Infectious Disease Institute, Makerere University, Kampala, Uganda.
Division of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
AIDS Res Hum Retroviruses. 2021 Jul;37(7):529-533. doi: 10.1089/AID.2020.0202. Epub 2021 Apr 12.
Early antiretroviral therapy (ART) initiation after cryptococcal meningitis increases mortality, and those unmasking cryptococcosis after <2 weeks of ART have higher mortality. However, it is unknown if those presenting as ART experienced are actually adherent to their ART. Unknowingly, restarting ART in persons, who have discontinued ART, may be a fatal iatrogenic error. To evaluate ART adherence in an exploratory analysis, we collected dried blood spots on 44 HIV-infected persons presenting with cryptococcal meningitis. We quantified tenofovir diphosphate (TFV-DP) and lamivudine (3TC) from dried blood spots. We quantified cumulative ART adherence over the preceding 6-8 weeks based on TFV-DP concentrations and adherence over the last few days based on 3TC concentrations. Of 22 ART experienced, 20 (91%) had quantifiable concentrations. Of 18 receiving tenofovir, 15 (83%) had TFV-DP consistent with drug intake of ≥4 doses/week or moderate adherence. With 3TC, 72% (18/22) had detectable levels consistent with adherence over the last 3 days before measurement. Only three ART-experienced subjects were alive and virally suppressed at 4 months ( = 2 on ART for <30 days; = 1 with undetectable antiretrovirals). Surprisingly, of 22 who reported not receiving ART, 4 (18%) had quantifiable tenofovir. Most ART-experienced subjects were taking their ART with moderate to good adherence with the majority likely having viral resistance given generally at good ART levels, receipt of intensive adherence counseling, and lack of subsequent viral suppression. The World Health Organization (WHO) guidelines recommend adherence counseling with ART continuation and repeat viral loads in 1-3 months before switching to second-line ART. These recommendations are likely inappropriate in those with central nervous system infections given the additional possible harm of central nervous system immune reconstitution syndrome. Further study to evaluate continuation of ART regimens when presenting with cryptococcosis has benefit, with checking blood levels at presentation potentially being a helpful option. ClinicalTrials.gov Identifier: NCT01802385.
早期抗逆转录病毒治疗 (ART) 启动后 cryptococcal 脑膜炎增加死亡率,和那些 unmasking cryptococcosis 后 < 2 周的 ART 有更高的死亡率。然而,目前尚不清楚是否那些呈现为 ART 经历实际上是坚持他们的 ART。无意中,重新启动 ART 的人,他们已经停止了 ART,可能是致命的医源性错误。为了评估在探索性分析中的 ART 遵守情况,我们收集了 44 例 HIV 感染患者的 cryptococcal 脑膜炎干血斑。我们从干血斑中定量了替诺福韦二磷酸 (TFV-DP) 和拉米夫定 (3TC)。我们根据 TFV-DP 浓度定量了过去 6-8 周的累积 ART 遵守情况,并根据 3TC 浓度定量了过去几天的遵守情况。在 22 例有 ART 经验的患者中,有 20 例 (91%) 有可量化的浓度。在 18 例接受替诺福韦的患者中,有 15 例 (83%) 的 TFV-DP 与每周 ≥4 剂或中度依从性的药物摄入一致。用 3TC,72% (18/22) 在测量前的最后 3 天有可检测到的水平,这与依从性一致。只有 3 例有 ART 经验的患者在 4 个月时存活并病毒抑制 ( = 2 例在 ART 上接受治疗 <30 天; = 1 例抗病毒药物不可检测)。令人惊讶的是,在 22 例未接受 ART 的患者中,有 4 例 (18%) 有可量化的替诺福韦。大多数有 ART 经验的患者以中度至良好的依从性服用他们的 ART,大多数患者可能因一般良好的 ART 水平、接受强化依从性咨询以及随后缺乏病毒抑制而具有病毒耐药性。世界卫生组织 (WHO) 指南建议在开始二线 ART 前,对服用 ART 的患者进行依从性咨询,并在 1-3 个月内重复病毒载量。鉴于中枢神经系统免疫重建综合征可能带来的额外危害,这些建议在中枢神经系统感染患者中可能不合适。进一步研究在 cryptococcosis 出现时继续 ART 方案的益处,在出现时检查血液水平可能是一个有用的选择。临床试验.gov 标识符:NCT01802385。