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Intraoperative Esketamine and Postpartum Depression Among Women With Cesarean Delivery: A Randomized Clinical Trial

Li Ren, Ting Zhang, B Zou, Xiaomei Su, Yuan Tao, Jixing Yang, Fangfang Lv, Peining Li, Fei Peng, Guodong Wu

Obstetric Anesthesia Digest November 18, 2025 DOI: 10.1097/01.aoa.0001171036.71757.fb (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Randomized clinical trial Peer reviewed
Population New mothers who had cesarean birth
Intervention Esketamine
Topics Depression Esketamine
Keywords Postpartum depression Randomized controlled trial Incidence geometry Depression economics Clinical trial Postpartum period Obstetrics Pregnancy Pediatrics Cesarean delivery
Citations 1
Key findings Esketamine may reduce the risk of postpartum depression following cesarean birth, but prior randomized clinical trials have shown mixed results.

Abstract

( JAMA Network Open . 2025;8(2):e2459331. doi: 10.1001/jamanetworkopen.2024.59331) Postpartum depression (PPD) is a widespread condition affecting about 17.7% of new mothers globally, with an even higher incidence of 21.4% reported in China. Cesarean birth (CB) appears to increase the risk of developing PPD compared to vaginal births. Given the growing recognition of esketamine, a derivative of ketamine, as a rapid-acting antidepressant, its potential use in PPD prevention has become a subject of interest. While prior randomized clinical trials (RCTs) have shown mixed results, there has been limited real-world evidence of its efficacy in typical clinical settings. The objective of this study was to examine the practical impact of esketamine in reducing the risk of PPD following CB.