Three Generic Nevirapine-Based Antiretroviral Treatments in Chinese HIV/AIDS Patients: Multicentric Observation Cohort Generic NVP-Based ART Study
2008

Three Nevirapine-Based Treatments for HIV in China

Sample size: 198 publication 10 minutes Evidence: moderate

Author Information

Author(s): Li Taisheng, Dai Yi, Kuang Jiqiu, Jiang Jingmei, Han Yang, Qiu Zhifeng, Xie Jing, Zuo Lingyan, Li Yanling

Primary Institution: Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China

Hypothesis

The study aimed to evaluate the efficacy and safety of three nevirapine-based antiretroviral treatments for adult antiretroviral-naïve Chinese patients with HIV-1 infection.

Conclusion

The study found that 3TC+d4T and 3TC+AZT are effective combinations for HIV treatment, while AZT+ddI+NVP showed poor virological response, especially in patients with higher CD4 counts.

Supporting Evidence

  • The regimen of AZT+ddI+NVP produced poor virological response especially in patients with CD4 count more than 200/ul.
  • 68.2% of patients in group B and 69% in group C achieved suppression of plasma HIV-1 RNA to less than 50 copies/ml.
  • Hepatotoxicity was significantly associated with higher CD4 baseline and HCV-Ab positive status.

Takeaway

This study looked at three different treatments for HIV and found that two of them worked better than the third one.

Methodology

A prospective, multicenter study where 198 HIV-1 positive patients were randomized into three treatment groups and monitored for viral and immunologic responses.

Potential Biases

Potential bias due to the study being conducted in a specific population and the randomization process.

Limitations

The study was limited to antiretroviral-naïve patients and may not be generalizable to those with prior treatment.

Participant Demographics

Participants were adult HIV-1 positive patients with CD4 counts between 100/ul and 350/ul.

Statistical Information

P-Value

p<0.001

Confidence Interval

95%CI: 1.106–3.973

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1371/journal.pone.0003918

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