Effectiveness of chronic hepatitis C treatment with direct-acting antivirals in the Public Health System in Brazil

被引:15
作者
Holzmann, Iandra [1 ]
Tovo, Cristiane V. [1 ]
Minme, Roseline [1 ]
Leal, Monica P. [2 ]
Kliemann, Michele L. [2 ]
Ubirajara, Camila [2 ]
Aquino, Amanda A. [1 ]
Araujo, Bruna [1 ]
Almeida, Paulo R. L. [1 ]
机构
[1] UFCSPA, Porto Alegre, RS, Brazil
[2] Hosp Sanat Partenon, Porto Alegre, RS, Brazil
关键词
Sofosbuvir; Daclatasvir; Simeprevir; DAA; Sustained virological response; DACLATASVIR PLUS SOFOSBUVIR; TREATMENT-NAIVE PATIENTS; ADVANCED LIVER-DISEASE; VIRUS GENOTYPE 3; HCV INFECTION; RIBAVIRIN; INTERFERON; EFFICACY;
D O I
10.1016/j.bjid.2018.06.004
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Chronic hepatitis C virus infection is one of the major causes of cirrhosis, hepatocellular carcinoma and liver transplantation. Treatment using direct-acting antivirals has revolutionized the treatment of hepatitis C virus, increasing long-term prognosis after cure. The goal of the present study was to evaluate the effectiveness of direct-acting antivirals in a Public Health System in southern Brazil. Methods: A retrospective study evaluated all patients with chronic hepatitis C virus infection who underwent treatment at one center of the Public Health Department of the State of Rio Grande do Sul - Brazil, according to the Brazilian Clinical Protocol and Therapeutic Guidelines. The effectiveness was assessed in terms sustained virological response 12 weeks after the end of treatment. Results: A total of 1002 patients who were treated for chronic hepatitis C virus infection were evaluated. The mean age was 58.6 years, 557 patients (55.6%) were male and 550 (54.9%) were cirrhotic. Overall sustained virological response was observed in 936 (93.4%) patients. There was a difference in sustained virological response rate varied according to sex, 91.6% in men and 95.7% in women (p = 0.009), length of treatment in genotype 1, 92.7% with 12 weeks and 99.1 with 24 weeks (p = 0.040), and genotype, 94.7% in genotype 1, 91.7% in genotype 2, and 91.4% in genotype 3 (p = 0.047). Conclusion: The treatment of chronic hepatitis C virus infection for genotypes 1, 2 or 3 with the therapeutic regimens established by the Brazilian guidelines showed high rates of SVR, even in cirrhotic patients. (C) 2018 Sociedade Brasileira de Infectologia. Published by Elsevier Editora Ltda.
引用
收藏
页码:317 / 322
页数:6
相关论文
共 50 条
[21]   Direct-acting antivirals for children and adolescents with chronic hepatitis C [J].
Indolfi, Giuseppe ;
Serranti, Daniele ;
Resti, Massimo .
LANCET CHILD & ADOLESCENT HEALTH, 2018, 2 (04) :298-304
[22]   Treatment of chronic hepatitis C with direct-acting antivirals: The role of resistance [J].
Jimenez-Perez, Miguel ;
Gonzalez-Grande, Rocio ;
Espana Contreras, Pilar ;
Pinazo Martinez, Isabel ;
de la Cruz Lombardo, Jesus ;
Olmedo Martin, Raul .
WORLD JOURNAL OF GASTROENTEROLOGY, 2016, 22 (29) :6573-6581
[23]   New direct-acting antivirals' combination for the treatment of chronic hepatitis C [J].
Asselah, Tarik ;
Marcellin, Patrick .
LIVER INTERNATIONAL, 2011, 31 :68-77
[24]   A review of direct-acting antivirals for the treatment of hepatitis C in patients with advanced chronic kidney disease [J].
Maruyama, Anna ;
Partovi, Nilufar ;
Yoshida, Eric M. ;
Erb, Siegfried R. ;
Azalgara, Vladimir Marquez ;
Hussaini, Trana .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2017, 32 (01) :35-41
[25]   Effects of Age on Treatment of Chronic Hepatitis C with Direct Acting Antivirals [J].
Pariente, Alexandre ;
Arpurt, Jean-Pierre ;
Remy, Andre-Jean ;
Rosa-Hezode, Isabelle ;
Causse, Xavier ;
Heluwaert, Frederic ;
Macaigne, Gilles ;
Henrion, Jean ;
Renou, Christophe ;
Schnee, Matthieu ;
Salloum, Hatem ;
Hommel, Severine ;
Pilette, Christophe ;
Arotcarena, Ramuntxo ;
Barjonet, Georges ;
Lison, Hortensia ;
Bourhis, Frangois ;
Jouannaud, Vincent ;
Pauwels, Arnaud ;
Le-Bricquir, Yann ;
Geagea, Edmond ;
Condat, Bertrand ;
Ripault, Marie-Pierre ;
Zanditenas, David ;
de Montigny-Lenhardt, Stephanie ;
Labadie, Helene ;
Tissot, Bertrand ;
Maringe, Eric ;
Cadranel, Jean-Francois ;
Hagege, Herve ;
Lesgourgues, Bruno .
ANNALS OF HEPATOLOGY, 2019, 18 (01) :193-202
[26]   Peginterferon alfa-2a for the treatment of chronic hepatitis C in the era of direct-acting antivirals [J].
Huang, Yan ;
Li, Ming-Hui ;
Hou, Min ;
Xie, Yao .
HEPATOBILIARY & PANCREATIC DISEASES INTERNATIONAL, 2017, 16 (05) :470-479
[27]   Effectiveness and safety of generic and brand direct acting antivirals for treatment of chronic hepatitis C [J].
Abdulla, Maheeba ;
Al Ghareeb, Aysha Mohamed ;
Husain, Hamed Ali Hasan Yusuf ;
Mohammed, Nafeesa ;
Al Qamish, Jehad .
WORLD JOURNAL OF CLINICAL CASES, 2022, 10 (34) :12566-12577
[28]   Newer direct-acting antivirals for hepatitis C virus infection: Perspectives for India [J].
Gupta, Varun ;
Kumar, Ashish ;
Sharma, Praveen ;
Arora, Anil .
INDIAN JOURNAL OF MEDICAL RESEARCH, 2017, 146 :22-32
[29]   Cost-effectiveness of the highly effective direct-acting antivirals in the treatment of chronic hepatitis C in Hong Kong [J].
Lo, Angeline Oi-Shan ;
Chan, Henry Lik-Yuen ;
Wong, Vincent Wai-Sun ;
Wong, Grace Lai-Hung .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2017, 32 (05) :1071-1078
[30]   Direct-acting antivirals for hepatitis C treatment: effectiveness versus cost-effectiveness [J].
Chhatwal, Jagpreet .
FUTURE VIROLOGY, 2015, 10 (08) :929-932