Mucopolysaccharidoses (MPSs) are a group of uncommon genetic diseases of connective tissue metabolism. It is well established that the elective treatment of subjects affected by MPS is multidisciplinary and must be carried out by experienced personnel in highly specialist centers. However, there is the possibility to perform an anesthesia in a peripheral center, where anesthesiologists might not have a large experience of MPS. Various attempts to produce guidelines have been made for MPS. There has been an increasing interest in the topic as it is demonstrated by the number of scientific studies published in the last few years (peak in 2011). We want to provide a summary of anesthetic management, reviewing the current literature on the topic in a procedural algorithm for these high-risk patients, who require surgical procedures and diagnostic examinations under sedation with a higher frequency than the general population. 1. Introduction The necessity of codified and univocal guidelines, suitable for all patients, is a common challenge in the field of rare diseases. The first difficulty arises from the lack of cases to study, so as to identify without excessive variety the clinical features of the conditions in study and from the consequent poor literature and the differences between worldwide centers in diagnosis, treatment, and management protocols. Various attempts to produce guidelines of this kind have been made for mucopolysaccharidoses (MPSs). There has been an increasing interest in the topic as it is demonstrated by the number of scientific studies published in the last few years (peak in 2011). It is well established that the elective treatment for subjects affected by MPS is multidisciplinary and must be carried out by experienced personnel in highly specialized centers. However, there is the possibility to perform an anesthesia for these kinds of pediatric patients in a peripheral center, where anesthesiologists might not have a large experience of MPS. Our intent is to review the current literature on this topic in a procedural algorithm of anesthetic management for these high-risk patients, requiring surgical procedures and diagnostic examinations under sedation with a higher frequency than the general population. Particularly, we are focusing on perioperative (pre-, intra-, and post-) anesthetic management. Our final aim is to improve the quality of care offered and, as a consequence, the quality of life of subjects affected by MPS. 2. Mucopolysaccharidoses Mucopolysaccharidoses are uncommon [1] genetic diseases related to the metabolism
References
[1]
U. Linstedt, C. Maier, H. Joehnk, and U. Stephani, “Threatening spinal cord compression during anesthesia in a child with mucopolysaccharidosis VI,” Anesthesiology, vol. 80, no. 1, pp. 227–229, 1994.
[2]
J. H. Diaz and K. G. Belani, “Perioperative management of children with mucopolysaccharidoses,” Anesthesia and Analgesia, vol. 77, no. 6, pp. 1261–1270, 1993.
[3]
J. E. Wraith, “The mucopolysaccharidoses: a clinical review and guide to management,” Archives of Disease in Childhood, vol. 72, no. 3, pp. 263–267, 1995.
[4]
M. S. Muhlebach, W. Wooten, and J. Muenzer, “Respiratory manifestations in mucopolysaccharidoses,” Paediatric Respiratory Reviews, vol. 12, no. 2, pp. 133–138, 2011.
[5]
J. Sam, A. R. Baluch, R. S. Niaz, L. Lonadier, and A. D. Kaye, “Mucopolysaccharidoses: anesthetic considerations and clinical manifestations,” Middle East Journal of Anesthesiology, vol. 21, no. 2, pp. 243–250, 2011.
[6]
A. H. Yeung, M. J. Cowan, B. Horn, and K. W. Rosbe, “Airway management in children with mucopolysaccharidoses,” Archives of Otolaryngology, vol. 135, no. 1, pp. 73–79, 2009.
[7]
V. McKunsick and E. Neufeld, “The mucopolysaccharide storage diseases,” in The Metabolic Basis of Inherited Diseases, J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson, Eds., pp. 342–365, McGraw-Hill Book, New York, NY, USA, 5th edition, 1983.
[8]
V. A. McKusick, “Allelism, non-allelismand genetic compounds among the mucopolysaccharidoses,” Transactions of the Association of American Physicians, vol. 85, pp. 15–25, 1972.
[9]
I. Young and P. S. Harper, “Mild form of Hunter's syndrome: clinical delineation based on 31 cases,” Archives of Disease in Childhood, vol. 57, no. 11, pp. 828–836, 1982.
