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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Hepatitis C transmission from seropositive, nonviremic donors to non–hepatitis C liver transplant recipients
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Hepatitis C transmission from seropositive, nonviremic donors to non–hepatitis C liver transplant recipients

机译:丙型肝炎从血清阳性,非血液捐献者到非丙型肝炎肝移植受者的传播

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Breakthroughs in hepatitis C virus (HCV) treatment and rising rates of intravenous drug use have led to an increase in the number of organ donors who are HCV antibody–positive but serum nucleic acid test (NAT)–negative. The risk of HCV transmission from the liver grafts of these donors to recipients is unknown. To estimate the incidence of HCV transmission, we prospectively followed 26 consecutive HCV antibody–negative (n = 25) or NAT‐negative (n = 1) transplant recipients who received a liver graft from donors who were HCV antibody–positive but serum NAT‐negative between March 2016 and March 2017. HCV transmission was considered to have occurred if recipients exhibited a positive HCV PCR test by 3 months following transplantation. Drug overdose was listed as the cause of death in 15 (60%) of the donors. One recipient died 18 days after transplantation from primary graft nonfunction and was excluded. Of the remaining 25 recipients, HCV transmission occurred in 4 (16%), at a median follow‐up of 11 months, all from donors who died of drug overdose. Three of these patients were treated with direct‐acting antiviral therapy, with two achieving a sustained virologic response and one an end‐of‐treatment response. One patient with HCV transmission died after a complicated postoperative course and did not receive antiviral therapy. Conclusion: In this prospective cohort of non‐HCV liver recipients receiving grafts from HCV antibody–positive/NAT‐negative donors, the incidence of HCV transmission was 16%, with the highest risk conferred by donors who died of drug overdose; given the availability of safe and highly effective antiviral therapies, use of such organs could be considered to expand the donor pool. (H epatology 2018;67:1673‐1682).
机译:丙型肝炎病毒(HCV)治疗和静脉注射药物的上升率的突破导致了HCV抗体阳性但血清核酸试验(NAT)的器官供体数量的增加。这些捐赠者的肝脏移植物与接受者的HCV传播风险是未知的。为了估算HCV透射的发病率,我们前瞻性地遵循26个连续的HCV抗体 - 阴性(n = 25)或NAT阴性(n = 1)移植接受者,其接受来自作为HCV抗体阳性但血清NAT-的供体的肝移植物2016年3月至2017年3月间否定。如果在移植后3个月,接受者呈阳性HCV PCR试验,则考虑发生HCV传播。药物过量被列为15(60%)捐助者死亡原因。一个受体从初级接枝非功能移植后18天死亡,并被排除在外。在剩下的25名受者中,HCV传播在4(16%)发生,中位随访11个月,来自死亡药物过量的捐助者。这些患者中的三种患者用直效抗病毒治疗治疗,两种达到持续的病毒学反应和治疗结束反应。在复杂的术后课程后,一名患有HCV传播的患者死亡并且没有接受抗病毒治疗。结论:在这种未经HCV肝脏受体的前瞻性群体接受来自HCV抗体阳性/ NAT阴性供体的移植物,HCV传播的发病率为16%,捐赠者赋予了药物过量的捐赠者的最高风险;鉴于安全性和高效的抗病毒疗法的可用性,可以考虑使用这种器官扩大捐助池。 (2018年Hopatology; 67:1673-1682)。

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