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Abnormal one-year post-lung transplant spirometry is a significant predictor of increased mortality and chronic lung allograft dysfunction.

Authors :
Paraskeva MA
Borg BM
Paul E
Fuller J
Westall GP
Snell GI
Source :
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation [J Heart Lung Transplant] 2021 Dec; Vol. 40 (12), pp. 1649-1657. Date of Electronic Publication: 2021 Aug 21.
Publication Year :
2021

Abstract

Background: The prognostic value of evaluating spirometry at a fixed time point using standardized population reference has not previously been evaluated. Our aim was to assess the association between spirometric phenotype at 12 months (Spiro <subscript>12M</subscript> ), survival and incidence of chronic lung allograft dysfunction (CLAD) in bilateral lung transplant recipients.<br />Methods: We conducted a retrospective cohort study of bilateral lung transplant recipients transplanted between January 2003 and September 2012. We defined Spiro <subscript>12M</subscript> as the mean of the 2 prebronchodilator FEV <subscript>1</subscript> measurements 12-month post-transplant. Normal spirometry was defined as FEV <subscript>1</subscript> /FVC ≥0.7 and FEV1≥80% and FVC≥80% predicted population-based values for that recipient. Abnormal spirometry was defined as failure to attain normal function by 12-months. We used a Cox regression model to assess the association between Spiro <subscript>12M</subscript> , survival, and CLAD. We used logistic regression to assess potential pretransplant donor and recipient factors associated with abnormal Spiro <subscript>12M</subscript> RESULTS: One hundred and eleven (51%) lung transplant recipients normalized their Spiro <subscript>12M</subscript> . Normal Spiro <subscript>12M</subscript> was associated improved survival (hazard ratio [HR] 0.60, 95% confidence interval [CI] 0.41-0.88], p = 0.009. Each 10% decrement in FEV <subscript>1</subscript> increased the risk of death in a stepwise fashion. Additionally, CLAD was reduced in those with normal Spiro <subscript>12M</subscript> (HR:0.65, 95%CI:0.46-0.92, p = 0.016). Donor smoking history (OR:2.93, 95% CI:1.21-7.09; p = 0.018) and mechanical ventilation time in hours (OR:1.03, 95% CI:1.004-1.05; p = 0.02) were identified as independent predictors of abnormal Spiro <subscript>12M</subscript> .<br />Conclusions: Abnormal Spiro <subscript>12M</subscript> is associated with increased mortality and the development of CLAD. The effect is dose dependent with increased dysfunction corresponding to increased risk. This assessment of phenotype at 12-months can easily be incorporated into standard of care.<br /> (Copyright © 2021 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1557-3117
Volume :
40
Issue :
12
Database :
MEDLINE
Journal :
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
Publication Type :
Academic Journal
Accession number :
34548197
Full Text :
https://doi.org/10.1016/j.healun.2021.08.003