School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
Public Health Scotland, Glasgow, UK.
Addiction. 2024 Feb;119(2):369-378. doi: 10.1111/add.16344. Epub 2023 Sep 19.
Direct-acting antiviral (DAA) treatment has an established positive effect on liver outcomes in people with hepatitis C infection; however, there is insufficient evidence regarding its effects on the 'extra-hepatic' outcomes of drug-related hospitalization and mortality (DRM) among people who inject drugs (PWID). We investigated associations between these outcomes and DAA treatment by comparing post-treatment to baseline periods using a within-subjects design to minimize selection bias concerns with cohort or case-control designs.
This was a self-controlled case-series study.
Scotland, 1 January 2015-30 November 2020.
The study population of non-cirrhotic, DAA-treated PWID was identified using a data set linking Scotland's hepatitis C diagnosis, HCV clinical databases, national inpatient/day-case hospital records and the national deaths register. Three principal outcomes (drug overdose admission, non-viral injecting related admission and drug-related mortality) were defined using ICD codes.
Self-controlled case-series methodology was used to estimate the relative incidence (RI) of each outcome associated with time on treatment and up to six 90-day exposure risk periods thereafter.
A total of 6050 PWID were treated with DAAs in the sampling time-frame. Compared with the baseline period, there was a significantly lowered risk of a drug overdose hospital admission in the second to fifth exposure risk periods only [relative incidence (RI) = 0.86, 95% confidence interval (CI) = 0.80-0.99; 0.89, 95% CI = 0.80-0.99; 0.86, 95% CI = 0.77-0.96; 0.88, 95% CI = 0.78-0.99, respectively]. For non-viral injecting-related admission, there was a reduced risk in the first, third and fourth exposure risk periods (RI = 0.76, 95% CI = 0.64-0.90; 0.75, 95% CI = 0.62-0.90; 0.79, 95% CI = 0.66-0.96, respectively). There was no evidence for reduced DRM risk in any period following treatment end.
Among people who inject drugs in Scotland, direct-acting antiviral treatment appears to be associated with a small, non-durable reduction in the risk of drug-related hospital admission, but not drug-related mortality. Direct-acting antiviral therapy, despite high effectiveness against liver disease, does not appear to offer a panacea for reducing other drug-related health harms.
直接作用抗病毒 (DAA) 治疗对丙型肝炎感染患者的肝脏结局具有明确的积极影响;然而,在注射毒品者(PWID)中,关于药物相关住院和死亡率(DRM)的“肝外”结局的证据不足。我们通过使用个体内设计来比较治疗后的时期与基线时期,以最小化队列或病例对照设计中选择偏差的问题,研究了这些结局与 DAA 治疗之间的关联。
这是一项自身对照病例系列研究。
苏格兰,2015 年 1 月 1 日至 2020 年 11 月 30 日。
使用一个链接苏格兰丙型肝炎诊断、HCV 临床数据库、全国住院/日间病例医院记录和国家死亡登记处的数据集,确定非肝硬化、接受 DAA 治疗的 PWID 研究人群。使用 ICD 代码定义了三个主要结局(药物过量入院、非病毒性注射相关入院和药物相关死亡)。
使用自身对照病例系列方法估计与治疗时间相关的每个结局的相对发病率(RI)以及之后最多六个 90 天暴露风险期。
在采样时间范围内,共有 6050 名 PWID 接受了 DAA 治疗。与基线期相比,仅在第二至第五个暴露风险期,药物过量入院的风险显著降低(相对发病率(RI)=0.86,95%置信区间(CI)=0.80-0.99;0.89,95%CI=0.80-0.99;0.86,95%CI=0.77-0.96;0.88,95%CI=0.78-0.99,分别)。对于非病毒性注射相关入院,在第一个、第三个和第四个暴露风险期风险降低(RI=0.76,95%CI=0.64-0.90;0.75,95%CI=0.62-0.90;0.79,95%CI=0.66-0.96,分别)。在治疗结束后的任何时期,都没有证据表明 DRM 风险降低。
在苏格兰注射毒品者中,直接作用抗病毒治疗似乎与药物相关住院风险的小而不持久的降低相关,但与药物相关死亡率无关。尽管对肝脏疾病具有高度有效性,但直接作用抗病毒疗法似乎并不能提供解决其他药物相关健康危害的万能药。