自发性蛛网膜下腔出血并发急性脑积水的相关因素分析
Analysis of the Related Factors of Acute Hydrocephalus Complicated with Spontaneous Subarachnoid Hemorrhage
摘要: 目的:探讨自发性蛛网膜下腔出血后并发急性脑积水的相关危险因素。方法:选取西安市中心医院神经外科收治的162例蛛网膜下腔出血的患者作为研究对象,统计患者的年龄、性别、饮酒史、吸烟史、高血压病史、糖尿病史、入院时是否昏迷、入院时是否呕吐、GCS评分、脑室出血、早期腰大池引流术、早期锥颅置管引流术、颅内动脉瘤等相关资料,本研究采用二元Logistic回归模型,深入剖析自发性蛛网膜下腔出血(SAH)患者并发急性脑积水(AHC)的相关危险因素。P < 0.05为差异有统计学意义。结果:发生急性脑积水的患者平均年龄大于未患急性脑积水患者平均年龄;女性患急性脑积水的比例大于男性;无饮酒史的患者患急性脑积水的比率大于有饮酒史的患者;不吸烟的患者患急性脑积水的比例大于吸烟患者;有高血压病史的患者患急性脑积水的比例大于无高血压病史的患者;有糖尿病病史的患者患急性脑积水的比例大于无糖尿病病史的患者;入院时昏迷的患者发生急性脑积水的概率高;入院时呕吐的患者发生急性脑积水的概率高;GCS评分 ≥ 8分的患者患急性脑积水的概率更高;早期脑室积血的患者患急性脑积水的概率更高;早期未接受锥颅置管引流术治疗的患者患急性脑积水的比例更高。早期腰大池引流术、糖尿病史无统计学意义,P > 0.05。是否有动脉瘤与急性脑积水的发生无统计学意义,P = 0.663。Hunt-Hess分级更高的患者发生急性脑积水的比例Hunt-Hess分级低的患者;患急性脑积水的患者动脉瘤直径大于未患急性脑积水的患者;动脉瘤位置、是否接受动脉瘤栓塞术无统计学意义,P > 0.05。多因素Logistic回归分析显示,年龄、GCS < 8分、脑室积血、入院时呕吐、入院时昏迷是自发性蛛网膜下腔出血患者并发急性脑积水的危险因素。讨论:自发性蛛网膜下腔出血患者并发急性脑积水的相关因素为年龄、GCS < 8分、脑室积血、入院时呕吐、入院时昏迷,动脉瘤性蛛网膜下腔出血患者并发急性脑积水的相关因素为动脉瘤的大小、Hunt-Hess分级。
Abstract: Objective: To explore the associated risk factors for the development of acute hydrocephalus following spontaneous subarachnoid hemorrhage. Methods: A total of 162 patients with spontaneous subarachnoid hemorrhage admitted to the Department of Neurosurgery at Xi’an Central Hospital were selected as the subjects of this study. Data including patient age, gender, drinking history, smoking history, history of hypertension, history of diabetes, coma on admission, vomiting on admission, GCS score, intracerebral hemorrhage, early ventricular hemorrhage, early lumbar puncture, early placement of external ventricular drainage, intracranial aneurysm, and other relevant information were collected. Multifactor Logistic regression analysis was used to assess the associated risk factors for the development of acute hydrocephalus in patients with spontaneous subarachnoid hemorrhage. A P-value of less than 0.05 was considered to indicate statistical significance. Results: Patients who developed acute hydrocephalus had a higher average age than those who did not; the proportion of females with acute hydrocephalus was greater than that of males; the rate of acute hydrocephalus in patients without a history of alcohol consumption was higher than those with a history of alcohol consumption; the proportion of patients who did not smoke and developed acute hydrocephalus was greater than those who smoked; patients with a history of hypertension had a higher proportion of acute hydrocephalus than those without a history of hypertension; the proportion of patients with a history of diabetes developing acute hydrocephalus was greater than those without a history of diabetes; patients who were comatose on admission had a higher probability of developing acute hydrocephalus; patients who vomited on admission had a higher likelihood of developing acute hydrocephalus; patients with a GCS score of 8 or higher had a higher probability of developing acute hydrocephalus; patients with early ventricular hemorrhage had a higher probability of developing acute hydrocephalus; the proportion of patients who did not receive early placement of external ventricular drainage and developed acute hydrocephalus was higher. Early lumbar puncture, a history of diabetes, did not show statistical significance, P > 0.05. The presence of an aneurysm was not statistically significant in relation to the occurrence of acute hydrocephalus, P = 0.663. Patients with a higher Hunt-Hess grade had a higher proportion of acute hydrocephalus; patients with acute hydrocephalus had a larger aneurysm diameter than those without acute hydrocephalus; the location of the aneurysm, and whether they received aneurysm occlusion surgery did not show statistical significance, P > 0.05. Multivariate Logistic regression analysis showed that age, GCS score less than 8, ventricular hemorrhage, vomiting on admission, and coma on admission were risk factors for the development of acute hydrocephalus in patients with spontaneous subarachnoid hemorrhage. Discussion: The associated risk factors for the development of acute hydrocephalus in patients with spontaneous subarachnoid hemorrhage include age, GCS score less than 1, ventricular hemorrhage, vomiting on admission, and coma on admission. For aneurysmal subarachnoid hemorrhage patients, the associated risk factors for the development of acute hydrocephalus include the size and Hunt-Hess grade.
