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右美托咪定对气腹时抑制交感神经反应所需七氟烷最低肺泡有效浓度的影响:一项随机试验
Authors Yuan Y, Zheng G, Guan J, Zhou C, Gao W , Li J , Dai D , Yao Y
Received 14 April 2025
Accepted for publication 29 June 2025
Published 9 July 2025 Volume 2025:19 Pages 5899—5909
DOI https://doi.org/10.2147/DDDT.S529767
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Georgios Panos
Yan Yuan,1,* Guanlin Zheng,2,* Jinsheng Guan,2,* Chenye Zhou,3 Weitao Gao,3 Junyu Li,3 Dongsheng Dai,3 Yusheng Yao3
1Department of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, People’s Republic of China; 2Department of Anesthesiology, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, People’s Republic of China; 3Department of Anesthesiology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, People’s Republic of China
*These authors contributed equally to this work
Correspondence: Dongsheng Dai, Email fjdaidongsheng@fjmu.edu.cn Yusheng Yao, Email fjslyys@fjmu.edu.cn
Purpose: Laparoscopic procedures require abdominal inflation (pneumoperitoneum), which triggers strong stress responses that typically need high concentrations of sevoflurane to manage. Despite dexmedetomidine’s known anesthetic-sparing properties, its specific effects on sevoflurane minimum alveolar concentration for blunting sympathetic response (MACBAR) during pneumoperitoneum remain incompletely characterized. This study evaluates dexmedetomidine’s impact on sevoflurane requirements for blocking sympathetic responses during laparoscopic pneumoperitoneum.
Patients and Methods: This prospective, randomized, double-blind, placebo-controlled trial enrolled 90 adults (aged 18– 45 years) classified as American Society of Anesthesiologists physical status I–II scheduled for elective laparoscopic cholecystectomy. Participants received either saline, low-dose dexmedetomidine (target 0.3 ng/mL), or high-dose dexmedetomidine (target 0.6 ng/mL). We determined sevoflurane MACBAR using Dixon’s up-and-down method, defined as the concentration preventing ≥ 20% increase in heart rate or mean arterial pressure following pneumoperitoneum. Secondary outcomes included hemodynamic responses, emergence time, adverse events, and plasma catecholamine levels.
Results: Dexmedetomidine significantly reduced sevoflurane MACBAR compared to control (4.70% ± 0.18%; 95% confidence interval [CI], 4.61– 4.80): to 2.90% ± 0.19% (95% CI, 2.80– 3.00) in the low-dose group and to 1.90% ± 0.16% (95% CI, 1.82– 1.98) in the high-dose group (both p < 0.001). Patients receiving dexmedetomidine had significantly lower plasma epinephrine and norepinephrine levels following pneumoperitoneum compared to control (p < 0.001), with better hemodynamic stability. Emergence times and adverse event rates remained comparable between groups.
Conclusion: Dexmedetomidine produces dose-dependent reductions in sevoflurane requirements for controlling sympathetic responses during pneumoperitoneum while maintaining hemodynamic stability, making it a valuable adjunct for anesthesia in laparoscopic surgery.
Registration: The Chinese Clinical Trials Registry, ChiCTR2300071257.
Keywords: dexmedetomidine, sevoflurane, minimum alveolar concentration, pneumoperitoneum, laparoscopic cholecystectomy