Espey 2000.
Methods | Design: retrospective chart review Location: 3 Indian Health Service facilities in southwestern USA Time frame: first injection of DMPA from December 1992 to June 1995 Sample size estimation and outcome of focus: no information |
|
Participants | Female members of Navajo tribe Inclusion criteria: 18 to 40 years old; completed at least 5 consecutive injections of DMPA at 10‐ to 14‐week intervals; had weights recorded at 1‐ or 2‐year intervals Exclusion criteria: history of diabetes or thyroid disease; women in postpartum group who had pre‐eclampsia or multiple gestations within index pregnancy |
|
Interventions | DMPA initiation 1) Interval (N = 115): first injection ≥ 20 weeks past pregnancy of ≥ 20 weeks gestation 2) Postpartum (N = 57): first injection at 5 to 8 weeks after delivery of singleton pregnancy of ≥ 20 weeks gestation | |
Outcomes | Mean weight gain (lb) for DMPA by initiation group Time frame: 1 and 2 years |
|
Notes | For another group, not included in this review, investigators reportedly extracted method of contraception from charts but did not provide specifics. Discussion noted that group "more frequently used" IUC or tubal ligation and included COC users. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | DMPA users by choice |
NOS selection (NRS) | Low risk | Exposed: clinic population of Navajo women Non‐exposed: same population as exposed Exposure: clinic records of DMPA injections |
NOS comparability (NRS) | Low risk | Analysis: adjusted for age, parity, and initial weight |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not feasible due to differences in insertion times |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No information; objective outcome measure |
Incomplete outcome data (attrition bias) All outcomes | High risk | Loss to follow‐up: for 1 year, only complete records included in retrospective review; does not account for discontinuation and loss; at 2 years, no weight data for 70% of interval group and 49% of postpartum group |