Paper Details 
Original Abstract of the Article :
Multidrug-resistance hepatitis B virus (MDR HBV), defined as those with mutations resistant to both nucleoside analogs lamivudine/telbivudine/entecavir (LAM/LdT/ETV) and nucleotide analog adefovir (ADV), has potential to cause treatment difficulty. To clarify clinical prevalence and virological feat...See full text at original site
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引用元:
https://doi.org/10.1016/j.antiviral.2021.105058

データ提供:米国国立医学図書館(NLM)

Navigating the Desert of Multidrug-Resistant Hepatitis B

Hepatitis B virus (HBV) infection can lead to chronic liver disease and is a significant global health concern. This study investigates the prevalence and characteristics of multidrug-resistant (MDR) HBV, a strain of the virus that has evolved to resist multiple antiviral medications. Imagine a camel caravan encountering a desert oasis guarded by fierce and resistant creatures. This is the challenge of MDR HBV, which can be difficult to treat with conventional medications.

The researchers analyzed a large cohort of chronic HBV-infected patients undergoing antiviral therapy. They identified a small percentage of patients with MDR HBV, highlighting the importance of ongoing monitoring and resistance testing. The study also provides valuable information about the characteristics and treatment strategies for MDR HBV, emphasizing the need for personalized medicine and tailored therapeutic approaches.

A Shifting Landscape: Understanding and Combating MDR HBV

This study underscores the dynamic nature of viral evolution, highlighting the emergence of MDR HBV and the need for ongoing vigilance in managing chronic HBV infection. It emphasizes the importance of personalized medicine, tailored treatment strategies, and continuous monitoring to combat the evolving threat of drug resistance.

Dr. Camel's Conclusion

This research provides a glimpse into the ongoing battle against HBV infection, highlighting the emergence of MDR HBV and the challenges it poses. It emphasizes the need for robust surveillance, innovative treatment approaches, and a concerted effort to combat this complex and evolving viral threat.

Date :
  1. Date Completed 2021-10-08
  2. Date Revised 2021-10-08
Further Info :

Pubmed ID

33711338

DOI: Digital Object Identifier

10.1016/j.antiviral.2021.105058

Related Literature

SNS
PICO Info
in preparation
Languages

English

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