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Volumn 17, Issue 8, 2007, Pages 738-748

Cardiac arrhythmias following anesthesia induction in infantile-onset Pompe disease: A case series

Author keywords

Anesthesia; Arrhythmia; Cardiomyopathy; GSD II; Pompe disease; rhGAA enzyme replacement therapy

Indexed keywords

ADRENALIN; ALIMEMAZINE TARTRATE; AMBROXOL; AMIODARONE; ANTIANEMIC AGENT; ATROPINE; BICARBONATE; CALCIUM; DOPAMINE; ETOMIDATE; FENTANYL; FEREDETATE SODIUM; GLUCAN 1,4 ALPHA GLUCOSIDASE; KETAMINE; LIDOCAINE; MAGNESIUM; MESNA; MIDAZOLAM; MORPHINE SULFATE; PHENYLEPHRINE; PROPOFOL; RECOMBINANT GLUCAN 1,4 ALPHA GLUCOSIDASE; ROCURONIUM; SEVOFLURANE; SUXAMETHONIUM; THIOPENTAL; TRICLOFOS; UNCLASSIFIED DRUG; UNINDEXED DRUG; VASODILATOR AGENT; VASOPRESSIN; VECURONIUM; VERAPAMIL;

EID: 34347209936     PISSN: 11555645     EISSN: 14609592     Source Type: Journal    
DOI: 10.1111/j.1460-9592.2007.02215.x     Document Type: Article
Times cited : (54)

