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The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review

Fourth ventricle outlet obstruction (FVOO) is a rare cause of hydrocephalus. In the last century, the standard treatment was the suboccipital craniotomy with magendieplasty or ventriculoperitoneal shunt (VP shunt). Since the beginning of the 21st century, the endoscopic third ventriculostomy (ETV) h...

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Autores principales: Mulhem, Ali, Alsulaiman, Abdul Masih, Hammersen, Stefanie, Kantelhardt, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683030/
https://www.ncbi.nlm.nih.gov/pubmed/38033697
http://dx.doi.org/10.1002/ccr3.8234
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author Mulhem, Ali
Alsulaiman, Abdul Masih
Hammersen, Stefanie
Kantelhardt, Sven
author_facet Mulhem, Ali
Alsulaiman, Abdul Masih
Hammersen, Stefanie
Kantelhardt, Sven
author_sort Mulhem, Ali
collection PubMed
description Fourth ventricle outlet obstruction (FVOO) is a rare cause of hydrocephalus. In the last century, the standard treatment was the suboccipital craniotomy with magendieplasty or ventriculoperitoneal shunt (VP shunt). Since the beginning of the 21st century, the endoscopic third ventriculostomy (ETV) has been considered a less invasive alternative. The medical literature lacks sufficient reports of FVOO cases and strong evidence about ETV's efficacy in treating this condition. We report two cases of FVOO treated with ETV and review published similar cases. Clinical and radiological findings of two FVOO cases with outcomes after ETV were presented. Moreover, we conducted a systematic review after protocol registration in PROSPERO (CRD42021281474). MEDLINE, Embase, Scopus, and Web of Science were searched from inception till December 31, 2022. Studies were included if they reported cases of FVOO treated initially with ETV. Cases with Chiari malformation, Dandy‐Walker malformation, tuberous sclerosis, trapped fourth ventricle, or space‐occupying lesions were excluded. Two reviewers independently examined title/abstract records in the first stage and full‐text publications in the second for eligibility. The primary outcome was the recurrence rate, defined by the need for re‐ETV or other invasive treatments (e.g., VP shunt or magendieplasty). Other outcomes included clinical state at follow‐up and mortality. Two cases, a 3‐year‐old male and 3.5‐year‐old female, with FVOO, were treated with ETV in our department by the same neurosurgeon (SH) in 2013 and 2021. Both cases improved significantly after ETV, and there was no recurrence through the follow‐up. Besides the present cases, we found 57 other cases of FVOO treated with ETV reported in 17 studies between 2001 and 2021. The median age was 26 years, with an IQR from 2.4 to 59 years, and 56% of cases were females. The recurrence rate was 32% in the sample (19 out of 59), with a 95% CI from 21% to 46%. The median time to recure was 2 months with IQR from 1.25 to 26. A VP shunt was the treatment for recurrence in 68% and a re‐ETV in 32%. At the follow‐up (41 ± 29 months), only one case died, and one deteriorated clinically. FVOO is a rare cause of hydrocephalus encountered mainly in the first or sixth decades of life. ETV provides the first reasonable treatment. Despite the moderate recurrence rate, the outcomes are favorable.
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spelling pubmed-106830302023-11-30 The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review Mulhem, Ali Alsulaiman, Abdul Masih Hammersen, Stefanie Kantelhardt, Sven Clin Case Rep Case Report Fourth ventricle outlet obstruction (FVOO) is a rare cause of hydrocephalus. In the last century, the standard treatment was the suboccipital craniotomy with magendieplasty or ventriculoperitoneal shunt (VP shunt). Since the beginning of the 21st century, the endoscopic third ventriculostomy (ETV) has been considered a less invasive alternative. The medical literature lacks sufficient reports of FVOO cases and strong evidence about ETV's efficacy in treating this condition. We report two cases of FVOO treated with ETV and review published similar cases. Clinical and radiological findings of two FVOO cases with outcomes after ETV were presented. Moreover, we conducted a systematic review after protocol registration in PROSPERO (CRD42021281474). MEDLINE, Embase, Scopus, and Web of Science were searched from inception till December 31, 2022. Studies were included if they reported cases of FVOO treated initially with ETV. Cases with Chiari malformation, Dandy‐Walker malformation, tuberous sclerosis, trapped fourth ventricle, or space‐occupying lesions were excluded. Two reviewers independently examined title/abstract records in the first stage and full‐text publications in the second for eligibility. The primary outcome was the recurrence rate, defined by the need for re‐ETV or other invasive treatments (e.g., VP shunt or magendieplasty). Other outcomes included clinical state at follow‐up and mortality. Two cases, a 3‐year‐old male and 3.5‐year‐old female, with FVOO, were treated with ETV in our department by the same neurosurgeon (SH) in 2013 and 2021. Both cases improved significantly after ETV, and there was no recurrence through the follow‐up. Besides the present cases, we found 57 other cases of FVOO treated with ETV reported in 17 studies between 2001 and 2021. The median age was 26 years, with an IQR from 2.4 to 59 years, and 56% of cases were females. The recurrence rate was 32% in the sample (19 out of 59), with a 95% CI from 21% to 46%. The median time to recure was 2 months with IQR from 1.25 to 26. A VP shunt was the treatment for recurrence in 68% and a re‐ETV in 32%. At the follow‐up (41 ± 29 months), only one case died, and one deteriorated clinically. FVOO is a rare cause of hydrocephalus encountered mainly in the first or sixth decades of life. ETV provides the first reasonable treatment. Despite the moderate recurrence rate, the outcomes are favorable. John Wiley and Sons Inc. 2023-11-28 /pmc/articles/PMC10683030/ /pubmed/38033697 http://dx.doi.org/10.1002/ccr3.8234 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mulhem, Ali
Alsulaiman, Abdul Masih
Hammersen, Stefanie
Kantelhardt, Sven
The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title_full The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title_fullStr The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title_full_unstemmed The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title_short The endoscopic treatment of fourth ventricle outlet obstruction: Report of two children and systematic review
title_sort endoscopic treatment of fourth ventricle outlet obstruction: report of two children and systematic review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683030/
https://www.ncbi.nlm.nih.gov/pubmed/38033697
http://dx.doi.org/10.1002/ccr3.8234
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