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小脑梗死以及与延迟就诊和误诊相关的因素

Cerebellar Infarction and Factors Associated with Delayed Presentation and Misdiagnosis.

作者信息

Calic Zeljka, Cappelen-Smith Cecilia, Anderson Craig S, Xuan Wei, Cordato Dennis J

机构信息

Department of Neurophysiology, Liverpool Hospital, Liverpool, N.S.W., Australia.

出版信息

Cerebrovasc Dis. 2016;42(5-6):476-484. doi: 10.1159/000448899. Epub 2016 Aug 27.

Abstract

BACKGROUND AND PURPOSE

The diagnosis of cerebellar infarction (CBI) is often challenging due to non-specific or subtle presenting symptoms and signs. We aimed to determine whether a common syndromic cluster of symptoms, signs or vascular risk factors were associated with delayed presentation or misdiagnosis to an Emergency Department (ED). The degree of misdiagnosis between ED and neurology physicians and the influence of delayed presentation or misdiagnosis on outcome were also investigated.

METHODS

A prospective study of CBI patients at a large tertiary-referral hospital with a comprehensive stroke service. Data are reported with OR and 95% CIs.

RESULTS

Of 115 consecutive CBI patients (mean age ± SD 66 ± 14 years, 51% male), infarction was isolated to the cerebellum in 46%; the remainder had additional vascular territory involvement ('mixed CBI'). Most patients (n = 79, 69%) had a mild stroke (National Institute of Health Stroke Scale score ≤4), and tended to present late to ED (>4.5 h; p = 0.05). Dysarthria (OR 3.9, 95% CI 1.6-9.6, p = 0.003) and prior history of atrial fibrillation (AF; OR 3.0, 95% CI 1.02-9.1, p = 0.047) predicted early presentation (<4.5 h; in 52%). Neurological signs (as determined by neurology physicians) were more commonly absent in patients with isolated CBI (OR 4.0, 95% CI 1.2-13.3, p = 0.03) who were also less likely to receive acute stroke therapy (p = 0.03). ED physicians detected fewer neurological signs than neurology physicians (mean 1 vs. 2 signs, p < 0.001), and 34% of CBI patients were misdiagnosed, with peripheral vestibulopathy being the most common alternative diagnosis. Nausea and vomiting (OR 2.3, 95% CI 1.01-5.5, p = 0.046), absence of neurological signs as determined by ED physicians (OR 3.5, 95% CI 1.5-8.0, p = 0.003) and isolated CBI (OR 2.2, 95% CI 1.01-4.8, p = 0.047) correlated with misdiagnosis. Vascular territory involvement did not correlate with time to presentation or misdiagnosis. At 3 months, 65% of patients were functionally independent (modified Rankin Scale (mRS) score 0-2). History of hypertension (p = 0.008), AF (p = 0.012), mixed CBI (p = 0.004) and in-hospital stroke-related complications (p < 0.001) were associated with patients having a poor outcome (mRS ≥3). At 3 months, mortality was 16%, and AF was the only predictor of death (OR 3.2, 95% CI 1.1-8.9, p = 0.03). Late presentation to ED and misdiagnosis did not significantly influence 3-month functional outcome.

CONCLUSIONS

Late ED presentation and misdiagnosis are common for CBI. Timely diagnosis of CBI may increase opportunity for acute stroke therapies and reduce risk of stroke-related complications.

摘要

背景与目的

由于小脑梗死(CBI)的症状和体征不具特异性或较为隐匿,其诊断往往具有挑战性。我们旨在确定是否存在一组常见的症状、体征或血管危险因素综合征与急诊科(ED)的延迟就诊或误诊相关。同时还研究了急诊科医生与神经科医生之间的误诊程度以及延迟就诊或误诊对预后的影响。

方法

在一家提供全面卒中服务的大型三级转诊医院对CBI患者进行前瞻性研究。数据以比值比(OR)和95%可信区间(CI)报告。

结果

在115例连续的CBI患者中(平均年龄±标准差66±14岁,51%为男性),46%的患者梗死局限于小脑;其余患者有其他血管区域受累(“混合型CBI”)。大多数患者(n = 79,69%)为轻度卒中(美国国立卫生研究院卒中量表评分≤4),且往往延迟就诊于急诊科(>4.5小时;p = 0.05)。构音障碍(OR 3.9,95% CI 1.6 - 9.6,p = 0.003)和房颤(AF)既往史(OR 3.0,95% CI 1.02 - 9.1,p = 0.047)提示早期就诊(<4.5小时;占52%)。孤立性CBI患者更常无神经体征(由神经科医生判定,OR 4.0,95% CI 1.2 - 13.3,p = 0.03),且接受急性卒中治疗的可能性也较小(p = 0.03)。急诊科医生检测到的神经体征少于神经科医生(平均1个对2个体征,p < 0.001),34%的CBI患者被误诊,最常见的误诊为外周前庭病变。恶心和呕吐(OR 2.3,95% CI 1.01 - 5.5,p = 0.046)、急诊科医生判定无神经体征(OR 3.5,95% CI 1.5 - 8.0,p = 0.003)和孤立性CBI(OR 2.2,95% CI 1.01 - 4.8,p = 0.047)与误诊相关。血管区域受累与就诊时间或误诊无关。3个月时,65%的患者功能独立(改良Rankin量表(mRS)评分0 - 2)。高血压病史(p = 0.008)、房颤(p = 0.012)、混合型CBI(p = 0.004)和院内卒中相关并发症(p < 0.001)与患者预后不良(mRS≥3)相关。3个月时,死亡率为16%,房颤是唯一的死亡预测因素(OR 3.2,95% CI 1.1 - 8.9,p = 0.03)。延迟就诊于急诊科和误诊对3个月功能预后无显著影响。

结论

CBI患者延迟就诊于急诊科和误诊情况常见。及时诊断CBI可能增加急性卒中治疗机会并降低卒中相关并发症风险。

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