Thirumurthy 2011.
Methods | CBA study | |
Participants | 1543 adult HIV+ persons, plus 54 caretakers and 67 children (Tamil Nadu, India) Index Group: 515 Control Group: 723 A total of 1238 participants were included in the final analysis. |
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Interventions | Intervention: Pharmacological, ART and home visits for ART adherence support
Control: All of the above except for ART and home visits for ART adherence support because CD4 counts were above 200 and ART was not indicated. |
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Outcomes | Employment:
Health status:
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Notes | ***Participants were not required to be employed at the time of the study, however the study measured economic outcomes related to ART. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
14. Blinding (Subjects) | Low risk | No blinding, however due to a dichotomous outcome of employment or non‐employment, this should not have affected the results. |
15. Blinding (outcome assessors) | Low risk | No blinding. Objective outcomes that should have been unaffected by blinding. |
16. Retrospective unplanned subgroup analysis | Low risk | No additional analysis. |
17. Follow‐up | Low risk | Same time period. 68.66% present for interviews at 24 months. |
18. Statistical tests | Unclear risk | Mean difference and standard error. Contacted authors for further interpertation but did not receive response. |
19. Compliance | Unclear risk | Compliance to ART was not reported. However, ART participants did receive home visits to encourage ART adherence. ART adherence is required for survival, therefore compliance, although not monitored, is likely. |
20. Outcome measures | Low risk | All previously determined outcomes were reported. |
21. Selection Bias (population) | Low risk | Selected from same population. (Tamil Nadu Family Continuum Care Program) |
22. Selection bias (time) | Low risk | Recruited at the same time. |
23. Randomization | High risk | Non‐randomized study. Participants were predetermined by health status and CD4 counts. |
24. Allocation concealment | Unclear risk | Non‐randomized. |
25. Adjustment for confounding | High risk | Adjusted for gender. No adjustment for differences in disease severity. No adjustments for differences for SES. No adjustments for differences in age. |
26. Incomplete outcome data | Unclear risk | 34.34% attrition in index group addressed. No attrition data reported for controls. |
Baseline comparability | Unclear risk | Female percentage was 42% in the index group and 65% in the reference group. Percentage of those who completed secondary education was 28% in the index group and 27% in the reference group. CD4 counts at baseline were 128.2 for the index group and 465.6 for the reference group. |
ART: antiretroviral therapy CBA: controlled before‐after study HIV+ persons: persons living with HIV RCT: randomized controlled trial SES: socioeconomic status WHO: World Health Organization