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Published on: October 14, 2022
Trapped fourth ventricle: a rare complication in children after supratentorial CSF shunting
Ahmed El Damaty1, Ahmed Eltanahy2,3, Andreas Unterberg4
1Department of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany. ahmed.eldamaty@med.uni-heidelberg.de.
Insights
Trapped fourth ventricle (TFV) is a complication in hydrocephalic children, often linked to post-hemorrhagic hydrocephalus (PHH) and prematurity. Early diagnosis and treatment, such as ventricular shunting or endoscopic aqueductoplasty, are crucial for better outcomes.
Area of Science:
- Pediatric Neurosurgery
- Neurology
- Medical Imaging
Background:
- Trapped fourth ventricle (TFV) is a recognized complication in pediatric hydrocephalus.
- Post-hemorrhagic hydrocephalus (PHH) is the most common etiology associated with TFV.
- TFV can lead to significant neurological deficits if not managed promptly.
Purpose of the Study:
- To identify predisposing factors for TFV in children.
- To describe the clinical presentation of TFV.
- To evaluate management strategies for TFV.
Main Methods:
- Retrospective review of a surgical database from 1991 to 2018.
- Analysis of patient demographics, hydrocephalus etiology, and treatment modalities.
- Correlation of clinical findings and MRI imaging with TFV diagnosis.
Main Results:
- Twenty-one patients with TFV were identified, predominantly with PHH (16/21) and prematurity (17/21).
- Brainstem dysfunction symptoms were present in 13 patients; 3 were asymptomatic.
- An additional fourth ventricular catheter was the primary treatment (18/21), with endoscopic aqueductoplasty also showing efficacy.
Conclusions:
- PHH and prematurity are significant risk factors for TFV.
- Both fourth ventricular shunting and endoscopic aqueductoplasty are effective treatments for TFV.
- Early detection and intervention are vital to prevent severe complications and improve neurological function.
Purpose:
Trapped fourth ventricle (TFV) is a well-identified problem in hydrocephalic children. Patients with post-hemorrhagic hydrocephalus (PHH) are mostly affected. We tried to find out predisposing factors and describe clinical findings to early diagnose TFV and manage it.
Methods:
We reviewed our database from 1991 to 2018 and included all patients with TFV who required surgery. We analyzed prematurity, cause of hydrocephalus, type of valve implanted, revision surgeries, modality of treatment of TFV, and their clinical examination and MRI imaging.
Results:
We found 21 patients. Most of patients suffered from PHH (16/21), tumor (2/21), post-meningitis hydrocephalus (2/21), and congenital hydrocephalus (1/21). Seventeen patients were preterm. Seven patients suffered from a chronic overdrainage with slit ventricles in MRI. Thirteen patients showed symptoms denoting brain stem dysfunction; in 3 patients, TFV was asymptomatic and in 5 patients, we did not have available information regarding presenting symptoms due to missing documentation. An extra fourth ventricular catheter was the treatment of choice in 18/21 patients. One patient was treated by cranio-cervical decompression. Endoscopic aqueductoplasty with stenting was done in last 2 cases.
Conclusion:
Diagnosis of clinically symptomatic TFV and its treatment is a challenge in our practice of pediatric neurosurgery. PHH and prematurity are risk factors for the development of such complication. Both fourth ventricular shunting and endoscopic aqueductoplasty with stenting are effective in managing TFV. Microsurgical fourth ventriculostomy is not recommended due to its high failure rate. Early detection and intervention may help in avoiding fatal complication and improving the neurological function.
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