Department of Internal Medicine, UT Southwestern Medical Center and Parkland Memorial Hospital, Parkland Health and Hospital System, Dallas, Texas, USA.
BMJ Open. 2013 Sep 3;3(9):e003231. doi: 10.1136/bmjopen-2013-003231.
To demonstrate the survival benefit from sustained virological response (SVR) in a safety net hospital population with limited resources for hepatitis C virus (HCV) therapy.
We conducted a retrospective study at an urban safety net hospital in the USA.
242 patients receiving standard HCV therapy between 2001 and 2006.
Response rates, including SVR, were recorded for each patient. Univariate and multivariate analyses were performed to identify predictors of SVR and 5-year survival.
A total of 242 eligible patients were treated. Treatment was completed in 197 (81%) patients, with 43 patients discontinuing therapy early-32 due to adverse events and 11 due to non-compliance. Complications on treatment were frequent, including three deaths. SVR was achieved in 83 patients (34%). On multivariate analysis, independent predictors of a decreased likelihood of achieving SVR included African-American race (OR 0.20, 95% CI 0.07 to 0.54), genotype 1 HCV infection (OR 0.25, 95% CI 0.13 to 0.50) and the presence of cirrhosis (OR 0.26, 95% CI 0.12 to 0.58). Survival was 98% in those achieving SVR (median follow-up 72 months) and 71% in non-responders and those discontinuing therapy (n=91, median known follow-up 65 and 36 months, respectively). On multivariate analysis, the only independent predictor of improved survival was SVR (HR 0.12, 95% CI 0.03 to 0.52). Both cirrhosis and hypoalbuminaemia were independent predictors of increased mortality.
Treatment before histological cirrhosis develops, in combination with careful selection, may improve long-term outcomes without compromising other healthcare endeavours in safety net hospitals and areas with financial limitations.
在资源有限的安全网医院人群中展示持续病毒学应答(SVR)带来的生存获益,这些人群患有丙型肝炎病毒(HCV)。
我们在美国的一家城市安全网医院进行了回顾性研究。
2001 年至 2006 年间接受标准 HCV 治疗的 242 例患者。
为每位患者记录了反应率,包括 SVR。进行了单变量和多变量分析,以确定 SVR 和 5 年生存率的预测因素。
共有 242 名符合条件的患者接受了治疗。197 例(81%)患者完成了治疗,32 例(32%)因不良反应和 11 例(11%)因不依从而提前中断治疗。治疗期间并发症频繁,包括 3 例死亡。83 例(34%)患者达到 SVR。多变量分析显示,SVR 可能性降低的独立预测因素包括非裔美国人种族(OR 0.20,95%CI 0.07 至 0.54)、基因型 1 HCV 感染(OR 0.25,95%CI 0.13 至 0.50)和肝硬化(OR 0.26,95%CI 0.12 至 0.58)。达到 SVR 的患者的生存率为 98%(中位随访 72 个月),未达到 SVR 和中断治疗的患者(n=91)的生存率分别为 71%和 65 个月和 36 个月。多变量分析显示,唯一改善生存的独立预测因素是 SVR(HR 0.12,95%CI 0.03 至 0.52)。肝硬化和低白蛋白血症都是死亡风险增加的独立预测因素。
在组织学肝硬化发生之前进行治疗,并结合精心选择,可能会在不影响安全网医院和资金有限地区的其他医疗保健工作的情况下,改善长期结果。