Design and implementation of a Type-2 hybrid, prospective randomized trial of opioid agonist therapies integration into primary care clinics in Ukraine

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
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引用次数: 0

Abstract

Introduction

Ukraine has high HIV prevalence, concentrated among people who inject drugs (PWID), mostly of opioids. Maintenance on opioid agonist therapies (OAT) is the most effective evidence-based treatment for opioid use disorder. As PWID experience high morbidity and mortality from preventable and treatable non-communicable diseases, international agencies recommend integrating OAT into primary care centers (PCC).

Methods

A randomized, type-2 hybrid implementation trial was carried out to compare outcomes of OAT integration in PCC to OAT delivery at specialty treatment centers (STC) – standard-of-care. Tele-education supporting PCC providers in managing OAT, HIV, tuberculosis and non-communicable diseases along with pay-for-performance incentives were used to facilitate implementation. Consenting patients underwent 1:2 randomization to either STC or PCC. Quality health indicators (QHIs), a composite percentage of recommended primary and specialty services accessed by patients (blood/urine tests, cancer screenings, etc.), were defined as efficacy outcomes and were assessed by participant self-report at baseline and every 6 months over 24 months and electronic chart reviews after the completion of the follow-up. The primary outcome is defined as the difference in composite QHI scores at 24 months, in which a repeated measures likelihood-based mixed model with missing at random assumptions will be used. Providers at PCC completed surveys at baseline, 12 and 24 months to assess implementation outcomes including changes in stigma and attitudes towards OAT and PWID.

Preliminary results

Among the 1459 participants allocated to STC (N = 509) or PCC (N = 950), there were no differences in clinical and demographic characteristics. Self-reported prevalences were available for HIV (42 %), HCV (57 %), and prior tuberculosis (17 %). Study retention at 6, 12, 18, and 24 months was as 91 %, 85 %, 80 %, and 74 %, respectively.

Conclusion

PWID have a high prevalence of medical comorbidities and integrating OAT into primary care settings has the potential to improve the health of PWID. Findings from this study can help guide implementation of integrated care in Ukraine and throughout similar low-resource, high-burden countries in the Eastern European and Central Asian region.

乌克兰将阿片类激动剂疗法纳入初级保健诊所的 2 型混合前瞻性随机试验的设计与实施
导言乌克兰的艾滋病毒感染率很高,主要集中在注射吸毒者中,其中大部分是阿片类药物注射者。阿片类药物激动剂疗法(OAT)是治疗阿片类药物使用障碍最有效的循证疗法。由于PWID在可预防和可治疗的非传染性疾病中发病率和死亡率较高,国际机构建议将阿片类激动剂疗法纳入初级保健中心(PCC)。方法:开展了一项随机、2型混合实施试验,以比较将阿片类激动剂疗法纳入初级保健中心与在专科治疗中心(STC)提供阿片类激动剂疗法(标准护理)的结果。通过远程教育支持 PCC 医疗服务提供者管理 OAT、艾滋病、结核病和非传染性疾病,并采用按绩效付费的激励措施来促进实施。获得同意的患者按 1:2 随机分配到 STC 或 PCC。质量健康指标(QHIs),即患者获得建议的初级和专科服务(血液/尿液检测、癌症筛查等)的综合百分比,被定义为疗效结果,通过参与者在基线和 24 个月内每 6 个月的自我报告以及随访结束后的电子病历审查进行评估。主要结果定义为 24 个月时 QHI 综合得分的差异,将采用基于似然法的重复测量混合模型和随机缺失假设。PCC 的提供者在基线、12 个月和 24 个月时完成了调查,以评估实施结果,包括对 OAT 和 PWID 的污名化和态度的变化。自我报告的患病率包括艾滋病毒(42%)、丙型肝炎病毒(57%)和既往结核病(17%)。6、12、18 和 24 个月的研究保留率分别为 91%、85%、80% 和 74%。这项研究的结果有助于指导乌克兰以及东欧和中亚地区类似的低资源、高负担国家实施综合护理。
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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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