Table 4.
What is the effectiveness of IUD insertion by auxiliary nurse midwives compared to IUD insertion by doctors? | ||||||
---|---|---|---|---|---|---|
Patient or population: patients with IUDs | ||||||
Settings: Primary health care setting in nine rural villages in Cubuk district, Turkey (Eren et al. [21] Study A) and Jose Fabella | ||||||
Memorial Hospital in Manila, Philippines (Eren et al. [21] Study B) | ||||||
Intervention: Auxiliary nurse-midwives inserting IUDs | ||||||
Comparison: Doctors inserting IUDs | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect | No of Participants | Certainty of the evidence | Comments | |
Assumed risk | Corresponding risk | |||||
Doctors inserting IUDs | Auxiliary nurse-midwives inserting IUDs | (95% CI) | (studies) | (GRADE) | ||
Continuation rates1 | 699 per 1000 | 727 per 1000 | RR 1.04 | 996 | ⊕⊕⊕⊝ | |
(671 to 783) | (0.96 to 1.12) | (2 studies) | moderate2 | |||
Removal rates | 107 per 1000 | 115 per 1000 | RR 1.08 | 996 | ⊕⊕⊕⊝ | |
(82 to 162) | (0.77 to 1.52) | (2 studies) | moderate2 | |||
Expulsion rates | 96 per 1000 | 81 per 1000 | RR 0.84 | 996 | ⊕⊕⊕⊝ | |
(54 to 121) | (0.56 to 1.26) | (2 studies) | moderate2 | |||
Unintended pregnancy rates | 20 per 1000 | 19 per 1000 | RR 0.95 | 996 | ⊕⊕⊝⊝ | |
(8 to 47) | (0.4 to 2.27) | (2 studies) | low2,3 | |||
Referral rate during IUD insertion4 | 65 per 1000 | 52 per 1000 | RR 0.80 | 1058 | ⊕⊕⊝⊝ | |
(33 to 84) | (0.50 to 1.29) | (2 studies) | low2,3 | |||
Referral rate after IUD insertion5 | 43 per 1000 | 64 per 1000 | RR 1.49 | 996 | ⊕⊕⊝⊝ | |
(38 to 109) | (0.88 to 2.54) | (2 studies) | low2,3 | |||
Uptake of contraceptives6 - not measured | See comment | See comment | Not estimable6 | - | See comment | |
Complication rates at insertion6 - not measured | See comment | See comment | Not estimable6 | - | See comment | |
Insertion failure rates6 - not measured | See comment | See comment | Not estimable6 | - | See comment |
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. 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; RR: Risk ratio;
GRADE Working Group grades of evidence.
High 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.
1Continuation rates were calculated from the number of discontinuations at 12 months.
2Downgraded because of unclear but potential risk of contamination and inadequate blinding and because of statistical heterogeneity.
3Downgraded because of imprecision (i.e. the confidence interval indicates both benefit and harm).
4In one study, women were referred because the health worker decided that they were unable to insert the IUD because of postpartum conditions or because they made a failed attempt (i.e. insertion failure). In the other study reasons for referral included: suspected pregnancy, suspected pelvic inflammatory disease, cervicitis and erosion and conditions interfering with IUD insertion (e.g. prolapsed uterus, cervical incompetence).
5Where women with IUDs were referred at follow-up visits, because of pregnancy, bleeding problems, suspected pelvic inflammatory diseases (PID), a missing IUD tail, difficulty with insertion or postpartum conditions (anaemia, episiotomy).
6The studies did not measure uptake of contraceptives, insertion failure rates or complication rates at insertion.