[10]
J. Muenzer, “The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations,” Journal of Pediatrics, vol. 144, no. 5, pp. S27–S34, 2004.
[11]
S. Rampini, “The Sanfilippo syndrome,” Helvetica Paediatrica Acta, vol. 24, no. 1, pp. 55–91, 1969.
[12]
S. Al Sawaf, E. Mayatepek, and B. Hoffmann, “Neurological findings in Hunter disease: pathology and possible therapeutic effects reviewed,” Journal of Inherited Metabolic Disease, vol. 31, no. 4, pp. 473–480, 2008.
[13]
M. Valstar, G. J. Ruijter, O. P. van Diggelen, and B. J. Poorthuis, “Sanfilippo syndrome: a mini-review,” Journal of Inherited Metabolic Disease, vol. 31, no. 2, pp. 240–252, 2008.
[14]
J. E. Davison, S. Kearney, J. Horton, K. Foster, A. C. Peet, and C. J. Hendriksz, “Intellectual and neurological functioning in Morquio syndrome (MPS IVa),” Journal of Inherited Metabolic Disease, vol. 36, no. 2, pp. 323–328, 2012.
[15]
R. Giugliani, A. Federhen, M. V. Rojas, et al., “Mucopolysaccharidosis I, II, and VI: brief review and guidelines for treatment,” Genetics and Molecular Biology, vol. 33, no. 4, pp. 589–604, 2010.
[16]
J. W. Spranger, F. Koch, V. A. McKusick, J. Natzschka, H. R. Wiedemann, and H. Zellweger, “Mucopolysaccharidosis VI (Maroteaux-Lamy's disease),” Helvetica Paediatrica Acta, vol. 25, no. 4, pp. 337–362, 1970.
[17]
J. Van Biervliet, “Un cas de maladie de Maroteaux-Lamy decouvert precocement,” Archives Francaises de Pediatrie, vol. 34, pp. 364–370, 1977.
[18]
V. Valayannopoulos and F. A. Wijburg, “Therapy for the mucopolysaccharidoses,” Rheumatology, vol. 50, supplement 5, pp. v49–v59, 2011.
[19]
S. Santos, L. López, L. González, and M. J. Domínguez, “Hearing loss and airway problems in children with mucopolysaccharidoses,” Acta Otorrinolaringológica Espa?ola, vol. 62, no. 6, pp. 411–417, 2011.
[20]
L. Bready, S. Noorily, and D. Dillman, Anestesiologia. Processo Decisionale, Elsevier, 2009.
[21]
R. W. M. Walker, M. Darowski, P. Morris, and J. E. Wraith, “Anaesthesia and mucopolysaccharidoses. A review of airway problems in children,” Anaesthesia, vol. 49, no. 12, pp. 1078–1084, 1994.
[22]
A. E. P. Jones and T. F. Croley, “Morquio syndrome and anesthesia,” Anesthesiology, vol. 51, no. 3, pp. 261–262, 1979.
[23]
G. A. Solanki, T. D. Alden, B. K. Burton, et al., “A multinational, multidisciplinary consensus for the diagnosis and management of spinal cord compression among patients with mucopolysaccharidosis VI,” Molecular Genetics and Metabolism, vol. 107, no. 1-2, pp. 15–24, 2012.
[24]
J. Muenzer, M. Beck, C. M. Eng et al., “Multidisciplinary management of Hunter syndrome,” Pediatrics, vol. 124, no. 6, pp. e1228–e1239, 2009.
[25]
P. Silvani, http://www.aimps.it/problemi anestesiologici.htm.
[26]
M. S. Muhlebach, C. B. Shaffer, L. Georges, K. Abode, and J. Muenzer, “Bronchoscopy and airway management in patients 7 with mucopolysaccharidoses (MPS),” Pediatric Pulmonology, vol. 48, pp. 601–607, 2013.
[27]
E. A. Braunlin and P. R. Harmatz, “Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management,” Journal of Inherited Metabolic Disease, vol. 34, no. 6, pp. 1183–1197, 2011.
