Evidence map›Paper›PMID 33974018›Full record

Trial reportJAMA2021

Effect of Antimicrobial Therapy on Respiratory Hospitalization or Death in Adults With Idiopathic Pulmonary Fibrosis: The CleanUP-IPF Randomized Clinical Trial.

Fernando J Martinez, 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 and 9 more

Registry-linked trialOpen access · bronzeAbstract readComparative StudyMulticenter StudyPragmatic Clinical Trial
In one paragraph

Trial report in JAMA, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02759120 (Study of Clinical Efficacy of Antimicrobial Therapy Strategy Using Pragmatic Design in Idiopathic Pulmonary Fibrosis), which is not on this map. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 pooled it
9.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02759120 phase3terminatednot on this map

Study of Clinical Efficacy of Antimicrobial Therapy Strategy Using Pragmatic Design in Idiopathic Pulmonary Fibrosis

TypeinterventionalSponsorWeill Medical College of Cornell UniversityRan2017 to 2020Enrolled513ConditionsIdiopathic Pulmonary FibrosisArmsAntimicrobial therapy: Co-trimoxazole or Doxycycline, No Intervention: Standard of Care
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 3 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Gut microbiota associate with disease severity and survival in idiopathic pulmonary fibrosis.American journal of respiratory and critical care medicine · 2026
    Article
  9. Inter-Organ Communication in Pulmonary Fibrosis: Systemic Modifiers of a Lung-Centered Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  10. Article
  11. Article
  12. The NHLBI lung transplant consortium 2025 steering committee report: Strategies to maximize the use of the consortium for advancing lung transplantation.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2026
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. The lung microbiome in interstitial lung disease.Breathe (Sheffield, England) · 2025
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 14 institutions in 3 countries.

Fernando J MartinezNew York Presbyterian Hospital/Weill Cornell Medicine, New York.
Eric YowDuke Clinical Research Institute, Duke University, Durham, North Carolina.
Kevin R FlahertyDivision of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor.
Laurie D SnyderDuke Clinical Research Institute, Duke University, Durham, North Carolina.
Michael T DurheimDuke Clinical Research Institute, Duke University, Durham, North Carolina.
Stephen R WisniewskiGraduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Frank C SciurbaGraduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Ganesh RaghuDivision of Pulmonary and Critical Care Medicine, University of Washington, Seattle.
Maria M BrooksGraduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Dong-Yun KimNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland.
Daniel F DillingDivision of Pulmonary and Critical Care Medicine, Loyola University Medical Center, Maywood, Illinois.
Gerard J CrinerDepartment of Thoracic Medicine and Surgery, Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania.
Hyun KimDivision of Pulmonary and Critical Care Medicine, University of Minnesota, Minneapolis.
Elizabeth A BelloliDivision of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor.
Anoop M NambiarDivision of Pulmonary and Critical Care Medicine, University of Texas Health San Antonio.
Mary Beth ScholandDivision of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City.
Kevin J AnstromDuke Clinical Research Institute, Duke University, Durham, North Carolina.
Imre NothDivision of Pulmonary and Critical Care Medicine, University of Virginia, Charlottesville.
CleanUP-IPF Investigators of the Pulmonary Trials Cooperative
The Ocean Cleanup · NLDuke University · USUniversity of Pittsburgh · USOslo University Hospital · NOUniversity of Michigan · USLoyola University Medical Center · USNational Institutes of Health · USNewYork–Presbyterian Hospital · USTemple University · USThe University of Texas Health Science Center at San Antonio · USUniversity of Minnesota · USUniversity of Utah · USUniversity of Virginia · USUniversity of Washington · US

Funding

Study of Co-trimoxazole and Proton Pump Inhibition Using Pragmatic Design in Idiopathic Pulmonary Fibrosis - CleanUP-IPFU01HL128964 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANSTROM, KEVIN J, MARTINEZ, FERNANDO J · 2015 to 2018
$1.6M
NHLBI NIH HHS U01 HL128964
6 · The paper itself

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 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.

Indexed as

AgedAnti-Bacterial AgentsDoxycyclineFemaleHospitalizationHumansIdiopathic Pulmonary FibrosisLungMaleMiddle AgedRespiratory Function TestsRespiratory Tract InfectionsTreatment OutcomeTrimethoprim, Sulfamethoxazole Drug CombinationAnti-Bacterial AgentsDoxycyclineTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID33974018
PMCPMC8114133
OpenAlexW3162861758

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.