Risk of prolonged ischemic time linked to use of cardiopulmonary bypass during implantation for lung transplantation in the United Kingdom.


Journal

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
ISSN: 1557-3117
Titre abrégé: J Heart Lung Transplant
Pays: United States
ID NLM: 9102703

Informations de publication

Date de publication:
10 2023
Historique:
received: 30 08 2022
revised: 28 03 2023
accepted: 26 04 2023
medline: 26 9 2023
pubmed: 2 5 2023
entrez: 1 5 2023
Statut: ppublish

Résumé

Some degree of ischemia is inevitable in organ transplantation, and for most, if not all organs, there is a relationship between ischemic time and transplant outcome. The contribution of ischemic time to lung injury is unclear, with conflicting recent data. In this study, we investigate the impact of ischemia time on survival after lung transplantation in a large national cohort. We studied the outcomes for 1,565 UK adult lung transplants over a 12-year period, for whom donor, transplant, and recipient data were available from the UK Transplant Registry. We examined the effect of ischemia time (defined as donor cross-clamp to recipient reperfusion) and whether standard cardiopulmonary bypass was used using Cox proportional hazards models, adjusting for other risk factors. The total ischemic time increased from a median under 5 hours in 2003 to over 6.2 hours in 2013. Our findings show that, when the cardiopulmonary bypass was used, there was an increase in the hazard of death (of 13% [95% CI: 5%-21%] for 1-year patient survival) for each hour of total ischemic time. However, if the cardiopulmonary bypass was not used for implantation, this link disappeared-there was no statistically significant change in mortality with increasing ischemic time. We document that avoidance of bypass may remove ischemic time, within the limits of our observed range of ischemic times, as a risk factor for poor outcomes. Our data add to the evidence that bypass may be harmful to the donor lung.

Sections du résumé

BACKGROUND
Some degree of ischemia is inevitable in organ transplantation, and for most, if not all organs, there is a relationship between ischemic time and transplant outcome. The contribution of ischemic time to lung injury is unclear, with conflicting recent data. In this study, we investigate the impact of ischemia time on survival after lung transplantation in a large national cohort.
METHODS
We studied the outcomes for 1,565 UK adult lung transplants over a 12-year period, for whom donor, transplant, and recipient data were available from the UK Transplant Registry. We examined the effect of ischemia time (defined as donor cross-clamp to recipient reperfusion) and whether standard cardiopulmonary bypass was used using Cox proportional hazards models, adjusting for other risk factors.
RESULTS
The total ischemic time increased from a median under 5 hours in 2003 to over 6.2 hours in 2013. Our findings show that, when the cardiopulmonary bypass was used, there was an increase in the hazard of death (of 13% [95% CI: 5%-21%] for 1-year patient survival) for each hour of total ischemic time. However, if the cardiopulmonary bypass was not used for implantation, this link disappeared-there was no statistically significant change in mortality with increasing ischemic time.
CONCLUSIONS
We document that avoidance of bypass may remove ischemic time, within the limits of our observed range of ischemic times, as a risk factor for poor outcomes. Our data add to the evidence that bypass may be harmful to the donor lung.

Identifiants

pubmed: 37127072
pii: S1053-2498(23)01845-4
doi: 10.1016/j.healun.2023.04.012
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1378-1396

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 International Society for the Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

Auteurs

Jennifer Dawn Mehew (JD)

Statistics and Clinical Research, NHS Blood and Transplant, UK.

Rachel Hogg (R)

Statistics and Clinical Research, NHS Blood and Transplant, UK.

Stephen Clark (S)

Cardiothoracic Centre, Freeman Hospital, Newcastle upon Tyne, UK.

Karthik Santhanakrishnan (K)

Transplant Unit, Wythenshawe Hospital, Manchester University Foundation Trust, UK.

Pedro Catarino (P)

Smidt Heart Institute, Cedars-Sinai Medical Center, USA.

Jorge Mascaro (J)

Queen Elizabeth Hospital Birmingham, University of Birmingham, UK.

Ulrich Stock (U)

Royal Brompton and Harefield Hospitals, Magdi Yacoub Institute, UK.

John Dark (J)

Translational and Clinical Research Institute, Newcastle University, UK. Electronic address: j.h.dark@ncl.ac.uk.

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Classifications MeSH