Talal Andrew H, Markatou Marianthi, Liu Anran, Perumalswami Ponni V, Dinani Amreen M, Tobin Jonathan N, Brown Lawrence S
Division of Gastroenterology, Hepatology, and Nutrition, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.
Department of Biostatistics, University at Buffalo, Buffalo, New York.
JAMA. 2024 Apr 23;331(16):1369-1378. doi: 10.1001/jama.2024.2452.
Facilitated telemedicine may promote hepatitis C virus elimination by mitigating geographic and temporal barriers.
To compare sustained virologic responses for hepatitis C virus among persons with opioid use disorder treated through facilitated telemedicine integrated into opioid treatment programs compared with off-site hepatitis specialist referral.
DESIGN, SETTING, AND PARTICIPANTS: Prospective, cluster randomized clinical trial using a stepped wedge design. Twelve programs throughout New York State included hepatitis C-infected participants (n = 602) enrolled between March 1, 2017, and February 29, 2020. Data were analyzed from December 1, 2022, through September 1, 2023.
Hepatitis C treatment with direct-acting antivirals through comanagement with a hepatitis specialist either through facilitated telemedicine integrated into opioid treatment programs (n = 290) or standard-of-care off-site referral (n = 312).
The primary outcome was hepatitis C virus cure. Twelve programs began with off-site referral, and every 9 months, 4 randomly selected sites transitioned to facilitated telemedicine during 3 steps without participant crossover. Participants completed 2-year follow-up for reinfection assessment. Inclusion criteria required 6-month enrollment in opioid treatment and insurance coverage of hepatitis C medications. Generalized linear mixed-effects models were used to test for the intervention effect, adjusted for time, clustering, and effect modification in individual-based intention-to-treat analysis.
Among 602 participants, 369 were male (61.3%); 296 (49.2%) were American Indian or Alaska Native, Asian, Black or African American, multiracial, or other (ie, no race category was selected, with race data collected according to the 5 standard National Institutes of Health categories); and 306 (50.8%) were White. The mean (SD) age of the enrolled participants in the telemedicine group was 47.1 (13.1) years; that of the referral group was 48.9 (12.8) years. In telemedicine, 268 of 290 participants (92.4%) initiated treatment compared with 126 of 312 participants (40.4%) in referral. Intention-to-treat cure percentages were 90.3% (262 of 290) in telemedicine and 39.4% (123 of 312) in referral, with an estimated logarithmic odds ratio of the study group effect of 2.9 (95% CI, 2.0-3.5; P < .001) with no effect modification. Observed cure percentages were 246 of 290 participants (84.8%) in telemedicine vs 106 of 312 participants (34.0%) in referral. Subgroup effects were not significant, including fibrosis stage, urban or rural participant residence location, or mental health (anxiety or depression) comorbid conditions. Illicit drug use decreased significantly (referral: 95% CI, 1.2-4.8; P = .001; telemedicine: 95% CI, 0.3-1.0; P < .001) among cured participants. Minimal reinfections (n = 13) occurred, with hepatitis C virus reinfection incidence of 2.5 per 100 person-years. Participants in both groups rated health care delivery satisfaction as high or very high.
Opioid treatment program-integrated facilitated telemedicine resulted in significantly higher hepatitis C virus cure rates compared with off-site referral, with high participant satisfaction. Illicit drug use declined significantly among cured participants with minimal reinfections.
ClinicalTrials.gov Identifier: NCT02933970.
便捷远程医疗可通过缓解地理和时间障碍来促进丙型肝炎病毒的消除。
比较通过整合到阿片类药物治疗项目中的便捷远程医疗接受治疗的阿片类药物使用障碍患者与非现场丙型肝炎专科转诊患者的丙型肝炎病毒持续病毒学应答情况。
设计、设置和参与者:采用阶梯楔形设计的前瞻性整群随机临床试验。纽约州的12个项目纳入了2017年3月1日至2020年2月29日期间登记的丙型肝炎感染参与者(n = 602)。对2022年12月1日至2023年9月1日期间的数据进行了分析。
通过与丙型肝炎专科医生共同管理,使用直接作用抗病毒药物进行丙型肝炎治疗,其中一组通过整合到阿片类药物治疗项目中的便捷远程医疗(n = 290),另一组为标准治疗的非现场转诊(n = 312)。
主要结局是丙型肝炎病毒治愈。12个项目从非现场转诊开始,每9个月,4个随机选择的地点在3个阶段过渡到便捷远程医疗,参与者不交叉。参与者完成了为期2年的随访以评估再感染情况。纳入标准要求在阿片类药物治疗中登记6个月且丙型肝炎药物有保险覆盖。在基于个体意向性治疗分析中,使用广义线性混合效应模型来检验干预效果,并对时间、聚类和效应修正进行了调整。
在602名参与者中,369名男性(61.3%);296名(49.2%)为美洲印第安人或阿拉斯加原住民、亚洲人、黑人或非裔美国人、多种族或其他(即未选择种族类别,种族数据根据美国国立卫生研究院5个标准类别收集);306名(50.8%)为白人。远程医疗组登记参与者的平均(标准差)年龄为47.1(13.1)岁;转诊组为48.9(12.8)岁。在远程医疗中,290名参与者中有268名(92.4%)开始治疗,而转诊组312名参与者中有126名(40.4%)开始治疗。意向性治疗治愈率在远程医疗中为90.3%(290名中的262名),在转诊中为39.4%(312名中的123名),研究组效应的估计对数比值比为2.9(95%CI,2.0 - 3.5;P <.001),无效应修正。观察到的治愈率在远程医疗中为290名参与者中的246名(84.8%),在转诊中为312名参与者中的106名(34.0%)。亚组效应不显著,包括纤维化阶段、城市或农村参与者居住地点或心理健康(焦虑或抑郁)合并症。治愈参与者中非法药物使用显著减少(转诊:95%CI,1.2 - 4.8;P =.001;远程医疗:95%CI,0.3 - 1.0;P <.001)。再感染极少(n = 13),丙型肝炎病毒再感染发生率为每100人年2.5例。两组参与者对医疗服务的满意度都评为高或非常高。
与非现场转诊相比,表示阿片类药物治疗项目中整合的便捷远程医疗使丙型肝炎病毒治愈率显著更高,参与者满意度高。治愈参与者中非法药物使用显著下降,再感染极少。
ClinicalTrials.gov标识符:NCT02933970