Outcomes | Illustrative comparative risks* (95 % CI) | Relative effect (95 % CI) | No of Participants (studies) | Quality of the evidence (GRADE) | |
---|---|---|---|---|---|
Assumed risk | Corresponding risk | ||||
AZT or d4T - containing combination antiretroviral regimens | ABC- containing combination antiretroviral regimens | ||||
Virologic suppression - ABC versus d4T (VL < 50–100 copies/ml) | 688 per 1000 | 881 per 1000 | RR 1.28 | 326 | ⊕ ⊕ ⊕⊝ |
Follow-up: mean 48 weeks | (461–1000) | (0.67–2.42 | (2 studies) | moderatea | |
Adverse events | 0 per 1000 | 0 per 1000 | RR 2.41 | 81 | ⊕ ⊕ ⊝⊝ |
Follow-up: mean 48 weeks | (0–0) | (0.1–57.52) | (1 study) | lowa,b | |
Death | 0 per 1000 | 0 per 1000 | RR 2.41 | 81 | ⊕ ⊕ ⊝⊝ |
Follow-up: mean 48 weeks | (0–0) | (0.1–57.52) | (1 study) | lowa,b |