In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs

Abstract Background Idiopathic pulmonary fibrosis (IPF) is a devastating condition characterized by progressive lung function decline and early mortality. While early accurate diagnosis is essential for IPF treatment, data evaluating the impact of hospital academic status on IPF-related mortality re...

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Main Authors: Shehabaldin Alqalyoobi, Evans R. Fernández Pérez, Justin M. Oldham
Format: Article
Language:English
Published: BMC 2020-11-01
Series:BMC Pulmonary Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12890-020-01328-y
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spelling doaj-97a52bc00d3448069c246698ba0f35f42020-11-25T04:07:01ZengBMCBMC Pulmonary Medicine1471-24662020-11-0120111110.1186/s12890-020-01328-yIn-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programsShehabaldin Alqalyoobi0Evans R. Fernández Pérez1Justin M. Oldham2Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, East Carolina University-Brody School of MedicineDivision of Pulmonary, Critical Care and Sleep Medicine, National Jewish HealthDepartment of Internal Medicine; Division of Pulmonary, Critical Care and Sleep Medicine, University of California at DavisAbstract Background Idiopathic pulmonary fibrosis (IPF) is a devastating condition characterized by progressive lung function decline and early mortality. While early accurate diagnosis is essential for IPF treatment, data evaluating the impact of hospital academic status on IPF-related mortality remains limited. Here we examined in-hospital mortality trends for patients with IPF from 2013 to 2017. We hypothesized that in-hospital IPF mortality would be influenced by hospital academic setting. Methods Hospitalization data was extracted from the National Inpatient Sample (NIS) for subjects with an international classification of disease code for IPF. In-hospital mortality stratified by hospital setting (academic versus non-academic) was the primary outcome of interest, with secondary analyses performed for subgroups with and without respiratory failure and requiring mechanical ventilation. Predictors of mortality were then assessed. Results Among 93,680 patients with IPF requiring hospitalization, 58,450 (62.4%) were admitted to academic institutions. In-hospital mortality decreased significantly in those admitted to an academic hospital (p < 0.001) but remained unchanged in patients admitted to a non-academic hospital. A plateau in-hospital mortality was observed among all hospitalized patients (p = 0.12), with a significant decrease observed for patients with admitted respiratory failure (p < 0.001) and those placed on mechanic ventilation (p < 0.001). Conclusion In-hospital mortality decreased significantly for patients with IPF admitted to an academic hospital, suggesting that management strategies may differ by hospital setting. Mortality among those with respiratory failure and those requiring mechanical ventilation has dropped significantly. Our findings may underscore the importance of promoting early referral to an academic institution and adherence to international treatment guidelines.http://link.springer.com/article/10.1186/s12890-020-01328-yIdiopathic pulmonary fibrosisMortalityAcademic hospitalRespiratory failureMechanical ventilation
collection DOAJ
language English
format Article
sources DOAJ
author Shehabaldin Alqalyoobi
Evans R. Fernández Pérez
Justin M. Oldham
spellingShingle Shehabaldin Alqalyoobi
Evans R. Fernández Pérez
Justin M. Oldham
In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
BMC Pulmonary Medicine
Idiopathic pulmonary fibrosis
Mortality
Academic hospital
Respiratory failure
Mechanical ventilation
author_facet Shehabaldin Alqalyoobi
Evans R. Fernández Pérez
Justin M. Oldham
author_sort Shehabaldin Alqalyoobi
title In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
title_short In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
title_full In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
title_fullStr In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
title_full_unstemmed In-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the United States between 2013-2017: a comparison of academic and non-academic programs
title_sort in-hospital mortality trends among patients with idiopathic pulmonary fibrosis in the united states between 2013-2017: a comparison of academic and non-academic programs
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2020-11-01
description Abstract Background Idiopathic pulmonary fibrosis (IPF) is a devastating condition characterized by progressive lung function decline and early mortality. While early accurate diagnosis is essential for IPF treatment, data evaluating the impact of hospital academic status on IPF-related mortality remains limited. Here we examined in-hospital mortality trends for patients with IPF from 2013 to 2017. We hypothesized that in-hospital IPF mortality would be influenced by hospital academic setting. Methods Hospitalization data was extracted from the National Inpatient Sample (NIS) for subjects with an international classification of disease code for IPF. In-hospital mortality stratified by hospital setting (academic versus non-academic) was the primary outcome of interest, with secondary analyses performed for subgroups with and without respiratory failure and requiring mechanical ventilation. Predictors of mortality were then assessed. Results Among 93,680 patients with IPF requiring hospitalization, 58,450 (62.4%) were admitted to academic institutions. In-hospital mortality decreased significantly in those admitted to an academic hospital (p < 0.001) but remained unchanged in patients admitted to a non-academic hospital. A plateau in-hospital mortality was observed among all hospitalized patients (p = 0.12), with a significant decrease observed for patients with admitted respiratory failure (p < 0.001) and those placed on mechanic ventilation (p < 0.001). Conclusion In-hospital mortality decreased significantly for patients with IPF admitted to an academic hospital, suggesting that management strategies may differ by hospital setting. Mortality among those with respiratory failure and those requiring mechanical ventilation has dropped significantly. Our findings may underscore the importance of promoting early referral to an academic institution and adherence to international treatment guidelines.
topic Idiopathic pulmonary fibrosis
Mortality
Academic hospital
Respiratory failure
Mechanical ventilation
url http://link.springer.com/article/10.1186/s12890-020-01328-y
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