Table 2.
Analysis | Participants, no. | Duration, person-years | Outcomes, no.a | 6-y Risk, % | 6-y RD (95% CI), % | HR (95% CI) |
---|---|---|---|---|---|---|
Crudeb | ||||||
EFV | 10 169 | 38 029.3 | 1097 | 14.2 | 0 | 1 |
InSTI | 5824 | 13 240.8 | 440 | 13.1 | −1.1 (−4.1 to 1.9) | 0.99 (.88–1.10) |
Intention to treatc | ||||||
EFV | 10 169 | 38 029.3 | 1097 | 14.3 | 0 | 1 |
InSTI | 5824 | 13 240.8 | 440 | 14.6 | 0.3 (−2.7 to 3.3) | 1.08 (.97– 1.19) |
Per protocold | ||||||
EFV | 10 169 | 25 100.8 | 672 | 11.9 | 0 | 1 |
InSTI | 5824 | 9313.0 | 325 | 12.2 | 0.3 (−3.0 to 3.7) | 1.09 (.96 –1.25) |
Abbreviations: CI, confidence interval; EFV, efavirenz; HR, hazard ratio; InSTI, integrase strand transfer inhibitor; RD, risk difference.
aThe composite outcome included AIDS-defining illnesses, acute myocardial infarction or stroke, end-stage renal disease, end-stage liver disease, or death.
bCrude analysis did not account for baseline confounding, differential loss to follow-up, or treatment changes (uncensored).
cIntention-to-treat analyses accounted for baseline confounding and differential loss to follow-up.
dPer-protocol analyses accounted for baseline confounding, differential loss to follow-up, and treatment changes (ie, treatment discontinuations or switches).