In-Hospital Mortality in Patients with Idiopathic Pulmonary Fibrosis: A US Cohort Study
- PMID: 31541276
- PMCID: PMC6861436
- DOI: 10.1007/s00408-019-00270-z
In-Hospital Mortality in Patients with Idiopathic Pulmonary Fibrosis: A US Cohort Study
Abstract
Purpose: In patients with idiopathic pulmonary fibrosis (IPF), hospitalizations are associated with high mortality. We sought to determine in-hospital mortality rates and factors associated with in-hospital mortality in patients with IPF.
Methods: Patients with IPF were identified from the Premier Healthcare Database, a representative administrative dataset that includes > 20% of hospital discharges in the US, using an algorithm based on diagnostic codes and billing data. We used logistic regression to analyze associations between patient-, hospital-, and treatment-related characteristics and a composite primary outcome of death during the index visit, lung transplant during the index visit and > 1 day after admission, or death during a readmission within 90 days.
Results: The cohort comprised 6665 patients with IPF hospitalized between October 2011 and October 2014. A total of 963 (14.4%) met the primary outcome. Factors significantly associated with a higher risk of the primary outcome included mechanical ventilation [odds ratio 4.65 (95% CI 3.73, 5.80)], admission to the intensive care unit [1.83 (1.52, 2.21)], treatment with opioids (3.06 [2.57, 3.65]), and a diagnosis of pneumonia [1.44 (1.21, 1.71)]. Factors significantly associated with a lower risk included concurrent chronic obstructive pulmonary disease [0.65 (0.55, 0.77)] and female sex [0.67 (0.57, 0.79)].
Conclusions: Patients with IPF, particularly those receiving mechanical ventilation or intensive care, are at substantial risk of death or lung transplant during hospitalization or death during a readmission within 90 days.
Keywords: Critical care; Hospitalization; Intensive care; Interstitial lung disease; Mechanical ventilation.
Conflict of interest statement
MTD, OM, BRS, and SMP are faculty members in the Duke Clinical Research Institute (DCRI), which received funding from Boehringer Ingelheim Pharmaceuticals, Inc (BIPI) to coordinate this project. MTD also reports grants and personal fees from Boehringer Ingelheim, and personal fees from Roche. JL was an employee of DCRI at the time that this research was conducted. JJ, DB, and SBR are employees of Premier, Inc which received funding from BIPI for work related to this project. SB, TL, and CSC are employees of BIPI
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