Young Jim, Rossi Carmine, Gill John, Walmsley Sharon, Cooper Curtis, Cox Joseph, Martel-Laferriere Valerie, Conway Brian, Pick Neora, Vachon Marie-Louise, Klein Marina B
Department of Medicine, Division of Infectious Diseases, McGill University Health Centre, Montreal, Canada.
Basel Institute for Clinical Epidemiology and Biostatistics, University Hospital Basel, Switzerland.
Clin Infect Dis. 2017 May 1;64(9):1154-1162. doi: 10.1093/cid/cix126.
Highly effective hepatitis C virus (HCV) therapies have spurred a scale-up of treatment to populations at greater risk of reinfection after sustained virologic response (SVR). Reinfection may be higher in HIV-HCV coinfection, but prior studies have considered small selected populations. We assessed risk factors for reinfection after SVR in a representative cohort of Canadian coinfected patients in clinical care.
All patients achieving SVR after HCV treatment were followed with HCV RNA measurements every 6 months in a prospective cohort study. We used Bayesian Cox regression to estimate reinfection rates according to patient reported injection drug use (IDU) and sexual activity among men who have sex with men (MSM).
Of 497 patients treated for HCV, 257 achieved SVR and had at least 1 subsequent RNA measurement. During 589 person-years of follow-up (PYFU) after SVR, 18 (7%) became HCV RNA positive. The adjusted reinfection rate (per 1000 PYFU) in the first year after SVR was highest in those who reported high-frequency IDU (58; 95% credible interval [CrI], 18-134) followed by MSM reporting high-risk sexual activity (26; 95% CrI, 6-66) and low-frequency IDU (22; 95% CrI, 4-68). The rate in low-risk MSM (16; 95% CrI, 4-38) was similar to that in reference patients (10; 95% CrI, 4-20). Reinfection rates did not diminish with time.
HCV reinfection rates varied according to risk. Measures are needed to reduce risk behaviors and increase monitoring in high-risk IDU and MSM if HCV elimination targets are to be realized.
高效的丙型肝炎病毒(HCV)治疗方法促使对持续病毒学应答(SVR)后再感染风险更高的人群扩大治疗规模。HIV-HCV合并感染患者的再感染率可能更高,但先前的研究关注的是经过挑选的小群体。我们在一个具有代表性的接受临床护理的加拿大合并感染患者队列中评估了SVR后再感染的风险因素。
在一项前瞻性队列研究中,对所有HCV治疗后实现SVR的患者每6个月进行一次HCV RNA检测随访。我们使用贝叶斯Cox回归,根据患者报告的注射吸毒(IDU)情况以及男男性行为者(MSM)的性行为来估计再感染率。
在497例接受HCV治疗的患者中,257例实现了SVR,并且至少进行了1次后续RNA检测。在SVR后的589人年随访(PYFU)期间,18例(7%)HCV RNA转为阳性。SVR后第一年的校正再感染率(每1000 PYFU)在报告高频IDU的患者中最高(58;95%可信区间[CrI],18 - 134),其次是报告高风险性行为的MSM(26;95% CrI,6 - 66)和低频IDU患者(22;95% CrI,4 - 68)。低风险MSM的再感染率(16;95% CrI,4 - 38)与对照患者相似(10;95% CrI,4 - 20)。再感染率并未随时间降低。
HCV再感染率因风险而异。如果要实现消除HCV的目标,需要采取措施减少风险行为,并加强对高风险IDU和MSM的监测。