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Updated: Jul 14, 2026

The Rabbit Blood-shunt Model for the Study of Acute and Late Sequelae of Subarachnoid Hemorrhage: Technical Aspects
Published on: October 2, 2014
Idiopathic subarachnoid hemorrhage: Pattern and long-term outcome
María Concepción García Ortiz1, Marcelino Sanchez Casado1, Francisco Javier Morán Gallego1
1Servicio de Medicina Intensiva, Hospital Universitario de Toledo, Toledo, España.
Objective:
To analyze the presentation characteristics of idiopathic subarachnoid hemorrhage (SAHi), its characteristics and its long-term evolution.
Patients And Methods:
Descriptive follow-up study. ICU in Hospital of III level. SAH admitted to the ICU with negative admission arteriography during the years 2007-2022. The main variables of interest were demographic data, prognostic and severity scales, ICU evolution data, radiological results, exitus and GOSE scale (Glasgow Outcome Scale Extended) until the last observation.
Results:
Seven hundred thirty-threepatients with SAH were admitted to the ICU, 149 with initial negative arteriography. After the verification test starting at 3 weeks, 114 patients (16.1%) remained without underlying lesion. 58.8% were male and the age was 57.1±12.8 years. If we compare SAH with vs without underlying lesion (SAHi), we observed differences in the male sex (38.7% vs 58.8%), Hunt-Hess [2 (2-4) vs 2 (1-2)], Fisher [4 (3-4) vs 3 (2-4)], mechanical ventilation (86.8% vs 21.1%), tracheostomy (24.9% vs 1.8%), ICU stay days [10 (5-21) vs 3 (2-5)] and ICU deaths (20.9% vs 1%). We followed up on SAHi: 70,5 (33-109) months, with mortality of 11.4% (13 patients), none to related causes. There has been no rebleeding or late brain injury. In survivors, the GOSE was 7 (7-8), with 82.3% of patients with GOSE between 5-8. 44.7% of the patients had perimesencephalic SAH, with a mortality in the follow-up period of 7.8% and GOSE 7 (6-8).
Conclusions:
SAH without underlying vascular lesion presents good results in terms of morbidity and mortality and long-term functional status, improving if it is a perimensencephalic SAH.
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