Durability of Stavudine, Lamivudine and Nevirapine among Advanced HIV-1 Infected Patients with/without Prior Co-administration of Rifampicin: A 144-week Prospective Study
2008

Effectiveness of HIV Treatment with Stavudine, Lamivudine, and Nevirapine

Sample size: 140 publication Evidence: moderate

Author Information

Author(s): Manosuthi Weerawat, Tantanathip Preecha, Prasithisirikul Wisit, Likanonsakul Sirirat, Sungkanuparph Somnuek

Primary Institution: Bamrasnaradura Infectious Diseases Institute, Ministry of Public Health, Nonthaburi, Thailand

Hypothesis

Does the co-administration of rifampicin affect the durability of HIV treatment with stavudine, lamivudine, and nevirapine?

Conclusion

The treatment regimen of stavudine, lamivudine, and nevirapine is effective for HIV-1 infected patients, regardless of rifampicin co-administration.

Supporting Evidence

  • 59.3% of patients achieved undetectable HIV-1 RNA levels after 144 weeks.
  • 61.4% of patients in the TB group achieved undetectable HIV-1 RNA.
  • 57.1% of patients in the control group achieved undetectable HIV-1 RNA.
  • 5.8% of patients discontinued treatment due to adverse effects.
  • The study included a diverse group of patients with varying tuberculosis diagnoses.

Takeaway

This study shows that a combination of three HIV medicines works well for patients, even if they are also being treated for tuberculosis.

Methodology

A prospective cohort study involving 140 HIV-infected patients, with 70 receiving rifampicin for tuberculosis and 70 not receiving it.

Potential Biases

Potential bias due to the study's design and the specific population studied.

Limitations

The sample size may not be sufficient to detect long-term differences in antiviral responses.

Participant Demographics

140 HIV-infected Thai patients, aged 15 and older, with a median baseline CD4 count of 31 cells/mm3.

Statistical Information

P-Value

0.731

Confidence Interval

95%CI = 0.608–2.346

Statistical Significance

p=0.731

Digital Object Identifier (DOI)

10.1186/1471-2334-8-136

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