References (32)
  • 1
    • 2342537868 scopus 로고    scopus 로고
    • Pompe disease in infants and children
    • Kishnani PS, Howell RR. Pompe disease in infants and children. J Pediatr 2004 144 : S35 S43.
    • (2004) J Pediatr , vol.144
    • Kishnani, P.S.1    Howell, R.R.2
  • 2
    • 0000995321 scopus 로고    scopus 로고
    • Glycogen storage disease type II: Acid alpha-glucosidase (acid maltase) deficiency
    • In: Scriver, C.R., Beaudet, A.L., Sly, W.S.*et al., eds. 8th edn. New York: McGraw-Hill
    • Hirschhorn R, Reuser AJ. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency. In : Scriver CR, Beaudet AL, Sly WS et al., eds. The Metabolic and Molecular Bases of Inherited Disease. 8th edn. New York : McGraw-Hill, 2001 : 3389 3420.
    • (2001) The Metabolic and Molecular Bases of Inherited Disease. , pp. 3389-3420
    • Hirschhorn, R.1    Reuser, A.J.2
  • 3
    • 0042131675 scopus 로고    scopus 로고
    • The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature
    • van den Hout HM, Hop W, van Diggelen OP et al. The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature. Pediatrics 2003 112 : 332 340.
    • (2003) Pediatrics , vol.112 , pp. 332-340
    • Van Den Hout, H.M.1    Hop, W.2    Van Diggelen, O.P.3
  • 4
    • 33646830132 scopus 로고    scopus 로고
    • A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease
    • Kishnani P, Hwu W-L, Mandel H et al. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J Pediatr 2006 148 : 671 676.
    • (2006) J Pediatr , vol.148 , pp. 671-676
    • Kishnani, P.1    Hwu, W.-L.2    Mandel, H.3
  • 5
    • 0032848015 scopus 로고    scopus 로고
    • Frequency of glycogen storage disease type II in the Netherlands: Implications for diagnosis and genetic counselling
    • Ausems MG, Verbiest J, Hermans MP et al. Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling. Eur J Hum Genet 1999 7 : 713 716.
    • (1999) Eur J Hum Genet , vol.7 , pp. 713-716
    • Ausems, M.G.1    Verbiest, J.2    Hermans, M.P.3
  • 6
    • 0031695078 scopus 로고    scopus 로고
    • Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease
    • Martiniuk F, Chen A, Mack A et al. Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease. Am J Med Genet 1998 79 : 69 72.
    • (1998) Am J Med Genet , vol.79 , pp. 69-72
    • Martiniuk, F.1    Chen, A.2    MacK, A.3
  • 7
    • 0033496795 scopus 로고    scopus 로고
    • Glycogen storage disease type II: Birth prevalence agrees with predicted genotype frequency
    • Ausems MG, ten Berg K, Kroos MA et al. Glycogen storage disease type II: birth prevalence agrees with predicted genotype frequency. Community Genet 1999 2 : 91 96.
    • (1999) Community Genet , vol.2 , pp. 91-96
    • Ausems, M.G.1    Ten Berg, K.2    Kroos, M.A.3
  • 8
    • 0032780351 scopus 로고    scopus 로고
    • The frequency of lysosomal storage diseases in the Netherlands
    • Poorthuis BJ, Wevers RA, Kleijer WJ et al. The frequency of lysosomal storage diseases in The Netherlands. Hum Genet 1999 105 : 151 156.
    • (1999) Hum Genet , vol.105 , pp. 151-156
    • Poorthuis, B.J.1    Wevers, R.A.2    Kleijer, W.J.3
  • 9
    • 0023151721 scopus 로고
    • Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity
    • Lin CY, Hwang B, Hsiao KJ, Jin YR. Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity. J Inherit Metab Dis 1987 10 : 11 17.
    • (1987) J Inherit Metab Dis , vol.10 , pp. 11-17
    • Lin, C.Y.1    Hwang, B.2    Hsiao, K.J.3    Jin, Y.R.4
  • 10
    • 0035746540 scopus 로고    scopus 로고
    • Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial
    • Amalfitano A, Bengur AR, Morse RP et al. Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial. Genet Med 2001 3 : 132 138.
    • (2001) Genet Med , vol.3 , pp. 132-138
    • Amalfitano, A.1    Bengur, A.R.2    Morse, R.P.3
  • 11
    • 33746151202 scopus 로고    scopus 로고
    • Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease
    • Kishnani PS, Nicolino M, Voit T et al. Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease. J Pediatr 2006 149 : 89 97.
    • (2006) J Pediatr , vol.149 , pp. 89-97
