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Ombitasvir, paritaprevir co-dosed with ritonavir, dasabuvir, and ribavirin for hepatitis C in patients co-infected with HIV-1: a randomized trial.
Author: BhattiLaveeza, BlickGary, BredeekFritz, BrennanRobert, CampbellAndrew L, Da Silva-TillmannBarbara, ElionRichard, EronJoseph J, FredrickLinda, GatheJoseph, GibbonsKrystal, HuYiran B, KhatriAmit, LalezariJay, McGovernBarbara, Pilot-MatiasTami, PodsadeckiThomas, RuanePeter J, SchnellGretja, SlimJihad, SulkowskiMark S, TrinhRoger, TripathiRakesh, WangChia, WylesDavid
Original Abstract of the Article :
IMPORTANCE: Patients co-infected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) are at high risk for liver disease progression. However, interferon-based treatments for HCV infection have significant toxicities, limiting treatment uptake. OBJECTIVE: To assess the all-oral 3 dir...See full text at original site
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引用元:
https://doi.org/10.1001/jama.2015.1328
データ提供:米国国立医学図書館(NLM)
Combating Hepatitis C: A New Treatment Regimen for HIV-Co-infected Patients
Hepatitis C virus (HCV) infection is a major global health concern, particularly in individuals co-infected with human immunodeficiency virus (HIV). This article explores the efficacy of a novel all-oral 3 direct-acting antiviral (3D) regimen, consisting of ombitasvir, paritaprevir (co-dosed with ritonavir), dasabuvir, and ribavirin, in treating HCV genotype 1 infection in adults with HIV-1 co-infection. The researchers conducted a randomized, open-label pilot study to assess the effectiveness of this regimen.
A Promising Approach to HCV Treatment
The study found that the 3D plus ribavirin regimen resulted in high sustained virologic response (SVR) rates in HCV genotype 1-infected adults with HIV-1 co-infection, regardless of whether they received 12 or 24 weeks of treatment. The regimen was generally well-tolerated, with few serious adverse events. The researchers emphasize the importance of further phase 3 studies to confirm these findings and to evaluate the long-term effectiveness of this regimen.
Hope for Improved HCV Treatment
This study provides encouraging evidence for the effectiveness of a novel all-oral, interferon-free regimen for HCV infection in HIV-1 co-infected patients. The findings offer hope for improved treatment outcomes and a better quality of life for individuals with this co-infection. Continued research is crucial to confirm the long-term efficacy and safety of this regimen, paving the way for more effective and convenient treatment options.
Dr.Camel's Conclusion
Just as a camel adapts to the harsh desert environment, individuals with HCV infection need to find ways to navigate the challenges of this condition. This study highlights a promising new treatment regimen for HCV in HIV-co-infected patients, offering hope for improved outcomes and enhanced quality of life. It's a reminder that ongoing research and development are essential for finding more effective and tolerable treatments for complex medical conditions.
Date :
- Date Completed 2015-04-07
- Date Revised 2022-04-08
Further Info :
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