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Preference for Sayana? Press versus intramuscular Depo-Provera among HIV-positive women in Rakai, Uganda: A randomized crossover trial

机译:更喜欢Sayana?乌干达拉凯艾滋病毒呈阳性妇女的新闻报道与肌肉注射Depo-Provera:一项随机交叉试验

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Introduction Sayana Press (SP), a subcutaneous formulation of depot medroxyprogesterone acetate (DMPA) prefilled in a Uniject injection system, could potentially improve and expand contraceptive injection services, but acceptability of SP is unknown. HIV-positive women need contraception to avoid unintended pregnancy and risk of vertical HIV transmission. We assessed acceptability of SP versus intramuscular DMPA (DMPA-IM) among HIV-positive women and their care providers in Rakai, Uganda. Methods Women were randomized to DMPA-IM or SP at baseline, received the alternate product at 3 months, and chose their preferred method at 6 months. We determined preferences among new and experienced contraceptive injectable users who had tried both types of injection during the trial, and from providers before and after providing both types of injectables to clients. Results Among 357 women randomized, 314 were followed up at 6 months (88%). Although SP caused more skin irritation than DMPA-IM (3.8% vs. 0% at 6 months, p=.03), it was associated with marginally fewer side effects (30.4% vs. 40.4% at 6 months, p=.06). Participants reported high levels of willingness to recommend the DMPA contraception to a friend and satisfaction with the injection received, and these did not differ by injection type. Sixty-four percent of women and 73% of providers preferred SP to DMPA-IM at 6 months; women's preferences did not differ by previous experience with injectable contraception. Conclusions SP is acceptable to HIV-positive women and health care providers in this rural Ugandan population. Implications SP appears to be acceptable to HIV-positive women and their care providers in Rakai, Uganda, and strategies for appropriate rollout of this innovative technology should be explored.
机译:简介Sayana Press(SP)是一种预填充在Uniject注射系统中的醋酸甲羟孕酮长效制剂(DMPA)的皮下制剂,可以潜在地改善和扩大避孕注射服务,但SP的可接受性尚不清楚。艾滋病毒抗体阳性的妇女需要避孕,以避免意外怀孕和艾滋病毒垂直传播的风险。我们评估了乌干达拉凯市HIV阳性妇女及其护理人员的SP与肌内DMPA(DMPA-IM)的可接受性。方法在基线时将女性随机分为DMPA-IM或SP,在3个月时接受替代产品,并在6个月时选择其偏爱的方法。我们确定了在试验期间尝试过两种注射剂的新的和经验丰富的避孕注射剂使用者以及在向客户提供两种注射剂之前和之后都从提供者那里得到的偏好。结果在357名随机分组的妇女中,有314名在6个月时得到了随访(88%)。尽管SP引起的皮肤刺激性比DMPA-IM更高(3.8%vs. 6%,0%,p = .03),但其副作用略少(60.4个月,30.4%,40.4%,p = .06)。 )。参与者报告了向朋友推荐DMPA避孕的高水平意愿和对收到的注射剂的满意度,并且这些注射剂类型没有差异。在6个月时,有64%的女性和73%的服务提供者更喜欢DMPA-IM。妇女的喜好与以前使用注射避孕药的经验并无不同。结论在乌干达农村人口中,艾滋病毒抗体阳性的妇女和卫生保健提供者可以接受SP。含义SP在乌干达拉凯的HIV阳性妇女及其护理提供者看来是可以接受的,应探索适当推广这种创新技术的策略。

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