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DOI 10.1097/js9.0000000000003501

Медицинская библиотека · International journal of surgery (London, England) · 2025

Effect of intraoperative low-dose esketamine on postoperative quality of recovery in patients undergoing laparotomy for gynecologic malignancy: a randomized controlled trial.

Geng Zhi-Yu, Zhang Yan, Bi Hui, Yan Xin, Song Lin-Lin, Song Hui-Cheng

СтатьяРандомизированное исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Gynecologic malignancy surgery with long midline incision and extensive surgical field often causes severe pain. We aimed to evaluate the benefit of low-dose esketamine on postoperative recovery after gynecologic malignancy laparotomy.

MATERIALS AND

METHODS

In total, 140 female patients scheduled for elective gynecologic malignancy laparotomy were randomly assigned to the esketamine group ( n = 70) or control group ( n = 70). Patients in the esketamine group received an intraoperative infusion of 0.25 mg/kg/h esketamine while those in the control group received an equivalent volume of saline. Both groups received a standard multimodal analgesic regimen that consisted of transversus abdominis plane block, acetaminophen, nonsteroidal anti-inflammatory drugs, and patient-controlled morphine. The primary outcome was the Quality of Recovery-40 (QoR-40) score at 48 hours postoperatively. Secondary outcomes included morphine consumption, pain scores, adverse effects, time to post-anesthesia care unit (PACU) discharge, postoperative depressive symptom on postoperative day 7, quality of life, and chronic pain at 3 months after surgery.

RESULTS

The median QoR-40 score at 48 hours was 179 (164-190) in the esketamine group, which was not significantly different from 178.5 (163-186) in the control group (median difference, 1; 95% CI, -4 to 7; P = 0.643). Secondary outcomes were comparable between the two groups. Patients in the esketamine group had more over-sedation (20/69 [29.0%] vs. 8/70 [11.4%]; absolute risk difference (ARD), 17.6% [95% CI, 4.2-30.4%]; P = 0.010), and delayed discharge from PACU (19/69 [27.5%] vs. 4/70 [5.7%]; ARD, 21.8% [95% CI, 9.6-33.8%]; P = 0.001) compared to the control group.

CONCLUSIONS

Intraoperative low-dose esketamine failed to further improve the QoR-40 score after gynecologic malignancy laparotomy when used as part of a multimodal analgesic regimen. Further research is needed to explore the optimal dosage and indications of esketamine in this patient population.

Для цитирования: Geng Zhi-Yu, Zhang Yan, Bi Hui, Yan Xin, Song Lin-Lin, Song Hui-Cheng. Effect of intraoperative low-dose esketamine on postoperative quality of recovery in patients undergoing laparotomy for gynecologic malignancy: a randomized controlled trial.. International journal of surgery (London, England). 2025. DOI: 10.1097/js9.0000000000003501.

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