文章引用:邓力芝, 张国来. 自发性蛛网膜下腔出血并发急性脑积水的相关因素分析[J]. 临床医学进展, 2025, 15(2): 1218-1227. https://doi.org/10.12677/acm.2025.152465

参考文献

[1] Claassen, J. and Park, S. (2022) Spontaneous Subarachnoid Haemorrhage. The Lancet, 400, 846-862. [Google Scholar] [CrossRef] [PubMed]
[2] van Gijn, J., Kerr, R.S. and Rinkel, G.J. (2007) Subarachnoid Haemorrhage. The Lancet, 369, 306-318. [Google Scholar] [CrossRef] [PubMed]
[3] Hop, J.W., Rinkel, G.J.E., Algra, A. and van Gijn, J. (1997) Case-Fatality Rates and Functional Outcome after Subarachnoid Hemorrhage: A Systematic Review. Stroke, 28, 660-664. [Google Scholar] [CrossRef] [PubMed]
[4] Feigin, V.L., Lawes, C.M., Bennett, D.A., Barker-Collo, S.L. and Parag, V. (2009) Worldwide Stroke Incidence and Early Case Fatality Reported in 56 Population-Based Studies: A Systematic Review. The Lancet Neurology, 8, 355-369. [Google Scholar] [CrossRef] [PubMed]
[5] Korja, M., Lehto, H., Juvela, S. and Kaprio, J. (2016) Incidence of Subarachnoid Hemorrhage Is Decreasing Together with Decreasing Smoking Rates. Neurology, 87, 1118-1123. [Google Scholar] [CrossRef] [PubMed]
[6] Korja, M., Silventoinen, K., Laatikainen, T., Jousilahti, P., Salomaa, V. and Kaprio, J. (2013) Cause-Specific Mortality of 1-Year Survivors of Subarachnoid Hemorrhage. Neurology, 80, 481-486. [Google Scholar] [CrossRef] [PubMed]
[7] Raimondi, A.J. and Torres, H. (1973) Acute Hydrocephalus as a Complication of Subarachnoid Hemorrhage. Surgical Neurology, 1, 23-26.
[8] Kusske, J.A., Turner, P.T., Ojemann, G.A. and Harris, A.B. (1973) Ventriculostomy for the Treatment of Acute Hydrocephalus Following Subarachnoid Hemorrhage. Journal of Neurosurgery, 38, 591-595. [Google Scholar] [CrossRef] [PubMed]
[9] Vale, F.L., Bradley, E.L. and Fisher, W.S. (1997) The Relationship of Subarachnoid Hemorrhage and the Need for Postoperative Shunting. Journal of Neurosurgery, 86, 462-466. [Google Scholar] [CrossRef] [PubMed]
[10] Rajshekhar, V. and Harbaugh, R.E. (1992) Results of Routine Ventriculostomy with External Ventricular Drainage for Acute Hydrocephalus Following Subarachnoid Haemorrhage. Acta Neurochirurgica, 115, 8-14. [Google Scholar] [CrossRef] [PubMed]
[11] Zaidi, H.A., Montoure, A., Elhadi, A., Nakaji, P., McDougall, C.G., Albuquerque, F.C., et al. (2015) Long-Term Functional Outcomes and Predictors of Shunt-Dependent Hydrocephalus after Treatment of Ruptured Intracranial Aneurysms in the BRAT Trial. Neurosurgery, 76, 608-615. [Google Scholar] [CrossRef] [PubMed]
[12] Suarez-Rivera, O. (1998) Acute Hydrocephalus after Subarachnoid Hemorrhage. Surgical Neurology, 49, 563-565. [Google Scholar] [CrossRef] [PubMed]
[13] de Oliveira, J.G., Beck, J., Setzer, M., Gerlach, R., Vatter, H., Seifert, V., et al. (2007) Risk of Shunt-Dependent Hydrocephalus after Occlusion of Ruptured Intracranial Aneurysms by Surgical Clipping or Endovascular Coiling. Neurosurgery, 61, 924-934. [Google Scholar] [CrossRef] [PubMed]
[14] Paisan, G.M., Ding, D., Starke, R.M., Crowley, R.W. and Liu, K.C. (2017) Shunt-Dependent Hydrocephalus after Aneurysmal Subarachnoid Hemorrhage: Predictors and Long-Term Functional Outcomes. Neurosurgery, 83, 393-402. [Google Scholar] [CrossRef] [PubMed]
