Centre for Research on Drugs and Health Behaviour, Department of Social and Environmental Health Research, London School of Hygiene and Tropical Medicine, London, UK.
Department of Epidemiology, Lazio Regional Health Service, Rome, Italy.
Addiction. 2018 Mar;113(3):545-563. doi: 10.1111/add.14012. Epub 2017 Oct 23.
To estimate the effects of needle and syringe programmes (NSP) and opioid substitution therapy (OST), alone or in combination, for preventing acquisition of hepatitis C virus (HCV) in people who inject drugs (PWID).
Systematic review and meta-analysis. Bibliographic databases were searched for studies measuring concurrent exposure to current OST (within the last 6 months) and/or NSP and HCV incidence among PWID. High NSP coverage was defined as regular NSP attendance or ≥ 100% coverage (receiving sufficient or greater number of needles and syringes per reported injecting frequency). Studies were assessed using the Cochrane risk of bias in non-randomized studies tool. Random-effects models were used in meta-analysis.
We identified 28 studies (n = 6279) in North America (13), United Kingdom (five), Europe (four), Australia (five) and China (one). Studies were at moderate (two), serious (17) critical (seven) and non-assessable risk of bias (two). Current OST is associated with 50% [risk ratio (RR) =0.50, 95% confidence interval (CI) = 0.40-0.63] reduction in HCV acquisition risk, consistent across region and with low heterogeneity (I = 0, P = 0.889). Weaker evidence was found for high NSP coverage (RR = 0.79, 95% CI = 0.39-1.61) with high heterogeneity (I = 77%, P = 0.002). After stratifying by region, high NSP coverage in Europe was associated with a 56% reduction in HCV acquisition risk (RR = 0.44, 95% CI = 0.24-0.80) with low heterogeneity (I = 12.3%, P = 0.337), but not in North America (RR = 1.58, I = 89.5%, P = < 0.001). Combined OST/NSP is associated with a 74% reduction in HCV acquisition risk (RR = 0.26, 95% CI = 0.07-0.89, I = 80% P = 0.007). According to Grades of Recommendation Assessment, Development and Evaluation (GRADE) criteria, the evidence on OST and combined OST/NSP is low quality, while NSP is very low.
Opioid substitution therapy reduces risk of hepatitis C acquisition and is strengthened in combination with needle and syringe programmes (NSP). There is weaker evidence for the impact of needle syringe programmes alone, although stronger evidence that high coverage is associated with reduced risk in Europe.
评估单独或联合使用针具和注射器计划(NSP)和阿片类药物替代疗法(OST),预防注射吸毒者(PWID)中丙型肝炎病毒(HCV)感染的效果。
系统评价和荟萃分析。检索了测量当前 OST(在过去 6 个月内)和/或 NSP 同时暴露以及 PWID 中 HCV 发病率的研究。高 NSP 覆盖率定义为定期参加 NSP 或覆盖率达到 100%(根据报告的注射频率,获得足够或更多数量的针和注射器)。使用 Cochrane 非随机研究工具评估研究的偏倚风险。使用随机效应模型进行荟萃分析。
我们在北美(13 项)、英国(5 项)、欧洲(4 项)、澳大利亚(5 项)和中国(1 项)确定了 28 项研究(n=6279)。研究的偏倚风险为中度(2 项)、严重(17 项)、关键(7 项)和不可评估(2 项)。当前的 OST 与 HCV 感染风险降低 50%(风险比 [RR] =0.50,95%置信区间 [CI] =0.40-0.63)相关,这在不同地区和低异质性(I=0,P=0.889)中是一致的。高 NSP 覆盖率的证据较弱(RR=0.79,95%CI=0.39-1.61),异质性很高(I=77%,P=0.002)。按地区分层后,欧洲高 NSP 覆盖率与 HCV 感染风险降低 56%相关(RR=0.44,95%CI=0.24-0.80),异质性低(I=12.3%,P=0.337),但在北美没有(RR=1.58,I=89.5%,P<0.001)。联合 OST/NSP 与 HCV 感染风险降低 74%相关(RR=0.26,95%CI=0.07-0.89,I=80%,P=0.007)。根据推荐评估、制定和评估(GRADE)标准,OST 和联合 OST/NSP 的证据质量低,而 NSP 的证据质量极低。
阿片类药物替代疗法降低了丙型肝炎感染的风险,并且与针具和注射器计划(NSP)联合使用时得到了加强。单独使用 NSP 的证据较弱,但在欧洲,高覆盖率与降低风险的相关性更强。