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Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival

Although pulmonary function testing (PFT) is typically performed for heart transplant evaluation, the prognostic utility of PFTs after transplantation is unknown. We evaluated whether PFT parameters were correlated with outcomes following heart transplantation. METHODS. International Society for Hea...

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Autores principales: Lundgren, Scott W., Lowes, Brian D., Lyden, Elizabeth, Zolty, Ronald, Burdorf, Adam, Hyden, Marshall, Um, John, Stoller, Douglas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425848/
https://www.ncbi.nlm.nih.gov/pubmed/34514107
http://dx.doi.org/10.1097/TXD.0000000000001177
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author Lundgren, Scott W.
Lowes, Brian D.
Lyden, Elizabeth
Zolty, Ronald
Burdorf, Adam
Hyden, Marshall
Um, John
Stoller, Douglas A.
author_facet Lundgren, Scott W.
Lowes, Brian D.
Lyden, Elizabeth
Zolty, Ronald
Burdorf, Adam
Hyden, Marshall
Um, John
Stoller, Douglas A.
author_sort Lundgren, Scott W.
collection PubMed
description Although pulmonary function testing (PFT) is typically performed for heart transplant evaluation, the prognostic utility of PFTs after transplantation is unknown. We evaluated whether PFT parameters were correlated with outcomes following heart transplantation. METHODS. International Society for Heart and Lung Transplantation Thoracic Organ Transplant Registry data were utilized. Survival was assessed using Kaplan-Meier method and compared via log-rank test. Cox proportional hazard modeling was used to evaluate univariate and multivariate predictors of survival. RESULTS. Eight hundred two patients pretransplant PFT data were available for evaluation. Forced expiratory volume in 1 s (FEV1) < 50% predicted (P < 0.0001), and forced vital capacity (FVC) < 50% predicted each had significantly higher mortality (P = 0.001) compared with patients with FEV1 or FVC 50%–80% or >80%. FEV1/FVC < 0.7 was not associated with increased mortality. FEV1 and FVC below 50% both predicted longer lengths of stay (P = 0.028 for FEV1 and P = 0.0075 for FVC). After adjusting for male gender, age, body mass index, smoking history, chronic obstructive pulmonary disease, creatinine, albumin, and total bilirubin, FEV1 < 50% (hazard ratio, 4.91; P < 0.0001; 95% confidence interval, 2.69-8.94) and FVC < 50% (hazard ratio, 2.75; P = 0.003; 95% confidence interval, 1.4-5.4) both remained independent predictors of mortality. CONCLUSIONS. Abnormal pulmonary function (FEV1 or FVC below 50% of predicted) pre–heart transplantation is associated with increased mortality and longer lengths of stay posttransplant.
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spelling pubmed-84258482021-09-10 Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival Lundgren, Scott W. Lowes, Brian D. Lyden, Elizabeth Zolty, Ronald Burdorf, Adam Hyden, Marshall Um, John Stoller, Douglas A. Transplant Direct Heart Transplantation Although pulmonary function testing (PFT) is typically performed for heart transplant evaluation, the prognostic utility of PFTs after transplantation is unknown. We evaluated whether PFT parameters were correlated with outcomes following heart transplantation. METHODS. International Society for Heart and Lung Transplantation Thoracic Organ Transplant Registry data were utilized. Survival was assessed using Kaplan-Meier method and compared via log-rank test. Cox proportional hazard modeling was used to evaluate univariate and multivariate predictors of survival. RESULTS. Eight hundred two patients pretransplant PFT data were available for evaluation. Forced expiratory volume in 1 s (FEV1) < 50% predicted (P < 0.0001), and forced vital capacity (FVC) < 50% predicted each had significantly higher mortality (P = 0.001) compared with patients with FEV1 or FVC 50%–80% or >80%. FEV1/FVC < 0.7 was not associated with increased mortality. FEV1 and FVC below 50% both predicted longer lengths of stay (P = 0.028 for FEV1 and P = 0.0075 for FVC). After adjusting for male gender, age, body mass index, smoking history, chronic obstructive pulmonary disease, creatinine, albumin, and total bilirubin, FEV1 < 50% (hazard ratio, 4.91; P < 0.0001; 95% confidence interval, 2.69-8.94) and FVC < 50% (hazard ratio, 2.75; P = 0.003; 95% confidence interval, 1.4-5.4) both remained independent predictors of mortality. CONCLUSIONS. Abnormal pulmonary function (FEV1 or FVC below 50% of predicted) pre–heart transplantation is associated with increased mortality and longer lengths of stay posttransplant. Lippincott Williams & Wilkins 2021-09-07 /pmc/articles/PMC8425848/ /pubmed/34514107 http://dx.doi.org/10.1097/TXD.0000000000001177 Text en Copyright © 2021 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Heart Transplantation
Lundgren, Scott W.
Lowes, Brian D.
Lyden, Elizabeth
Zolty, Ronald
Burdorf, Adam
Hyden, Marshall
Um, John
Stoller, Douglas A.
Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title_full Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title_fullStr Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title_full_unstemmed Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title_short Pulmonary Function Testing Pre–heart Transplant Predicts Posttransplant Survival
title_sort pulmonary function testing pre–heart transplant predicts posttransplant survival
topic Heart Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425848/
https://www.ncbi.nlm.nih.gov/pubmed/34514107
http://dx.doi.org/10.1097/TXD.0000000000001177
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