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Effect of Intraoperative Intravenous Infusion of Esketamine Combined with Dexmedetomidine on Postoperative Sleep Disturbance in Patients Undergoing Radical Mastectomy.

Xingyu Geng, Yutian Pu, Ziwei Hu, Heling Zhang, Maosan Wang, Can Fang, Gaochao Lv, Wanting Li, Xinyue Zhang, Xiaoxuan Fan, Su Liu, Xiuxia Chen, Jingru Wu

Drug design, development and therapy January 1, 2025 DOI: 10.2147/DDDT.S510222 via PubMed

Summary

AI-generated from the abstract

Postoperative sleep disturbance (POSD) is common after breast cancer surgery. In a randomized trial of 100 patients, intraoperative infusion of esketamine combined with dexmedetomidine did not significantly reduce the incidence of POSD compared to control or either drug alone over the first three days. However, on postoperative day 3, each drug alone reduced POSD risk when the other was absent. Dexmedetomidine decreased rapid eye movement (REM) sleep on day 1, while esketamine reduced nighttime awakening time on days 1 and 3. The combination showed no added benefit for POSD, but each drug had distinct effects on sleep architecture.

Study at a glance

Characteristics Randomized controlled trial Double-blind Peer reviewed
Sample size 100
Population Breast cancer patients after surgery
Interventions Esketamine Dexmedetomidine Esketamine combined with dexmedetomidine
Duration First three postoperative days
Topics Esketamine
Keywords Dexmedetomidine Sleep disturbance Sleep medicine Post-surgical recovery
Citations 7
Key finding Intraoperative esketamine combined with dexmedetomidine did not significantly reduce the incidence of postoperative sleep disturbance, but dexmedetomidine reduced REM sleep and esketamine reduced nocturnal awakening time.

Abstract

Postoperative sleep disturbance(POSD) is a problem in breast cancer patients after surgery. Little is known about the differences in the treatment of POSD with esketamine combined with dexmedetomidine under the same circumstances. We investigated the effects of intraoperative esketamine combined with intravenous dexmedetomidine on the incidence of POSD and postoperative sleep architecture. A single-center, randomized, double-blind controlled trial was conducted. A total of 100 participants were randomly assigned to four groups: the esketamine group (Group E), the dexmedetomidine group (Group D), the esketamine combined with dexmedetomidine group (Group ED), and the control group (Group S) (n=25 each). The intervention drugs were continuously infused until the placement of the drainage tube. The primary outcome measure was the incidence of POSD, defined as an Athens Insomnia Scale (AIS) score >6 on at least one of the first three postoperative days. The secondary outcome measure was the duration of sleep structure, which was collected using the Fitbit Charge 2® smartwatch (Fitbit, Inc. San Francisco, California, USA). In the first three postoperative days, the incidence of POSD was similar across the four groups (P=0.947). However, on postoperative day 3 (POD3), there was a significant interaction between esketamine and dexmedetomidine (P=0.004). Further simple effect analysis revealed that, in the absence of esketamine, dexmedetomidine had a significant effect on POSD on POD3 (OR=0.196, [0.056-0.691]; P=0.019). In the absence of dexmedetomidine, esketamine had a significant effect on POSD on POD3 (OR=0.248, [0.074-0.833]; P=0.042). Dexmedetomidine reduced rapid eye movement (REM) sleep on postoperative day 1 (P=0.042). Esketamine reduced nighttime awakening time on POD1 (P=0.036) and POD3 (P=0.020). Intraoperative infusion of esketamine combined with dexmedetomidine had no significant effect on POSD, but dexmedetomidine reduced REM sleep, and esketamine reduced the nocturnal awakening time.

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