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Effect of Low-Dose Esketamine on Postoperative Delirium in Elderly Patients Undergoing Total Hip or Knee Arthroplasty: A Randomized Controlled Trial.

Chao-Bang Ma, Cheng-Yang Zhang, Cai-Li Gou, Zeng-Hui Liang, Jing-Xian Zhang, Fei Xing, Jing-Jing Yuan, Xin Wei, Ya-Bing Zhang, Zhong-Yu Wang

Drug design, development and therapy January 1, 2024 DOI: 10.2147/DDDT.S477342 via PubMed

Summary

AI-generated from the abstract

A randomized controlled trial tested whether low-dose esketamine reduces postoperative delirium in elderly patients after total hip or knee replacement. Two hundred sixty participants received either esketamine (a loading dose of 0.20 mg/kg, infusion of 0.125 mg/kg/h, and 0.5 mg/kg for postoperative pain) or a placebo of normal saline. Delirium occurred in 8.5% of the esketamine group and 10.8% of the placebo group, a difference that was not statistically significant. The timing, duration, and subtype of delirium also did not differ between groups. Esketamine provided more stable blood pressure after anesthesia induction and lowered pain with movement during the first two days after surgery, but increased dizziness. Repeated low-dose esketamine did not reduce delirium in the first three days after surgery.

Study at a glance

Characteristics Randomized controlled trial Peer reviewed
Sample size 260
Population Elderly patients undergoing total hip or knee arthroplasty
Intervention Esketamine
Dose 0.20 mg/kg loading, 0.125 mg/kg/h infusion, 0.5 mg/kg for postoperative analgesia
Duration Initial three postoperative days
Topics Esketamine Ketamine
Keywords Aged Delirium Pain management Elderly care Senior medicine
Citations 27
Key finding Low-dose esketamine did not significantly reduce the incidence of postoperative delirium compared to placebo in elderly patients after total hip or knee arthroplasty.

Abstract

Postoperative delirium (POD) is a prevalent and severe complication in elderly patients undergoing major surgery, associated with increased morbidity and mortality. This randomized controlled trial aimed to investigate the effects of low-dose esketamine on the incidence of POD in elderly patients underwent total hip or knee arthroplasty. Two hundred and sixty elderly participants were randomly assigned to either the esketamine group (Group E) (0.20mg/kg loading, 0.125mg/kg/h infusion, 0.5 mg/kg for postoperative analgesia) or the placebo group (Group P) (received normal saline). The primary outcome was the incidence of POD, with secondary outcomes including delirium subtypes, duration, intraoperative analgesic consumption, operative and anesthesia times, hemodynamic changes, postoperative pain scores, sleep quality, and common postoperative adverse events. There was no significant difference in the incidence of POD between Group E (8.5%) and Group P (10.8%). No significant differences were observed for the time of delirium onset, duration of delirium, and delirium subtype between the two groups. Patients in the esketamine group had more stable hemodynamic profile after induction and reduced the pain score of motion on the first two days postoperatively but increased the incidence of postoperative dizziness. The repeated infusion of low-dose esketamine did not reduce the incidence of POD during the initial three postoperative days in elderly patients following total hip or knee arthroplasty.

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