Parotidektomi Yapılan Charcot-Marie-Tooth Hastasında Anestezi Yönetimi
Özet
Charcot-Marie-Tooth hastalığı sensörinöral bir periferik polinöropati olup periferik sinir sisteminin en yaygın kalıtsal bozukluğudur. İlerleyici kas güçsüzlüğü tipik olarak ergenlikte veya erken yetişkinlikte fark edilir hale gelir. Hem duyusal hem de motor sinirleri etkiler. Etkilenen sinirler yavaşça dejenere olur ve uzaktaki hedefleriyle iletişim kurma yeteneğini kaybeder, bu da kollarda, bacaklarda, ellerde veya ayaklarda kas güçsüzlüğü ve atrofiye neden olur. Bu olgu sunumunda kulak burun ve boğaz hastalıkları (KBB) tarafından parotidektomi yapılan 57 yaşındaki Charcot-Marie-Tooth tanılı erkek hastanın anestezi yönetimi tartışılmıştır.
Charcot-Marie-Tooth disease is a sensorineural peripheral polyneuropathy and the most common inherited disorder of the peripheral nervous system. Progressive muscle weakness typically becomes noticeable in adolescence or early adulthood. It affects both sensory and motor nerves. Affected nerves slowly degenerate and lose the ability to communicate with their distant targets, resulting in muscle weakness and atrophy in the arms, legs, hands or feet. In this case report, we discuss the anesthetic management of a 57-year-old male patient with Charcot-Marie-Tooth who underwent parotidectomy by Otorhinolaryngology.
Referanslar
Nagappa M, Sharma S, Taly AB. Charcot-Marie-Tooth Disease. 2023 Aug 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024.
Timmerman V, Strickland AV, Züchner S. Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success. Genes. 2014; 22(1):13-32. doi: 10.3390/genes5010013.
Ohshita N, Oka S, Tsuji K et al. Anesthetic Management of a Patient With Charcot-Marie-Tooth Disease. Anesth Prog. 2016;63(2):80-3. doi: 10.2344/15-00010R1.1.
Ortiz-Gómez J, Palacio-Abizanda F, Fornet I. Rocuronium induced neuromuscular blockade reversion with sugammadex in a patient with Charcot-Marie-Tooth disease. Anestezjologia i Ratownictwo. 2010; 4. 307-309.
Greenwood JJ, Scott WE. Charcot-Marie-Tooth disease: peripartum management of two contrasting clinical cases. Int J Obstet Anesth. 2007;16(2):149-54. doi: 10.1016/j.ijoa.2006.10.005.
Aboussouan LS, Lewis RA, Shy ME. Disorders of pulmonary function, sleep, and the upper airway in Charcot-Marie-Tooth disease. Lung. 2007;185(1):1-7. doi: 10.1007/s00408-006-0053-9.
Ramchandren S, Tirella C. Dysautonomia in Charcot-Marie-Tooth Disease and Correlations with Patient-Reported Disability (P2.112). Neurology. 2018. doi: 10.1212/WNL.90.15_supplement.P2.11.
Neal JM, Barrington MJ, Brull R et al. The Second ASRA Practice Advisory on Neurologic Complications Associated With Regional Anesthesia and Pain Medicine: Executive Summary 2015. Reg Anesth Pain Med. 2015;40(5):401-30. doi: 10.1097/AAP.0000000000000286.
McClain RL, Rubin DI, Bais KS et al. Regional anesthesia in patients with Charcot-Marie-Tooth disease: a historical cohort study of 53 patients. Can J Anaesth. 2022;69(7):880-884. doi: 10.1007/s12630-022-02258-5.
Brock M, Guinn C, Jones M. Anesthetic management of an obstetric patient with Charcot-Marie-Tooth disease: a case study. AANA J. 2009;77(5):335-7.
Esteban RO, Estefanía M, Julia M et al. Spinal anesthesia in a patient with Charcot–Marie–Tooth disease undergoing orthopedic surgery: case report. Rev Colomb Anestesiol. 2019;47(3): 180-183. doi: 10.1097/CJ9.0000000000000115.
