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1.
J Spinal Cord Med ; 33(4): 410-9, 2010.
Article in English | MEDLINE | ID: mdl-21061901

ABSTRACT

OBJECTIVE: To evaluate the appropriate use of arm span measurements as a substitute for height/linear length to evaluate obesity in people with myelomeningocele by comparing calculated body mass indices (BMIs) with recently published BMI graphs by the Centers for Disease Control and Prevention (CDC) and National Center for Health Statistics standards (NCHS) published in 2000. STUDY DESIGN: Retrospective analysis of collected data on patients seen in the University of Washington Birth Defects Clinic from July 1, 1965, through June 1, 2008. Observations included degree of paralysis, presence of scoliosis, height (linear length), weight, and arm span. We compared published CDC/NCHS BMIs with our data using both height and arm span in place of height/linear length. There were 14,701 measures collected during 4968 visits from 709 patients. Mean values were calculated using age, gender, and lesion level as independent variables. RESULTS: Comparison of BMI means of patients with myelomeningocele suggests that our observations using arm span and height are comparable with the CDC/NCHS BMI means using height for the 2 least paralyzed groups but not for those groups with paralysis from high-level lesions that are more likely to exhibit lower extremity deformities or scoliosis. CONCLUSIONS: Published CDC/NCHS graphs, with their percentiles, are appropriate for estimating normal growth by BMI for children born with myelomeningocele when arm span is substituted for length if severe body differences due to high-level paralysis are taken into consideration.


Subject(s)
Anthropometry , Child Development/physiology , Meningomyelocele/epidemiology , Meningomyelocele/pathology , Obesity/epidemiology , Obesity/pathology , Adolescent , Age Factors , Body Mass Index , Body Weight , Centers for Disease Control and Prevention, U.S. , Child , Child, Preschool , Female , Humans , Longitudinal Studies , Male , National Center for Health Statistics, U.S. , Retrospective Studies , Sex Factors , United States , Young Adult
2.
Spine (Phila Pa 1976) ; 35(13): 1294-9, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20354477

ABSTRACT

STUDY DESIGN: This is a retrospective review of all children with myelomeningocele (MMC) who were undergoing surgery for scoliosis at our institution. OBJECTIVE: Our aim was to investigate possible correlations between poor nutritional indexes and/or positive urinary cultures before surgery to perioperative infection risk. SUMMARY OF BACKGROUND DATA: Patients who have scoliosis secondary to MMC have been shown to have a high rate of infectious complications. Many children with MMC have been found to have asymptomatic urinary tact infections due to their neurogenic bladder. There is little literature on risk factors for and ways to prevent postoperative infections for these patients. METHODS: We reviewed a comprehensive database for the outcome for spinal fusion surgeries of 59 patients with MMC treated at our institution over the past 45 years. Perioperative infections were correlated to preoperative nutritional status (measured by patient hematocrit [Hct]) and presence of active infection using Fisher Exact Probability Test. RESULTS: A total of 84 different spinal fusion operations for 59 patients were recorded. Patients presenting with poor preoperative nutrition (Hct

Subject(s)
Meningomyelocele/complications , Postoperative Complications/etiology , Scoliosis/surgery , Spinal Fusion/adverse effects , Bacterial Infections/complications , Bacterial Infections/urine , Child , Humans , Malnutrition/complications , Nutritional Status , Preoperative Period , Retrospective Studies , Risk Assessment/methods , Risk Factors , Scoliosis/complications , Spinal Fusion/methods
3.
Dev Med Child Neurol ; 48(4): 253-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16542511

ABSTRACT

This study describes ages of acquisition (AOA) of typical adolescent autonomy skills in a regional cohort of individuals with myelomeningocele (MM), aged 12 to 18 years, with a mean age of 14 years 11 months (SD 2y 5mo). Prospectively collected data over 10 years were analyzed. Regression analysis, using Generalized Estimation Equation, provided 50th centile and 75th centile AOA for each skill. One hundred and fifty-eight participants (90 males, 68 females) attended 378 annual patient visits. Patient contacts were equally distributed across age and physical severity groupings. Twenty-four percent of participants had functional lesion levels at or above L2, and 38% between L3-L5, 38% at S1 or below. Eighty-four percent had shunted hydrocephalus, 24% were independent in ambulation, and 69% achieved toileting independence before adolescence. AOA for autonomy skills were delayed by 25 to 30% when compared with typically developing adolescents. Differences in cognitive ability explained the variance in median ages for skill acquisition (p=0.01) more than physical lesion level. Participants acquired community skills at a median age of 16 years 6 months. Twelve percent of 18-year-olds drove cars (9% with supervision, 3% independently), regardless of physical lesion severity. We conclude that adolescents with MM acquire the majority of autonomy skills 2 to 5 years later than their typically developing peers. This study establishes AOA timelines for autonomy skills in adolescents with MM.


Subject(s)
Learning , Meningomyelocele/complications , Meningomyelocele/physiopathology , Motor Skills Disorders/etiology , Motor Skills Disorders/physiopathology , Personal Autonomy , Adolescent , Cohort Studies , Demography , Disability Evaluation , Female , Humans , Male , Motor Skills Disorders/diagnosis , Prospective Studies
4.
Pediatr Neurosurg ; 41(4): 186-91, 2005.
Article in English | MEDLINE | ID: mdl-16088253

ABSTRACT

The objectives of this study were to extend survival analysis into adulthood for patients with myelomeningocele (MM) and to compare survival curves for patients born with varying defect severity before and after 1975. We have reviewed existing data for 904 patients with MM seen in a large multidisciplinary children's clinic over 43 years. Before 1975, a major contributor to decreased survival is death during infancy. The presence of cerebral spinal fluid shunting is a major contributor to increased survival. After 1975, survival to adolescence is similar regardless of shunt status (p = 0.17). For all patients alive at age 16, a significant decrease in survival probability after age 34 years was found for individuals with shunted hydrocephalus compared to those without a shunt (p = 0.03). Although childhood survival for individuals born after 1975 is not related to shunt status, adults with MM and shunted hydrocephalus may be at risk for decreased longevity.


Subject(s)
Meningomyelocele/mortality , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Cerebrospinal Fluid Shunts , Child , Child, Preschool , Cohort Studies , Female , Humans , Hydrocephalus/etiology , Hydrocephalus/mortality , Hydrocephalus/therapy , Infant , Male , Meningomyelocele/complications , Meningomyelocele/therapy , Middle Aged , Retrospective Studies , Severity of Illness Index , Survival Analysis , Survival Rate
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