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Effect of Antimicrobial Therapy on Respiratory Hospitalization or Death in Adults With Idiopathic Pulmonary Fibrosis

医学 随机对照试验 内科学 临床终点 安慰剂 抗菌剂 儿科 外科 病理 有机化学 化学 替代医学
作者
Fernando J. Martínez,Eric Yow,Kevin R. Flaherty,Laurie D. Snyder,Michael T. Durheim,Stephen R. Wisniewski,Frank C. Sciurba,Ganesh Raghu,Maria M. Brooks,Dong‐Yun Kim,Daniel F. Dilling,Gerard J. Criner,Hyun Kim,Elizabeth A. Belloli,Anoop M. Nambiar,Mary Beth Scholand,Kevin J. Anstrom,Imre Noth,Rebecca Bascom,Scott Beegle
出处
期刊:JAMA [American Medical Association]
卷期号:325 (18): 1841-1841 被引量:66
标识
DOI:10.1001/jama.2021.4956
摘要

Importance

Alteration in lung microbes is associated with disease progression in idiopathic pulmonary fibrosis.

Objective

To assess the effect of antimicrobial therapy on clinical outcomes.

Design, Setting, and Participants

Pragmatic, randomized, unblinded clinical trial conducted across 35 US sites. A total of 513 patients older than 40 years were randomized from August 2017 to June 2019 (final follow-up was January 2020).

Interventions

Patients were randomized in a 1:1 allocation ratio to receive antimicrobials (n = 254) or usual care alone (n = 259). Antimicrobials included co-trimoxazole (trimethoprim 160 mg/sulfamethoxazole 800 mg twice daily plus folic acid 5 mg daily, n = 128) or doxycycline (100 mg once daily if body weight <50 kg or 100 mg twice daily if ≥50 kg, n = 126). No placebo was administered in the usual care alone group.

Main Outcomes and Measures

The primary end point was time to first nonelective respiratory hospitalization or all-cause mortality.

Results

Among the 513 patients who were randomized (mean age, 71 years; 23.6% women), all (100%) were included in the analysis. The study was terminated for futility on December 18, 2019. After a mean follow-up time of 13.1 months (median, 12.7 months), a total of 108 primary end point events occurred: 52 events (20.4 events per 100 patient-years [95% CI, 14.8-25.9]) in the usual care plus antimicrobial therapy group and 56 events (18.4 events per 100 patient-years [95% CI, 13.2-23.6]) in the usual care group, with no significant difference between groups (adjusted HR, 1.04 [95% CI, 0.71-1.53;P = .83]. There was no statistically significant interaction between the effect of the prespecified antimicrobial agent (co-trimoxazole vs doxycycline) on the primary end point (adjusted HR, 1.15 [95% CI 0.68-1.95] in the co-trimoxazole group vs 0.82 [95% CI, 0.46-1.47] in the doxycycline group;P = .66). Serious adverse events occurring at 5% or greater among those treated with usual care plus antimicrobials vs usual care alone included respiratory events (16.5% vs 10.0%) and infections (2.8% vs 6.6%); adverse events of special interest included diarrhea (10.2% vs 3.1%) and rash (6.7% vs 0%).

Conclusions and Relevance

Among adults with idiopathic pulmonary fibrosis, the addition of co-trimoxazole or doxycycline to usual care, compared with usual care alone, did not significantly improve time to nonelective respiratory hospitalization or death. These findings do not support treatment with these antibiotics for the underlying disease.

Trial Registration

ClinicalTrials.gov Identifier:NCT02759120
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