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Esketamine combined with low-dose propofol induction strategy for category-1 cesarean section: a case series.

Guang-Qiu Zhu, Yu Wang, Xiao-Xia Wang, Hai-Tao Cong, Wan-Lan Mou

BMC anesthesiology May 8, 2025 DOI: 10.1186/s12871-025-03098-8 via PubMed

Summary

AI-generated from the abstract

A low-dose combination of esketamine and propofol for general anesthesia induction during category-1 emergency cesarean sections maintained maternal hemodynamic stability without causing neonatal depression. In a case series of 11 patients, the median 1-minute Apgar score was 9 and the 5-minute Apgar score was 10 for all newborns. The mean decision-to-delivery interval was 10.9 minutes. Only one newborn required temporary mask ventilation due to acute fetal distress from placental abruption; no newborns were admitted to the ICU. No episodes of hypotension, intraoperative awareness, reflux aspiration, or adverse psychiatric effects occurred. The strategy appears suitable, but randomized controlled trials are needed to confirm these findings.

Study at a glance

Characteristics Case series Randomized Case report Peer reviewed
Sample size 11
Population Patients undergoing category-1 emergency cesarean section
Interventions Esketamine Propofol Rocuronium
Dose 0.5 mg/kg esketamine, 1 mg/kg propofol, 1 mg/kg rocuronium
Topics Esketamine
Keywords Emergency General anesthesia Propofol Caesarean section
Citations 1
Key finding An esketamine-based combined low-dose propofol induction strategy effectively maintained maternal hemodynamic stability without neonatal depression in category-1 emergency cesarean sections.

Abstract

General anesthesia (GA) is the most accepted option for category-1 emergency cesarean sections (CSs). A low dose of esketamine has been used as an excellent adjunct to neuraxial anesthesia (NA) with little effect on newborns. However, literature on the use of esketamine for GA induction in emergency CS is limited. This case series describes our experience with an esketamine-based combined low-dose propofol induction strategy for category-1 CS. We retrospectively analyzed esketamine-based anesthesia induction for category-1 emergency CS at our hospital between November 2022 and November 2024. Modified rapid sequence induction included 0.5 mg/kg esketamine, 1 mg/kg propofol, and 1 mg/kg rocuronium, respectively. Anesthesia was maintained by propofol infusion at 4 mg/kg/h and inhalation of 1.5% sevoflurane. The dose of propofol and sevoflurane was adjusted to maintain the BIS value at 40-60. The final cohort comprised 11 patients. The median 1-minute Apgar score was 9 points [range, 6-10], and the 5-minute Apgar score was 10 points for all newborns. The mean decision-to-delivery interval (DDI) was 10.9 ± 2.4 min. Only one newborn required temporary mask ventilation due to acute fetal distress, mainly caused by major placental abruption. No newborns were admitted to the intensive care unit (ICU). No episodes of hypotension (MAP < 70 mmHg) were observed from anesthesia induction to delivery of the newborns. In all cases, there was no intraoperative awareness, reflux aspiration, or adverse psychiatric effects. The esketamine-based combination low-dose propofol induction strategy can effectively maintain maternal hemodynamic stability without causing neonatal depression, making it suitable for category-1 emergency CSs. However, further randomized controlled trials are needed to confirm these findings.

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