...
首页> 外文期刊>AIDS Research and Human Retroviruses >Virological Response and Drug Resistance 1 and 2 Years Post-Partum in HIV-Infected Women Initiated on Life-Long Antiretroviral Therapy in Malawi
【24h】

Virological Response and Drug Resistance 1 and 2 Years Post-Partum in HIV-Infected Women Initiated on Life-Long Antiretroviral Therapy in Malawi

机译:马拉维终身抗逆转录病毒疗法启动的艾滋病毒感染妇女的产后1年和2年的病毒学应答和耐药性

获取原文
获取原文并翻译 | 示例

摘要

The objective of this study was to determine the virological response and the possible emergence of drug resistance at 1 and 2 years postpartum in HIV-positive pregnant women enrolled under the Option B approach and meeting the criteria for treatment. In the study, women with baseline CD4+ < 350/mm 3 received a combination of stavudine, lamivudine, and nevirapine during pregnancy (from week 25 of gestation) and continued it indefinitely after delivery. HIV-RNA was measured at 12 and 24 months postpartum. Drug resistance mutations were assessed in those with HIV-RNA > 50 copies/ml. Baseline resistance mutations were assessed in the entire cohort. A total of 107 women were studied. At baseline, resistance mutations were seen in 6.6% of the women. At 12 months, 26.7% of the women had > 50 copies/ml and among them 12.9% had virological failure (HIV-RNA > 1,000 copies/ml). At 24 months, detectable HIV-RNA was seen in 28.3% of the women and virological failure in 10.1% of the women. Resistance mutations (mainly non-nucleoside reverse transcriptase inhibitors mutations) were seen in 40% of the women with detectable HIV-RNA. Baseline mutations did not correlate with virological failure or the emergence of resistance at later time points. Virological failure 2 years postpartum and emergence of resistance were rare in this cohort of HIV-infected women. These findings are reassuring in the light of the new strategies for the prevention of mother-to-child HIV transmission, recommending life-long antiretroviral therapy administration.
机译:这项研究的目的是确定在选择B方法下接受治疗并符合治疗标准的HIV阳性孕妇在产后1年和2年时的病毒学应答和耐药性的可能出现。在该研究中,基线CD4 + <350 / mm 3的妇女在妊娠期间(从妊娠第25周开始)接受司他夫定,拉米夫定和奈韦拉平的联合治疗,并在分娩后无限期继续服用。在产后12和24个月测量HIV-RNA。在HIV-RNA> 50拷贝/ ml的患者中评估了耐药性突变。在整个队列中评估基线耐药性突变。共研究了107名妇女。基线时,在6.6%的女性中发现了耐药性突变。在12个月时,有26.7%的妇女有> 50个拷贝/毫升,其中12.9%的人有病毒学衰竭(HIV-RNA> 1,000拷贝/毫升)。在24个月时,有28.3%的女性发现了可检测到的HIV-RNA,而有10.1%的女性出现了病毒学衰竭。在40%带有可检测HIV-RNA的女性中观察到耐药性突变(主要是非核苷类逆转录酶抑制剂突变)。基线突变与病毒学失败或在稍后的时间点出现耐药性无关。在这组感染了HIV的女性中,产后2年的病毒学衰竭和抵抗力的出现很少见。鉴于新的预防母婴HIV传播的策略,这些发现令人放心,建议终身使用抗逆转录病毒疗法。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号