单中心评估并启动HIV感染者使用长效卡博特韦/利匹韦林的经验。

Single-center experience evaluating and initiating people with HIV on long-acting cabotegravir/rilpivirine.

作者信息

Hill Lucas A, Abulhosn Kari K, Yin Jeffrey F, Bamford Laura P

机构信息

University of California San Diego, San Diego, CA, USA.

出版信息

AIDS. 2023 Mar 15;37(4):605-609. doi: 10.1097/QAD.0000000000003446. Epub 2022 Nov 28.

Abstract

OBJECTIVE

To describe our experience evaluating and initiating individuals on long-acting injectable (LAI) cabotegravir/rilpivirine (CAB/RPV) and evaluate factors associated with starting LAI CAB/RPV and reasons for not starting.

DESIGN

We conducted a retrospective single-center study at the UC San Diego Owen Clinic.

METHODS

We included all individuals who expressed interest in treatment with LAI CAB/RPV between April 2021 and June 2022 who had a definitive decision made on starting LAI CAB/RPV.

RESULTS

In total, 383 individuals were included with 201 (52.5%) initiating LAI CAB/RPV. Those who initiated LAI CAB/RPV were younger ( P  = 0.02) and were more likely to be on a two-drug regimen or first-generation integrase inhibitor regimen and less likely to be on a protease inhibitor or multiclass regimen. The most common reasons for not starting LAI CAB/RPV were inconsistent clinic attendance or difficulty being contacted and patient choice not to start. Of those who had a proviral DNA resistance test as workup for LAI CAB/RPV ( n  = 135), 18.5% had a resistance mutation identified that may have impacted the activity of LAI CAB/RPV.

CONCLUSION

Despite novel challenges over half of our cohort initiated LAI CAB/RPV. Evaluating for potential non-nucleoside reverse transcriptase inhibitor resistance is an important part of the workup for LAI CAB/RPV and proviral DNA resistance testing can be an additional tool to identify potential resistance.

摘要

目的

描述我们评估并启动使用长效注射用卡博特韦/利匹韦林(CAB/RPV)治疗个体的经验,并评估与开始使用长效注射用CAB/RPV相关的因素以及未开始使用的原因。

设计

我们在加州大学圣地亚哥分校欧文诊所进行了一项回顾性单中心研究。

方法

我们纳入了2021年4月至2022年6月期间所有对长效注射用CAB/RPV治疗表示感兴趣且已就是否开始使用长效注射用CAB/RPV做出明确决定的个体。

结果

总共纳入了383名个体,其中201名(52.5%)开始使用长效注射用CAB/RPV。开始使用长效注射用CAB/RPV的个体更年轻(P = 0.02),更有可能采用双药方案或第一代整合酶抑制剂方案,而采用蛋白酶抑制剂或多类药物方案的可能性较小。未开始使用长效注射用CAB/RPV的最常见原因是就诊不规律或难以联系到以及患者选择不开始使用。在那些接受过作为长效注射用CAB/RPV检查的前病毒DNA耐药性检测的个体中(n = 135),18.5%检测出可能影响长效注射用CAB/RPV活性的耐药突变。

结论

尽管存在新的挑战,但我们队列中超过一半的个体开始使用了长效注射用CAB/RPV。评估潜在的非核苷类逆转录酶抑制剂耐药性是长效注射用CAB/RPV检查的重要组成部分,前病毒DNA耐药性检测可以作为识别潜在耐药性的额外工具。

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