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A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018
Hospitalizations are common in patients with idiopathic pulmonary fibrosis (IPF) and are associated with high mortality. We used data from the Premier Healthcare Database to determine in-hospital mortality rates and the factors associated with in-hospital mortality in patients with IPF in the era of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676591/ https://www.ncbi.nlm.nih.gov/pubmed/33217820 http://dx.doi.org/10.1097/MD.0000000000023143 |
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author | Durheim, Michael T. Judy, Jennifer Bender, Shaun Neely, Megan L. Baumer, Dorothy Robinson, Scott B. Conoscenti, Craig S. Leonard, Thomas B. Lazarus, Howard M. Palmer, Scott M. |
author_facet | Durheim, Michael T. Judy, Jennifer Bender, Shaun Neely, Megan L. Baumer, Dorothy Robinson, Scott B. Conoscenti, Craig S. Leonard, Thomas B. Lazarus, Howard M. Palmer, Scott M. |
author_sort | Durheim, Michael T. |
collection | PubMed |
description | Hospitalizations are common in patients with idiopathic pulmonary fibrosis (IPF) and are associated with high mortality. We used data from the Premier Healthcare Database to determine in-hospital mortality rates and the factors associated with in-hospital mortality in patients with IPF in the era of approved antifibrotic drugs. The Premier Healthcare Database is a detailed and broadly representative database of hospital admissions and discharges in the US. Patients with IPF who were hospitalized between 1 January 2015 and 28 February 2018 were identified using a diagnostic algorithm comprising International Classification of Diseases -9 and International Classification of Diseases -10 diagnostic codes and billing data. Associations between patient-, hospital- and treatment-related factors and a composite outcome of death during the index visit, lung transplant during the index visit but >1 day after admission, or death during a readmission within 90 days of the index visit were analyzed using logistic regression. The cohort comprised 9667 hospitalized patients with IPF. In total, 1414 patients (14.6%) met the composite outcome: 1036 (10.7%) died during the index visit, 371 (3.8%) died during a readmission within 90 days; 7 (0.1%) underwent lung transplant >1 day after admission. Factors significantly associated with a higher risk of the composite outcome included mechanical ventilation (odds ratio 6.41 [95% CI: 5.24, 7.84]), admission to the intensive care unit (1.73 [1.49, 2.00]), attendance by a critical care physician (2.12 [1.33, 3.38]), older age (1.20 [1.12, 1.28] per 10-year increase), and use of intravenous steroids (1.16 [1.00, 1.34]), intravenous antibiotics (1.49 [1.22, 1.83]) and opioids (3.41 [2.95, 3.93]). Factors significantly associated with a lower risk of the composite outcome included female sex (0.70 [0.61, 0.80]), comorbid chronic obstructive pulmonary disease (0.69 [0.60, 0.78]), attendance by a family medicine physician (0.67 [0.48, 0.94]) or internal medicine physician (0.59 [0.46, 0.75]), and use of oral steroids (0.62 [0.51, 0.77]), statins (0.76 [0.67, 0.87]) and proton pump inhibitors (0.80 [0.70, 0.92]). In conclusion, patients with IPF are at risk of mortality during a hospital stay or readmission within 90 days, particularly those who receive mechanical ventilation. |
format | Online Article Text |
id | pubmed-7676591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-76765912020-11-24 A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 Durheim, Michael T. Judy, Jennifer Bender, Shaun Neely, Megan L. Baumer, Dorothy Robinson, Scott B. Conoscenti, Craig S. Leonard, Thomas B. Lazarus, Howard M. Palmer, Scott M. Medicine (Baltimore) 6700 Hospitalizations are common in patients with idiopathic pulmonary fibrosis (IPF) and are associated with high mortality. We used data from the Premier Healthcare Database to determine in-hospital mortality rates and the factors associated with in-hospital mortality in patients with IPF in the era of approved antifibrotic drugs. The Premier Healthcare Database is a detailed and broadly representative database of hospital admissions and discharges in the US. Patients with IPF who were hospitalized between 1 January 2015 and 28 February 2018 were identified using a diagnostic algorithm comprising International Classification of Diseases -9 and International Classification of Diseases -10 diagnostic codes and billing data. Associations between patient-, hospital- and treatment-related factors and a composite outcome of death during the index visit, lung transplant during the index visit but >1 day after admission, or death during a readmission within 90 days of the index visit were analyzed using logistic regression. The cohort comprised 9667 hospitalized patients with IPF. In total, 1414 patients (14.6%) met the composite outcome: 1036 (10.7%) died during the index visit, 371 (3.8%) died during a readmission within 90 days; 7 (0.1%) underwent lung transplant >1 day after admission. Factors significantly associated with a higher risk of the composite outcome included mechanical ventilation (odds ratio 6.41 [95% CI: 5.24, 7.84]), admission to the intensive care unit (1.73 [1.49, 2.00]), attendance by a critical care physician (2.12 [1.33, 3.38]), older age (1.20 [1.12, 1.28] per 10-year increase), and use of intravenous steroids (1.16 [1.00, 1.34]), intravenous antibiotics (1.49 [1.22, 1.83]) and opioids (3.41 [2.95, 3.93]). Factors significantly associated with a lower risk of the composite outcome included female sex (0.70 [0.61, 0.80]), comorbid chronic obstructive pulmonary disease (0.69 [0.60, 0.78]), attendance by a family medicine physician (0.67 [0.48, 0.94]) or internal medicine physician (0.59 [0.46, 0.75]), and use of oral steroids (0.62 [0.51, 0.77]), statins (0.76 [0.67, 0.87]) and proton pump inhibitors (0.80 [0.70, 0.92]). In conclusion, patients with IPF are at risk of mortality during a hospital stay or readmission within 90 days, particularly those who receive mechanical ventilation. Lippincott Williams & Wilkins 2020-11-20 /pmc/articles/PMC7676591/ /pubmed/33217820 http://dx.doi.org/10.1097/MD.0000000000023143 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6700 Durheim, Michael T. Judy, Jennifer Bender, Shaun Neely, Megan L. Baumer, Dorothy Robinson, Scott B. Conoscenti, Craig S. Leonard, Thomas B. Lazarus, Howard M. Palmer, Scott M. A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title | A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title_full | A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title_fullStr | A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title_full_unstemmed | A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title_short | A retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
title_sort | retrospective study of in-hospital mortality in patients with idiopathic pulmonary fibrosis between 2015 and 2018 |
topic | 6700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676591/ https://www.ncbi.nlm.nih.gov/pubmed/33217820 http://dx.doi.org/10.1097/MD.0000000000023143 |
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