Evidence map›Paper›PMID 42207991›Full record

ArticleAnesthesia and analgesia2026

Dexmedetomidine Preemptive Analgesia on Intra- and Postoperative Pain in Noncardiac Surgery: A Randomized, Double-Blind, Controlled Study.

Xiaohua Wang, Haosheng Chang, Wenwei Qi, Hongmei Wang, Yi Huang, Zhiwei Wu, Qian Wang, Wei Jiang, Tianlong Wang

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Article in Anesthesia and analgesia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Xiaohua WangFrom the Department of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Haosheng ChangDepartment of Surgery, Beijing Armed Police Corps Hospital, Beijing, China.
Wenwei QiNational Clinical Research Center for Cardiovascular Diseases, Beijing, China.
Hongmei WangXinjiang Changji Vocational and Technical College, Xinjiang, China.
Yi HuangDepartment of Radiology, South Branch of Peking University Cancer Hospital, Beijing, China.
Zhiwei WuFrom the Department of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Qian WangFrom the Department of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wei JiangDepartment of Anesthesiology, Third Medical Center of People`s Liberation Army General Hospital, Beijing, China.
Tianlong WangFrom the Department of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInadequate pain management affects over half of the 230 million major surgeries performed annually. Preemptive analgesia aims to prevent peripheral and central sensitization. Dexmedetomidine (DEX) offers non-opioid analgesia and opioid-sparing effects. This study evaluated the efficacy of preemptive DEX using the nociception index (NOX) for objective intraoperative monitoring and assessed its impact on perioperative outcomes.

methodsIn this single-center, double-blind, randomized controlled trial, 220 eligible patients were assigned to receive either intravenous DEX (1.5 µg·kg-1·h-1) (DEX group) or placebo (normal saline) (PO group) from 15 minutes before anesthesia induction until 15 minutes post-induction. The co-primary outcomes were the intraoperative NOX compliance rate (mean NOX ≤60 during nociceptive stimulation) and the incidence of moderate-to-severe postoperative pain (pNRS > 3) at 0, 24, 48 hours, and 7 days. Secondary outcomes included hemodynamic parameters, postoperative nausea and vomiting (mPONV), dizziness, analgesic consumption, and safety events.

resultsThe DEX group demonstrated a significantly higher NOX compliance rate compared to the placebo group (98/108, 90.7% vs 14/112, 12.5%; P <.001). The incidence of NRS>3 was significantly lower in the DEX group at all postoperative time points (3/108, 2.8% vs 29/112, 25.9% at 0 hour; 6/108, 5.6% vs 33/112, 29.5% at 24 hours; 1/108, 0.9% vs 19/112, 17% at 48 hours; 0/108, 0% vs 6/112, 5.4% at 7 d; P = .000). DEX also reduced rescue opioid consumption (z = -2.428, P = .004), decreased mPONV (z = -4.901, P = .001), and improved hemodynamic stability. Safety profiles were favorable in DEX group.

conclusionPreemptive analgesia with DEX significantly improves both intraoperative nociceptive control as objectively measured by the NOX and postoperative pain control. It validates the role in optimizing perioperative analgesia and enhancing recovery.

Identifiers

PMID42207991
PMCPMC13668036

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.