Hepatic decompensation/serious adverse events in post-liver transplantation recipients on sofosbuvir for recurrent hepatitis C virus

被引:4
|
作者
Patel, Neal [1 ]
Bichoupan, Kian [1 ]
Ku, Lawrence [1 ]
Yalamanchili, Rachana [1 ]
Harty, Alyson [1 ]
Gardenier, Donald [1 ]
Ng, Michel [1 ]
Motamed, David [1 ,2 ]
Khaitova, Viktoriya [1 ,2 ]
Bach, Nancy [1 ,2 ]
Chang, Charissa [1 ,2 ]
Grewal, Priya [1 ,2 ]
Bansal, Meena [1 ]
Agarwal, Ritu [1 ]
Liu, Lawrence [1 ,2 ]
Im, Gene [1 ,2 ]
Leong, Jennifer [1 ,2 ]
Kim-Schluger, Leona [1 ,2 ]
Odin, Joseph [1 ,2 ]
Ahmad, Jawad [1 ,2 ]
Friedman, Scott [1 ]
Dieterich, Douglas [1 ]
Schiano, Thomas [1 ,2 ]
Perumalswami, Ponni [1 ,2 ]
Branch, Andrea [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Div Liver Dis, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Recanati Miller Transplant Inst, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
Hepatitis C virus; Sofosbuvir; Ribavirin; Anemia; Hepatic decompensation; Serious adverse event; Liver transplant; GENOTYPE; 1; INFECTION; COMBINATION THERAPY; VIRAL-HEPATITIS; RIBAVIRIN; HCV; INTERFERON; LEDIPASVIR; DISEASE; MULTICENTER; INHIBITOR;
D O I
10.3748/wjg.v22.i9.2844
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To determine the safety profile of new hepatitis C virus (HCV) treatments in liver transplant (LT) recipients with recurrent HCV infection. METHODS: Forty-two patients were identified with recurrent HCV infection that underwent LT at least 12 mo prior to initiating treatment with a Sofosbuvir-based regimen during December 2013-June 2014. Cases were patients who experienced hepatic decompensation and/or serious adverse events (SAE) during or within one month of completing treatment. Controls had no evidence of hepatic decompensation and/or SAE. HIV-infected patients were excluded. Cumulative incidence of decompensation/SAE was calculated using the Kaplan Meier method. Exact logistic regression analysis was used to identify factors associated with the composite outcome. RESULTS: Median age of the 42 patients was 60 years [Interquartile Range (IQR): 56-65 years], 33% (14/42) were female, 21% (9/42) were Hispanic, and 9% (4/42) were Black. The median time from transplant to treatment initiation was 5.4 years (IQR: 2.1-8.8 years). Thirteen patients experienced one or more episodes of hepatic decompensation and/or SAE. Anemia requiring transfusion, the most common event, occurred in 62% (8/13) patients, while 54% (7/13) decompensated. The cumulative incidence of hepatic decompensation/ SAE was 31% (95% CI: 16%-41%). Risk factors for decompensation/SAE included lower pre-treatment hemoglobin (OR = 0.61 per g/dL, 95% CI: 0.40-0.88, P < 0.01), estimated glomerular filtration rate (OR = 0.95 per mL/min per 1.73 m(2), 95% CI: 0.90-0.99, P = 0.01), and higher baseline serum total bilirubin (OR = 2.43 per mg/dL, 95% CI: 1.17-8.65, P < 0.01). The sustained virological response rate for the cohort of 42 patients was 45%, while it was 31% for cases. CONCLUSION: Sofosbuvir/ribavirin will continue to be used in the post-transplant population, including those with HCV genotypes 2 and 3. Management of anemia remains an important clinical challenge.
引用
收藏
页码:2844 / 2854
页数:11
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