Treated hydrocephalus in individuals with myelomeningocele in the National Spina Bifida Patient Registry

Author:

Kim Irene1,Hopson Betsy2,Aban Inmaculada3,Rizk Elias B.4,Dias Mark S.4,Bowman Robin5,Ackerman Laurie L.6,Partington Michael D.7,Castillo Heidi8,Castillo Jonathan8,Peterson Paula R.9,Blount Jeffrey P.2,Rocque Brandon G.2

Affiliation:

1. Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin;

2. Department of Neurosurgery, University of Alabama at Birmingham, Children’s of Alabama, Birmingham;

3. Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama;

4. Department of Neurological Surgery, Penn State College of Medicine, Hershey, Pennsylvania;

5. Pediatric Neurosurgery, Lurie Children’s Hospital of Chicago, Illinois;

6. Goodman Campbell Brain and Spine Division of Pediatric Neurosurgery, Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana;

7. Department of Neurosurgery, University of Kansas, Kansas City, Kansas;

8. Department of Pediatrics, Baylor College of Medicine, Houston, Texas; and

9. Department of Neurology, University of Utah, Salt Lake City, Utah

Abstract

OBJECTIVEAlthough the majority of patients with myelomeningocele have hydrocephalus, reported rates of hydrocephalus treatment vary widely. The purpose of this study was to determine the rate of surgical treatment for hydrocephalus in patients with myelomeningocele in the National Spina Bifida Patient Registry (NSBPR). In addition, the authors explored the variation in shunting rates across NSBPR institutions, examined the relationship between hydrocephalus, and the functional lesion level of the myelomeningocele, and evaluated for temporal trends in rates of treated hydrocephalus.METHODSThe authors queried the NSBPR to identify all patients with myelomeningoceles. Individuals were identified as having been treated for hydrocephalus if they had undergone at least 1 hydrocephalus-related operation. For each participating NSBPR institution, the authors calculated the proportion of patients with treated hydrocephalus who were enrolled at that site. Logistic regression was performed to analyze the relationship between hydrocephalus and the functional lesion level of the myelomeningocele and to compare the rate of treated hydrocephalus in children born before 2005 with those born in 2005 or later.RESULTSA total of 4448 patients with myelomeningocele were identified from 26 institutions, of whom 3558 patients (79.99%) had undergone at least 1 hydrocephalus-related operation. The rate of treated hydrocephalus ranged from 72% to 96% among institutions enrolling more than 10 patients. This difference in treatment rates between centers was statistically significant (p < 0.001). Insufficient data were available in the NSBPR to analyze reasons for the different rates of hydrocephalus treatment between sites. Multivariate logistic regression demonstrated that more rostral functional lesion levels were associated with higher rates of treated hydrocephalus (p < 0.001) but demonstrated no significant difference in hydrocephalus treatment rates between children born before versus after 2005.CONCLUSIONSThe rate of hydrocephalus treatment in patients with myelomeningocele in the NSBPR is 79.99%, which is consistent with the rates in previously published literature. The authors’ data demonstrate a clear association between functional lesion level of the myelomeningocele and the need for hydrocephalus treatment.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference28 articles.

1. Decompression for Chiari malformation type II in individuals with myelomeningocele in the National Spina Bifida Patient Registry;Kim;J Neurosurg Pediatr [epub ahead of print,August 24, 2018

2. Reducing CSF shunt placement in patients with spinal myelomeningocele;Sankhla;J Pediatr Neurosci,2009

3. Fetal myelomeningocele repair: short-term clinical outcomes;Johnson;Am J Obstet Gynecol,2003

4. Predictors of the need for cerebrospinal fluid diversion in patients with myelomeningocele;Phillips;J Neurosurg Pediatr,2014

5. A randomized trial of prenatal versus postnatal repair of myelomeningocele;Adzick;N Engl J Med,2011

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