Intraoperative dexmedetomidine reduces postoperative sleep disturbance in older adults undergoing major abdominal surgery: a single-center, randomized, double-blind, placebo-controlled trial
5 affiliations
- 1Department of Anesthesiology, First Affiliated Hospital of Soochow University, Suzhou, China
- 2Institute of Anesthesiology, Soochow University, Suzhou, China
- 3Jintan Traditional Chinese Medicine Hospital, Changzhou, China
- 4Department of Anesthesiology and Pain Medicine, University of California Davis Health, Sacramento, CA USA
- 5Anesthesia and Critical Care, National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Trust, London, UK
Abstract
Background:: Postoperative sleep disturbance (PSD) after major abdominal surgery in older adults is common and impairs recovery. Dexmedetomidine is a selective α2-adrenergic agonist with sedative, analgesic, and anti-inflammatory properties that promotes natural sleep. We hypothesized that intraoperative dexmedetomidine would reduce PSD in this population.
Methods:: In this randomized, double-blind, placebo-controlled trial, 210 older adults undergoing major abdominal surgery were randomly assigned (1:1:1) to receive intraoperative normal saline, dexmedetomidine 0.3 μg/kg/h, or 0.6 μg/kg/h. The primary outcome was PSD on the first postoperative night (Athens Insomnia Scale score ≥ 6). Secondary outcomes included PSD on until nights 30; pain at 24 and 48 h; delirium and depressive symptoms within 7 days; and recovery quality on postoperative days 1‒3. Sleep patterns on nights 1 and 2 were assessed using wrist actigraphy. This trial was registered on the Chinese Clinical Trial Registry (Identifier: ChiCTR2300073163; principal investigator: Ke Peng; dated July 23, 2023; https://www.chictr.org.cn/showproj.html?proj=199410).
Results:: 203 patients (median age 71 years; 67.5% male) completed this trial. Compared with normal saline (n = 67), both low-dose (n = 68) and high-dose dexmedetomidine (n = 68) significantly reduced first-night PSD (20.6% vs 65.7%; relative risk 0.31, 95% CI 0.19–0.50; NNT 2.2; P < 0.001; and 11.8% vs 65.7%; relative risk 0.18, 95% CI 0.09–0.34; NNT 1.8; P < 0.001, respectively). The two doses did not differ. Dexmedetomidine was associated with lower sleep disturbance on night 2 and higher recovery quality, without between-group differences in hypotension, bradycardia, delirium, or 30-day mortality. Exploratory actigraphy analysis (n = 20 per group) showed longer total sleep time and lower wake-time percentage associated with dexmedetomidine.
Conclusions:: Intraoperative dexmedetomidine infusion reduced the relative risk of first-night PSD by 70–80% among older adults undergoing major abdominal surgery. These findings require confirmation in multicenter trials.
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BibTeX
@article{peng2026intraoperative,
title = {{Intraoperative dexmedetomidine reduces postoperative sleep disturbance in older adults undergoing major abdominal surgery: a single-center, randomized, double-blind, placebo-controlled trial}},
author = {Hui-ping Peng and Jing-hui Hu and Li-ping Fan and Xiu Yang and Hua-yue Liu and Xi-sheng Shan and Hong Liu and Nazneen Sudhan and Fu-hai Ji and Ke Peng},
journal = {Communications Medicine},
year = {2026},
month = jul,
doi = {10.1038/s43856-026-01769-2},
url = {https://doi.org/10.1038/s43856-026-01769-2},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Intraoperative dexmedetomidine reduces postoperative sleep disturbance in older adults undergoing major abdominal surgery: a single-center, randomized, double-blind, placebo-controlled trial
AU - Hui-ping Peng
AU - Jing-hui Hu
AU - Li-ping Fan
AU - Xiu Yang
AU - Hua-yue Liu
AU - Xi-sheng Shan
AU - Hong Liu
AU - Nazneen Sudhan
AU - Fu-hai Ji
AU - Ke Peng
PY - 2026
DA - 2026/07/03
JO - Communications Medicine
DO - 10.1038/s43856-026-01769-2
UR - https://doi.org/10.1038/s43856-026-01769-2
AB - Background:: Postoperative sleep disturbance (PSD) after major abdominal surgery in older adults is common and impairs recovery. Dexmedetomidine is a selective α2-adrenergic agonist with sedative, analgesic, and anti-inflammatory properties that promotes natural sleep. We hypothesized that intraoperative dexmedetomidine would reduce PSD in this population. Methods:: In this randomized, double-blind, placebo-controlled trial, 210 older adults undergoing major abdominal surgery were randomly assigned (1:1:1) to receive intraoperative normal saline, dexmedetomidine 0.3 μg/kg/h, or 0.6 μg/kg/h. The primary outcome was PSD on the first postoperative night (Athens Insomnia Scale score ≥ 6). Secondary outcomes included PSD on until nights 30; pain at 24 and 48 h; delirium and depressive symptoms within 7 days; and recovery quality on postoperative days 1‒3. Sleep patterns on nights 1 and 2 were assessed using wrist actigraphy. This trial was registered on the Chinese Clinical Trial Registry (Identifier: ChiCTR2300073163; principal investigator: Ke Peng; dated July 23, 2023; https://www.chictr.org.cn/showproj.html?proj=199410). Results:: 203 patients (median age 71 years; 67.5% male) completed this trial. Compared with normal saline (n = 67), both low-dose (n = 68) and high-dose dexmedetomidine (n = 68) significantly reduced first-night PSD (20.6% vs 65.7%; relative risk 0.31, 95% CI 0.19–0.50; NNT 2.2; P < 0.001; and 11.8% vs 65.7%; relative risk 0.18, 95% CI 0.09–0.34; NNT 1.8; P < 0.001, respectively). The two doses did not differ. Dexmedetomidine was associated with lower sleep disturbance on night 2 and higher recovery quality, without between-group differences in hypotension, bradycardia, delirium, or 30-day mortality. Exploratory actigraphy analysis (n = 20 per group) showed longer total sleep time and lower wake-time percentage associated with dexmedetomidine. Conclusions:: Intraoperative dexmedetomidine infusion reduced the relative risk of first-night PSD by 70–80% among older adults undergoing major abdominal surgery. These findings require confirmation in multicenter trials.
SN - 2730-664X
ER -