[15] Hoh, B.L., Ko, N.U., Amin-Hanjani, S., Chou, S.H., Cruz-Flores, S., Dangayach, N.S., et al. (2023) 2023 Guideline for the Management of Patients with Aneurysmal Subarachnoid Hemorrhage: A Guideline from the American Heart Association/American Stroke Association. Stroke, 54, e314-e370. [Google Scholar] [CrossRef] [PubMed]
[16] Hua, C. and Zhao, G. (2017) Biomarkers in Adult Posthemorrhagic Hydrocephalus. International Journal of Stroke, 12, 574-579. [Google Scholar] [CrossRef] [PubMed]
[17] Fang, Y., Liu, Y., Chen, L., Wang, J., Zhang, J., Zhang, H., et al. (2024) Cerebrospinal Fluid Markers of Neuroinflammation and Coagulation in Severe Cerebral Edema and Chronic Hydrocephalus after Subarachnoid Hemorrhage: A Prospective Study. Journal of Neuroinflammation, 21, Article No. 237. [Google Scholar] [CrossRef] [PubMed]
[18] Dandy, W.E. (1919) Experimental Hydrocephalus. Annals of Surgery, 70, 129-142. [Google Scholar] [CrossRef] [PubMed]
[19] Andeweg, J. (1991) Concepts of Cerebral Venous Drainage and the Aetiology of Hydrocephalus. Journal of Neurology, Neurosurgery & Psychiatry, 54, 830-831. [Google Scholar] [CrossRef] [PubMed]
[20] Orešković, D., Klarica, M. and Vukić, M. (2002) The Formation and Circulation of Cerebrospinal Fluid Inside the Cat Brain Ventricles: A Fact or an Illusion? Neuroscience Letters, 327, 103-106. [Google Scholar] [CrossRef] [PubMed]
[21] Bulat, M. and Klarica, M. (2011) Recent Insights into a New Hydrodynamics of the Cerebrospinal Fluid. Brain Research Reviews, 65, 99-112. [Google Scholar] [CrossRef] [PubMed]
[22] Sakka, L., Coll, G. and Chazal, J. (2011) Anatomy and Physiology of Cerebrospinal Fluid. European Annals of Otorhinolaryngology, Head and Neck Diseases, 128, 309-316. [Google Scholar] [CrossRef] [PubMed]
[23] Thompson, D., Brissette, C.A. and Watt, J.A. (2022) The Choroid Plexus and Its Role in the Pathogenesis of Neurological Infections. Fluids and Barriers of the CNS, 19, Article No. 75. [Google Scholar] [CrossRef] [PubMed]
[24] Chen, Y., Luo, Z., Sun, Y., Li, F., Han, Z., Qi, B., et al. (2022) Exercise Improves Choroid Plexus Epithelial Cells Metabolism to Prevent Glial Cell-Associated Neurodegeneration. Frontiers in Pharmacology, 13, Article 1010785. [Google Scholar] [CrossRef] [PubMed]
[25] Faure, G.C. (2003) Choroid Plexus Ageing of the Brain and Alzheimer S Disease. Frontiers in Bioscience, 8, s515-s521. [Google Scholar] [CrossRef] [PubMed]
[26] Redzic, Z.B., Preston, J.E., Duncan, J.A., Chodobski, A. and Szmydynger‐Chodobska, J. (2005) The Choroid Plexus‐cerebrospinal Fluid System: From Development to Aging. Current Topics in Developmental Biology, 71, 1-52. [Google Scholar] [CrossRef] [PubMed]
[27] Preston, J.E. (2001) Ageing Choroid Plexus‐cerebrospinal Fluid System. Microscopy Research and Technique, 52, 31-37. [Google Scholar] [CrossRef
[28] Jartti, P., Karttunen, A., Jartti, A., Ukkola, V., Sajanti, J. and Pyhtinen, J. (2004) Factors Related to Acute Hydrocephalus after Subarachnoid Hemorrhage. Acta Radiologica, 45, 333-339. [Google Scholar] [CrossRef] [PubMed]