Kim SU, Kim S, Jung KT. Neuromuscular monitoring of a patient with Charcot-Marie-Tooth disease; which monitoring technique is adequate? - A case report and literature review. Anesth Pain Med. 2024;19(1):54-61. doi: 10.17085/apm.23111.
Schmitt HJ, Münster T. Mivacurium-induced neuromuscular block in adult patients suffering from Charcot-Marie-Tooth disease. Can J Anaesth. 2006;53(10):984-8. doi: 10.1007/BF03022526.
Gálvez-Cañellas JL, Errando CL, Martínez-Torrente F et al. Anaesthesia and orphan disease: difficult monitoring of neuromuscular blockade in a patient with severe Charcot-Marie-Tooth disease type I. Eur J Anaesthesiol. 2013;30(12):772-5. doi: 10.1097/EJA.0b013e3283623dea.
Pasha TM, Knowles A. Anaesthetic management of a patient with Charcot-Marie-Tooth disease for staged diaphragmatic plication. Br J Anaesth. 2013;110(6):1061-3. doi: 10.1093/bja/aet142.
Antognini JF. Anaesthesia for Charcot-Marie-Tooth disease: a review of 86 cases. Can J Anaesth. 1992;39(4):398-400. doi: 10.1007/BF03009054.
Jae WK, Jin HC, Goo K et al. Anesthetic Management of Charcot-Marie-Tooth Disease. Arch Clin Med Case Rep. 2020; (4):138-152. doi:10.26502/acmcr.96550179.
Errando CL, Muñoz L. Anaesthesia recommendations for Charcot-Marie-Tooth disease. Available from: https://www.orphananesthesia.eu/en/rare-diseases/published-guidelines/charcot-marie-tooth-disease/1598-charcot-marie-tooth-disease-2/file.html (Accessed 26th May 2024).
Isbister GK, Burns J, Prior F et al. Safety of nitrous oxide administration in patients with Charcot-Marie-Tooth disease. J Neurol Sci. 2008;15;268(1-2):160-2. doi: 10.1016/j.jns.2007.12.004.
Itoh N, Hoshijima H, Takeuchi R et al. Use of sugammadex in a patient with Charcot-Marie-Tooth disease under general anesthesia. Stomatological Dis Sci. 2018; 2: 2. doi: 10.20517/2573-0002.2017.14.
Hiramatsu S, Moriwaki K, Nakao M et al. Rocuronium-induced respiratory paralysis refractory to sugammadex in Charcot-Marie-Tooth disease. Can J Anaesth. 2022;69(3):364-368. doi: 10.1007/s12630-021-02168-y.
Referanslar
Nagappa M, Sharma S, Taly AB. Charcot-Marie-Tooth Disease. 2023 Aug 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024.
Timmerman V, Strickland AV, Züchner S. Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success. Genes. 2014; 22(1):13-32. doi: 10.3390/genes5010013.
Ohshita N, Oka S, Tsuji K et al. Anesthetic Management of a Patient With Charcot-Marie-Tooth Disease. Anesth Prog. 2016;63(2):80-3. doi: 10.2344/15-00010R1.1.
Ortiz-Gómez J, Palacio-Abizanda F, Fornet I. Rocuronium induced neuromuscular blockade reversion with sugammadex in a patient with Charcot-Marie-Tooth disease. Anestezjologia i Ratownictwo. 2010; 4. 307-309.
Greenwood JJ, Scott WE. Charcot-Marie-Tooth disease: peripartum management of two contrasting clinical cases. Int J Obstet Anesth. 2007;16(2):149-54. doi: 10.1016/j.ijoa.2006.10.005.
Aboussouan LS, Lewis RA, Shy ME. Disorders of pulmonary function, sleep, and the upper airway in Charcot-Marie-Tooth disease. Lung. 2007;185(1):1-7. doi: 10.1007/s00408-006-0053-9.
