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Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death
BACKGROUND: The donor’s mode of brain death (BD), being associated with impairment of myocardial function and hemodynamic performance, impacts the prognosis of the heart transplantation (HTx) recipient. METHODS: All patients who underwent HTx between 1996 and 2017 were categorized according to donor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647135/ https://www.ncbi.nlm.nih.gov/pubmed/31331354 http://dx.doi.org/10.1186/s13019-019-0963-2 |
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author | Ram, Eilon Lavee, Jacob Freimark, Dov Maor, Elad Kassif, Yigal Sternik, Leonid Kogan, Alexander Peled, Yael |
author_facet | Ram, Eilon Lavee, Jacob Freimark, Dov Maor, Elad Kassif, Yigal Sternik, Leonid Kogan, Alexander Peled, Yael |
author_sort | Ram, Eilon |
collection | PubMed |
description | BACKGROUND: The donor’s mode of brain death (BD), being associated with impairment of myocardial function and hemodynamic performance, impacts the prognosis of the heart transplantation (HTx) recipient. METHODS: All patients who underwent HTx between 1996 and 2017 were categorized according to donor’s BD mechanism: traumatic BD (TBD) versus non-traumatic BD (NTBD). RESULTS: The TBD group included 105 recipients, and the NTBD group, 85 recipients. Kaplan-Meier survival analysis showed that overall survival was significantly higher for recipients of TBD hearts (10-year survival 58.1 vs. 37.6%, p = 0.044). Consistently, multivariate analysis showed that TBD was independently associated with a significant 43% reduction in mortality [95% confidence interval (CI) 0.42–0.75, p = 0.033]. Rejection rate was lower in the TBD group (total rejection score 0.44 ± 0.32 vs. 0.51 ± 0.38, p = 0.04; any rejection score 0.38 ± 0.26 vs. 0.45 ± 0.31, p = 0.030), and freedom from cardiac allograft vasculopathy (CAV) was significantly higher in recipients of traumatic vs. non-traumatic donors (10 years: 82.9 vs. 62.4%, log-rank p-value = 0.024). Multivariate analysis showed a significant 42% reduction in CAV [hazard ratio (HR) = 0.58, 95% CI 0.51–0.85, p = 0.022). CONCLUSION: Mode of brain death significantly impacts HTx outcomes, with TBD being associated with reduced mortality, rejections and CAV. |
format | Online Article Text |
id | pubmed-6647135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66471352019-07-31 Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death Ram, Eilon Lavee, Jacob Freimark, Dov Maor, Elad Kassif, Yigal Sternik, Leonid Kogan, Alexander Peled, Yael J Cardiothorac Surg Research Article BACKGROUND: The donor’s mode of brain death (BD), being associated with impairment of myocardial function and hemodynamic performance, impacts the prognosis of the heart transplantation (HTx) recipient. METHODS: All patients who underwent HTx between 1996 and 2017 were categorized according to donor’s BD mechanism: traumatic BD (TBD) versus non-traumatic BD (NTBD). RESULTS: The TBD group included 105 recipients, and the NTBD group, 85 recipients. Kaplan-Meier survival analysis showed that overall survival was significantly higher for recipients of TBD hearts (10-year survival 58.1 vs. 37.6%, p = 0.044). Consistently, multivariate analysis showed that TBD was independently associated with a significant 43% reduction in mortality [95% confidence interval (CI) 0.42–0.75, p = 0.033]. Rejection rate was lower in the TBD group (total rejection score 0.44 ± 0.32 vs. 0.51 ± 0.38, p = 0.04; any rejection score 0.38 ± 0.26 vs. 0.45 ± 0.31, p = 0.030), and freedom from cardiac allograft vasculopathy (CAV) was significantly higher in recipients of traumatic vs. non-traumatic donors (10 years: 82.9 vs. 62.4%, log-rank p-value = 0.024). Multivariate analysis showed a significant 42% reduction in CAV [hazard ratio (HR) = 0.58, 95% CI 0.51–0.85, p = 0.022). CONCLUSION: Mode of brain death significantly impacts HTx outcomes, with TBD being associated with reduced mortality, rejections and CAV. BioMed Central 2019-07-22 /pmc/articles/PMC6647135/ /pubmed/31331354 http://dx.doi.org/10.1186/s13019-019-0963-2 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ram, Eilon Lavee, Jacob Freimark, Dov Maor, Elad Kassif, Yigal Sternik, Leonid Kogan, Alexander Peled, Yael Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title | Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title_full | Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title_fullStr | Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title_full_unstemmed | Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title_short | Improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
title_sort | improved long-term outcomes after heart transplantation utilizing donors with a traumatic mode of brain death |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647135/ https://www.ncbi.nlm.nih.gov/pubmed/31331354 http://dx.doi.org/10.1186/s13019-019-0963-2 |
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