TY - JOUR
T1 - Risk factors for shunt malfunction in pediatric hydrocephalus
T2 - A multicenter prospective cohort study
AU - for the Hydrocephalus Clinical Research Network
AU - Riva-Cambrin, Jay
AU - Kestle, John R.W.
AU - Holubkov, Richard
AU - Butler, Jerry
AU - Kulkarni, Abhaya V.
AU - Drake, James
AU - Whitehead, William E.
AU - Wellons, John C.
AU - Shannon, Chevis N.
AU - Tamber, Mandeep S.
AU - Limbrick, David D.
AU - Rozzelle, Curtis
AU - Browd, Samuel R.
AU - Simon, Tamara D.
N1 - Funding Information:
We thank the Hydrocephalus Association for their continued support of the HCRN, and Kristin Kraus, MSc, for editorial assistance with the paper. The HCRN has been funded by private philanthropy and National Institute of Neurological Disorders and Stroke (NINDS) Grant No. 1RC1NS068943-01. Dr. Simon is supported by Award K23NS062900 from the National Institute of Neurological Disorders and Stroke, the Child Health Corporation of America via the Pediatric Research in Inpatient Setting Network Executive Council, and the Seattle Children's Center for Clinical and Translational Research. None of the sponsors participated in design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript. Its contents are solely the responsibility of the authors and do not necessarily represent the official view of the sponsors. The authors would like to thank their colleagues who kindly agreed to participate in this HCRN project and allow collection of patient data for the purpose of this publication: Douglas Brockmeyer, Rob Bollo, Jeff Blount, James Johnston, Brandon Rocque, Leslie Ackacpo-Satchivi, Peter Dirks, James Rutka, Michael Taylor, Daniel Curry, Robert Dauser, Andrew Jea, Sandi Lam, Richard Ellenbogen, Jeffery Ojemann, Amy Lee, Anthony Avellino, R. Aaron Robison, Ian Pollack, Stephanie Greene, Elizabeth Tyler-Kabara, T. S. Park, Jeffrey Leonard, Matthew Smyth, Noel Tulipan, Robert Naftel, Ash Signhal, Paul Steinbok. In addition, this work would not have been possible without the outstanding support of the dedicated personnel at each clinical site and the data coordinating center. Special thanks goes to Tracey Bach (Salt Lake City), Anastasia Arynchyna (Birmingham), Homa Ashrafpour (Toronto), Sheila Ryan (Houston), Amy Anderson (Seattle), Arlene Luther (Pittsburgh), Deanna Mercer (St. Louis), Angela Davis, (Nashville), Ross Hengel (British Columbia), and Marcie Langley, Nichol Nunn, and Tyler Hunt (Utah Data Coordinating Center). The authors thank them for their hard work and contributions to the HCRN.
Publisher Copyright:
©AANS, 2016.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Objective The rate of CSF shunt failure remains unacceptably high. The Hydrocephalus Clinical Research Network (HCRN) conducted a comprehensive prospective observational study of hydrocephalus management, the aim of which was to isolate specific risk factors for shunt failure. Methods The study followed all first-time shunt insertions in children younger than 19 years at 6 HCRN centers. The HCRN Investigator Committee selected, a priori, 21 variables to be examined, including clinical, radiographic, and shunt design variables. Shunt failure was defined as shunt revision, subsequent endoscopic third ventriculostomy, or shunt infection. Important a priori-defined risk factors as well as those significant in univariate analyses were then tested for independence using multivariate Cox proportional hazard modeling. Results A total of 1036 children underwent initial CSF shunt placement between April 2008 and December 2011. Of these, 344 patients experienced shunt failure, including 265 malfunctions and 79 infections. The mean and median length of follow-up for the entire cohort was 400 days and 264 days, respectively. The Cox model found that age younger than 6 months at first shunt placement (HR 1.6 [95% CI 1.1-2.1]), a cardiac comorbidity (HR 1.4 [95% CI 1.0-2.1]), and endoscopic placement (HR 1.9 [95% CI 1.2-2.9]) were independently associated with reduced shunt survival. The following had no independent associations with shunt survival: etiology, payer, center, valve design, valve programmability, the use of ultrasound or stereotactic guidance, and surgeon experience and volume. Conclusions This is the largest prospective study reported on children with CSF shunts for hydrocephalus. It confirms that a young age and the use of the endoscope are risk factors for first shunt failure and that valve type has no impact. A new risk factor-an existing cardiac comorbidity-was also associated with shunt failure.
AB - Objective The rate of CSF shunt failure remains unacceptably high. The Hydrocephalus Clinical Research Network (HCRN) conducted a comprehensive prospective observational study of hydrocephalus management, the aim of which was to isolate specific risk factors for shunt failure. Methods The study followed all first-time shunt insertions in children younger than 19 years at 6 HCRN centers. The HCRN Investigator Committee selected, a priori, 21 variables to be examined, including clinical, radiographic, and shunt design variables. Shunt failure was defined as shunt revision, subsequent endoscopic third ventriculostomy, or shunt infection. Important a priori-defined risk factors as well as those significant in univariate analyses were then tested for independence using multivariate Cox proportional hazard modeling. Results A total of 1036 children underwent initial CSF shunt placement between April 2008 and December 2011. Of these, 344 patients experienced shunt failure, including 265 malfunctions and 79 infections. The mean and median length of follow-up for the entire cohort was 400 days and 264 days, respectively. The Cox model found that age younger than 6 months at first shunt placement (HR 1.6 [95% CI 1.1-2.1]), a cardiac comorbidity (HR 1.4 [95% CI 1.0-2.1]), and endoscopic placement (HR 1.9 [95% CI 1.2-2.9]) were independently associated with reduced shunt survival. The following had no independent associations with shunt survival: etiology, payer, center, valve design, valve programmability, the use of ultrasound or stereotactic guidance, and surgeon experience and volume. Conclusions This is the largest prospective study reported on children with CSF shunts for hydrocephalus. It confirms that a young age and the use of the endoscope are risk factors for first shunt failure and that valve type has no impact. A new risk factor-an existing cardiac comorbidity-was also associated with shunt failure.
KW - Csf shunt
KW - Hydrocephalus
KW - Hydrocephalus clinical research network
KW - Pediatric
KW - Prospective
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=84973365080&partnerID=8YFLogxK
U2 - 10.3171/2015.6.PEDS14670
DO - 10.3171/2015.6.PEDS14670
M3 - Article
C2 - 26636251
AN - SCOPUS:84973365080
SN - 1933-0707
VL - 17
SP - 382
EP - 390
JO - Journal of Neurosurgery: Pediatrics
JF - Journal of Neurosurgery: Pediatrics
IS - 4
ER -