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直接作用抗病毒药物对肝、肾移植成本和结局的影响。

The impact of direct-acting antiviral agents on liver and kidney transplant costs and outcomes.

机构信息

Lahey Hospital & Medical Center, Burlington, MA, USA.

Saint Louis University Center for Abdominal Transplantation, St. Louis, MO, USA.

出版信息

Am J Transplant. 2018 Oct;18(10):2473-2482. doi: 10.1111/ajt.14895. Epub 2018 May 29.

Abstract

Direct-acting antiviral medications (DAAs) have revolutionized care for hepatitis C positive (HCV+) liver (LT) and kidney (KT) transplant recipients. Scientific Registry of Transplant Recipients registry data were integrated with national pharmaceutical claims (2007-2016) to identify HCV treatments before January 2014 (pre-DAA) and after (post-DAA), stratified by donor (D) and recipient (R) serostatus and payer. Pre-DAA, 18% of HCV+ LT recipients were treated within 3 years and without differences by donor serostatus or payer. Post-DAA, only 6% of D-/R+ recipients, 19.8% of D+/R+ recipients with public insurance, and 11.3% with private insurance were treated within 3 years (P < .0001). LT recipients treated for HCV pre-DAA experienced higher rates of graft loss (adjusted hazard ratio [aHR] 1.85 , P < .0001) and death (aHR 1.68 , P < .0001). Post-DAA, HCV treatment was not associated with death (aHR 0.67 , P = .25) or graft failure (aHR 0.64 , P = .20) in D+R+ LT recipients. Treatment increased in D+R+ KT recipients (5.5% pre-DAA vs 12.9% post-DAA), but did not differ by payer status. DAAs reduced the risk of death after D+/R+ KT by 57% ( 0.43 , P = .04) and graft loss by 46% ( 0.54 , P = .08). HCV treatment with DAAs appears to improve HCV+ LT and KT outcomes; however, access to these medications appears limited in both LT and KT recipients.

摘要

直接作用抗病毒药物 (DAA) 彻底改变了丙型肝炎阳性 (HCV+) 肝 (LT) 和肾 (KT) 移植受者的治疗方法。通过整合科学注册移植受者登记数据和全国药品索赔数据(2007-2016 年),按供体 (D) 和受者 (R) 的血清学状态和支付方来确定 DAA 治疗前 (DAA 前) 和 DAA 治疗后 (DAA 后) 的 HCV 治疗情况。DAA 前,18%的 HCV+LT 受者在 3 年内接受治疗,供体血清学状态或支付方无差异。DAA 后,只有 6%的 D-/R+受者、19.8%有公共保险的 D+/R+受者和 11.3%有私人保险的 D+/R+受者在 3 年内接受治疗 (P<.0001)。DAA 前接受 HCV 治疗的 LT 受者出现移植物丢失的比率更高 (校正风险比 [aHR] 1.85,P<.0001) 和死亡 (aHR 1.68,P<.0001)。DAA 后,D+/R+LT 受者的 HCV 治疗与死亡 (aHR 0.67,P=.25) 或移植物衰竭 (aHR 0.64,P=.20) 无关。D+/R+KT 受者的治疗有所增加 (DAA 前 5.5%,DAA 后 12.9%),但支付方状态无差异。DAA 降低了 D+/R+KT 受者死亡风险 57% (0.43,P=.04) 和移植物丢失风险 46% (0.54,P=.08)。DAA 治疗 HCV 似乎改善了 HCV+LT 和 KT 的结果;然而,LT 和 KT 受者获得这些药物的机会似乎有限。

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