Abstract | BACKGROUND: Antiretroviral therapy is associated with adverse events (AEs). The most frequently reported AE associated with lopinavir/ ritonavir (LPV/r) containing regimens is diarrhea. The objective of this meta-analysis is to describe the incidence, prevalence, and duration of diarrhea in individuals taking LPV/r. METHODS: This is a meta-analysis of Abbott-conducted clinical trials. Inclusion criteria included prospective randomized clinical trials with the LPV/r tablet formulation and had AE data (moderate/severe diarrhea) available through 48 weeks of treatment. RESULTS: Three trials (total 1469 participants) met the inclusion criteria. In all, 11.2% of participants reported moderate/severe diarrhea by week 8, with median time to resolution of 7.4 weeks. The overall 48-week incidence of moderate/severe diarrhea was 15.5%. The discontinuation rate due to moderate/severe diarrhea was 1.3%. CONCLUSIONS: Moderate/severe diarrhea occurred in less than 1 in 6 participants taking LPV/r, typically started in the first 8 weeks of treatment and infrequently resulted in premature discontinuation.
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Authors | Colleen M Wegzyn, Linda M Fredrick, Roxann O Stubbs, William C Woodward, Michael Norton |
Journal | Journal of the International Association of Physicians in AIDS Care (Chicago, Ill. : 2002)
(J Int Assoc Physicians AIDS Care (Chic))
2012 Jul-Aug
Vol. 11
Issue 4
Pg. 252-9
ISSN: 1545-1097 [Print] United States |
PMID | 22544446
(Publication Type: Journal Article, Meta-Analysis)
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Chemical References |
- Anti-HIV Agents
- Antidiarrheals
- Drug Combinations
- Lopinavir
- Ritonavir
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Topics |
- Anti-HIV Agents
(adverse effects)
- Antidiarrheals
(therapeutic use)
- Diarrhea
(chemically induced, drug therapy, epidemiology)
- Drug Combinations
- Drug Therapy, Combination
- HIV Infections
(drug therapy, virology)
- HIV-1
- Humans
- Incidence
- Lopinavir
(adverse effects)
- Prevalence
- Risk Factors
- Ritonavir
(adverse effects)
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