性侵犯儿童和青少年的暴露后预防和随访。

IF 2 Q1 MEDICINE, GENERAL & INTERNAL
Sarah Hui Wen Yao, Karen Nadua, Chia Yin Chong, Koh Cheng Thoon, Chee Fu Yung, Natalie Woon Hui Tan, Kai-Qian Kam, Peter Wong, Juliet Tan, Jiahui Li
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引用次数: 0

摘要

儿科性侵犯(SA)受害者应评估暴露后预防(PEP),以减少性传播感染(sti)的风险。我们描述了在新加坡KK妇女和儿童医院出现SA的儿童和青少年(CYPs)的临床特征,病毒PEP(人类免疫缺陷病毒[HIV]和乙型肝炎病毒[HBV])处方实践,以及随访时的性传播感染评估。方法:回顾2022年1月至2023年8月期间出现SA的年龄≤16岁的CYPs患者的医疗记录,包括攻击和攻击者特征、基线和随访STI筛查、PEP处方、依从性和随访出席率。具有高危特征的HIV阳性或HIV状态未知的攻击者在前72小时内发生SA的CYPs符合HIV PEP的条件。结果:我们分析了278例进行了292次SA就诊的CYPs。有40例(13.7%)符合HIV PEP条件,其中29例(82.9%)接受了PEP。在基线检测中,分别有9%和34.9%的CYPs沙眼衣原体和阴道加德纳菌检测呈阳性。淋病奈瑟菌、阴道毛滴虫、HIV、HBV和丙型肝炎均未检测出阳性。大多数CYPs检测为HBV非免疫(n=167, 67.6%);只有77人(46.1%)接种了疫苗。在符合HBV PEP免疫球蛋白治疗条件的27例CYPs中,只有21例(77.7%)接受了免疫球蛋白治疗。共有37名CYPs接受了HIV PEP,其中8人回顾性地被认为不合格。只有10人(27%)完成了课程。总体而言,153名(57.7%)cyp参加了随访,没有HIV或HBV血清转化。结论:我们报告在儿童SA受害者中,HBV暴露后疫苗接种率不理想,HIV PEP和随访依从性低。应审查导致依从性差的因素,以优化对这一弱势群体的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-exposure prophylaxis and follow-up in children and young persons presenting with sexual assault.

Introduction: Paediatric sexual assault (SA) victims should be assessed for post-exposure prophylaxis (PEP) to mitigate the risk of sexually transmitted infections (STIs). We describe the clinical characteristics of children and young persons (CYPs) presenting with SA at KK Women's and Children's Hospital in Singapore, viral PEP (human immunodeficiency virus [HIV] and hepatitis B virus [HBV]) prescribing practices, and STI evaluation at follow-up.

Method: Medical records of CYPs ≤16 years who presented with SA between January 2022 and August 2023 were reviewed, including assault and assailant characteristics, baseline and follow-up STI screening, PEP prescription, adherence and follow-up attendance. CYPs with SA in the preceding 72 hours by HIV-positive or HIV-status unknown assailants with high-risk characteris-tics were eligible for HIV PEP.

Results: We analysed 278 CYPs who made 292 SA visits. There were 40 (13.7%) CYPs eligible for HIV PEP, of whom 29 (82.9%) received it. Among those tested at baseline, 9% and 34.9% of CYPs tested positive for Chlamydia trachomatis and Gardnerella vaginalis, respectively. None tested positive for Neisseria gonorrhoeae, Trichomonas vaginalis, HIV, HBV or hepatitis C. Majority of CYPs tested were HBV non-immune (n=167, 67.6%); only 77 (46.1%) received the vaccine. Out of 27 CYPs eligible for HBV PEP with immunoglobulin, only 21 (77.7%) received immunoglobulin. A total of 37 CYPs received HIV PEP, including 8 who were retrospectively deemed ineligible. Only 10 (27%) completed the course. Overall, 153 (57.7%) CYPs attended follow-up, and none seroconverted for HIV or HBV.

Conclusion: We report suboptimal rates of HBV post-exposure vaccination, and low compliance to HIV PEP and follow-up among paediatric SA victims. Factors contri-buting to poor compliance should be examined to optimise care for this vulnerable population.

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