Evidence map›Paper›PMID 39761062›Full record

ArticleJAMA internal medicine2025

Doxycycline Postexposure Prophylaxis and Bacterial Sexually Transmitted Infections Among Individuals Using HIV Preexposure Prophylaxis.

Michael W Traeger, Wendy A Leyden, Jonathan E Volk, Michael J Silverberg, Michael A Horberg, Teaniese L Davis, Kenneth H Mayer, Douglas S Krakower, Jessica G Young, Samuel M Jenness and 1 more

Abstract read
In one paragraph

Article in JAMA internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sustained Effectiveness of Doxycycline Post-Exposure-Prophylaxis in a Large Sexual Health Clinic Over 96 Weeks: An Interrupted Time Series Analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. High prevalence of tetracycline resistance inEuro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2026
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Tetracycline-resistantJAC-antimicrobial resistance · 2025
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Michael W TraegerDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
Wendy A LeydenDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Jonathan E VolkDepartment of Infectious Diseases, Kaiser Permanente San Francisco, San Francisco, California.
Michael J SilverbergDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Michael A HorbergDepartment of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California.
Teaniese L DavisCenter for Research and Evaluation, Kaiser Permanente Georgia, Atlanta.
Kenneth H MayerThe Fenway Institute, Fenway Health, Boston, Massachusetts.
Douglas S KrakowerDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
Jessica G YoungDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.
Samuel M JennessDepartment of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia.
Julia L MarcusDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts.

Funding

Cabotegravir PrEP: Actionable Robust Evidence for Translation into Practice (CABARET)R01AI174862 · NIAID · HARVARD PILGRIM HEALTH CARE, INC. · PI MARCUS, JULIA L. · 2022 to 2025
$3.3M
NIAID NIH HHS R01 AI174862
6 · The paper itself

Abstract

Importance: Doxycycline postexposure prophylaxis (doxyPEP) has been shown to decrease the incidence of bacterial sexually transmitted infections (STIs) among people assigned male sex at birth in clinical trials, but data from clinical practice are limited. Objective: To describe early uptake of doxyPEP and evaluate changes in STI incidence following doxyPEP initiation. Design, Setting, and Participants: This retrospective cohort study of adults (aged ≥18 years) dispensed HIV preexposure prophylaxis (PrEP) at Kaiser Permanente Northern California during November 1, 2022, to December 31, 2023, examined electronic health record data to compare HIV PrEP users dispensed and not dispensed doxyPEP and rates of bacterial STIs before and after starting doxyPEP. Individuals were followed up from their first recorded STI test on or after November 1, 2020, until December 31, 2023, or discontinuation of health plan membership. Exposure: Pharmacy dispensing data were used to define doxyPEP recipients. Main Outcomes and Measures: Demographic and clinical characteristics were compared between individuals dispensed and not dispensed doxyPEP. Primary outcomes were incident chlamydia, gonorrhea, or infectious syphilis measured as quarterly STI positivity (proportion of individuals testing positive at least once per quarter). Among doxyPEP recipients, rate ratios (RRs) compared mean quarterly STI positivity from 24 months before to 12 months after starting doxyPEP. In an exploratory analysis, STI trends were evaluated for the full cohort, stratified by receipt of doxyPEP. Results: Among 11 551 HIV PrEP users (mean [SD] age, 39.9 [12.1] years; 95.1% male), 2253 (19.5%) were dispensed doxyPEP, of whom 2228 (98.9%) were male and 1096 (48.6%) had an STI in the year before starting doxyPEP. Compared with individuals not dispensed doxyPEP, doxyPEP recipients were older (mean [SD] age, 40.4 [10.8] vs 39.8 [12.4] years; P = .04) and had used HIV PrEP longer (mean [SD], 4.2 [2.8] vs 3.4 [2.6] years; P < .001), and a higher proportion were commercially insured (2091 [92.8%] vs 8270 [88.9%]; P < .001). Among doxyPEP recipients, quarterly chlamydia positivity decreased from 9.6% (95% CI, 9.0%-10.3%) before starting doxyPEP to 2.0% (95% CI, 1.5%-2.6%) after starting doxyPEP (RR, 0.21; 95% CI, 0.16-0.27; P < .001), with significant declines for each anatomic site of infection. Quarterly gonorrhea positivity decreased from 10.2% (95% CI, 9.6%-10.9%) before starting doxyPEP to 9.0% (95% CI, 8.0%-10.1%) after starting doxyPEP (RR, 0.88; 95% CI, 0.77-1.00; P = .048); site-specific declines were significant for rectal (RR, 0.81; 95% CI, 0.67-0.97; P = .02) and urethral (RR, 0.56; 95% CI, 0.40-0.79; P = .001) gonorrhea, but not pharyngeal gonorrhea. Quarterly syphilis positivity decreased from 1.7% (95% CI, 1.4%-1.9%) before starting doxyPEP to 0.3% (95% CI, 0.2%-0.6%) after starting doxyPEP (RR, 0.20; 95% CI, 0.11-0.37; P < .001). Positivity for STIs remained stable in individuals not dispensed doxyPEP. Conclusions and Relevance: This study found that receipt of doxyPEP was associated with substantial declines in chlamydia and syphilis incidence and modest declines in urethral and rectal gonorrhea incidence among individuals using HIV PrEP. These findings suggest that doxyPEP may offer substantial benefits for reducing population-level STI transmission with broader implementation.

Indexed as

Anti-Bacterial AgentsDoxycyclineHIV InfectionsPost-Exposure ProphylaxisPre-Exposure ProphylaxisSexually Transmitted DiseasesSexually Transmitted Diseases, BacterialAdultCaliforniaChlamydia InfectionsFemaleGonorrheaHumansIncidenceMaleMiddle AgedAnti-Bacterial AgentsDoxycycline

Identifiers

PMID39761062
PMCPMC11877173

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Registered trials

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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.