Prophylactic esketamine for postpartum depression after cesarean section: a systematic review and meta-analysis.
Haibin Shi, Caihong Zheng, Bin Zhu
Journal of affective disorders June 10, 2025 DOI: 10.1016/j.jad.2025.119631 via PubMed
Summary
AI-generated from the abstractA meta-analysis of 13 studies with 2,716 patients found that perioperative esketamine lowers the risk of postpartum depression and reduces Edinburgh Postnatal Depression Scale scores at 1 and 6 weeks after cesarean section, and decreases pain scores within 48 hours during movement and 24 hours at rest. However, esketamine increases adverse effects such as hallucinations, dizziness, blurred vision, and diplopia. Prenatal body mass index is inversely correlated with mood response to esketamine one week after surgery. The studies had clinical heterogeneity, used different EPDS thresholds for diagnosing postpartum depression, and lacked racial diversity.
Study at a glance
| Characteristics | Meta-analysis Peer reviewed |
|---|---|
| Sample size | 2,716 |
| Population | Patients undergoing cesarean section |
| Intervention | Esketamine |
| Topics | Esketamine |
| Keywords | Meta-analysis Postpartum depression ppd Postnatal depression Cesarean section c-section Surgical birth |
| Citations | 5 |
| Key finding | Perioperative esketamine reduces the risk of postpartum depression and pain after cesarean section but increases short-term adverse effects, and higher prenatal body mass index predicts weaker antidepressant response. |
Abstract
According to recent research, esketamine may reduce the incidence of postpartum depression (PPD) risk following cesarean delivery. To further assess this potential benefit, a meta-analysis was conducted. Embase, Web of Science, the Cochrane Library, and PubMed were searched from inception through March 2025. Meta-analysis was performed using random-effects models to calculate risk ratios (RRs) and mean differences along with their corresponding 95 % confidence intervals (CIs). The primary outcome was the incidence of PPD risk as measured by the Edinburgh Postnatal Depression Scale (EPDS). Secondary outcomes were EPDS score, Numeric Rating Scale (NRS) postoperative pain score, and the incidence of adverse events. Thirteen studies with 2716 patients were analyzed. Esketamine used perioperatively lowers the risk of PPD and EPDS scores at 1 and 6 weeks after cesarean section and reduces NRS pain scores within 48 h during movement and 24 h at rest. However, it also increases adverse effects like hallucinations, dizziness, blurred vision, and diplopia. Additionally, prenatal body mass index (BMI) is inversely correlated with mood response to esketamine one week after surgery. There was clinical heterogeneity, diagnostic interview for PPD with different EPDS score, and sample was not racially diverse among studies. Current research suggests that esketamine may reduce the incidence of PPD risk, EPDS score, and NRS pain score after cesarean section with short-term complications. Prenatal BMI was a negative predictor of the antidepressant efficacy of esketamine.