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Effectiveness of a fixed combination formula of ombitasvir/paritaprevir/ritonavir for hepatitis C virus infection in patients on maintenance haemodialysis.
Morisawa, Norihiko; Koshima, Yohei; Kuriyama, Satoru; Matsuyama, Momoko; Hayashi, Naomi; Satoh, Jun-Ichi; Amemiya, Morimasa; Yokoo, Takashi.
Afiliação
  • Morisawa N; Division of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
  • Koshima Y; Division of Nephrology, Department of Internal Medicine, Saitama Red Cross Hospital, Saitama, Japan.
  • Kuriyama S; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Saitama Red Cross Hospital, Saitama, Japan.
  • Matsuyama M; Division of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
  • Hayashi N; Division of Nephrology, Department of Internal Medicine, Saitama Red Cross Hospital, Saitama, Japan.
  • Satoh JI; Division of Nephrology and Hypertension, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
  • Amemiya M; Division of Nephrology, Department of Internal Medicine, Saitama Red Cross Hospital, Saitama, Japan.
  • Yokoo T; Division of Nephrology, Department of Internal Medicine, Saitama Red Cross Hospital, Saitama, Japan.
Nephrology (Carlton) ; 22(7): 562-565, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28621007
A fixed-dose formula that combines Ombitasvir (OBV), Paritaprevir (PTV) and Ritonavir (RTV) has been launched into the field of anti-HCV therapy in Japan for patients infected with HCV genotypes 1 and 2 in 2015. However, little is yet known as to the efficacy and safety of this novel therapy in patients on maintenance haemodialysis (HD). The present report describes a preliminary experience in 10 patients (five males and five females) who underwent maintenance HD. All of them had HCV genotype 1b, without having the resistance-associated variants at Y93 or L31 in the nonstructural proteins 5A (NS5A) region. After the treatment, eight patients successfully achieved virus eradication and sustained a virological response at 12 weeks (SVR12). In addition, mac-2 binding protein glycosylation isomer (M2BPGi), a biomarker for liver fibrosis, was reduced after the therapy. Two patients withdrew from the therapy due to the development of erythema multiforme and a strong drowsiness, respectively. These results suggest that triple therapy combining OBV, PTV and RTV is effective in achieving SVR12 in most of the HCV-infected patients on HD. In addition, this combination therapy contributed to retard the progression of liver fibrosis. However, we suggest that further trial will be required to establish its clinical efficacy and safety.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Carbamatos / Diálise Renal / Hepatite C / Hepacivirus / Ritonavir / Compostos Macrocíclicos / Insuficiência Renal Crônica / Anilidas Tipo de estudo: Diagnostic_studies Limite: Aged80 País/Região como assunto: Asia Idioma: En Revista: Nephrology (Carlton) Assunto da revista: NEFROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Carbamatos / Diálise Renal / Hepatite C / Hepacivirus / Ritonavir / Compostos Macrocíclicos / Insuficiência Renal Crônica / Anilidas Tipo de estudo: Diagnostic_studies Limite: Aged80 País/Região como assunto: Asia Idioma: En Revista: Nephrology (Carlton) Assunto da revista: NEFROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão