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Delayed perihematomal hypoperfusion is associated with poor outcome in intracerebral haemorrhage

改良兰金量表 医学 置信区间 脑血流 灌注 优势比 灌注扫描 内科学 脑出血 混淆 心脏病学 前瞻性队列研究 逻辑回归 麻醉 核医学 蛛网膜下腔出血 缺血 缺血性中风
作者
Andrea Morotti,Giorgio Busto,Grégoire Boulouis,Elisa Scola,Andrea Bernardoni,Alessandro Fiorenza,Tommaso Amadori,Federico Carbone,Ilaria Casetta,Fabrizio Montecucco,Enrico Fainardi
出处
期刊:European Journal of Clinical Investigation [Wiley]
卷期号:52 (4) 被引量:9
标识
DOI:10.1111/eci.13696
摘要

The aim of this study was to characterize the temporal evolution and prognostic significance of perihematomal perfusion in acute intracerebral haemorrhage (ICH).A single-centre prospective cohort of patients with primary spontaneous ICH receives computed tomography perfusion (CTP) within 6 h from onset (T0) and at 7 days (T7). Cerebral blood flow (CBF), cerebral blood volume (CBV) and mean transit time (MTT) were measured in the manually outlined perihematomal low-density area. Poor functional prognosis (modified Rankin Scale 3-6) at 90 days was the outcome of interest, and predictors were explored with multivariable logistic regression.A total of 150 patients were studied, of whom 52 (34.7%) had a mRS 3-6 at 90 days. Perihematomal perfusion decreased from T0 to T7 in all patients, but the magnitude of CBF and CBV reduction was larger in patients with unfavourable outcome (median CBF change -7.8 vs. -6.0 ml/100 g/min, p < .001, and median CBV change -0.5 vs. -0.4 ml/100 g, p = .010, respectively). This finding remained significant after adjustment for confounders (odds ratio [OR] for 1 ml/100 g/min CBF reduction: 1.33, 95% confidence interval [CI] (1.15-1.55), p < .001; OR for 0.1 ml/100 g CBV reduction: 1.67, 95% CI 1.18-2.35, p = .004). The presence of CBF < 20 ml/100 g/min at T7 was then demonstrated as an independent predictor of poor functional outcome (adjusted OR: 2.45, 95% CI 1.08-5-54, p = .032).Perihaemorrhagic hypoperfusion becomes more severe in the days following acute ICH and is independently associated with poorer outcome. Understanding the underlying biological mechanisms responsible for delayed decrease in perihematomal perfusion is a necessary step towards outcome improvement in patients with ICH.
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