Summary of findings for the main comparison. Enhanced patient referral compared with simple patient referral for partner notification for STIs, including HIV.
Enhanced patient referral compared with simple patient referral for partner notification for STIs, including HIV | ||||||
Health problem: partner notification for STIs, including HIV Settings: people in rural and urban areas, given a diagnosis of STI (clinically or by a laboratory) in health services Intervention: enhanced patient referral Comparison: simple patient referral | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No of Participants (studies) | Quality of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
Simple patient referral | Enhanced patient referral | |||||
Re‐infection in index patient ‐ home sampling vs. simple patient referral Follow‐up: 12 months | Study population | RR 2.14 (0.91 to 5.05) | 220 (1 study) | ⊕⊕⊝⊝ low1,2 | ||
64 per 1000 | 136 per 1000 (58 to 321) | |||||
Moderate | ||||||
64 per 1000 | 137 per 1000 (58 to 323) | |||||
Re‐infection in index patient ‐ information booklet vs. simple patient referral Follow‐up: 8 weeks | Study population | RR 0.55 (0.22 to 1.33) | 942 (2 studies) | ⊕⊕⊝⊝ low3,4 | ||
180 per 1000 | 99 per 1000 (40 to 239) | |||||
Moderate | ||||||
156 per 1000 | 86 per 1000 (34 to 207) | |||||
Re‐infection in index patient ‐ patient referral (DIS/health advisor) vs. patient referral (nurse) Follow‐up: 6 weeks | Study population | RR 0.35 (0.01 to 8.51) | 140 (1 study) | ⊕⊕⊝⊝ low5 | ||
14 per 1000 | 5 per 1000 (0 to 118) | |||||
Moderate | ||||||
14 per 1000 | 5 per 1000 (0 to 119) | |||||
Re‐infection in index patient ‐ disease‐specific website vs. simple referral Follow‐up: 1 weeks | Study population | RR 3.12 (0.17 to 58.73) | 105 (1 study) | ⊕⊕⊝⊝ low6 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Re‐infection in index patient ‐ additional counselling vs. simple patient referral Follow‐up: 6 months | Study population | RR 0.49 (0.27 to 0.89) | 600 (1 study) | ⊕⊕⊕⊝ moderate7 | ||
101 per 1000 | 50 per 1000 (27 to 90) | |||||
Moderate | ||||||
101 per 1000 | 49 per 1000 (27 to 90) | |||||
The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: confidence interval; DIS: disease intervention specialist; RR: risk ratio; STI: sexually transmitted infection. | ||||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |
1 Method of allocation concealment was not reported. 70% completed follow‐up, some were lost to follow‐up and some withdrew from the study, reasons for withdrawal were not reported. Study was not blinded. 2 Assuming alpha of 0.05 and beta of 0.2. For relative risk reduction of 20% with best estimate of control event rate of 0.2 approximately 3000 participants were required. The total sample size was 220 and did not meet the optimal information size. 3 High attrition rate and no information given on method of allocation concealment in one of the studies. Different methods were used for outcome assessment 4 I2 = 76% (P value = 0.06) and minimal overlap of CIs. 5 Sample size less than 400, there were very few events and CIs around both relative and absolute estimates include both appreciable benefit and appreciable harm. 6 Sample size was very small and optimal information size was not met. There were very few events and CIs overlapped, therefore, no effect both for absolute and relative estimates. 7 Risk for selective reporting and unclear method of allocation concealment.