Regional anesthetic techniques are an alternative to general anesthesia for infants with Pompe's disease
Summary Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these p...
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Published in | Pediatric anesthesia Vol. 17; no. 7; pp. 697 - 702 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.07.2007
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Abstract | Summary
Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established. |
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AbstractList | Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established. Summary Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established. Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established.Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross hypertrophic cardiomegaly and death in the early years. General anesthesia is associated with potential major morbidity in these patients. We present our experience of regional anesthetic blocks used in five patients with the infantile form of glycogen storage disease type II with and without sedation for 11 surgical procedures during a clinical trial of replacement therapy for this condition. Both femoral nerve blockade and caudal epidural blockade were used with good result. The relative merits of the type of block are discussed in addition to the choice of sedation and risks of general anesthesia. The avoidance of general anesthesia in the newly presenting patient with Pompe's disease may reduce potential morbidity until enzyme replacement has been established. |
Author | BRUCE, JAMES WALKER, ROBERT W.M. BRIGGS, GERAINT WRAITH, E.D. FLETCHER, JOAN |
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References | 1980; 7 1932; 76 2001; 3 1986; 41 1999; 7 2000; 356 1980; 52 1986; 33 2003; 53 2004; 14 e_1_2_4_12_2 Kishnani P (e_1_2_4_6_2) 2003; 53 e_1_2_4_4_2 e_1_2_4_3_2 e_1_2_4_5_2 Kaplan R (e_1_2_4_10_2) 1980; 7 e_1_2_4_8_2 Genzyme Corporation (e_1_2_4_11_2) e_1_2_4_7_2 Pompe JC (e_1_2_4_2_2) 1932; 76 e_1_2_4_9_2 |
References_xml | – volume: 53 start-page: 259A year: 2003 article-title: Enzyme replacement therapy with human recombinant acid alpha glucosidase (rhGAA) in infantile Pompe disease: results from a phase II clinical study publication-title: Pediatr Res – volume: 7 start-page: 713 year: 1999 end-page: 716 article-title: Frequency of glycogen storage disease type II in the Netherlands: implications for genetic counselling publication-title: Eur J Hum Genet – volume: 52 start-page: 153 year: 1980 end-page: 164 article-title: Inherited muscle disease publication-title: Br J Anaesth – volume: 41 start-page: 1219 year: 1986 end-page: 1224 article-title: Pompe's disease and anaesthesia publication-title: Anaesthesia – volume: 14 start-page: 514 year: 2004 end-page: 519 article-title: Anesthetic management of infant with glycogen storage disease type II: a physiological approach publication-title: Pediatr Anesth – volume: 3 start-page: 132 year: 2001 end-page: 138 article-title: Recombinant human acid glucosidase enzyme therapy for infantile glycogen storage disease type II: results of phase I/II clinical trial publication-title: Genet Med – volume: 76 start-page: 304 year: 1932 end-page: 311 article-title: Over idiopathische hypertrophie von het hart publication-title: Ned Tijdschr Geneeskd – volume: 7 start-page: 21 year: 1980 end-page: 28 article-title: Pompe's disease presenting for anesthesia. Two case reports publication-title: Anesthesiol Rev – volume: 356 start-page: 397 year: 2000 end-page: 398 article-title: Recombinant human glucosidase from rabbit milk in Pompe patients publication-title: Lancet – volume: 33 start-page: 790 year: 1986 end-page: 794 article-title: Anaesthesia for diagnostic muscle biopsy in an infant with Pompe's disease publication-title: Can Anaesth Soc J – volume: 7 start-page: 21 year: 1980 ident: e_1_2_4_10_2 article-title: Pompe's disease presenting for anesthesia. Two case reports publication-title: Anesthesiol Rev – ident: e_1_2_4_3_2 doi: 10.1038/sj.ejhg.5200367 – ident: e_1_2_4_4_2 doi: 10.1097/00125817-200103000-00008 – ident: e_1_2_4_9_2 doi: 10.1093/bja/52.2.153 – ident: e_1_2_4_7_2 doi: 10.1111/j.1460-9592.2004.01242.x – volume: 53 start-page: 259A year: 2003 ident: e_1_2_4_6_2 article-title: Enzyme replacement therapy with human recombinant acid alpha glucosidase (rhGAA) in infantile Pompe disease: results from a phase II clinical study publication-title: Pediatr Res – ident: e_1_2_4_8_2 doi: 10.1111/j.1365-2044.1986.tb13007.x – ident: e_1_2_4_12_2 doi: 10.1007/BF03027132 – ident: e_1_2_4_5_2 doi: 10.1016/S0140-6736(00)02533-2 – volume: 76 start-page: 304 year: 1932 ident: e_1_2_4_2_2 article-title: Over idiopathische hypertrophie von het hart publication-title: Ned Tijdschr Geneeskd – volume-title: Investigators Brochure for Myozyme ident: e_1_2_4_11_2 |
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Snippet | Summary
Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with... Pompe's disease or glycogen storage disease type II is a genetic disorder affecting skeletal and cardiac muscle. The infantile form is associated with gross... |
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SubjectTerms | Anesthesia, Conduction Anesthesia, General Anesthetics, Combined Biopsy Catheters, Indwelling caudal epidural block Child, Preschool Conscious Sedation Female Femoral Nerve femoral nerve block Glycogen - metabolism glycogen storage disease type II Glycogen Storage Disease Type II - diagnosis Glycogen Storage Disease Type II - pathology Humans hypertrophic cardiomyopathy Infant Lidocaine Male Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Nerve Block Pompe's disease Prilocaine regional anesthesia Treatment Outcome |
Title | Regional anesthetic techniques are an alternative to general anesthesia for infants with Pompe's disease |
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