    • Kishnani, P.S.1    Nicolino, M.2    Voit, T.3
  • 12
    • 15044345490 scopus 로고    scopus 로고
    • Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: Results of a phase II clinical trial
    • Klinge L, Straub V, Neudorf U et al. Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial. Neuromuscul Disord 2005 15 : 24 31.
    • (2005) Neuromuscul Disord , vol.15 , pp. 24-31
    • Klinge, L.1    Straub, V.2    Neudorf, U.3
  • 13
    • 0034729963 scopus 로고    scopus 로고
    • Recombinant human alpha-glucosidase from rabbit milk in Pompe patients
    • van den Hout H, Reuser AJ, Vulto AG et al. Recombinant human alpha-glucosidase from rabbit milk in Pompe patients. Lancet 2000 356 : 397 398.
    • (2000) Lancet , vol.356 , pp. 397-398
    • Van Den Hout, H.1    Reuser, A.J.2    Vulto, A.G.3
  • 14
    • 2942570942 scopus 로고    scopus 로고
    • Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk
    • van den Hout JM, Kamphoven JH, Winkel LP et al. Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk. Pediatrics 2004 113 : e448 e457.
    • (2004) Pediatrics , vol.113
    • Van Den Hout, J.M.1    Kamphoven, J.H.2    Winkel, L.P.3
  • 15
    • 0035009304 scopus 로고    scopus 로고
    • Enzyme therapy for Pompe disease with recombinant human alpha-glucosidase from rabbit milk
    • van den Hout JM, Reuser AJ, de Klerk JB et al. Enzyme therapy for Pompe disease with recombinant human alpha-glucosidase from rabbit milk. J Inherit Metab Dis 2001 24 : 266 274.
    • (2001) J Inherit Metab Dis , vol.24 , pp. 266-274
    • Van Den Hout, J.M.1    Reuser, A.J.2    De Klerk, J.B.3
  • 16
    • 0038546958 scopus 로고    scopus 로고
    • Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy
    • Winkel LP, Kamphoven JH, van den Hout HJ et al. Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy. Muscle Nerve 2003 27 : 743 751.
    • (2003) Muscle Nerve , vol.27 , pp. 743-751
    • Winkel, L.P.1    Kamphoven, J.H.2    Van Den Hout, H.J.3
  • 17
    • 2942548954 scopus 로고    scopus 로고
    • Anaesthetic management of infants with glycogen storage disease type II: A physiological approach
    • Ing RJ, Cook DR, Bengur RA et al. Anaesthetic management of infants with glycogen storage disease type II: a physiological approach. Pediatr Anesth 2004 14 : 514 519.
    • (2004) Pediatr Anesth , vol.14 , pp. 514-519
    • Ing, R.J.1    Cook, D.R.2    Bengur, R.A.3
  • 18
  • 19
    • 33745584427 scopus 로고    scopus 로고
    • Ambulatory electrocardiogram analysis in infants treated with recombinant human acid alpha glucosidase enzyme replacement therapy for Pompe disease
    • Cook AL, Kishnani PS, Carboni MP et al. Ambulatory electrocardiogram analysis in infants treated with recombinant human acid alpha glucosidase enzyme replacement therapy for Pompe disease. Genet Med 2006 8 : 313 317.
    • (2006) Genet Med , vol.8 , pp. 313-317
    • Cook, A.L.1    Kishnani, P.S.2    Carboni, M.P.3
  • 20
    • 33745634913 scopus 로고    scopus 로고
    • Electrocardiographic response to enzyme replacement therapy for Pompe disease
    • Ansong AK, Li JS, Nozik-Grayck E et al. Electrocardiographic response to enzyme replacement therapy for Pompe disease. Genet Med 2006 8 : 297 301.
    • (2006) Genet Med , vol.8 , pp. 297-301
    • Ansong, A.K.1    Li, J.S.2    Nozik-Grayck, E.3
  • 21
    • 0026525414 scopus 로고
    • Comparison of propofol vs ketamine for anesthesia in pediatric patients undergoing cardiac catheterization
    • Lebovic S, Reich DL, Steinberg LG et al. Comparison of propofol vs ketamine for anesthesia in pediatric patients undergoing cardiac catheterization. Anesth Analg 1992 74 : 490 494.
    • (1992) Anesth Analg , vol.74 , pp. 490-494
    • Lebovic, S.1    Reich, D.L.2    Steinberg, L.G.3
  • 22
    • 0347716456 scopus 로고    scopus 로고
    • Which anesthetic agent alters the hemodynamic status during pediatric catheterization? Comparison of propofol vs ketamine
    • Oklu E, Bulutcu FS, Yalcin Y et al. Which anesthetic agent alters the hemodynamic status during pediatric catheterization? Comparison of propofol vs ketamine. J Cardiothorac Vasc Anesth 2003 17 : 686 690.
