Characterization of Surgical Procedures in Patients with Mucopolysaccharidosis Type I: Findings from the MPS I Registry

被引:34
作者
Arn, Pamela [1 ]
Wraith, J. Edmond [2 ]
Underhill, Lisa [3 ]
机构
[1] Nemours Childrens Clin, Dept Pediat, Jacksonville, FL 32207 USA
[2] Royal Manchester Childrens Hosp, Willink Biochem Genet Unit, Manchester M27 1HA, Lancs, England
[3] Genzyme Corp, Global Med Affairs, Cambridge, MA USA
关键词
ENZYME REPLACEMENT THERAPY; L-IDURONIDASE LARONIDASE; CELL TRANSPLANTATION; CHILDREN; EXPERIENCE; ANESTHESIA; OUTCOMES;
D O I
10.1016/j.jpeds.2008.12.024
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To clarify the extent mid chronology of surgical burden in relation to symptom onset and diagnosis in patients with mucopolysaccharidosis I (MPS I) as reported in the MPS I Registry, an international observational database. Study design Analysis of surgical data from 544 patients enrolled in the MPS I Registry. Among all patients with at least I reported surgery, the number and frequency of procedures, and age at procedure, diagnosis, and symptom onset were collected overall, by patient, and by reported phenotype (Hurler, Hurler-Scheie, Scheie). Results Overall and by phenotype, similar to 75% of patients in the MPS I Registry reported at least I surgery. The most common were myringotomies and related procedures, hernia repair, adenoidectomy/tonsillectomy, and carpal-tunnel release. Median age at first surgery was <5 years. A median of 3 to 4 surgeries was reported per patient. By age 1.5, 4, and 10 years, respectively, 22%, 44%, and 54% of patients reported >= 2 surgeries. At least I surgery preceded diagnosis in 36%, 46%, and 63% of patients with Hurler, Hurler-Scheie, and Scheie, respectively. Conclusions Pediatricians and pediatric surgeons need to be aware of the surgical burden of MPS I and be alert to its presenting signs and symptoms in children scheduled for surgery. (J Pediatr 2009;154:859-64)
引用
收藏
页码:859 / 864
页数:6
相关论文
共 17 条
[1]   ANESTHETIC IMPLICATIONS OF THE MUCOPOLYSACCHARIDOSES - A 15-YEAR EXPERIENCE IN A CHILDRENS HOSPITAL [J].
BAINES, D ;
KENEALLY, J .
ANAESTHESIA AND INTENSIVE CARE, 1983, 11 (03) :198-202
[2]   Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure [J].
Boelens, J. J. ;
Wynn, R. F. ;
O'Meara, A. ;
Veys, P. ;
Bertrand, Y. ;
Souillet, G. ;
Wraith, J. E. ;
Fischer, A. ;
Cavazzana-Calvo, M. ;
Sykora, K. W. ;
Sedlacek, P. ;
Rovelli, A. ;
Uiterwaal, C. S. P. M. ;
Wulffraat, N. .
BONE MARROW TRANSPLANTATION, 2007, 40 (03) :225-233
[3]   Airway management in infants and children [J].
Brambrink, Ansgar M. ;
Braun, Ulrich .
BEST PRACTICE & RESEARCH-CLINICAL ANAESTHESIOLOGY, 2005, 19 (04) :675-697
[4]   Carpal tunnel syndrome in children [J].
Lamberti, PM ;
Light, TR .
HAND CLINICS, 2002, 18 (02) :331-+
[5]   Anaesthesia for children with mucopolysaccharidoses [J].
Moores, C ;
Rogers, JG ;
McKenzie, IM ;
Brown, TCK .
ANAESTHESIA AND INTENSIVE CARE, 1996, 24 (04) :459-463
[6]  
Neufeld EF., 2001, The Metabolic and Molecular Bases of Inherited Disease, P3421, DOI DOI 10.1036/OMMBID.165
[7]   The MPS I registry: Design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I [J].
Pastores, Gregory M. ;
Arn, Pamela ;
Beck, Michael ;
Clarke, Joe T. R. ;
Guffon, Nathalie ;
Kaplan, Paige ;
Muenzer, Joseph ;
Norato, Denise Y. J. ;
Shapiro, Elsa ;
Thomas, Janet ;
Viskochil, David ;
Wraith, J. Edmond .
MOLECULAR GENETICS AND METABOLISM, 2007, 91 (01) :37-47
[8]   Hematopoietic cell transplantation for inherited metabolic diseases: an overview of outcomes and practice guidelines [J].
Peters, C ;
Steward, CG .
BONE MARROW TRANSPLANTATION, 2003, 31 (04) :229-239
[9]   Inguinal hernia repair: Incidence of elective and emergency surgery, readmission and mortality [J].
Primatesta, P ;
Goldacre, MJ .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1996, 25 (04) :835-839
[10]  
RUSSO CA, 2007, AHRQ PUBL