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Effect of Antimicrobial Therapy on Respiratory Hospitalization or Death in Adults With Idiopathic Pulmonary Fibrosis: The CleanUP-IPF Randomized Clinical Trial.
Martinez, Fernando J; Yow, Eric; Flaherty, Kevin R; Snyder, Laurie D; Durheim, Michael T; Wisniewski, Stephen R; Sciurba, Frank C; Raghu, Ganesh; Brooks, Maria M; Kim, Dong-Yun; Dilling, Daniel F; Criner, Gerard J; Kim, Hyun; Belloli, Elizabeth A; Nambiar, Anoop M; Scholand, Mary Beth; Anstrom, Kevin J; Noth, Imre.
  • Martinez FJ; New York Presbyterian Hospital/Weill Cornell Medicine, New York.
  • Yow E; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Flaherty KR; Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor.
  • Snyder LD; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Durheim MT; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
  • Wisniewski SR; Department of Respiratory Medicine, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
  • Sciurba FC; Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Raghu G; Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Brooks MM; Division of Pulmonary and Critical Care Medicine, University of Washington, Seattle.
  • Kim DY; Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Dilling DF; National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
  • Criner GJ; Division of Pulmonary and Critical Care Medicine, Loyola University Medical Center, Maywood, Illinois.
  • Kim H; Department of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania.
  • Belloli EA; Division of Pulmonary and Critical Care Medicine, University of Minnesota, Minneapolis.
  • Nambiar AM; Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor.
  • Scholand MB; Division of Pulmonary and Critical Care Medicine, University of Texas Health San Antonio.
  • Anstrom KJ; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City.
  • Noth I; Duke Clinical Research Institute, Duke University, Durham, North Carolina.
JAMA ; 325(18): 1841-1851, 2021 05 11.
Article in English | MEDLINE | ID: covidwho-1237391
ABSTRACT
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 11 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.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Trimethoprim, Sulfamethoxazole Drug Combination / Doxycycline / Idiopathic Pulmonary Fibrosis / Anti-Bacterial Agents Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: JAMA Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Trimethoprim, Sulfamethoxazole Drug Combination / Doxycycline / Idiopathic Pulmonary Fibrosis / Anti-Bacterial Agents Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: JAMA Year: 2021 Document Type: Article