Chronic postsurgical pain after nitrous oxide anesthesia

被引:88
作者
Chan, Matthew T. V. [1 ]
Wan, Alex C. M. [1 ]
Gin, Tony [1 ]
Leslie, Kate [2 ,3 ]
Myles, Paul S. [4 ,5 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Anaesthesia & Intens Care, Shatin, Hong Kong, Peoples R China
[2] Royal Melbourne Hosp, Dept Anaesthesia & Pain Management, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Pharmacol, Melbourne, Vic, Australia
[4] Alfred Hosp, Dept Anaesthesia & Perioperat Med, Melbourne, Vic, Australia
[5] Monash Univ, Acad Board Anaesthesia & Perioperat Med, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
Chronic postsurgical pain; Nitrous oxide; Anesthesia; Postoperative complication; Quality of life; Impact of chronic pain; D-ASPARTATE RECEPTOR; NEUROPATHIC PAIN; PLASMA HOMOCYSTEINE; RISK-FACTORS; TRANSMISSION; INSTABILITY; MECHANISMS; SURGERY; TARGETS; FOLATE;
D O I
10.1016/j.pain.2011.07.015
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Nitrous oxide is an antagonist at the N-methyl-D-aspartate receptor and may prevent the development of chronic postsurgical pain. We conducted a follow-up study in the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA) trial patients to evaluate the preventive analgesic efficacy of nitrous oxide after major surgery. The ENIGMA trial was a randomized controlled trial of nitrous oxide-based or nitrous oxide-free general anesthesia in patients presenting for noncardiac surgery lasting more than 2 hours. Using a structured telephone interview, we contacted all ENIGMA trial patients recruited in Hong Kong (n = 640). We recorded the severity of postsurgical pain of at least 3 months' duration that was not due to disease recurrence or a pre-existing pain syndrome, using the modified Brief Pain Inventory. The impact of postsurgical pain on quality of life was also measured. Pain intensity, opioid and other analgesic requirements during the first week of surgery, were retrieved from the trial case report form and medical records. A total of 46 (10.9%) patients reported pain that persisted from the index surgery, and 39 (9.2%) patients had severe pain. In addition, patients with chronic pain rated poorly in all attributes of the quality-of-life measures compared with those who were pain free. In a multivariate analysis, nitrous oxide decreased the risk of chronic postsurgical pain. In addition, severe pain in the first postoperative week, wound complication, and abdominal incision increased the risk of chronic pain. In conclusion, chronic postsurgical pain was common after major surgery in the ENIGMA trial. Intraoperative nitrous oxide administration was associated with a reduced risk of chronic postsurgical pain. (C) 2011 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2514 / 2520
页数:7
相关论文
共 45 条
[1]
Chemokines and pain mechanisms [J].
Abbadie, Catherine ;
Bhangoo, Sonia ;
De Koninck, Yves ;
Malcangio, Marzia ;
Melik-Parsadaniantz, Stephane ;
White, Fletcher A. .
BRAIN RESEARCH REVIEWS, 2009, 60 (01) :125-134
[2]
[Anonymous], 1986, Pain Suppl, V3, pS1
[3]
Bennett GJ, 2000, J PAIN SYMPTOM MANAG, V19, pS2
[4]
Nitrous oxide (N2O) prevents latent pain sensitization and long-term anxiety-like behavior in pain and opioid-experienced rats [J].
Bessiere, Baptiste ;
Richebe, Philippe ;
Laboureyras, Emilie ;
Laulin, Jean-Paul ;
Contarino, Angelo ;
Simonnet, Guy .
NEUROPHARMACOLOGY, 2007, 53 (06) :733-740
[5]
A Single Nitrous Oxide (N2O) Exposure Leads to Persistent Alleviation of Neuropathic Pain in Rats [J].
Bessiere, Baptiste ;
Laboureyras, Emilie ;
Chateauraynaud, Jeremy ;
Laulin, Jean-Paul ;
Simonnet, Guy .
JOURNAL OF PAIN, 2010, 11 (01) :13-23
[6]
Development and validation of the neuropathic pain symptom inventory [J].
Bouhassira, D ;
Attal, N ;
Fermanian, J ;
Alchaar, H ;
Gautron, M ;
Masquelier, E ;
Rostaing, S ;
Lanteri-Minet, M ;
Collin, E ;
Grisart, J ;
Boureau, F .
PAIN, 2004, 108 (03) :248-257
[7]
NMDA antagonists and neuropathic pain - Multiple drug targets and multiple uses [J].
Chizh, BA ;
Headley, PM .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (23) :2977-2994
[8]
DNA instability (strand breakage, uracil misincorporation, and defective repair) is increased by folic acid depletion in human lymphocytes in vitro [J].
Duthie, SJ ;
Hawdon, A .
FASEB JOURNAL, 1998, 12 (14) :1491-1497
[9]
Wind-up and the NMDA receptor complex from a clinical perspective [J].
Eide, PK .
EUROPEAN JOURNAL OF PAIN, 2000, 4 (01) :5-15
[10]
Nutritional treatment of genome instability: a paradigm shift in disease prevention and in the setting of recommended dietary allowances [J].
Fenech, M .
NUTRITION RESEARCH REVIEWS, 2003, 16 (01) :109-122