[29] Strahle, J., Garton, H.J.L., Maher, C.O., Muraszko, K.M., Keep, R.F. and Xi, G. (2012) Mechanisms of Hydrocephalus after Neonatal and Adult Intraventricular Hemorrhage. Translational Stroke Research, 3, 25-38. [Google Scholar] [CrossRef] [PubMed]
[30] Klarica, M., Orešković, D., Božić, B., Vukić, M., Butković, V. and Bulat, M. (2009) New Experimental Model of Acute Aqueductal Blockage in Cats: Effects on Cerebrospinal Fluid Pressure and the Size of Brain Ventricles. Neuroscience, 158, 1397-1405. [Google Scholar] [CrossRef] [PubMed]
[31] Karimy, J.K., Zhang, J., Kurland, D.B., Theriault, B.C., Duran, D., Stokum, J.A., et al. (2017) Inflammation-Dependent Cerebrospinal Fluid Hypersecretion by the Choroid Plexus Epithelium in Posthemorrhagic Hydrocephalus. Nature Medicine, 23, 997-1003. [Google Scholar] [CrossRef] [PubMed]
[32] Miller, B.A., Turan, N., Chau, M. and Pradilla, G. (2014) Inflammation, Vasospasm, and Brain Injury after Subarachnoid Hemorrhage. BioMed Research International, 2014, 1-16. [Google Scholar] [CrossRef] [PubMed]
[33] Lauzier, D.C., Jayaraman, K., Yuan, J.Y., Diwan, D., Vellimana, A.K., Osbun, J.W., et al. (2023) Early Brain Injury after Subarachnoid Hemorrhage: Incidence and Mechanisms. Stroke, 54, 1426-1440. [Google Scholar] [CrossRef] [PubMed]
[34] Ostrowski, R.P., Colohan, A.R. and Zhang, J.H. (2006) Molecular Mechanisms of Early Brain Injury after Subarachnoid Hemorrhage. Neurological Research, 28, 399-414. [Google Scholar] [CrossRef] [PubMed]
[35] Sehba, F.A., Schwartz, A.Y., Chereshnev, I. and Bederson, J.B. (2000) Acute Decrease in Cerebral Nitric Oxide Levels after Subarachnoid Hemorrhage. Journal of Cerebral Blood Flow & Metabolism, 20, 604-611. [Google Scholar] [CrossRef] [PubMed]
[36] Li, Y., Wu, P., Bihl, J.C. and Shi, H. (2020) Underlying Mechanisms and Potential Therapeutic Molecular Targets in Blood-Brain Barrier Disruption after Subarachnoid Hemorrhage. Current Neuropharmacology, 18, 1168-1179. [Google Scholar] [CrossRef] [PubMed]
[37] Hayman, E.G., Wessell, A., Gerzanich, V., Sheth, K.N. and Simard, J.M. (2016) Mechanisms of Global Cerebral Edema Formation in Aneurysmal Subarachnoid Hemorrhage. Neurocritical Care, 26, 301-310. [Google Scholar] [CrossRef] [PubMed]
[38] Macdonald, R.L. and Schweizer, T.A. (2017) Spontaneous Subarachnoid Haemorrhage. The Lancet, 389, 655-666. [Google Scholar] [CrossRef] [PubMed]
[39] Shishido, H., Zhang, H., Okubo, S., Hua, Y., Keep, R.F. and Xi, G. (2016) The Effect of Gender on Acute Hydrocephalus after Experimental Subarachnoid Hemorrhage. In: Applegate, R., Chen, G., Feng, H. and Zhang, J., Eds., Brain Edema XVI, Springer, 335-339. [Google Scholar] [CrossRef] [PubMed]
[40] Demirgil, B.T., Tugcu, B., Postalci, L., Guclu, G., Dalgic, A. and Oral, Z. (2003) Factors Leading to Hydrocephalus after Aneurysmal Sub-Arachnoid Hemorrhage. Minimally Invasive Neurosurgery, 46, 344-348.
[41] Rincon, F., Gordon, E., Starke, R.M., Buitrago, M.M., Fernandez, A., Schmidt, J.M., et al. (2010) Predictors of Long-Term Shunt-Dependent Hydrocephalus after Aneurysmal Subarachnoid Hemorrhage. Journal of Neurosurgery, 113, 774-780. [Google Scholar] [CrossRef] [PubMed]