[28]
P. M. Ingelmo, R. Parini, M. Grimaldi et al., “Multidetector computed tomography (MDCT) for preoperative airway assessment in children with mucopolysaccharidoses,” Minerva Anestesiologica, vol. 77, no. 8, pp. 774–780, 2011.
[29]
L. Kadic and J. J. Driessen, “General anaesthesia in an adult patient with Morquio syndrom with emphasis on airway issues,” Bosnian Journal of Basic Medical Sciences, vol. 12, no. 2, pp. 130–133, 2012.
[30]
G. L. Semenza and R. E. Pyeritz, “Respiratory complications of mucopolysaccharide storage disorders,” Medicine, vol. 67, no. 4, pp. 209–219, 1988.
[31]
C. Moores, J. G. Rogers, I. M. Mckenzie, and T. C. K. Brown, “Anaesthesia for children with mucopolysaccharidoses,” Anaesthesia and Intensive Care, vol. 24, no. 4, pp. 459–463, 1996.
[32]
C. Scriver and A. Baudet, Eds., The Metabolic and Molecular Bases of Inherited Disease, McGraw-Hill, 8 edition, 2001.
[33]
E. D. Bothun, A. Decanini, C. G. Summers, P. J. Orchard, and J. Tolar, “Outcome of penetrating keratoplasty for mucopolysaccharidoses,” Archives of Ophthalmology, vol. 129, no. 2, pp. 138–144, 2011.
[34]
R. J. Gorlin and M. Meyer, Syndromes of the Head and Neck.
[35]
B. Link, L. L. de Camargo Pinto, R. Giugliani, et al., “Orthopedic manifestations in patients with muco—polysaccharidosis type II (Hunter syndrome) enrolled in the Hunter Outcome Survey,” Orthopedic Reviews, vol. 2, no. 2, article e16, 2010.
[36]
J. L. Ashworth, S. Biswas, E. Wraith, and I. C. Lloyd, “Mucopolysaccharidoses and the eye,” Survey of Ophthalmology, vol. 51, no. 1, pp. 1–17, 2006.
[37]
J. Spranger, M. Cantz, and J. Gehler, “Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrum,” European Journal of Pediatrics, vol. 129, no. 1, pp. 11–16, 1978.
[38]
H. Y. Lin, M. R. Chen, C. C. Lin et al., “Polysomnographic characteristics in patients with mucopolysaccharidoses,” Pediatric Pulmonology, vol. 45, no. 12, pp. 1205–1212, 2010.
[39]
R. G. Hulsebos, C. J. Zeebregts, and Z. J. De Langen, “Perforation of a congenital umbilical hernia in a patient with Hurler's syndrome,” Journal of Pediatric Surgery, vol. 39, no. 9, pp. 1426–1427, 2004.
[40]
J. E. Wraith, M. Beck, R. Giugliani, J. Clarke, R. Martin, and J. Muenzer, “Initial report from the Hunter Outcome Survey,” Genetics in Medicine, vol. 10, no. 7, pp. 508–516, 2008.
[41]
J. D. Tobias, “Anesthetic care for the child with Morquio syndrome: general versus regional anesthesia,” Journal of Clinical Anesthesia, vol. 11, no. 3, pp. 242–246, 1999.
[42]
W. A. Osthaus, T. Harendza, L. H. Witt, et al., “Paediatric airway management in mucopolysaccharidosis 1: a retrospective case review,” European Journal of Anaesthesiology, vol. 29, pp. 204–207, 2012.
[43]
M. G. Butler, B. G. Hayes, M. M. Hathaway, and M. L. Begleiter, “Specific genetic diseases at risk for sedation/anesthesia complications,” Anesthesia and Analgesia, vol. 91, no. 4, pp. 837–855, 2000.
[44]
J. L. Ard, A. Bekker, and A. K. Frempong-Boadu, “Anesthesia for an adult with mucopolysaccharidosis I,” Journal of Clinical Anesthesia, vol. 17, no. 8, pp. 624–626, 2005.
