Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil

Abstract Background Advanced lung disease in adult cystic fibrosis (CF) drives most clinical care requirements. The aim was to evaluate outcome (time to death while in the study) in a cohort of adult CF patients with severe lung disease, and to determine the association among baseline patient charac...

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Main Authors: Guilherme Figueiredo Silva, Nicholas J. Simmonds, Paulo de Tarso Roth Dalcin
Format: Article
Language:English
Published: BMC 2020-07-01
Series:BMC Pulmonary Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12890-020-01223-6
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spelling doaj-a1446fe8d79e45ed9584689469b753562020-11-25T03:20:52ZengBMCBMC Pulmonary Medicine1471-24662020-07-012011810.1186/s12890-020-01223-6Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern BrazilGuilherme Figueiredo Silva0Nicholas J. Simmonds1Paulo de Tarso Roth Dalcin2Programa de Pós-Graduação em Ciências Pneumológicas, UFRGS; Serviço de Pneumologia, HCPADepartment of Cystic Fibrosis, Royal Brompton Hospital and Imperial CollegePrograma de Pós-Graduação em Ciências Pneumológicas, UFRGSAbstract Background Advanced lung disease in adult cystic fibrosis (CF) drives most clinical care requirements. The aim was to evaluate outcome (time to death while in the study) in a cohort of adult CF patients with severe lung disease, and to determine the association among baseline patient characteristics and outcome. Methods A retrospective cohort study was performed and clinical records between 2000 and 2015 were reviewed. Severe lung disease was defined as forced expiratory volume in the first second (FEV1) < 30% of predicted. Outcomes of all patients, including their date of death or transplantation, were determined till January 1st, 2016. Clinical data were recorded at the entry date. Results Among 39 subjects included in the study, 20 (51.3%) died, 16 (41.0%) underwent bilateral lung transplantation, and 3 were alive at the end of the study period. Two variables were independently associated with death: body mass index (BMI ≥ 18.5 kg/m2) (HR = 0.78, 95% CI = 0.64–0.96 and p = 0.017) and use of tobramycin inhalation therapy (HR = 3.82, 95% CI = 1.38–10.6 and p = 0.010). Median survival was 37 (95% CI = 16.4–57.6) months. The best cut-off point for BMI was 18.5 kg/m2. Median survival in patients with BMI < 18.5 kg/m2 was 36 months (95% CI = 18.7–53.3). Conclusion Median survival of CF subjects with FEV1 < 30% was 37 months. BMI and tobramycin inhalation therapy were independently associated with death. Median survival in patients with BMI < 18.5 kg/m2 was significantly lower than in patients with BMI ≥ 18.5 kg/m2. The association of tobramycin inhalation with death was interpreted as confounding by severity (use was reserved for advanced lung disease).http://link.springer.com/article/10.1186/s12890-020-01223-6Cystic fibrosisFEV1Advanced lung diseaseSurvival
collection DOAJ
language English
format Article
sources DOAJ
author Guilherme Figueiredo Silva
Nicholas J. Simmonds
Paulo de Tarso Roth Dalcin
spellingShingle Guilherme Figueiredo Silva
Nicholas J. Simmonds
Paulo de Tarso Roth Dalcin
Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
BMC Pulmonary Medicine
Cystic fibrosis
FEV1
Advanced lung disease
Survival
author_facet Guilherme Figueiredo Silva
Nicholas J. Simmonds
Paulo de Tarso Roth Dalcin
author_sort Guilherme Figueiredo Silva
title Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
title_short Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
title_full Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
title_fullStr Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
title_full_unstemmed Clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in Porto Alegre, southern Brazil
title_sort clinical characteristics and outcomes in adult cystic fibrosis patients with severe lung disease in porto alegre, southern brazil
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2020-07-01
description Abstract Background Advanced lung disease in adult cystic fibrosis (CF) drives most clinical care requirements. The aim was to evaluate outcome (time to death while in the study) in a cohort of adult CF patients with severe lung disease, and to determine the association among baseline patient characteristics and outcome. Methods A retrospective cohort study was performed and clinical records between 2000 and 2015 were reviewed. Severe lung disease was defined as forced expiratory volume in the first second (FEV1) < 30% of predicted. Outcomes of all patients, including their date of death or transplantation, were determined till January 1st, 2016. Clinical data were recorded at the entry date. Results Among 39 subjects included in the study, 20 (51.3%) died, 16 (41.0%) underwent bilateral lung transplantation, and 3 were alive at the end of the study period. Two variables were independently associated with death: body mass index (BMI ≥ 18.5 kg/m2) (HR = 0.78, 95% CI = 0.64–0.96 and p = 0.017) and use of tobramycin inhalation therapy (HR = 3.82, 95% CI = 1.38–10.6 and p = 0.010). Median survival was 37 (95% CI = 16.4–57.6) months. The best cut-off point for BMI was 18.5 kg/m2. Median survival in patients with BMI < 18.5 kg/m2 was 36 months (95% CI = 18.7–53.3). Conclusion Median survival of CF subjects with FEV1 < 30% was 37 months. BMI and tobramycin inhalation therapy were independently associated with death. Median survival in patients with BMI < 18.5 kg/m2 was significantly lower than in patients with BMI ≥ 18.5 kg/m2. The association of tobramycin inhalation with death was interpreted as confounding by severity (use was reserved for advanced lung disease).
topic Cystic fibrosis
FEV1
Advanced lung disease
Survival
url http://link.springer.com/article/10.1186/s12890-020-01223-6
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