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Arch Pediatr Adolesc Med · Nov 2008
Subsequent sexually transmitted infection after outpatient treatment of pelvic inflammatory disease.
- Maria Trent, Shang-en Chung, Lynette Forrest, and Jonathan M Ellen.
- Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD 21287, USA. mtrent2@jhmi.edu
- Arch Pediatr Adolesc Med. 2008 Nov 1;162(11):1022-5.
ObjectiveTo determine the frequency of recurrent sexually transmitted infections (STIs) and/or pelvic inflammatory disease (PID), the average time until subsequent infection following a baseline PID diagnosis, and age- and insurance-related associations with subsequent diagnoses.DesignThis study used prospective longitudinal follow-up of STI and/or PID outcome data from electronic medical records.SettingAn urban academic hospital system.ParticipantsA total of 110 adolescent girls treated for PID as outpatients in pediatric ambulatory sites. Main Exposure Electronic medical records used to assess subsequent PID diagnoses and/or infections with Neisseria gonorrhoeae or Chlamydia trachomatis during the study window.Main Outcome MeasuresDemographic, health care use, and STI and/or PID outcome data were examined. Incidence of an STI and/or PID was calculated as incident cases per person-months of exposure. Cox proportional hazard modeling was performed to evaluate the incidence of STI by age or insurance status.ResultsThe mean (SD) age was 16.8 (1.9) years, 89% of patients were black, and 39% had laboratory results that were positive for N gonorrhoeae or C trachomatis at baseline. Thirty-four percent of patients had an additional diagnosis of an STI during the 48-month follow-up window (incidence, 3.1 per 100 person-months) and the mean (SD) time to a subsequent STI and/or PID was 377 (297) days. Of those patients, 67% (n = 18) had chlamydia, 11% had gonorrhoeae, and 44% had PID. There were no differences based on age or insurance status.ConclusionsAdolescents treated for PID are at risk for subsequent STI and/or PID for a 48-month period. Given the need to prevent future infections in these vulnerable youths, efforts to explore the value of ongoing strategies for risk reduction after diagnosis are warranted.
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