Ramchandren S, Tirella C. Dysautonomia in Charcot-Marie-Tooth Disease and Correlations with Patient-Reported Disability (P2.112). Neurology. 2018. doi: 10.1212/WNL.90.15_supplement.P2.11.
Neal JM, Barrington MJ, Brull R et al. The Second ASRA Practice Advisory on Neurologic Complications Associated With Regional Anesthesia and Pain Medicine: Executive Summary 2015. Reg Anesth Pain Med. 2015;40(5):401-30. doi: 10.1097/AAP.0000000000000286.
McClain RL, Rubin DI, Bais KS et al. Regional anesthesia in patients with Charcot-Marie-Tooth disease: a historical cohort study of 53 patients. Can J Anaesth. 2022;69(7):880-884. doi: 10.1007/s12630-022-02258-5.
Brock M, Guinn C, Jones M. Anesthetic management of an obstetric patient with Charcot-Marie-Tooth disease: a case study. AANA J. 2009;77(5):335-7.
Esteban RO, Estefanía M, Julia M et al. Spinal anesthesia in a patient with Charcot–Marie–Tooth disease undergoing orthopedic surgery: case report. Rev Colomb Anestesiol. 2019;47(3): 180-183. doi: 10.1097/CJ9.0000000000000115.
Kim SU, Kim S, Jung KT. Neuromuscular monitoring of a patient with Charcot-Marie-Tooth disease; which monitoring technique is adequate? - A case report and literature review. Anesth Pain Med. 2024;19(1):54-61. doi: 10.17085/apm.23111.
Schmitt HJ, Münster T. Mivacurium-induced neuromuscular block in adult patients suffering from Charcot-Marie-Tooth disease. Can J Anaesth. 2006;53(10):984-8. doi: 10.1007/BF03022526.
Gálvez-Cañellas JL, Errando CL, Martínez-Torrente F et al. Anaesthesia and orphan disease: difficult monitoring of neuromuscular blockade in a patient with severe Charcot-Marie-Tooth disease type I. Eur J Anaesthesiol. 2013;30(12):772-5. doi: 10.1097/EJA.0b013e3283623dea.
Pasha TM, Knowles A. Anaesthetic management of a patient with Charcot-Marie-Tooth disease for staged diaphragmatic plication. Br J Anaesth. 2013;110(6):1061-3. doi: 10.1093/bja/aet142.
Antognini JF. Anaesthesia for Charcot-Marie-Tooth disease: a review of 86 cases. Can J Anaesth. 1992;39(4):398-400. doi: 10.1007/BF03009054.
Jae WK, Jin HC, Goo K et al. Anesthetic Management of Charcot-Marie-Tooth Disease. Arch Clin Med Case Rep. 2020; (4):138-152. doi:10.26502/acmcr.96550179.
Errando CL, Muñoz L. Anaesthesia recommendations for Charcot-Marie-Tooth disease. Available from: https://www.orphananesthesia.eu/en/rare-diseases/published-guidelines/charcot-marie-tooth-disease/1598-charcot-marie-tooth-disease-2/file.html (Accessed 26th May 2024).
Isbister GK, Burns J, Prior F et al. Safety of nitrous oxide administration in patients with Charcot-Marie-Tooth disease. J Neurol Sci. 2008;15;268(1-2):160-2. doi: 10.1016/j.jns.2007.12.004.
Itoh N, Hoshijima H, Takeuchi R et al. Use of sugammadex in a patient with Charcot-Marie-Tooth disease under general anesthesia. Stomatological Dis Sci. 2018; 2: 2. doi: 10.20517/2573-0002.2017.14.
Hiramatsu S, Moriwaki K, Nakao M et al. Rocuronium-induced respiratory paralysis refractory to sugammadex in Charcot-Marie-Tooth disease. Can J Anaesth. 2022;69(3):364-368. doi: 10.1007/s12630-021-02168-y.