    • (2003) J Cardiothorac Vasc Anesth , vol.17 , pp. 686-690
    • Oklu, E.1    Bulutcu, F.S.2    Yalcin, Y.3
  • 23
    • 0022980630 scopus 로고
    • Pompe's disease and anaesthesia
    • McFarlane HJ, Soni N. Pompe's disease and anaesthesia. Anaesthesia 1986 41 : 1219 1224.
    • (1986) Anaesthesia , vol.41 , pp. 1219-1224
    • McFarlane, H.J.1    Soni, N.2
  • 24
    • 33745605564 scopus 로고    scopus 로고
    • A comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease
    • Zhang H, Kallwass H, Young SP et al. A comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid alpha-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease. Genet Med 2006 8 : 302 306.
    • (2006) Genet Med , vol.8 , pp. 302-306
    • Zhang, H.1    Kallwass, H.2    Young, S.P.3
  • 25
    • 4143095952 scopus 로고    scopus 로고
    • Glycogen storage disease type II: Enzymatic screening in dried blood spots on filter paper
    • Chamoles NA, Niizawa G, Blanco M et al. Glycogen storage disease type II: enzymatic screening in dried blood spots on filter paper. Clin Chim Acta 2004 347 : 97 102.
    • (2004) Clin Chim Acta , vol.347 , pp. 97-102
    • Chamoles, N.A.1    Niizawa, G.2    Blanco, M.3
  • 26
    • 4644273798 scopus 로고    scopus 로고
    • Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening
    • Li Y, Scott CR, Chamoles NA et al. Direct multiplex assay of lysosomal enzymes in dried blood spots for newborn screening. Clin Chem 2004 50 : 1785 1796.
    • (2004) Clin Chem , vol.50 , pp. 1785-1796
    • Li, Y.1    Scott, C.R.2    Chamoles, N.A.3
  • 27
    • 0034911699 scopus 로고    scopus 로고
    • Determination of acid alpha-glucosidase activity in blood spots as a diagnostic test for Pompe disease
    • Umapathysivam K, Hopwood JJ, Meikle PJ. Determination of acid alpha-glucosidase activity in blood spots as a diagnostic test for Pompe disease. Clin Chem 2001 47 : 1378 1383.
    • (2001) Clin Chem , vol.47 , pp. 1378-1383
    • Umapathysivam, K.1    Hopwood, J.J.2    Meikle, P.J.3
  • 28
    • 0021815441 scopus 로고
    • Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-alpha-glucosidase in human fetal and adult tissues and cultured cells
    • Shin YS, Endres W, Unterreithmeier J et al. Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-alpha-glucosidase in human fetal and adult tissues and cultured cells. Clin Chim Acta 1985 148 : 9 19.
    • (1985) Clin Chim Acta , vol.148 , pp. 9-19
    • Shin, Y.S.1    Endres, W.2    Unterreithmeier, J.3
  • 29
    • 0018222503 scopus 로고
    • Alpha glucosidases in white blood cells, with reference to the detection of acid alpha 1-4 glucosidase deficiency
    • Dreyfus JC, Poenaru L. Alpha glucosidases in white blood cells, with reference to the detection of acid alpha 1-4 glucosidase deficiency. Biochem Biophys Res Commun 1978 85 : 615 622.
    • (1978) Biochem Biophys Res Commun , vol.85 , pp. 615-622
    • Dreyfus, J.C.1    Poenaru, L.2
  • 30
    • 33745585382 scopus 로고    scopus 로고
    • The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease
    • Jack RM, Gordon C, Scott CR et al. The use of acarbose inhibition in the measurement of acid alpha-glucosidase activity in blood lymphocytes for the diagnosis of Pompe disease. Genet Med 2006 8 : 307 312.
    • (2006) Genet Med , vol.8 , pp. 307-312
    • Jack, R.M.1    Gordon, C.2    Scott, C.R.3
  • 31
    • 0023005703 scopus 로고
    • Anaesthesia for diagnostic muscle biopsy in an infant with Pompe's disease
    • Rosen KR, Broadman LM. Anaesthesia for diagnostic muscle biopsy in an infant with Pompe's disease. Can Anaesth Soc J 1986 33 : 790 794.
    • (1986) Can Anaesth Soc J , vol.33 , pp. 790-794
    • Rosen, K.R.1    Broadman, L.M.2
  • 32
    • 33745589302 scopus 로고    scopus 로고
    • Pompe disease diagnosis and management guidelines
    • Kishnani PS, Steiner RD, Bali D et al. Pompe disease diagnosis and management guidelines. Genet Med 2006 8 : 267 288.
    • (2006) Genet Med , vol.8 , pp. 267-288
    • Kishnani, P.S.1    Steiner, R.D.2    Bali, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.