Shunt-dependent hydrocephalus

The pathogenesis of shunt-dependent hydrocephalus involves obstruction of blood products or adhesions which blocks cerebrospinal fluid circulation within the ventricular system, fibrillation of aseptic inflammation after aneurysmal subarachnoid hemorrhage which may cause CSF mal-absorption 1) 2) 3).

Patients with shunt-dependent hydrocephalus require regular monitoring to ensure the proper functioning of the shunt. Complications such as infections, blockages, or malfunctions can occur and may require prompt medical attention.

Lifelong Management:

Shunt-dependent hydrocephalus often requires lifelong management. Regular follow-ups with healthcare providers, imaging studies, and adjustments to the shunt system may be necessary over time.

Subarachnoid Hemorrhage Volume, intraventricular hemorrhage volume, intracerebral hemorrhage volume, and total hemorrhage (TH) were computed from brain CT scans utilizing AW Server analytical software. ROC curves and multivariate analyses were employed to determine the association between hemorrhage volumes and SDAHC. The study included 170 patients, of whom 111 (65.3%) were women, with a mean age of 58.5 years (SD: 14.6). Fifty-five patients (32.4%) presented SDAHC. intraventricular hemorrhage volumes had an area under the ROC curve of 0.757 (95% CI: 0.674-0.839; p <0.001). An IVH volume > 2.7 cm³ showed a sensitivity of 70.9% and a specificity of 77.2% for predicting SDAHC, while TH volumes > 29.5 cm³ demonstrated a sensitivity of 69.1% and a specificity of 61.4%. Multivariate analysis revealed that IVH volumes > 2.7 cm³ (OR 5.373; 95% CI: 2.477-11.657), TH volumes > 29.5 cm³ (OR 2.232; 95% CI: 1.008-4.942), and a bicaudate index ≥0.2 were significantly associated with SDAHC, adjusting for confounders. In aSAH patients, semiautomatic measurement of hemorrhage volumes using specialized software is independently associated with SDAHC. This method could facilitate early prediction and timely intervention 4).


This is a well-conceived and clinically relevant study that contributes meaningfully to the literature on aSAH complications. While its methodological rigor is commendable, future studies should aim to validate and refine the thresholds in larger, multicentric cohorts, and integrate clinical, radiological, and biochemical markers into comprehensive SDAHC prediction tools.


An observational retrospective analytic study of the patients with spontaneous SAH admitted to Miguel Servet University Hospital between 2017 and 2022. Patients' clinical and radiological characteristics, type of treatment, diagnoses and treatment of hydrocephalus, complications of ventriculoperitoneal shunts, and mortality are some of the data achieved in this study. A descriptive study of these variables has been done and, subsequently, the most relevant variables have been statistically analyzed to identify patients with an increasing risk of shunting for hydrocephalus. This study was authorized by the Ethics Committee before its elaboration.

Results: A total of 359 patients with spontaneous SAH were admitted to Miguel Servet University Hospital between 2017 and 2022, with an intrahospital death rate of 25.3%. 66.3% of the total of patients with SAH were due to intracranial aneurysm rupture (n = 238). 45.3% of the patients with aneurysmal SAH required an external ventricular drain (EVD) to treat acute hydrocephalus. 11.7% (n = 28) developed a shunt-dependent hydrocephalus. Statistical significance was found between shunt-dependent hydrocephalus and the following: high score in modified Fisher scale and placement of EVD. The mean interval from EVD to ventriculoperitoneal shunt placement was 26.1 days. The mean rate of reoperation of patients after shunt was 17.7%, mostly due to infection.

The most significant risk factor for shunt-dependent hydrocephalus after aneurysmal subarachnoid hemorrhage was high Fisher scale and previous need for external ventricular drainage. Shunt infections are the main cause of shunt reoperation. Early shunt placement in selected patients might reduce the rate of infectious complications 5).


1)
Hasan D, Herve L, Tanghe J. Distribution of cisternal blood in patients with acute hydrocephalus after subarachnoid hemorrhage. Ann Neurol 1992;31:374–8.
2)
Donauer E, Reif J, al-Khalaf B, et al. Intraventricular hemorrhage caused by aneurysms and angiomas. Acta Neurochir (Wien) 1993;122:23–31.
3)
Ishii M. Subarachnoid hemorrhage and circulation disturbance of cerebrospinal fluid scanning electron microscopic study in clinical and autopsy case. No Shinkei Geka 1979;7:579–88.
4)
Bravo-Garrido G, Vargas-Lopez A, Fernández-Gómez M, Gomar-Alba M, Urreta-Juárez G, Martínez-Sánchez P. Cerebral Hemorrhage Volume Threshold and Shunt-Dependent Acute Hydrocephalus in Aneurysmal Subarachnoid Hemorrhage: A Semiautomated Measurement Study. J Neurol Surg A Cent Eur Neurosurg. 2025 Mar 28. doi: 10.1055/a-2568-4732. Epub ahead of print. PMID: 40154533.
5)
Esteban Estallo L, Casado Pellejero J, Vázquez Sufuentes S, López López LB, Fustero de Miguel D, González Martínez LM. Risk factors for shunt-dependent hydrocephalus after spontaneous subarachnoid hemorrhage. Neurocirugia (Astur : Engl Ed). 2024 Mar 6:S2529-8496(24)00015-7. doi: 10.1016/j.neucie.2024.03.002. Epub ahead of print. PMID: 38452929.
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