Endoscopic third ventriculostomy in previously shunt-treated patients.

ETV revision Hydrocephalus Clinical Research Network endoscopic third ventriculostomy ventriculoperitoneal shunt

Journal

Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759

Informations de publication

Date de publication:
29 Jul 2022
Historique:
received: 05 05 2022
accepted: 30 06 2022
pmc-release: 29 01 2024
entrez: 30 7 2022
pubmed: 31 7 2022
medline: 31 7 2022
Statut: aheadofprint

Résumé

Endoscopic third ventriculostomy (ETV) is an option for treatment of hydrocephalus, including for patients who have a history of previous treatment with CSF shunt insertion. The purpose of this study was to report the success of postshunt ETV by using data from a multicenter prospective registry. Prospectively collected data in the Hydrocephalus Clinical Research Network (HCRN) Core Data Project (i.e., HCRN Registry) were reviewed. Children who underwent ETV between 2008 and 2019 and had a history of previous treatment with a CSF shunt were included. A Kaplan-Meier survival curve was created for the primary outcome: time from postshunt ETV to subsequent CSF shunt placement or revision. Univariable Cox proportional hazards models were created to evaluate for an association between clinical and demographic variables and subsequent shunt surgery. Postshunt ETV complications were also identified and categorized. A total of 203 children were included: 57% male and 43% female; 74% White, 23% Black, and 4% other race. The most common hydrocephalus etiologies were postintraventricular hemorrhage secondary to prematurity (56, 28%) and aqueductal stenosis (42, 21%). The ETV Success Score ranged from 10 to 80. The median patient age was 4.1 years. The overall success of postshunt ETV at 6 months was 41%. Only the surgeon's report of a clear view of the basilar artery was associated with a lower likelihood of postshunt ETV failure (HR 0.43, 95% CI 0.23-0.82, p = 0.009). None of the following variables were associated with postshunt ETV success: age at the time of postshunt ETV, etiology of hydrocephalus, sex, race, ventricle size, number of previous shunt operations, ETV performed at time of shunt infection, and use of external ventricular drainage. Overall, complications were reported in 22% of patients, with CSF leak (8.6%) being the most common complication. Postshunt ETV was successful in treating hydrocephalus, without subsequent need for a CSF shunt, in 41% of patients, with a clear view of the basilar artery being the only variable significantly associated with success. Complications occurred in 22% of patients. ETV is an option for treatment of hydrocephalus in children who have previously undergone shunt placement, but with a lower than expected likelihood of success.

Identifiants

pubmed: 35907200
doi: 10.3171/2022.6.PEDS22177
pmc: PMC9884313
mid: NIHMS1831811
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Subventions

Organisme : NINDS NIH HHS
ID : RC1 NS068943
Pays : United States

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Auteurs

Brandon G Rocque (BG)

1Department of Neurosurgery, Children's of Alabama, The University of Alabama at Birmingham, Alabama.

Hailey Jensen (H)

Departments of2Pediatrics and.

Ron W Reeder (RW)

Departments of2Pediatrics and.

Abhaya V Kulkarni (AV)

3Division of Neurosurgery, Hospital for Sick Children, Toronto, Ontario, Canada.

Ian F Pollack (IF)

4Department of Neurosurgery, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh, Pennsylvania.

John C Wellons (JC)

5Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee.
6Surgical Outcomes Center for Kids, Monroe Carell Jr. Children's Hospital at Vanderbilt University, Nashville, Tennessee.

Robert P Naftel (RP)

5Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee.
6Surgical Outcomes Center for Kids, Monroe Carell Jr. Children's Hospital at Vanderbilt University, Nashville, Tennessee.

Eric M Jackson (EM)

7Department of Neurosurgery, The Johns Hopkins Hospital, Johns Hopkins University, Baltimore, Maryland.

William E Whitehead (WE)

8Department of Neurosurgery, Texas Children's Hospital, Houston, Texas.

Jonathan A Pindrik (JA)

9Department of Neurosurgery, The Ohio State University College of Medicine, Columbus, Ohio.

David D Limbrick (DD)

10Department of Neurosurgery, Washington University School of Medicine in St. Louis, Missouri.

Patrick J McDonald (PJ)

11Division of Neurosurgery, British Columbia Children's Hospital, The University of British Columbia, Vancouver, British Columbia, Canada.

Mandeep S Tamber (MS)

11Division of Neurosurgery, British Columbia Children's Hospital, The University of British Columbia, Vancouver, British Columbia, Canada.

Todd C Hankinson (TC)

12Department of Neurosurgery, Children's Hospital Colorado, Colorado Springs, Colorado.

Jason S Hauptman (JS)

13Department of Neurosurgery, Seattle Children's Hospital, University of Washington, Seattle, Washington.

Mark D Krieger (MD)

Departments of14Neurosurgery and.

Jason Chu (J)

Departments of14Neurosurgery and.

Tamara D Simon (TD)

15Pediatrics, Children's Hospital Los Angeles, University of Southern California, Los Angeles, California; and.

Jay Riva-Cambrin (J)

16Division of Neurosurgery, Alberta Children's Hospital, University of Calgary, Alberta, Canada.

John R W Kestle (JRW)

17Neurosurgery, University of Utah, Salt Lake City, Utah.

Curtis J Rozzelle (CJ)

1Department of Neurosurgery, Children's of Alabama, The University of Alabama at Birmingham, Alabama.

Classifications MeSH