Criterion | Risk of bias | ||
---|---|---|---|
Low | Moderate | High | |
Eligibility | · Recruited from general HIV-infected population, eg. HIV clinics | · Recruited from moderately selected population, eg. STI clinics | · Highly selected population (eg. FSW, active GUD) |
· Unclear selection criteria applied | |||
HSV-2 ascertainment | · High quality type-specific serology assay | · Culture-based diagnosis | · Methods unclear |
· PCR assay | · Clinical diagnosis | ||
Endpoint ascertainment | · Similar between groups | · Similar between groups | · Methods unclear |
· Regular timing | · Irregular timing | ||
Confounding | · Accounted for ART, and | · Some of these confounders accounted for | · None of these confounders accounted for or unclear |
· Accounted for acyclovir, and | |||
· Accounted for CD4/stage of HIV disease | |||
Analysis | · Sample size or power calculation done, and | · No concerns with analysis | · Problems identified with analysis |
· No concerns with analysis | |||
Attrition | · Minimal attrition (<10%) and | · Moderate attrition (10-20%) | · High attrition (>20%) |
· Attrition explained | · Attrition not explained | ||
OVERALL | · Most items at low risk of bias, including both HSV-2 ascertainment and confounding | · Most items at low to moderate risk of bias | · Most items at moderate risk of bias |
· Not more than two items at moderate risk of bias | · No item at high risk of bias | · At least one item at high risk of bias |