Single low-dose esketamine improves postpartum depression symptoms and recovery quality in cesarean section women.
American journal of translational research January 1, 2026 DOI: 10.62347/euok7911 via PubMed
Summary
AI-generated from the abstractA single low dose of esketamine (0.2 mg/kg) given intravenously for 40 minutes right after fetal delivery, combined with standard patient-controlled intravenous analgesia, reduces early postpartum depression symptoms and speeds recovery in women having cesarean sections. In a randomized controlled trial of 136 women, those receiving esketamine had lower Edinburgh Postnatal Depression Scale scores on days 2 and 7 after surgery, higher Obstetric Quality of Recovery-10 scores, shorter times to first walking, passing gas, and breastfeeding, and more frequent breastfeeding within 48 hours, compared with a placebo group. Adverse reactions did not differ significantly between groups.
Study at a glance
| Characteristics | Randomized controlled trial Peer reviewed |
|---|---|
| Sample size | 136 |
| Population | Women scheduled for elective cesarean section |
| Interventions | Esketamine Patient-controlled intravenous analgesia |
| Dose | 0.2 mg/kg |
| Topics | Esketamine |
| Keywords | Low dose Cesarean section Patient-controlled intravenous analgesia Postpartum depression |
| Key finding | A single low-dose esketamine combined with PCIA significantly lowers early postpartum depression symptoms and improves recovery quality after cesarean section, with no increase in adverse reactions. |
Abstract
To investigate the effects of single low-dose esketamine combined with patient-controlled intravenous analgesia (PCIA) on early postpartum depression symptoms and recovery quality in women undergoing cesarean section. This prospective, randomized, controlled study enrolled 136 women scheduled for elective cesarean section, who were randomly assigned in a 1:1 ratio to the study group (esketamine group, n=68) or the control group (placebo group, n=68). In the study group, esketamine (0.2 mg/kg) was intravenously infused for 40 minutes immediately after fetal delivery. In the control group, an equal volume of normal saline was given. Both groups then received PCIA for pain relief maintenance after the operation. The Edinburgh Postnatal Depression Scale (EPDS) scores, Obstetric Quality of Recovery-10 (ObsQoR-10) scores, and postoperative recovery indicators were compared between groups at different time points after surgery. Compared with the control group, the study group showed significantly lower EPDS scores at postoperative days 2 and 7, higher ObsQoR-10 scores, shorter times to first ambulation, flatus, and breastfeeding, as well as increased breastfeeding frequency within 48 hours (all P<0.05). The incidence of adverse reactions revealed no statistically significant difference (P>0.05). A single low-dose esketamine combined with PCIA effectively alleviates early postpartum depression symptoms, enhances postoperative recovery in women undergoing cesarean section, and demonstrates good safety and clinical applicability.