Extragenital Gonorrhea and Chlamydia Testing Among Women Reporting Extragenital Exposure at an Urban STD Clinic: Is It Worth the Cost?

Author:

Caragol Laura1,Voegeli Christopher2,Mettenbrink Christie3,Wendel Karen4,Rietmeijer Cornelis5

Affiliation:

1. Infectious Diseases, University of Colorado – Anschutz Medical Campus, Aurora, Colorado; HIV and STD Prevention, Denver Public Health Department, Denver Health and Hospital, Denver, Colorado

2. STD and HIV Prevention, Denver Public Health Department, Denver Health and Hospital, Denver, Colorado

3. Public Health Informatics Group, Denver Public Health Department, Denver Health and Hospital, Denver, Colorado

4. STD Prevention Training Center, Denver Public Health Department, Denver Health and Hospital, Denver, Colorado

5. President, ASTDA, Rietmeijer Consulting, Denver, Colorado, Denver, Colorado; Denver Public Health Department, Denver Health and Hospital, Denver, Colorado; Colorado School of Public Health, University of Colorado, Aurora, Colorado

Abstract

Abstract Background Current guidelines only recommend screening for gonorrhea (GC) and chlamydia (CT) at extragenital sites of exposure in men who have sex with men (MSM). With Medicaid reimbursement for GC/CT nucleic acid amplification testing (NAAT) at approximately $48/test, expanding testing to women requires a value assessment. We report the prevalence of extragenital GC/CT in women with extragenital exposure, determine the proportion of disease missed by urogenital NAAT, and estimate additional cost per infection identified by extragenital testing in women vs MSM. Methods We conducted a retrospective analysis of women undergoing extragenital NAAT for GC and CT at Denver Metro Health Clinic. Data were analyzed for all women with extragenital testing from 9/11/2015 to 7/8/2016, and for MSM from 9/3/2013 to 7/8/2016. Statistical Package for the Social Sciences and Excel programs were used for data analysis. Results In a total 804 female visits, the mean age was 29 (13–67years); 46% were White non-Hispanic; 37% were Hispanic; and 15% were Black. In women, the prevalence of extragenital GC and CT was 2% (16/804) and 5% (38/804), respectively. The rate of GC infection in women was the same at genital and pharyngeal sites (2%, 16/804) but lower at the rectum (0.25%, 2/804). Female chlamydia rates were 11% genital (85/804), 4% pharyngeal (30/804), and 1.4% rectal (11/804). If only urogenital testing had been performed in women, 27% (6/22) of GC infections and 14% (14/99) of CT infections would have been missed. Overall, isolated extragenital infection accounted for 18% (20/111, 95% CI 12–26%) and 65% (943/1453, 95% CI 62–67%) of the combined GC and CT burden in women and MSM, respectively. On average, 40 women and five MSM were screened with extragenital tests to identify one isolated extragenital infection. Estimated additional Medicaid costs for isolated extragenital infection identified in women was $3,851 and in men was $480 for pharyngeal and rectal testing. Conclusion Urogenital screening misses a significant number of extragenital infections in women. However, given the high cost of extragenital screening in women, further work is needed to determine whether screening can be limited to the pharynx or if risk factors can be used to target screening for cost savings. Disclosures All authors: No reported disclosures.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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