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. 2013 Oct 3;2013(10):CD002843. doi: 10.1002/14651858.CD002843.pub2

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.