Butt Zahid A, Wong Stanley, Rossi Carmine, Binka Mawuena, Wong Jason, Yu Amanda, Darvishian Maryam, Alvarez Maria, Chapinal Nuria, Mckee Geoff, Gilbert Mark, Tyndall Mark W, Krajden Mel, Janjua Naveed Z
School of Public Health and Health Systems, University of Waterloo, Waterloo, Ontario, Canada.
British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
Open Forum Infect Dis. 2020 Aug 13;7(9):ofaa347. doi: 10.1093/ofid/ofaa347. eCollection 2020 Sep.
Hepatitis C virus (HCV), hepatitis B virus (HBV), and human immunodeficiency virus (HIV) infections are associated with significant mortality globally and in North America. However, data on impact of concurrent multiple infections on mortality risk are limited. We evaluated the effect of HCV, HBV, and HIV infections and coinfections and associated factors on all-cause mortality in British Columbia (BC), Canada.
The BC Hepatitis Testers Cohort includes ~1.7 million individuals tested for HCV or HIV, or reported as a case of HCV, HIV, or HBV from 1990 to 2015, linked to administrative databases. We followed people with HCV, HBV, or HIV monoinfection, coinfections, and triple infections from their negative status to date of death or December 31, 2016. Extended Cox proportional hazards regression was used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for factors associated with all-cause mortality.
Of 658 704 individuals tested for HCV, HBV, and HIV, there were 33 804 (5.13%) deaths. In multivariable Cox regression analysis, individuals with HCV/HBV/HIV (HR, 8.9; 95% CI, 8.2-9.7) infections had the highest risk of mortality followed by HCV/HIV (HR, 4.8; 95% CI, 4.4-5.1), HBV/HIV (HR, 4.1; 95% CI, 3.5-4.8), HCV/HBV (HR, 3.9; 95% CI, 3.7-4.2), HCV (HR, 2.6; 95% CI, 2.6-2.7), HBV (HR, 2.2; 95% CI, 2.0-2.3), and HIV (HR, 1.6; 95% CI, 1.5-1.7). Additional factors associated with mortality included injection drug use, problematic alcohol use, material deprivation, diabetes, chronic kidney disease, heart failure, and hypertension.
Concurrent multiple infections are associated with high mortality risk. Substance use, comorbidities, and material disadvantage were significantly associated with mortality independent of coinfection. Preventive interventions, including harm reduction combined with coinfection treatments, can significantly reduce mortality.
丙型肝炎病毒(HCV)、乙型肝炎病毒(HBV)和人类免疫缺陷病毒(HIV)感染在全球和北美均与显著的死亡率相关。然而,关于同时发生多种感染对死亡风险影响的数据有限。我们评估了HCV、HBV和HIV感染、合并感染及相关因素对加拿大不列颠哥伦比亚省(BC)全因死亡率的影响。
BC肝炎检测队列包括1990年至2015年期间接受HCV或HIV检测,或报告为HCV、HIV或HBV病例的约170万人,这些数据与行政数据库相关联。我们追踪了HCV、HBV或HIV单一感染、合并感染和三重感染的人群,从其阴性状态直至死亡日期或2016年12月31日。采用扩展的Cox比例风险回归来估计与全因死亡率相关因素的风险比(HRs)和95%置信区间(CIs)。
在658704名接受HCV、HBV和HIV检测的个体中,有33804人(5.13%)死亡。在多变量Cox回归分析中,HCV/HBV/HIV感染个体(HR,8.9;95%CI,8.2 - 9.7)的死亡风险最高,其次是HCV/HIV(HR,4.8;95%CI,4.4 - 5.1)、HBV/HIV(HR,4.1;95%CI,3.5 - 4.8)、HCV/HBV(HR,3.9;95%CI,3.7 - 4.2)、HCV(HR,2.6;95%CI,2.6 - 2.7)、HBV(HR,2.2;95%CI,2.0 - 2.3)和HIV(HR,1.6;95%CI,1.5 - 1.7)。与死亡率相关的其他因素包括注射吸毒、有问题的饮酒、物质匮乏、糖尿病、慢性肾病、心力衰竭和高血压。
同时发生多种感染与高死亡风险相关。物质使用、合并症和物质劣势与死亡率显著相关,且独立于合并感染。包括减少伤害与合并感染治疗相结合的预防性干预措施可显著降低死亡率。