Leukocyte DNA Damage and Wound Infection after Nitrous Oxide Administration A Randomized Controlled Trial

被引:40
作者
Chen, Yan [1 ]
Liu, Xiaodong [1 ]
Cheng, Christopher H. K. [2 ]
Gin, Tony [1 ]
Leslie, Kate [3 ,4 ]
Myles, Paul [5 ,6 ]
Chan, Matthew T. V. [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Anaesthesia & Intens Care, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Sch Biomed Sci, Hong Kong, Hong Kong, Peoples R China
[3] Royal Melbourne Hosp, Dept Anaesthesia & Pain Management, Melbourne, Vic, Australia
[4] Univ Melbourne, Dept Pharmacol, Melbourne, Vic, Australia
[5] Alfred Hosp, Dept Anaesthesia & Perioperat Med, Melbourne, Vic, Australia
[6] Monash Univ, Acad Board Anaesthesia & Perioperat Med, Melbourne, Vic 3004, Australia
关键词
SUPPLEMENTAL PERIOPERATIVE OXYGEN; SURGICAL SITE INFECTION; HOMOCYSTEINE STATUS; GENOME INSTABILITY; ANESTHETIC AGENTS; COMET ASSAY; FOLATE; SURGERY; SEVOFLURANE; LYMPHOCYTES;
D O I
10.1097/ALN.0b013e31829107b8
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Nitrous oxide inactivates methionine synthase and may lead to DNA damage and wound infection. By using single-cell gel electrophoresis (comet assay), the authors determined the effect of nitrous oxide on DNA damage in circulating leukocytes. Methods: In this double-blind, randomized controlled trial, 91 patients undergoing major colorectal surgery were randomized to receive 70% nitrous oxide (n = 31) or nitrous oxide-free anesthesia using 30 (n = 30) or 80% (n = 30) oxygen. Venous blood was collected before and 24 h after surgery. The primary outcome was extent of DNA damage, quantified as the percentage of DNA staining intensity in the comet tail using digital fluorescence microscopy. Incidence of postoperative wound infection was also recorded. Results: Nitrous oxide exposure was associated with a two-fold increase in the percentage of DNA intensity in tail (P = 0.0003), but not in the 30 (P = 0.181) or 80% oxygen groups (P = 0.419). There was a positive correlation between the duration of nitrous oxide exposure and extent of DNA damage, r = 0.33, P = 0.029. However, no correlation was observed in nitrous oxide-free patients. The proportions of postoperative wound infection, using the Centers for Disease Control and Prevention criteria, were 19.4% (6 of 31) in the 70% nitrous oxide group and 6.7% (2 of 30) in both the 30 and 80% oxygen groups, P = 0.21. An increase in DNA damage was associated with a higher risk of wound infection, adjusted odds ratio (95% CIs): 1.19 (1.07-1.34), P = 0.003. Conclusions: Nitrous oxide increased DNA damage compared with nitrous oxide-free anesthesia and was associated with postoperative wound infection.
引用
收藏
页码:1322 / 1331
页数:10
相关论文
共 44 条
  • [1] OXYGEN-DEPENDENT MICROBIAL KILLING BY PHAGOCYTES .1.
    BABIOR, BM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (12) : 659 - 668
  • [2] Supplemental perioperative oxygen and the risk of surgical wound infection -: A randomized controlled trial
    Belda, FJ
    Aguilera, L
    de la Asunción, JG
    Alberti, J
    Vicente, R
    Ferrándiz, L
    Rodríguez, R
    Company, R
    Sessler, DI
    Aguilar, G
    Botello, SG
    Ortí, R
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (16): : 2035 - 2042
  • [3] Is Antibiotic Prophylaxis in Surgery a Generally Effective Intervention? Testing a Generic Hypothesis Over a Set of Meta-Analyses
    Bowater, Russell J.
    Stirling, Seonaid A.
    Lilford, Richard J.
    [J]. ANNALS OF SURGERY, 2009, 249 (04) : 551 - 556
  • [4] DNA damage in patients who underwent minimally invasive surgery under inhalation or intravenous anesthesia
    Braz, Mariana G.
    Braz, Leandro G.
    Barbosa, Barbara S.
    Giacobino, Juliana
    Orosz, Jose E. B.
    Salvadori, Daisy M. F.
    Braz, Jose R. C.
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2011, 726 (02) : 251 - 254
  • [5] REACTIONS OF OXYL RADICALS WITH DNA
    BREEN, AP
    MURPHY, JA
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1995, 18 (06) : 1033 - 1077
  • [6] SURGICAL WOUND-INFECTION RATES BY WOUND CLASS, OPERATIVE PROCEDURE, AND PATIENT RISK INDEX
    CULVER, DH
    HORAN, TC
    GAYNES, RP
    MARTONE, WJ
    JARVIS, WR
    EMORI, TG
    BANERJEE, SN
    EDWARDS, JR
    TOLSON, JS
    HENDERSON, TS
    HUGHES, JM
    [J]. AMERICAN JOURNAL OF MEDICINE, 1991, 91 : S152 - S157
  • [7] Dean RT, 1997, BIOCHEM J, V324, P1
  • [8] DNA stability and genomic methylation status in colonocytes isolated from methyl-donor-deficient rats
    Duthie, SJ
    Narayanan, S
    Brand, GM
    Grant, G
    [J]. EUROPEAN JOURNAL OF NUTRITION, 2000, 39 (03) : 106 - 111
  • [9] DNA instability (strand breakage, uracil misincorporation, and defective repair) is increased by folic acid depletion in human lymphocytes in vitro
    Duthie, SJ
    Hawdon, A
    [J]. FASEB JOURNAL, 1998, 12 (14) : 1491 - 1497
  • [10] Low intake of calcium, folate, nicotinic acid, vitamin E, retinol, β-carotene and high intake of pantothenic acid, biotin and riboflavin are significantly associated with increased genome instability -: results from a dietary intake and micronucleus index survey in South Australia
    Fenech, M
    Baghurst, P
    Luderer, W
    Turner, J
    Record, S
    Ceppi, M
    Bonassi, S
    [J]. CARCINOGENESIS, 2005, 26 (05) : 991 - 999