Key result
DOAC use linked to ~344% greater risk of hospitalization for acute-onset interstitial lung disease.
Why the study?
DOACs offer advantages over warfarin, but concerns exist regarding their association with acute interstitial lung diseases.
Does DOAC use increase the risk of hospitalization for acute-onset interstitial lung diseases in adult patients?
Case-Control (n=178)
Does DOAC use increase the risk of hospitalization for acute-onset interstitial lung diseases in adult patients?
Answers are grounded in this paper and cite their sources.
DOAC use is associated with a significantly increased risk of hospitalization for acute-onset interstitial lung diseases, highlighting the need for clinical monitoring of respiratory symptoms in DOAC users.
BACKGROUND: Direct oral anticoagulants (DOACs) offer advantages over warfarin; however, concerns exist regarding their association with acute interstitial lung diseases (ILDs). This study investigated the risk of acute-onset ILDs associated with DOAC use. METHODS: We conducted a case-crossover study to assess the risk of hospitalization for acute-onset ILDs following DOAC initiation using the JMDC database, a Japanese administrative claims database. Patients aged ≥ 18 years hospitalized for acute-onset ILDs (April 2011-February 2023) were included. DOAC exposure was defined as ≥ 14 days within predefined 30-day windows: 1-30 days before admission (exposure period) and 60-90 and 120-150 days before admission (reference periods). The primary outcome was hospitalizations for acute-onset ILD, identified using a validated algorithm. Conditional logistic regression estimated odds ratios (ORs). Sensitivity analyses included a bidirectional case-crossover design, a case-crossover analysis with warfarin as an active comparator, weighted case-crossover analysis, and a case-case-time-control design. A descriptive cohort analysis of new DOAC and warfarin users examined ILD frequency and prognosis. RESULTS: The main case-crossover analysis included 178 patients, showing an association between DOAC use and acute-onset ILDs (adjusted OR, 4.44 [95% CI, 1.58-12.5]). Sensitivity analyses demonstrated a consistent direction of association (adjusted ORs: 3.37-6.85). In descriptive cohort analysis (52 021 DOAC and 12 026 warfarin initiators), ILD incidence was low (0.24% vs. 0.20%), but 90-day mortality was higher in the DOAC group (21% vs. 0%). CONCLUSIONS: DOAC use was associated with an increased risk of hospitalization for acute-onset ILDs. Clinicians should monitor patients on DOACs for ILD symptoms.
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Anan et al. (2026) conducted a case-control in Acute interstitial lung diseases (ILDs) (n=178). Direct oral anticoagulants (DOACs) vs. Reference periods (60-90 and 120-150 days before admission) was evaluated on Hospitalizations for acute-onset ILD (adjusted OR 4.44, 95% CI 1.58-12.5). DOAC use was associated with an increased risk of hospitalization for acute-onset interstitial lung diseases (adjusted OR 4.44; 95% CI 1.58-12.5).
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