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

Summary of findings 2. Reminders (+/‐ educational information) compared to usual family planning care for improving adherence and continuation of shorter‐term hormonal methods of contraception.

Reminders (+/‐ educational information) 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: Reminders (+/‐ educational information)
 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 reminders (+/‐ educational information)
Continuation of hormonal contraceptive method 516 per 1000 587 per 1000
(524 to 649)
OR 1.33
(1.03 to 1.73)
933
 (2 RCTs) ⊕⊝⊝⊝
 VERY LOW 1 2 3 High unexplained heterogeneity (I2 = 69%) (unable to determine whether heterogeneity was due to differences in type of contraception, or in type of intervention)
Rates of discontinuation due to adverse events Not reported  
Adherence to method use as indicated by missed pills per cycle The mean adherence was 5.8 MD 0.8 higher
 (1.22 lower to 2.82 higher) 73
 (1 RCT) ⊕⊕⊝⊝
 LOW 4 5  
Adherence to method use as indicated by on‐time injections overall 50 per 100 46 per 100
 (35 to 56) OR 0.84
 (0.54 to 1.29) 350
 (2 RCTs) ⊕⊕⊝⊝
 LOW 1 5  
Pregnancy Not reported  
*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 were at high risk of bias due to lack of blinding and/or rates of attrition > 20%

2 Downgraded one level for serious inconsistency due to some heterogeneity (I2 > 50% indicating some variation between point estimates due to between‐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 small sample size

5 Downgraded one level for serious imprecision as 95% confidence interval included the null effect, and included appreciable benefit or harm