Related Experiment Video
Updated: Jan 13, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Association of Pulse Dose Corticosteroids With Outcomes Among Patients With Acute Exacerbations of Idiopathic
Divya A Shankar1, Nicholas A Bosch1, S Reza Jafarzadeh1
1The Pulmonary Center (D. A. S., N. A. B., R. S. W., K. C. W., F. J. H., K.-D. A., A. J. W., and A. C. L.), the Evans Center for Implementation and Improvement Sciences, Department of Medicine (D. A. S., N. A. B., and M.-L. D.), and the Section of Rheumatology (S. R. J.), Boston University Chobanian and Avedisian School of Medicine; the Section of Infectious Diseases (M.-L. D.), Department of Medicine, Boston Medical Center & Boston University Chobanian & Avedisian School of Medicine; the Department of Health Law Policy & Management (M.-L. D.), Boston University School of Public Health; the Center for Health Optimization & Implementation Research (R. S. W.), VA Boston Healthcare System; and the Division of Health Systems Science (A. J. W.), University of Massachusetts Chan Medical School, Boston, MA.
Background:
Corticosteroids are a mainstay of treatment for acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF), but dosing practices vary. We leveraged between-hospital variation in propensity to administer pulse dose corticosteroids to determine the association between pulse dose corticosteroids and patient outcomes in AE-IPF.
Research Question:
Do outcomes differ for hospitalized patients who recieve pulse dose corticosteroids vs low dose corticosteroids for AE-IPF?
Study Design And Methods:
We designed an instrumental variable study informed by a target trial framework using the Premier Healthcare Database (2016-2022). We identified adults ≥ 50 years of age with AE-IPF who received a dose of IV methylprednisolone within 2 days of admission. Our exposure of interest was receipt of pulse dose methylprednisolone (≥ 250 mg); our instrument was admission to a hospital with high use of pulse dosing. We assessed association with in-hospital death/discharge to hospice and discharge home without invasive mechanical ventilation. In subgroup analyses, we tested for interaction with unit of admission (admission to ICU/intermediate care units vs ward units).
Results:
We identified 3,049 patients with AE-IPF at 177 US hospitals (pulse dose: n = 1,094; low dose: n = 1,955). Patients who received a pulse dose vs low dose had a risk difference for death/hospice of 1.2% (95% CI, -6.0% to 8.5%); for discharge home without invasive mechanical ventilation, this was 5.3% (95% CI, -2.6% to 13.1%). In subgroup analysis, receipt of pulse dosing was associated with differential risk of death/hospice by admission unit (risk difference: ICU/intermediate care: 26.3%; 95% CI, 10.1%-42.6% vs ward units: 0.1%; 95% CI, -11.1% to 11.3%; P interaction = .009), but not with differential risk of discharge home without invasive mechanical ventilation (P interaction = .18).
Interpretation:
We observed no significant benefit or harm associated with the receipt of pulse dose corticosteroids for patients with AE-IPF. However, in the subgroup of patients admitted to ICU/intermediate care, there was an increased risk of in-hospital death/discharge to hospice. Future studies should explore the use of pulse vs low-dose corticosteroids in critically ill populations with AE-IPF.
Related Concept Videos
COPD: Management Using Bronchodilators and Corticosteroids
Antiasthma Drugs: Inhaled Corticosteroids and Glucocorticoids
ICS work through a multifaceted mechanism of action. They suppress the inflammatory response caused by the proliferation of TH cells. They also reduce the transcription of the IL-2 gene, which is involved in the...
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies
Medical History
COPD: Pathogenesis and Clinical Features
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...
Chronic Obstructive Pulmonary Disease-V: Management
Smoking Cessation