[45]
A. Mahoney, N. Soni, and A. Vellodi, “Anaesthesia and the mucopolysaccharidoses: a review of patients treated by bone marrow transplantation,” Pediatric Anesthesia, vol. 2, pp. 317–324, 1992.
[46]
D. R. Hillman, P. R. Platt, and P. R. Eastwood, “The upper airway during anaesthesia,” British Journal of Anaesthesia, vol. 91, no. 1, pp. 31–39, 2003.
[47]
R. W. M. Walker, V. Colovic, D. N. Robinson, and O. R. Dearlove, “Postobstructive pulmonary oedema during anaesthesia in children with mucopolysaccharidoses,” Paediatric Anaesthesia, vol. 13, no. 5, pp. 441–447, 2003.
[48]
R. Giugliani, P. Harmatz, and J. E. Wraith, “Management guidelines for mucopolysaccharidosis VI,” Pediatrics, vol. 120, no. 2, pp. 405–418, 2007.
[49]
M. Scarpa, Z. Almássy, M. Beck, et al., “Mucopolysaccharidosis type II: european recommendations for the diagnosis and multidisciplinary management of a rare disease,” Orphanet Journal of Rare Diseases, vol. 6, article 72, 2011.
[50]
Y. Toda, M. Takeuchi, K. Morita et al., “Complete heart block during anesthetic management in a patient with mucopolysaccharidosis type VII,” Anesthesiology, vol. 95, no. 4, pp. 1035–1037, 2001.
[51]
J. A. Thorne, M. Javadpour, D. G. Hughes, E. Wraith, and R. A. Cowie, “Craniovertebral abnormalities in type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome),” Neurosurgery, vol. 48, no. 4, pp. 849–853, 2001.
[52]
S. L. Thomas, M. H. Childress, and B. Quinton, “Hypoplasia of the odontoid with atlanto-axial subluxation in Hurler's syndrome,” Pediatric Radiology, vol. 15, no. 5, pp. 353–354, 1985.
[53]
G. W?grzyn, J. Jakóbkiewicz-Banecka, M. Narajczyk, et al., “Why are behaviors of children suffering from various neuronopathic types of mucopolysaccharidoses different?” Medical Hypotheses, vol. 75, no. 6, pp. 605–609, 2010.
[54]
T. Aslam, S. Shakir, J. Wong, L. Au, and J. Ashworth, “Use of iris recognition camera technology for the quantification of corneal opacification in mucopolysaccharidoses,” British Journal of Ophthalmology, vol. 96, no. 12, pp. 1466–1468, 2012.
[55]
C. Summers and J. Ashworth, “Ocular manifestations as key features for diagnosing mucopolysaccharidoses,” Rheumatology, vol. 50, no. 5, pp. 34–40, 2011.
[56]
L. A. Clarke and J. Heppner, Mucopolysaccharidosis Type I, GeneReviews, 2002.
[57]
M. Scarpa, Mucopolysaccharidosis Type II, GeneReviews, 2007.
[58]
G. Frawley, D. Fuenzalida, S. Donath, J. Yaplito-Lee, and H. Peters, “A retrospective audit of anesthetic tecniques and complications in children with Mucopolysaccharidoses,” Pediatric Anesthesia, vol. 22, no. 8, pp. 737–744, 2012.
[59]
M. C. Theroux, T. Nerker, C. Ditro, and W. G. Mackenzie, “Anesthetic care and perioperative complications of children with Morquio syndrome,” Pediatric Anesthesia, vol. 22, no. 9, pp. 901–907, 2012.
[60]
A. Dullenkopf, D. Holzmann, R. Feurer, A. Gerber, and M. Weiss, “Tracheal intubation in children with Morquio syndrome using the angulated video-intubation laryngoscope,” Canadian Journal of Anesthesia, vol. 49, no. 2, pp. 198–202, 2002.
[61]
J. Brimacombe and A. Brain, The Laryngeal Mask Airway, Saunders, London, UK, 1st edition, 1997.
[62]
P. Busoni and G. Fognani, “Failure of the laryngeal mask to secure the airway in a patient with Hunter's syndrome (mucopolysaccharidosis type II),” Paediatric Anaesthesia, vol. 9, no. 2, pp. 153–155, 1999.
