Endoscopic third ventriculostomy in children: prospective, multicenter results from the Hydrocephalus Clinical Research Network

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Endoscopic third ventriculostomy in children: prospective, multicenter results from the Hydrocephalus Clinical Research Network

Abhaya V. KulkarniMD, PhD1, Jay Riva-CambrinMD, MSc2, Richard HolubkovPhD3, Samuel R. BrowdMD, PhD4, D. Douglas CochraneMD5, James M. DrakeFRCSC1, David D. LimbrickMD, PhD6, Curtis J. RozzelleMD10, Tamara D. SimonMD, MSPH4, Mandeep S. TamberMD, PhD7, John C. Wellons IIIMD, MSPH8, William E. WhiteheadMD9 and John R. W. KestleMD, MSc3 and 

INCLUDE WHEN CITING Published online June 3, 2016; DOI: 10.3171/2016.4.PEDS163.

Correspondence Abhaya V. Kulkarni, Division of Neurosurgery, Hospital for Sick Children, Rm. 1503, 555 University Ave., Toronto, ON M5G 1X8, Canada. email: abhaya.kulkarni@sickkids.ca.
Journal of Neurosurgery: Pediatrics
Pages. 1-7

(Issue publication date: June 2016)
DOI: 10.3171/2016.4.PEDS163
OBJECTIVE

Endoscopic third ventriculostomy (ETV) is now established as a viable treatment option for a subgroup of children with hydrocephalus. Here, the authors report prospective, multicenter results from the Hydrocephalus Clinical Research Network (HCRN) to provide the most accurate determination of morbidity, complication incidence, and efficacy of ETV in children and to determine if intraoperative predictors of ETV success add substantially to preoperative predictors.
METHODS

All children undergoing a first ETV (without choroid plexus cauterization) at 1 of 7 HCRN centers up to June 2013 were included in the study and followed up for a minimum of 18 months. Data, including detailed intraoperative data, were prospectively collected as part of the HCRN’s Core Data Project and included details of patient characteristics, ETV failure (need for repeat hydrocephalus surgery), and, in a subset of patients, postoperative complications up to the time of discharge.
RESULTS

Three hundred thirty-six eligible children underwent initial ETV, 18.8% of whom had undergone shunt placement prior to the ETV. The median age at ETV was 6.9 years (IQR 1.7–12.6), with 15.2% of the study cohort younger than 12 months of age. The most common etiologies were aqueductal stenosis (24.8%) and midbrain or tectal lesions (21.2%). Visible forniceal injury (16.6%) was more common than previously reported, whereas severe bleeding (1.8%), thalamic contusion (1.8%), venous injury (1.5%), hypothalamic contusion (1.5%), and major arterial injury (0.3%) were rare. The most common postoperative complications were CSF leak (4.4%), hyponatremia (3.9%), and pseudomeningocele (3.9%). New neurological deficit occurred in 1.5% cases, with 0.5% being permanent.
One hundred forty-one patients had documented failure of their ETV requiring repeat hydrocephalus surgery during follow-up, 117 of them during the first 6 months postprocedure. Kaplan-Meier rates of 30-day, 90-day, 6-month, 1-year, and 2-year failure-free survival were 73.7%, 66.7%, 64.8%, 61.7%, and 57.8%, respectively. According to multivariate modeling, the preoperative ETV Success Score (ETVSS) was associated with ETV success (p < 0.001), as was the intraoperative ability to visualize a “naked” basilar artery (p = 0.023).
CONCLUSIONS

The authors’ documented experience represents the most detailed account of ETV results in North America and provides the most accurate picture to date of ETV success and complications, based on contemporaneously collected prospective data. Serious complications with ETV are low. In addition to the ETVSS, visualization of a naked basilar artery is predictive of ETV success.
Keywords: pediatric; hydrocephalus; endoscopy; third ventriculostomy

Read more:  http://thejns.org/doi/abs/10.3171/2016.4.PEDS163