Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2021 Jul 27;326(4):324-331.
doi: 10.1001/jama.2021.9899.

Effect of 7 vs 14 Days of Antibiotic Therapy on Resolution of Symptoms Among Afebrile Men With Urinary Tract Infection: A Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Effect of 7 vs 14 Days of Antibiotic Therapy on Resolution of Symptoms Among Afebrile Men With Urinary Tract Infection: A Randomized Clinical Trial

Dimitri M Drekonja et al. JAMA. .

Abstract

Importance: Determination of optimal treatment durations for common infectious diseases is an important strategy to preserve antibiotic effectiveness.

Objective: To determine whether 7 days of treatment is noninferior to 14 days when using ciprofloxacin or trimethoprim/sulfamethoxazole to treat urinary tract infection (UTI) in afebrile men.

Design, setting, and participants: Randomized, double-blind, placebo-controlled noninferiority trial of afebrile men with presumed symptomatic UTI treated with ciprofloxacin or trimethoprim/sulfamethoxazole at 2 US Veterans Affairs medical centers (enrollment, April 2014 through December 2019; final follow-up, January 28, 2020). Of 1058 eligible men, 272 were randomized.

Interventions: Participants continued the antibiotic prescribed by their treating clinician for 7 days of treatment and were randomized to receive continued antibiotic therapy (n = 136) or placebo (n = 136) for days 8 to 14 of treatment.

Main outcomes and measures: The prespecified primary outcome was resolution of UTI symptoms by 14 days after completion of active antibiotic treatment. A noninferiority margin of 10% was selected. The as-treated population (participants who took ≥26 of 28 doses and missed no more than 2 consecutive doses) was used for the primary analysis, and a secondary analysis included all patients as randomized, regardless of treatment adherence. Secondary outcomes included recurrence of UTI symptoms and/or adverse events within 28 days of stopping study medication.

Results: Among 272 patients (median [interquartile range] age, 69 [62-73] years) who were randomized, 100% completed the trial and 254 (93.4%) were included in the primary as-treated analysis. Symptom resolution occurred in 122/131 (93.1%) participants in the 7-day group vs 111/123 (90.2%) in the 14-day group (difference, 2.9% [1-sided 97.5% CI, -5.2% to ∞]), meeting the noninferiority criterion. In the secondary as-randomized analysis, symptom resolution occurred in 125/136 (91.9%) participants in the 7-day group vs 123/136 (90.4%) in the 14-day group (difference, 1.5% [1-sided 97.5% CI, -5.8% to ∞]) Recurrence of UTI symptoms occurred in 13/131 (9.9%) participants in the 7-day group vs 15/123 (12.9%) in the 14-day group (difference, -3.0% [95% CI, -10.8% to 6.2%]; P = .70). Adverse events occurred in 28/136 (20.6%) participants in the 7-day group vs 33/136 (24.3%) in the 14-day group.

Conclusions and relevance: Among afebrile men with suspected UTI, treatment with ciprofloxacin or trimethoprim/sulfamethoxazole for 7 days was noninferior to 14 days of treatment with regard to resolution of UTI symptoms by 14 days after antibiotic therapy. The findings support the use of a 7-day course of ciprofloxacin or trimethoprim/sulfamethoxazole as an alternative to a 14-day course for treatment of afebrile men with UTI.

Trial registration: ClinicalTrials.gov identifier: NCT01994538.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: Dr Trautner reports research and consulting funding from Genentech and the National Institute of Allergy and Infectious Diseases for COVID trials; consultancy fees from Genentech; and grants from the US Department of Veterans Affairs (VA) Rehabilitation Research & Development Service and the Agency for Healthcare Research and Quality. Ms Amundson reports receiving salary support for this trial during the conduct of the study from VA Merit Review grants. Dr. Johnson reports grant support from Allergan/Actavis, Cipla/Achaogen, Melinta, Merck, Shionogi, Synitron, Tetraphase; consulting fees from Crucell/Janssen; and pending patents for 2 E coli strain tests. No other conflicts were reported.

Figures

Figure.
Figure.. Enrollment, Randomization, and Flow of Patients in the Trial
aAll participants received 7 days of trimethoprim/sulfamethoxazole or ciprofloxacin before being randomized to receive an additional 7 days of the same antimicrobial or placebo. bVarious reasons were given for disinterest; however, 29 expressed disinterest specifically because they did not want to change treatment duration. cRandomization was stratified by urinary catheter use, study drug, and study site. dIndicates that participants adhered to taking at least 26 of 28 assigned medication doses and missed no more than 2 consecutive doses. UTI indicates urinary tract infection.

Comment in

References

    1. Barlam TF, Cosgrove SE, Abbo LM, et al. Executive summary: implementing an antibiotic stewardship program: guidelines by the Infectious Diseases Society of America and the Society for Healthcare Epidemiology of America. Clin Infect Dis. 2016;62(10):1197-1202. doi: 10.1093/cid/ciw217 - DOI - PubMed
    1. Chastre J, Wolff M, Fagon JY, et al. ; PneumA Trial Group . Comparison of 8 vs 15 days of antibiotic therapy for ventilator-associated pneumonia in adults: a randomized trial. JAMA. 2003;290(19):2588-2598. doi: 10.1001/jama.290.19.2588 - DOI - PubMed
    1. Uranga A, España PP, Bilbao A, et al. Duration of antibiotic treatment in community-acquired pneumonia: a multicenter randomized clinical trial. JAMA Intern Med. 2016;176(9):1257-1265. doi: 10.1001/jamainternmed.2016.3633 - DOI - PubMed
    1. Sawyer RG, Claridge JA, Nathens AB, et al. ; STOP-IT Trial Investigators . Trial of short-course antimicrobial therapy for intraabdominal infection. N Engl J Med. 2015;372(21):1996-2005. doi: 10.1056/NEJMoa1411162 - DOI - PMC - PubMed
    1. Gariani K, Pham TT, Kressmann B, et al. Three versus six weeks of antibiotic therapy for diabetic foot osteomyelitis: a prospective, randomized, non-inferiority pilot trial. Clin Infect Dis. Published online November 26, 2020. doi: 10.1093/cid/ciaa1758 - DOI - PubMed

MeSH terms

Substances

Associated data