[63]
P. Michalek, P. Hodgkinson, and W. Donaldson, “Fiberoptic intubation through an I-Gel supraglottic airway in two patients with predicted difficult airway and intellectual disability,” Anesthesia and Analgesia, vol. 106, no. 5, pp. 1501–1504, 2008.
[64]
S. H. Suh, R. Okutani, M. Nakasuji, and K. Nakata, “Anesthesia in a patient with mucopolysaccharidosis type VI, (Maroteaux-Lamy syndrome),” Journal of Anesthesia, vol. 24, no. 6, pp. 945–948, 2010.
[65]
A. Yoskovitch, T. L. Tewfik, R. T. Brouillette, M. D. Schloss, and V. M. Der Kaloustian, “Acute airway obstruction in Hunter syndrome,” International Journal of Pediatric Otorhinolaryngology, vol. 44, no. 3, pp. 273–278, 1998.
[66]
M. Ingrosso, M. M. Picilli, A. Capasso, F. Cecere, V. Cirillo, and V. Merolla, “Anaestethic problems in Sanfilippo syndrome: a rare case of adult patient,” Minerva Anestesiologica, vol. 69, no. 7-8, pp. 641–645, 2003.
[67]
S. C. Nicolson, A. E. Black, and C. M. Kraras, “Management of a difficult airway in a patient with Hurler-Scheie syndrome during cardiac surgery,” Anesthesia and Analgesia, vol. 75, no. 5, pp. 830–832, 1992.
[68]
P. Sjogren, T. Pedersen, and H. Steinmetz, “Mucopolysaccharidoses and anaesthetic risks,” Acta Anaesthesiologica Scandinavica, vol. 31, no. 3, pp. 214–218, 1987.
[69]
M. A. Henderson, “Use of a laryngeal mask airway in an adult patient with the Hunter syndrome,” European Journal of Anaesthesiology, vol. 12, no. 6, pp. 613–616, 1995.
[70]
R. W. M. Walker, D. L. Allen, and M. R. Rothera, “A fibreoptic intubation technique for children with mucopolysaccharidoses using the laryngeal mask airway,” Paediatric Anaesthesia, vol. 7, no. 5, pp. 421–426, 1997.
[71]
R. Hopkins, J. A. Watson, J. H. Jones, and M. Walker, “Two cases of Hunter's syndrome. The anaesthetic and operative difficulties in oral surgery,” British Journal of Oral Surgery, vol. 10, no. 3, pp. 286–299, 1973.
[72]
J. Bredenkamp, M. Smith, and J. Dudley, “Otolaryngologic manifestations of mucopolysaccharidoses,” Annals of Otology, Rhinology, and Laryngology, vol. 101, no. 6, pp. 472–478, 1992.
[73]
M. J. Ruckenstein, R. E. MacDonald, J. T. R. Clarke, and V. Forte, “The management of otolaryngological problems in the mucopolysaccharidoses: a retrospective review,” Journal of Otolaryngology, vol. 20, no. 3, pp. 177–183, 1991.
[74]
A. H. Grosz, I. N. Jacobs, C. Cho, and G. J. Schears, “Use of helium-oxygen mixtures to relieve upper airway obstruction in a pediatric population,” Laryngoscope, vol. 111, no. 9, pp. 1512–1514, 2001.
[75]
D. R. Hillman, P. R. Platt, and P. R. Eastwood, “The upper airway during anaesthesia,” British Journal of Anaesthesia, vol. 91, no. 1, pp. 31–39, 2003.
[76]
G. Hoffmann and W. Nyhan, Inherited Metabolic Disease: A Clinical Approach.
[77]
I. M. Hayes, V. Collins, M. Sahhar, J. E. Wraith, and M. B. Delatycki, “Newborn screening for mucopolysaccharidoses: opinions of patients and their families,” Clinical Genetics, vol. 71, no. 5, pp. 446–450, 2007.