Boehme Amelia K, Kumar Andre D, Lyerly Michael J, Gillette Michael A, Siegler James E, Albright Karen C, Beasley T Mark, Martin-Schild Sheryl
Department of Epidemiology, University of Alabama at Birmingham; Department of Neurology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Stroke Program, Department of Neurology, Tulane University Hospital, New Orleans, Louisiana.
J Stroke Cerebrovasc Dis. 2014 Aug;23(7):1939-43. doi: 10.1016/j.jstrokecerebrovasdis.2014.02.004. Epub 2014 Apr 29.
In the setting of acute ischemic stroke (AIS), leukocytosis has been shown to be an indicator of inflammatory response. Although leukocytosis on admission has been shown to correlate with initial stroke severity in AIS patients, no work has been done to assess if there are differences in transient or persistent leukocytosis in patients without infection. The objective of this study is to determine the clinical significance of persistent versus transient leukocytosis during the early phase of AIS.
Patients who presented with AIS to our center within 48 hours of symptom onset between July 2008 and June 2010 were retrospectively identified by chart review. Patients were included if they had leukocytosis on admission (defined as white blood cell count >11,000/μL based on laboratory reference range values). A logistic regression model was used to evaluate persistent leukocytosis (leukocytosis 48 hours after admission) as a predictor of several outcome measures, including good functional outcome (discharge modified Rankin Scale score of 0-2). Marginal effects were used to estimate the probability of poor functional outcome.
Of the 438 patients screened, 49 had leukocytosis on admission and of those 24 (49%) had persistent leukocytosis. NIHSS score correlated significantly with persistence of leukocytosis (r = .306; P = .0044). More people with transient leukocytosis (leukocytosis lasting <48 hours) had a good functional outcome (44% versus 16%; P = .006). After adjusting for baseline NIHSS score, persistent leukocytosis was not a significant independent predictor of good functional outcome, but showed an association (OR, 2.5; 95% CI, .562-10.7; P = .2322). Persistent leukocytosis after adjusting for age and NIHSS score at admission is associated with a poor functional outcome, but it is not statistically significant (OR, 2.43; 95% CI, .59-9.87; P = .2151). After controlling for age and NIHSS score on admission, for patients with persistent leukocytosis, the probability of having poor functional outcome at discharge was increased by 16 percentage points.
Persistent leukocytosis is associated with higher baseline NIHSS scores. Persistent leukocytosis is tightly linked with baseline stroke severity and is associated with poor patient outcomes. Our study found that patients with persistent leukocytosis are more likely to present with severe strokes and maintain a high NIHSS score at 24 hours after admission, unlike patients without leukocytosis or patients with transient leukocytosis. Furthermore, it appears that persistent leukocytosis outside the setting of an infection negatively impacts the short-term functional outcome of AIS patients. Identifying patients with persistent leukocytosis could help to prognosticate and target patients that may benefit from future anti-inflammatory interventions.
在急性缺血性卒中(AIS)的情况下,白细胞增多已被证明是炎症反应的一个指标。虽然入院时白细胞增多已被证明与AIS患者的初始卒中严重程度相关,但尚未开展工作来评估无感染患者的短暂性或持续性白细胞增多是否存在差异。本研究的目的是确定AIS早期持续性与短暂性白细胞增多的临床意义。
通过病历回顾,对2008年7月至2010年6月期间在症状发作后48小时内就诊于我们中心的AIS患者进行回顾性识别。如果患者入院时白细胞增多(根据实验室参考范围值定义为白细胞计数>11,000/μL),则纳入研究。使用逻辑回归模型评估持续性白细胞增多(入院后48小时白细胞增多)作为几种结局指标的预测因素,包括良好的功能结局(出院时改良Rankin量表评分为0 - 2)。边际效应用于估计功能结局不良的概率。
在筛查的438例患者中,49例入院时白细胞增多,其中24例(49%)有持续性白细胞增多。美国国立卫生研究院卒中量表(NIHSS)评分与白细胞增多的持续性显著相关(r = 0.306;P = 0.0044)。短暂性白细胞增多(持续时间<48小时)的患者有更多获得良好功能结局的(44%对16%;P = 0.006)。在调整基线NIHSS评分后,持续性白细胞增多不是良好功能结局的显著独立预测因素,但显示出相关性(比值比,2.5;95%置信区间,0.562 - 10.7;P = 0.2322)。在调整年龄和入院时NIHSS评分后,持续性白细胞增多与功能结局不良相关,但无统计学意义(比值比,2.43;95%置信区间,0.59 - 9.87;P = 0.2151)。在控制年龄和入院时NIHSS评分后,对于持续性白细胞增多的患者,出院时功能结局不良的概率增加了16个百分点。
持续性白细胞增多与较高的基线NIHSS评分相关。持续性白细胞增多与基线卒中严重程度密切相关,并与患者预后不良相关。我们的研究发现,与无白细胞增多或短暂性白细胞增多的患者不同,持续性白细胞增多的患者更可能出现严重卒中,并在入院后24小时维持较高的NIHSS评分。此外,似乎在无感染情况下的持续性白细胞增多对AIS患者的短期功能结局有负面影响。识别持续性白细胞增多的患者有助于预测并确定可能从未来抗炎干预中获益的患者。