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DigiPrEP:一项评估数字药丸系统测量使用物质的男男性行为者中 PrEP 依从性的可行性、可接受性和准确性的试点研究。

DigiPrEP: A Pilot Trial to Evaluate the Feasibility, Acceptability, and Accuracy of a Digital Pill System to Measure PrEP Adherence in Men Who Have Sex With Men Who Use Substances.

机构信息

Division of Medical Toxicology, Department of Emergency Medicine, Brigham and Women's Hospital, Boston, MA.

The Fenway Institute, Fenway Health, Boston, MA.

出版信息

J Acquir Immune Defic Syndr. 2022 Feb 1;89(2):e5-e15. doi: 10.1097/QAI.0000000000002854.

Abstract

BACKGROUND

Adherence to once daily oral preexposure prophylaxis (PrEP) for HIV prevention can be challenging for men who have sex with men (MSM) with substance use. Digital pill systems (DPS) comprise a radiofrequency emitter integrated into a gelatin capsule containing PrEP, which transmits data to a wearable Reader following ingestion, thereby enabling direct, real-time adherence measurement. This study evaluated the feasibility, acceptability, and accuracy of a DPS to measure PrEP adherence.

METHODS

A 90-day, single-arm, open-label, pilot demonstration trial was conducted with adult, cisgender, HIV-negative MSM on PrEP with nonalcohol substance use. Feasibility was measured via DPS engagement and timeline followback. Acceptability was assessed via qualitative user experience interviews. Accuracy was evaluated via DPS performance metrics, pill counts, and DBS to quantify tenofovir diphosphate.

RESULTS

Sixteen MSM enrolled (median age, 32 years), and 15 completed the study. Engagement remained stable over time. Emergent nonadherence patterns included intercurrent substance use. The DPS was largely acceptable based on interviews; the predominant barrier to use was the Reader. DPS-recorded ingestions totaled 1099, including 83.9% were detected by Reader and 16.1% were reported manually. The DPS recorded 92.2% of 1192 total expected ingestions per pill counts. Point-biserial correlation (R = 0.58; 95% CI: 0.21 to 0.80; P = 0.047) and Pearson correlation (month 1: R = 0.85; 95% CI: 0.57 to 0.95; P = 0.0002; month 3: R = 0.75; 95% CI: 0.17 to 0.94; P = 0.0197) showed strong correlations between DPS-recorded adherence and tenofovir diphosphate in dried blood spots.

CONCLUSION

DPS are a feasible, acceptable, and accurate method of measuring PrEP adherence in MSM with substance use. Future investigations should incorporate DPS into behavioral interventions targeting nonadherence.

摘要

背景

对于有药物使用问题的男男性行为者(MSM),每日口服暴露前预防(PrEP)药物的依从性可能是一个挑战。数字药丸系统(DPS)由一个集成在含有 PrEP 胶囊中的射频发射器组成,服用后会将数据传输到可穿戴式读取器,从而能够直接、实时地测量药物依从性。本研究评估了 DPS 测量 PrEP 依从性的可行性、可接受性和准确性。

方法

一项为期 90 天的、单臂、开放标签、初步试验在使用非酒精类物质的成年、顺性别、HIV 阴性的 MSM 中进行。通过 DPS 参与和时间线随访来衡量可行性。通过定性用户体验访谈评估可接受性。通过 DPS 性能指标、药丸计数和 DBS 来定量检测替诺福韦二磷酸酯来评估准确性。

结果

16 名 MSM 入组(中位年龄 32 岁),15 名完成了研究。随着时间的推移,参与度保持稳定。出现的不依从模式包括并发的药物使用。根据访谈,DPS 基本上是可以接受的;使用的主要障碍是读取器。DPS 记录的摄入量共计 1099 次,其中 83.9%被读取器检测到,16.1%手动报告。DPS 记录了 1192 片预计每次摄入的 92.2%。点二项式相关系数(R = 0.58;95%置信区间:0.21 至 0.80;P = 0.047)和皮尔逊相关系数(第 1 个月:R = 0.85;95%置信区间:0.57 至 0.95;P = 0.0002;第 3 个月:R = 0.75;95%置信区间:0.17 至 0.94;P = 0.0197)表明 DPS 记录的依从性与干血斑中的替诺福韦二磷酸酯之间存在较强的相关性。

结论

DPS 是一种可行、可接受和准确的方法,可用于测量有药物使用问题的 MSM 的 PrEP 依从性。未来的研究应将 DPS 纳入针对不依从性的行为干预措施中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4de5/8740604/7a113e96ae89/qai-89-e5-g002.jpg

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