3.4. Analysis.
Comparison 3: Lay health worker‐led psychosocial interventions versus usual care in treating perinatal depression, Outcome 4: Adverse events
Adverse events | |
Study | Heading 1 |
Chibanda 2014 | 3 participants in pharmacological arm discontinued study drug due to adverse effects. |
Fuhr 2019 | Overall, 24 (17%) participants in the intervention group and 27 (19%) participants in the control group had at least one serious adverse event; the most common of these events were hospital admissions, experiences of physical violence, and stigmatisation. However, there was no evidence of any differences between the groups. |
Lund 2020 | There were no significant harms associated with the intervention, and no notable differences between the two arms in the number of adverse events. |
Sikander 2019 | Overall, 43 (15%) women in the intervention group and 47 (16%) women in the control group had at least one serious adverse event, which were evenly distributed between the groups (p=0·72). The most common serious adverse events were death of the child, hospital admissions (mainly of the child), and experience of physical violence; however, there was no evidence of any difference between the groups. |