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Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant

BACKGROUND: Previous studies suggest that infant heart transplant (HT) recipients are at higher risk of developing severe primary graft dysfunction (PGD) than older children. We sought to identify risk factors for developing severe PGD in infant HT recipients. METHODS AND RESULTS: We identified all...

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Autores principales: Singh, Tajinder P., Profita, Elizabeth L., Rycus, Peter, Thiagarajan, Ravi, Gauvreau, Kimberlee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403271/
https://www.ncbi.nlm.nih.gov/pubmed/34184543
http://dx.doi.org/10.1161/JAHA.121.021082
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author Singh, Tajinder P.
Profita, Elizabeth L.
Rycus, Peter
Thiagarajan, Ravi
Gauvreau, Kimberlee
author_facet Singh, Tajinder P.
Profita, Elizabeth L.
Rycus, Peter
Thiagarajan, Ravi
Gauvreau, Kimberlee
author_sort Singh, Tajinder P.
collection PubMed
description BACKGROUND: Previous studies suggest that infant heart transplant (HT) recipients are at higher risk of developing severe primary graft dysfunction (PGD) than older children. We sought to identify risk factors for developing severe PGD in infant HT recipients. METHODS AND RESULTS: We identified all HT recipients aged <1 year in the United States during 1996 to 2015 using the Organ Procurement and Transplant Network database. We linked their data to ELSO (Extracorporeal Life Support Organization) registry data to identify those with severe PGD, defined by initiation of extracorporeal membrane oxygenation support for PGD within 2 days following HT. We used multivariable logistic regression to assess risk factors for developing severe PGD. Of 1718 infants analyzed, 600 (35%) were <90 days old and 1079 (63%) had congenital heart disease. Overall, 134 (7.8%) developed severe PGD; 95 (71%) were initiated on extracorporeal membrane oxygenation support on the day of HT, 34 (25%) the next day, and 5 (4%) the following day. In adjusted analysis, recipient congenital heart disease, extracorporeal membrane oxygenation, or biventricular assist device support at transplant, recipient blood type AB, donor‐recipient weight ratio <0.9, and graft ischemic time ≥4 hours were independently associated with developing severe PGD whereas left ventricular assist device support at HT was not. One‐year graft survival was 48% in infants with severe PGD versus 87% without severe PGD. CONCLUSIONS: Infant HT recipients with severe PGD have poor graft survival. Although some recipient‐level risk factors are nonmodifiable, avoiding modifiable risk factors may mitigate further risk in infants at high risk of developing severe PGD.
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spelling pubmed-84032712021-09-03 Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant Singh, Tajinder P. Profita, Elizabeth L. Rycus, Peter Thiagarajan, Ravi Gauvreau, Kimberlee J Am Heart Assoc Original Research BACKGROUND: Previous studies suggest that infant heart transplant (HT) recipients are at higher risk of developing severe primary graft dysfunction (PGD) than older children. We sought to identify risk factors for developing severe PGD in infant HT recipients. METHODS AND RESULTS: We identified all HT recipients aged <1 year in the United States during 1996 to 2015 using the Organ Procurement and Transplant Network database. We linked their data to ELSO (Extracorporeal Life Support Organization) registry data to identify those with severe PGD, defined by initiation of extracorporeal membrane oxygenation support for PGD within 2 days following HT. We used multivariable logistic regression to assess risk factors for developing severe PGD. Of 1718 infants analyzed, 600 (35%) were <90 days old and 1079 (63%) had congenital heart disease. Overall, 134 (7.8%) developed severe PGD; 95 (71%) were initiated on extracorporeal membrane oxygenation support on the day of HT, 34 (25%) the next day, and 5 (4%) the following day. In adjusted analysis, recipient congenital heart disease, extracorporeal membrane oxygenation, or biventricular assist device support at transplant, recipient blood type AB, donor‐recipient weight ratio <0.9, and graft ischemic time ≥4 hours were independently associated with developing severe PGD whereas left ventricular assist device support at HT was not. One‐year graft survival was 48% in infants with severe PGD versus 87% without severe PGD. CONCLUSIONS: Infant HT recipients with severe PGD have poor graft survival. Although some recipient‐level risk factors are nonmodifiable, avoiding modifiable risk factors may mitigate further risk in infants at high risk of developing severe PGD. John Wiley and Sons Inc. 2021-06-29 /pmc/articles/PMC8403271/ /pubmed/34184543 http://dx.doi.org/10.1161/JAHA.121.021082 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Singh, Tajinder P.
Profita, Elizabeth L.
Rycus, Peter
Thiagarajan, Ravi
Gauvreau, Kimberlee
Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title_full Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title_fullStr Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title_full_unstemmed Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title_short Risk Factors for Severe Primary Graft Dysfunction in Infants Following Heart Transplant
title_sort risk factors for severe primary graft dysfunction in infants following heart transplant
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403271/
https://www.ncbi.nlm.nih.gov/pubmed/34184543
http://dx.doi.org/10.1161/JAHA.121.021082
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