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. 2019 Apr 23;2019(4):CD004317. doi: 10.1002/14651858.CD004317.pub5

Summary of findings for the main comparison. Intensive counseling compared to usual family planning care for improving adherence and continuation of shorter‐term hormonal methods of contraception.

Intensive counseling compared to usual family planning care for improving adherence and continuation of shorter‐term hormonal methods of contraception
Patient or population: Women of reproductive age seeking to avoid pregnancy
 Setting: Family planning clinics in middle‐ to high‐income countries
 Intervention: Intensive counseling
 Comparison: Usual family planning care
Outcomes Anticipated absolute effects* (95% CI) Relative effect
 (95% CI) № of participants
 (studies) Certainty of the evidence
 (GRADE) Comments
Risk with usual family planning care Risk with intensive counseling
Continuation of hormonal contraceptive method 392 per 1,000 452 per 1,000
 (408 to 498) OR 1.28
 (1.07 to 1.54) 2624
 (6 RCTs) ⊕⊝⊝⊝
 VERY LOW 1 2 3 I2 = 79%
Rate of discontinuation due to menstrual disturbances 320 per 1,000 86 per 1,000
 (49 to 148) OR 0.20
 (0.11 to 0.37) 350
 (1 RCT) ⊕⊕⊝⊝
 LOW 1 3  
Rate of discontinuation due to all other adverse events 549 per 1000 470 per 1000
 (304 to 641) OR 0.73
 (0.36 to 1.47) 350
 (1 RCT) ⊕⊕⊝⊝
 LOW 1 3  
Adherence to method use Not reported  
Pregnancy 18 per 100 21 per 100
 (18 to 25) OR 1.24
 (0.98 to 1.57) 1985
 (3 RCTs) ⊕⊝⊝⊝
 VERY LOW 1 3 4  
*The risk in the intervention group (and its 95% confidence interval) is based on the median risk in the comparison group (usual care) and the relative effect of the intervention (and its 95% CI). Calculations were done using GRADEpro.
 
 CI: Confidence interval; OR: Odds ratio
GRADE Working Group grades of evidenceHigh certainty: We are very confident that the true effect lies close to that of the estimate of the effect
 Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
 Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
 Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded one level for serious risk of bias as included trials had high risk of bias due to lack of blinding and/or rates of attrition > 20%

2 Downgraded one level for very serious inconsistency due to considerable heterogeneity (I2 = 79% indicating large variation between point estimates due to among‐study differences)

3 Downgraded one level for serious indirectness as differences in intervention or comparison could be sufficient to make a difference to the outcome

4 Downgraded one level for serious imprecision as 95% Confidence Interval included the null effect, and included appreciable benefit or harm