Safety of nitrous oxide administration in patients with Charcot-Marie-Tooth disease

被引:7
|
作者
Isbister, Geoffrey K. [2 ]
Burns, Joshua [1 ]
Prior, Felicity [3 ]
Ouvrier, Robert A. [1 ]
机构
[1] Univ Sydney, Childrens Hosp Westmead, Inst Neuromuscular Res, Discipline Paediat & Child Hlth,Fac Med, Westmead, NSW 2145, Australia
[2] Charles Darwin Univ, Childrens Hosp Westmead, Trop Toxinol Unit, Sch Hlth Res, Darwin, NT, Australia
[3] Calvary Mater Hosp, Hunter Drug Informat Serv, Newcastle, NSW, Australia
关键词
hereditary motor and sensory neuropathy; peripheral neuropathy; Charcot-Marie-Tooth; nitrous oxide;
D O I
10.1016/j.jns.2007.12.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Nitrous oxide is routinely administered to children and adults with Charcot-Marie-Tooth disease (CMT) as an anaesthetic for procedures such as nerve conduction studies and maintenance for general anaesthesia. However it is listed as a 'moderate to significant' risk of potential toxicity and worsening neuropathy in people with CMT by the CMT Association (USA), CMT Association of Australia, CMT International (Canada) and CMT United Kingdom. We performed a systematic review focussing on the use of nitrous oxide in patients with CMT to help clarify its safety. This identified I I studies reporting 41 exposures to therapeutically inhaled nitrous oxide as maintenance for general anaesthesia with no reports of adverse effects or worsening of CMT neuropathy. In the absence of a single case in the literature reporting worsening neuropathy in CMT patients receiving nitrous oxide, this review provides good evidence that nitrous oxide should be considered a safe agent for use in children and adults with CMT. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 162
页数:3
相关论文
共 50 条
  • [41] Clinical and genetic aspects of Charcot-Marie-Tooth disease subtypes
    Nam, Soo Hyun
    Choi, Byung-Ok
    PRECISION AND FUTURE MEDICINE, 2019, 3 (02): : 43 - 68
  • [42] Outcomes of Charcot-Marie-Tooth Disease Cavovarus Surgical Reconstruction
    Haupt, Edward Thomas
    Porter, Giselle Moriah
    Blough, Christian
    Michalski, Max P.
    Pfeffer, Glenn B.
    FOOT & ANKLE INTERNATIONAL, 2024, 45 (11) : 1175 - 1183
  • [43] Charcot-Marie-Tooth Disease Type 2B
    Durdu, Senay
    Koc, Kadriye
    Balaban, Deniz
    Karaoglu, Aynur
    TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, 2009, 43 (02): : 65 - 67
  • [44] Postural instability in Charcot-Marie-Tooth 1A disease
    Tozza, Stefano
    Aceto, Maria Gabriella
    Pisciotta, Chiara
    Bruzzese, Dario
    Iodice, Rosa
    Santoro, Lucio
    Manganelli, Fiore
    GAIT & POSTURE, 2016, 49 : 353 - 357
  • [45] Measuring Ankle Instability in Pediatric Charcot-Marie-Tooth Disease
    Mandarakas, Melissa
    Hiller, Claire E.
    Rose, Kristy J.
    Burns, Joshua
    JOURNAL OF CHILD NEUROLOGY, 2013, 28 (11) : 1456 - 1462
  • [46] Charcot-Marie-Tooth Disease as a Cause of Conductive Hearing Loss
    L'Heureux-Lebeau, Benedicte
    Alzahrani, Musaed
    Saliba, Issam
    OTOLOGY & NEUROTOLOGY, 2013, 34 (07) : E105 - E106
  • [47] Charcot-Marie-Tooth disease and pathways to molecular based therapies
    Harel, T.
    Lupski, J. R.
    CLINICAL GENETICS, 2014, 86 (05) : 422 - 431
  • [48] Correction of cavovarus foot deformity in Charcot-Marie-Tooth disease
    Azmaipairashvili, Z
    Riddle, EC
    Scavina, PSM
    Kumar, SJ
    JOURNAL OF PEDIATRIC ORTHOPAEDICS, 2005, 25 (03) : 360 - 365
  • [49] The impact of orthoses on gait in children with Charcot-Marie-Tooth disease
    Ounpuu, Sylvia
    Garibay, Erin
    Acsadi, Gyula
    Brimacombe, Michael
    Pierz, Kristan
    GAIT & POSTURE, 2021, 85 : 198 - 204
  • [50] Atypical presentation of Charcot-Marie-Tooth disease 1A: A case report
    Kulkarni, Shilpa D.
    Sayed, Rafat
    Garg, Meenal
    Patil, Varsha A.
    NEUROMUSCULAR DISORDERS, 2015, 25 (11) : 916 - 919