg
Pays: United States
ID NLM: 0376343

Informations de publication

Date de publication:
01 2023
Historique:
received: 25 08 2020
revised: 16 01 2021
accepted: 23 01 2021
pubmed: 12 3 2021
medline: 17 12 2022
entrez: 11 3 2021
Statut: ppublish

Résumé

Combined heart and lungs (CHL) procurement differs from isolated heart (IH) procurement in several aspects, including lung recruitment, cannulation, and preservation requirements. We aimed to investigate whether CHL versus IH procurement contributes to the development of primary graft dysfunction (PGD) after heart transplantation (HT). Between 1999 and 2019, we assessed 175 patients undergoing HT at a single center. Patients were divided into IH (n = 61) or CHL (n = 114) procurement groups. End points included PGD (defined according to the International Society for Heart and Lung Transplantation consensus statement) and long-term survival. The incidence of PGD was significantly greater in CHL recipients compared with IH recipients (53.5% vs 16.4%, P < .001). Multivariable analysis showed that CHL procurement was independently associated with a significant 4.6-fold increased risk for PGD (95% confidence interval, 2.1-11, P < .001). Univariable and multivariable analyses showed that the overall survival was not significantly affected by the procurement group (log-rank P = .150, hazard ratio, 1.13; 95% confidence interval, 0.68-1.88, P = .646). The simultaneous procurement of abdominal organs was not associated with an increased risk of PGD in HT recipients. These results remained consistent in a propensity-matched analysis. Combined procurement of heart and lungs is independently associated with an increased risk of PGD. Further prospective studies are needed to validate this hypothesis-generating study.

Identifiants

pubmed: 33691941
pii: S0022-5223(21)00189-6
doi: 10.1016/j.jtcvs.2021.01.090
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

186-195.e4

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Eilon Ram (E)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: Eilon.ram@sheba.health.gov.il.

Jacob Lavee (J)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yigal Kassif (Y)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yury Peysakhovich (Y)

Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel; Department of Cardiothoracic Surgery, Rabin Medical Center, Petah Tikva, Israel.

Leonid Sternik (L)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Amit Segev (A)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Jignesh Patel (J)

Cedars-Sinai Heart Institute and David Geffen School of Medicine at the University of California, Los Angeles, Calif.

Yael Peled (Y)

Leviev Cardiothoracic and Vascular Center, Sheba Medical Center, Tel Hashomer, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: Yael.Peled-Potashnik@sheba.health.gov.il.

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