医学
改良兰金量表
蛛网膜下腔出血
内科学
倾向得分匹配
入射(几何)
接收机工作特性
回顾性队列研究
贫血
胃肠病学
缺血
缺血性中风
光学
物理
作者
Runting Li,Fa Lin,Yú Chen,Junlin Lu,Heze Han,Li Ma,Yahui Zhao,Debin Yan,Ruinan Li,Jun Yang,Shihao He,Zhipeng Li,Haibin Zhang,Kexin Yuan,Ke Wang,Qiang Hao,Xun Ye,Hao Wang,Hongliang Li,Linlin Zhang
出处
期刊:Neurosurgical Review
[Springer Science+Business Media]
日期:2022-04-02
卷期号:45 (4): 2689-2699
被引量:6
标识
DOI:10.1007/s10143-022-01780-w
摘要
Hemoglobin (HGB), a potent spasmogen, may cause irreversible damage to the brain after aneurysm rupture. However, there is no clinical evidence to reveal the relationship between blood HGB concentrations on admission and the prognosis of patients with aneurysmal subarachnoid hemorrhage (aSAH). We retrospectively reviewed all aSAH patients admitted to our institution between January 2015 and December 2020. Functional outcome was assessed at 90 days after discharge using the modified Rankin scale (mRS). Independent risk factors associated with 90-day unfavorable outcomes were derived from a forward stepwise multivariate analysis. Receiver operating characteristic curve analysis was conducted to identify the best cutoff value of HGB to discriminate 90-day unfavorable outcomes. Then, patients were divided into two groups according to the cutoff value of HGB, and to account for imbalances in baseline characteristics, propensity score matching (PSM) was carried out to assess the impact of HGB on in-hospital complications. A total of 800 aSAH patients without anemia on admission were retrospectively enrolled in this study. Elevated blood HGB (OR = 1.02, 95% CI = 1.00-1.03, p = 0.018) on admission was identified as an independent risk factor associated with 90-day unfavorable outcomes, and the cutoff value was 149.5 g/L. After PSM, patients with an HGB > 149.5 g/L had a higher incidence of in-hospital delayed cerebral ischemia (DCI) (33.9% vs. 22.0%, p = 0.013) and deep vein thrombosis (DVT) (11.9% vs. 4.0%, p = 0.006). Patients with a blood HGB > 149.5 g/L on admission might develop more DCI and DVT during hospitalization, leading to 90-day unfavorable outcomes in aSAH patients. ClinicalTrials.gov Identifier: NCT04785976. 2021/03/05, retrospectively registered.
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