Traeger Michael W, Mayer Kenneth H, Krakower Douglas S, Gitin Sy, Jenness Samuel M, Marcus Julia L
Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts, United States.
The Fenway Institute, Fenway Health, Boston, Massachusetts, United States.
Clin Infect Dis. 2023 Aug 18. doi: 10.1093/cid/ciad488.
Doxycycline post-exposure prophylaxis (doxyPEP) reduces bacterial sexually transmitted infection (STI) incidence in people with HIV (PWH) or using HIV preexposure prophylaxis (PrEP). Given concerns about widespread antibiotic use, we identified doxyPEP prescribing strategies to minimize use while maximizing impact on STIs.
We used electronic health records of gay and bisexual men (GBM), transgender women, and non-binary people assigned male sex at birth with ≥2 STI tests (chlamydia, gonorrhea, syphilis) at an LGBTQ-focused health center during 2015-2020. We defined 10 hypothetical doxyPEP prescribing strategies based on PrEP use, HIV status, or STI history. We estimated doxyPEP use and STI diagnoses averted in counterfactual scenarios in which people meeting prescribing criteria received doxyPEP, assuming STI rates during use would have been reduced by clinical trial efficacy estimates.
Among 10,546 individuals (94% GBM), rate of any STI was 35.9/100 person-years. Prescribing doxyPEP to all individuals would have averted 71% of STI diagnoses (number needed to treat for one year to avert one STI diagnosis, NNT = 3.9); prescribing to PrEP users/PWH (52%/12% of individuals) would have averted 60% of STI diagnoses (NNT = 2.9). Prescribing doxyPEP for 12 months after STI diagnosis would have reduced the proportion using doxyPEP to 38% and averted 39% of STI diagnoses (NNT = 2.4). Prescribing after concurrent or repeated STIs would have maximized efficiency (lowest NNTs) but prevented fewer STIs.
Prescribing doxyPEP to individuals with STIs, particularly concurrent or repeated STIs, could avert a substantial proportion of all STI diagnoses. The most efficient prescribing strategies are based on STI history rather than HIV status or PrEP use.
多西环素暴露后预防(doxyPEP)可降低艾滋病毒感染者(PWH)或使用艾滋病毒暴露前预防(PrEP)者的细菌性性传播感染(STI)发病率。鉴于对广泛使用抗生素的担忧,我们确定了doxyPEP的处方策略,以尽量减少使用量,同时最大限度地提高对性传播感染的影响。
我们使用了2015年至2020年期间在一家以LGBTQ为重点的健康中心接受过≥2次性传播感染检测(衣原体、淋病、梅毒)的男同性恋者(GBM)、跨性别女性以及出生时被指定为男性性别的非二元性别人士的电子健康记录。我们根据PrEP使用情况、艾滋病毒状态或性传播感染病史定义了10种假设的doxyPEP处方策略。我们估计了在符合处方标准的人接受doxyPEP的反事实情景中doxyPEP的使用情况和避免的性传播感染诊断数,假设使用期间的性传播感染率会因临床试验疗效估计而降低。
在10546名个体(94%为GBM)中,任何性传播感染的发生率为35.9/100人年。对所有个体开具doxyPEP可避免71%的性传播感染诊断(为避免1例性传播感染诊断所需治疗的人数,NNT = 3.9);对PrEP使用者/艾滋病毒感染者(分别占个体的52%/12%)开具doxyPEP可避免60%的性传播感染诊断(NNT = 2.9)。在性传播感染诊断后开具12个月的doxyPEP会将使用doxyPEP的比例降至38%,并避免39%的性传播感染诊断(NNT = 2.4)。在同时发生或反复发生性传播感染后开具doxyPEP可使效率最大化(NNT最低),但预防的性传播感染较少。
对性传播感染患者,尤其是同时发生或反复发生性传播感染的患者开具doxyPEP,可避免相当比例的所有性传播感染诊断。最有效的处方策略基于性传播感染病史,而非艾滋病毒状态或PrEP使用情况。