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Update to U.S. Medical Eligibility Criteria for Contraceptive Use 2016: Updated Recommendations for the Use of Contraception Among Women at High Risk for HIV Infection

机译:2016年美国避孕药医学合格标准的最新信息:关于艾滋病毒高危女性中使用避孕药的最新建议

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摘要

“U.S. Medical Eligibility Criteria for Contraceptive Use” (U.S. MEC) 2016 provides evidence-based guidance for the safe use of contraceptive methods among U.S. women with certain characteristics or medical conditions ( ). The U.S. MEC is adapted from global guidance from the World Health Organization (WHO) and kept up to date through continual review of published literature ( ). CDC recently evaluated the evidence and the updated WHO guidance on the risk for human immunodeficiency virus (HIV) acquisition among women using hormonal contraception and intrauterine devices (IUDs) ( ). After careful review, CDC adopted WHO’s 2019 updated guidance for inclusion in the U.S. MEC guidance; CDC’s updated guidance states that progestin-only injectable contraception (including depot medroxyprogesterone acetate [DMPA]) and IUDs (including levonorgestrel-releasing and copper-bearing) are safe for use without restriction among women at high risk for HIV infection (U.S. MEC category 1 [previously U.S. MEC category 2, advantages outweigh risks]) ( ). CDC’s guidance also adds an accompanying clarification for women who wish to use IUDs, which states “Many women at a high risk for HIV infection are also at risk for other sexually transmitted diseases (STDs). For these women, refer to the recommendations in the ‘U.S. Medical Eligibility Criteria for Contraceptive Use’ for women with other factors related to STDs, and the ‘U.S. Selected Practice Recommendations for Contraceptive Use’ on STD screening before IUD insertion” ( , ). Recommendations for other hormonal contraceptive methods (including combined hormonal methods, implants, and progestin-only pills) remain the same; there is also no restriction for their use among women at high risk for HIV infection (U.S. MEC category 1). Finally, CDC clarified that the U.S. MEC recommendations for concurrent use of hormonal contraceptives or IUDs and antiretroviral use for treatment of HIV infection also apply to use of antiretrovirals for prevention of HIV acquisition (preexposure prophylaxis [PrEP]).
机译:“我们。 《避孕药具医疗资格标准》(美国MEC)2016年为具有某些特征或医疗状况的美国妇女安全使用避孕方法提供了循证指南()。美国MEC改编自世界卫生组织(WHO)的全球指南,并通过不断审查已发表的文献()来保持最新。疾病预防控制中心(CDC)最近评估了有关使用激素避孕和宫内节育器(IUD)的妇女中获得人类免疫缺陷病毒(HIV)风险的证据和最新的WHO指南()。经过仔细审查,疾病预防控制中心通过了WHO的2019年更新指南,以将其纳入美国MEC指南;美国疾病预防控制中心(CDC)更新的指南指出,在高感染HIV的女性中,仅使用孕激素注射避孕药(包括醋酸甲羟孕酮[DMPA])和宫内节育器(包括左炔诺孕酮释放和含铜)是安全的,不受限制。 [以前是US MEC类别2,优势胜于风险])()。美国疾病预防控制中心(CDC)的指南还为希望使用宫内节育器的妇女增加了相应的说明,其中指出:“许多感染艾滋病毒的高风险妇女也有患其他性传播疾病(STD)的风险。对于这些女性,请参考“美国具有其他与性传播疾病相关的因素的女性的避孕药医学合格标准,以及“美国“在插入宫内节育器之前进行性病筛查的部分避孕方法建议”(,)。其他激素避孕方法的建议(包括联合激素方法,植入物和仅含孕激素的药丸)保持不变;在感染HIV的高风险女性中也没有使用限制(美国MEC第1类)。最后,疾病预防控制中心澄清说,美国MEC关于同时使用激素避孕药或宫内节育器以及抗逆转录病毒药物治疗HIV感染的建议也适用于抗逆转录病毒药物预防HIV的获得(预防性暴露[PrEP])。

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