Duchenne Musküler Distrofili Bir Olguda Kombine Spinal-Epidural Anestezi Altında Laparoskopik Kolesistektomi
Özet
Duchenne Musküler Distrofisi (DMD) tanılı, 24 yaşında, erkek hasta, preoperatif detaylı değerlendirme sonrası kombine spinal-epidural anestezi altında laparoskopik kolesistektomi operasyonuna alındı. Sorunsuz bir perioperatif süreç sonrasında 1 günü yoğun bakım ünitesinde olmak üzere günlük hastane yatışının ardından taburcu edildi.
Referanslar
Birnkrant DJ, Panitch HB, Benditt JO, Boitano LJ, Carter ER, Cwik VA, Finder JD, Iannaccone ST, Jacobson LE, Kohn GL, Motoyama EK, Moxley RT, Schroth MK, Sharma GD, Sussman MD.AmericanCollege of Chest Physicians consensus statement on the respiratory and related management of patients with Duchenne muscular dystrophy undergoing anesthesia or sedation. Chest 2007;132:1977–86.
Rodino-Klapac LR, Mendell JR, Sahenk Z. Update on the treatment of Duchenne muscular dystrophy. Curr Neurol Neurosci Rep 2013; 13: 332.
Morris P. Duchenne muscular dystrophy: a challenge for the anaesthetist. Paediatr Anaesth 1997;7(1):1-4.
Büget Mİ, Eren İ, Küçükay S. Regional anaesthesia in a Duchenne muscular dystrophy patient for upper extremity amputation. Agri. 2014;26(4):191-5.
Cripe LH, Tobias JD. Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr Anaesth. 2013 Sep;23(9):777-84.
Thrush PT, Allen HD, Viollet L et al. Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy. Am J Cardiol 2009; 103: 262–265.
Birnkrant DJ. The American College of Chest Physicians consensus statement on the respiratory and related management of patients with Duchenne muscular dystrophy undergoing anesthesia or sedation. Pediatrics 2009; 123(Suppl 4): S242–S244.
Litman RS, Rosenberg H. Malignant hyperthermia: update on susceptibility testing. JAMA 2005;293:2918–24.
Rosenberg H, Davis M, James D, Pollock N, Stowell K. Malig nant hyperthermia. Orphanet J Rare Dis 2007;2:21
Takagi A. [Malignant hyperthermia of Duchenne muscular dystrophy: application of clinical grading scale and caffeine contracture of skinned muscle fibers]. Rinsho Shinkeigaku 2000;40:423–7.
Morris P. Duchenne muscular dystrophy: a challenge for the anaesthetist. Paediatr Anaesth 1997;7:1–4.
Gurnaney H, Brown A, Litman RS. Malignant hyperthermia and muscular dystrophies. Anesth Analg. 2009 Oct;109(4):1043-8.
Muenster T, Mueller C, Forst J et al. Anaesthetic management in patients with Duchenne muscular dystrophy undergoing orthopaedic surgery: a review of 232 cases. Eur J Anaesthesiol 2012; 29: 489–494.
Caliskan E, Sener M, Kocum A et al. Duchenne muscular dystrophy: how I do it? Regional or general anesthesia? Pediatr Anesth 2009; 19: 624–625.
Mehta N, Gupta S, Sharma A, Dar MR. Thoracic combined spinal epidural anesthesia for laparoscopic cholecystectomy in a geriatric patient with ischemic heart disease and renal insufficiency. Local Reg Anesth. 2015 Dec 2;8:101-4.
O’Higashi T, Shirakami G, Sasai S, et al. Spinal anesthesia for patients with progressive muscular dystrophy. Jpn J Anesth 1995; 44: 723–728.
Shiraishi MA, Minami K, Kadaya T. Safe anesthetic method using caudal block and ketamine for the child with congenital myotonic dystrophy.
Referanslar
Birnkrant DJ, Panitch HB, Benditt JO, Boitano LJ, Carter ER, Cwik VA, Finder JD, Iannaccone ST, Jacobson LE, Kohn GL, Motoyama EK, Moxley RT, Schroth MK, Sharma GD, Sussman MD.AmericanCollege of Chest Physicians consensus statement on the respiratory and related management of patients with Duchenne muscular dystrophy undergoing anesthesia or sedation. Chest 2007;132:1977–86.
Rodino-Klapac LR, Mendell JR, Sahenk Z. Update on the treatment of Duchenne muscular dystrophy. Curr Neurol Neurosci Rep 2013; 13: 332.
Morris P. Duchenne muscular dystrophy: a challenge for the anaesthetist. Paediatr Anaesth 1997;7(1):1-4.
Büget Mİ, Eren İ, Küçükay S. Regional anaesthesia in a Duchenne muscular dystrophy patient for upper extremity amputation. Agri. 2014;26(4):191-5.
Cripe LH, Tobias JD. Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr Anaesth. 2013 Sep;23(9):777-84.
Thrush PT, Allen HD, Viollet L et al. Re-examination of the electrocardiogram in boys with Duchenne muscular dystrophy and correlation with its dilated cardiomyopathy. Am J Cardiol 2009; 103: 262–265.
Birnkrant DJ. The American College of Chest Physicians consensus statement on the respiratory and related management of patients with Duchenne muscular dystrophy undergoing anesthesia or sedation. Pediatrics 2009; 123(Suppl 4): S242–S244.
Litman RS, Rosenberg H. Malignant hyperthermia: update on susceptibility testing. JAMA 2005;293:2918–24.
Rosenberg H, Davis M, James D, Pollock N, Stowell K. Malig nant hyperthermia. Orphanet J Rare Dis 2007;2:21
Takagi A. [Malignant hyperthermia of Duchenne muscular dystrophy: application of clinical grading scale and caffeine contracture of skinned muscle fibers]. Rinsho Shinkeigaku 2000;40:423–7.
Morris P. Duchenne muscular dystrophy: a challenge for the anaesthetist. Paediatr Anaesth 1997;7:1–4.
Gurnaney H, Brown A, Litman RS. Malignant hyperthermia and muscular dystrophies. Anesth Analg. 2009 Oct;109(4):1043-8.
Muenster T, Mueller C, Forst J et al. Anaesthetic management in patients with Duchenne muscular dystrophy undergoing orthopaedic surgery: a review of 232 cases. Eur J Anaesthesiol 2012; 29: 489–494.
Caliskan E, Sener M, Kocum A et al. Duchenne muscular dystrophy: how I do it? Regional or general anesthesia? Pediatr Anesth 2009; 19: 624–625.
Mehta N, Gupta S, Sharma A, Dar MR. Thoracic combined spinal epidural anesthesia for laparoscopic cholecystectomy in a geriatric patient with ischemic heart disease and renal insufficiency. Local Reg Anesth. 2015 Dec 2;8:101-4.
O’Higashi T, Shirakami G, Sasai S, et al. Spinal anesthesia for patients with progressive muscular dystrophy. Jpn J Anesth 1995; 44: 723–728.
Shiraishi MA, Minami K, Kadaya T. Safe anesthetic method using caudal block and ketamine for the child with congenital myotonic dystrophy.
