# Comparative efficacy of cisternal drainage versus external ventricular drainage in severe aneurysmal subarachnoid hemorrhage

**Authors:** Mahamat Hamid Mahamat, Tuo Li, Jun Liu, Shusheng Zhang, Ye Miao, Zhongzhen Li, Yadan Li, Hua Yan, Guobin Zhang, Xiaoguang Tong, Eric Sribnick, Eric Sribnick, Eric Sribnick, Eric Sribnick, Eric Sribnick

PMC · DOI: 10.1371/journal.pone.0340013 · 2026-01-07

## TL;DR

This study compares two methods for managing brain pressure in severe aneurysmal subarachnoid hemorrhage patients and finds that combining both methods may improve recovery.

## Contribution

The study introduces cisternal drainage as a supplementary strategy to external ventricular drainage for better inflammatory clearance and reduced hospitalization.

## Key findings

- Combining EVD and CD reduced hospitalization duration by 22.8% compared to EVD alone.
- The EVD+CD group showed significantly lower levels of inflammatory markers and vascular injury factors by day 7.
- ICP monitoring accuracy was similar between the two groups.

## Abstract

The cerebrovascular emergency known as aneurysmal subarachnoid hemorrhage (aSAH) is potentially fatal. Although external ventricular drainage (EVD) is the gold standard for monitoring intracranial pressure (ICP), cisternal drainage (CD) should be considered as a supplementary strategy due to the limited effectiveness of EVD in removing inflammatory mediators and preventing vascular damage.

To compare ICP monitoring accuracy, cerebrospinal fluid (CSF) clearance, and clinical outcomes between EVD and CD in severe aSAH patients.

A retrospective study enrolled 47 Hunt-Hess IV–V grade aSAH patients, divided into EVD (n = 23) and EVD + CD (n = 24) groups. Daily ICP values (days 1/3/5/7), CSF biomarkers (cell count, protein, Interleukin-6, Interleukin-8, Tumor Necrosis Factor-α, Endothelin-1, Monocyte Chemoattractant Protein-1, Vascular Cell Adhesion Molecule-1), hospitalization duration, and 6-month Glasgow Outcome Scale (GOS) were analyzed.

ICP values showed no significant difference between the two groups (p > 0.05). EVD + CD group exhibited higher CSF cell count (394.68 ± 91.32 vs. 320.40 ± 75.49), protein (16.17 ± 2.27 vs. 13.74 ± 2.94 g/L), and cytokines (IL-6/IL-8, p < 0.05) on day 1, but significantly lower levels by day 7 (p < 0.05). Vascular injury factors (ET-1/MCP-1/VCAM-1) were reduced in the EVD + CD group by day 7 (p < 0.05). Hospitalization duration was 22.8% shorter in the EVD + CD group (27 vs. 35 days, p = 0.030); while 6-month GOS showed no difference (2.52 vs. 2.57, p = 0.148).

Compared with EVD, CD could not only provide accurate ICP readings and trend data but also enhance inflammatory clearance, reduce hospitalization time, and mitigate vascular injury in severe aSAH, warranting further validation in larger cohorts.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL8L1 (interleukin 8-like 1)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, CADM1 (cell adhesion molecule 1) [NCBI Gene 23705] {aka BL2, IGSF4, IGSF4A, NECL2, Necl-2, RA175}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}
- **Diseases:** cerebrovascular emergency (MESH:D002561), aSAH (MESH:D013345), inflammatory (MESH:D007249), Vascular injury (MESH:D057772)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12779065/full.md

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Source: https://tomesphere.com/paper/PMC12779065