Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1

Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1 - Hallo friend NEWS AN INSPIRATION, In the article you read this time with the title Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1, we have prepared well for this article you read and download the information therein. hopefully fill posts Article ECONOMY, Article HEALTH, Article POLITICS, Article SPORTS, Article TRAVELING, Article UPDATE, we write can understand. Well, happy reading.

Titre : Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1
link : Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1

Read also


Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1

Real-world effectiveness and safety of sofosbuvir and ledipasvir with or without ribavirin for patients with hepatitis C virus genotype 1 infection in Taiwan 
Chen-Hua Liu, Chun-Jen Liu, Tung-Hung Su, Hung-Chih Yang, Chun-Ming Hong, Tai-Chung Tseng, Pei-Jer Chen, Ding-Shinn Chen, Jia-Horng Kao

Published: December 21, 2018 http://bit.ly/2Gy889l

Full-Text Article
Download PDF

Abstract
Background
The real-world data for the effectiveness and safety of sofosbuvir/ledipasvir (SOF/LDV) with or without ribavirin (RBV) in patients with hepatitis C virus genotype 1 (HCV-1) infection remain limited in Taiwan.

Methods
A total of 273 chronic HCV-1 patients receiving 8, 12, or 24 weeks of SOF/LDV with or without RBV were enrolled. The sustained virologic response rate at week 12 off-therapy (SVR12) by evaluable population (EP) and per-protocol population (PP) were assessed for effectiveness. The treatment discontinuation rate due to adverse events (AEs) and serious AE rate were assessed for safety. Baseline patient characteristics and on-treatment HCV viral kinetics associated with SVR12 were analyzed.

Results
The SVR12 rates by EP and PP analyses were 96.7% (95% confidence interval [CI]: 93.9%-98.3%) and 97.5% (95% CI: 94.8%-98.8%), respectively. The rates of treatment discontinuation due to AE and serious AE were 0.4% and 4.4%, respectively. Seven patients with true virologic failure were relapsers. In 2 patients who were lost-to follow-up, one expired at treatment week 3 due to pneumonia which was considered not related to treatment, and one declined follow-up at off-therapy week 4. The SVR12 rates were comparable in terms of baseline patient characteristics and viral decline at week 4 of treatment.

Conclusions
SOF/LDV with or without RBV for 8–24 weeks is well tolerated and achieves a high SVR12 rate in patients with HCV-1 infection in Taiwan.


Thus articles Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1

that is all articles Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1 This time, hopefully can provide benefits to you all. Okay, see you in another article post.

You are now reading the article Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1 the link address https://newsaninpiration.blogspot.com/2018/12/real-world-effectiveness-and-safety-of.html

Subscribe to receive free email updates:

0 Response to "Real-world effectiveness and safety of Harvoni with/without ribavirin hepatitis C virus genotype 1"

Post a Comment