Pear Therapeutics Inc., Boston, MA, USA.
Curr Med Res Opin. 2021 Feb;37(2):175-183. doi: 10.1080/03007995.2020.1846023. Epub 2020 Dec 7.
To evaluate patient engagement and usage of a prescription digital therapeutic (PDT) and associated outcomes of opioid use and treatment retention in a large real-world dataset of patients with opioid use disorder (OUD) treated with buprenorphine medication for opioid use disorder (MOUD). PDTs are software-based disease treatments evaluated for safety and effectiveness in randomized clinical trials (RCTs), and authorized by the U.S. Food and Drug Administration (FDA) to treat disease with approved directions for use (label).
A real-world observational evaluation of an all-comer population of patients who redeemed a 12-week prescription for the reSET-O PDT. Engagement and therapeutic use data were collected and analysed on a population level. Substance use was evaluated as a composite of self-reports recorded with reSET-O and urine drug screens (UDS).
Data from 3144 individuals with OUD were evaluated. 45.5% were between ages 30 and 39 years. 80% completed at least 8 of the 67 possible therapeutic modules, 66% completed half of all modules, and 49% completed all modules. Abstinence during the last 4 weeks of treatment was calculated with two imputation methodologies: 66% abstinent using "missing data excluded (patients with no data as positive)", and 91% abstinent with "missing data removed (patients with no data excluded)". 91% of patients met the responder definition of ≥80% of self-report or UDS negative. 74.2% of patients were retained through the last 4 weeks of treatment. Subgroup analysis of patients using reSET-O appropriately (4 or more modules per week for the first 4 weeks) showed 88.1% abstinence using "missing data excluded (patients with no data as positive)", and retention at weeks 9-12 of 85.8%.
Results demonstrate that reSET-O is readily and broadly used by patients with OUD and that high real-world engagement with the therapeutic is positively associated with abstinence and retention in treatment. ReSET-O is a potentially valuable adjunct to buprenorphine MOUD therapy for patients with OUD.
评估患者对处方数字疗法(PDT)的参与度和使用情况,并结合接受丁丙诺啡药物治疗的阿片类药物使用障碍(OUD)患者的大型真实世界数据集,评估其对阿片类药物使用和治疗保留的影响。PDT 是一种基于软件的疾病治疗方法,在随机临床试验(RCT)中评估其安全性和有效性,并经美国食品和药物管理局(FDA)批准,按照已批准的使用说明(标签)治疗疾病。
对接受再 SET-O PDT 为期 12 周处方的所有患者进行真实世界观察性评估。在人群层面收集和分析参与度和治疗使用数据。药物使用情况通过 reSET-O 记录的自我报告和尿液药物检测(UDS)的综合情况进行评估。
共评估了 3144 名 OUD 患者的数据。45.5%的患者年龄在 30 到 39 岁之间。80%的患者完成了 67 个可能的治疗模块中的至少 8 个,66%的患者完成了一半的模块,49%的患者完成了所有模块。使用两种插补方法计算治疗最后 4 周的禁欲情况:66%的患者在“排除缺失数据(无数据患者为阳性)”时禁欲,91%的患者在“删除缺失数据(无数据患者排除)”时禁欲。91%的患者符合应答者定义,即自我报告或 UDS 阴性率≥80%。74.2%的患者在治疗最后 4 周内得到保留。对适当使用 reSET-O(前 4 周每周使用 4 个或更多模块)的患者进行亚组分析显示,66%的患者在“排除缺失数据(无数据患者为阳性)”时禁欲,85.8%的患者在第 9-12 周保留。
结果表明,reSET-O 易于被 OUD 患者广泛使用,而在治疗中与治疗高度相关的高真实世界参与度与禁欲和保留治疗呈正相关。reSET-O 可能是 OUD 患者丁丙诺啡 MOUD 治疗的有效辅助手段。