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立陶宛卒中患者队列中心律失常的高患病率。

High Prevalence of Atrial Fibrillation in a Lithuanian Stroke Patient Cohort.

机构信息

Center of Neurology, Vilnius University, 08661 Vilnius, Lithuania.

Faculty of Medicine, Vilnius University, 03101 Vilnius, Lithuania.

出版信息

Medicina (Kaunas). 2022 Jun 14;58(6):800. doi: 10.3390/medicina58060800.

DOI:10.3390/medicina58060800
PMID:35744063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9230037/
Abstract

Background and Objectives: Atrial fibrillation (AF) is the most common cardiac arrhythmia and is associated with a five-fold increased risk for acute ischemic stroke (AIS). We aimed to estimate the prevalence of AF in a Lithuanian cohort of stroke patients, and its impact on patients regarding case fatality, functional outcome, and health-related quality of life (HRQoL) at 90 days. Materials and Methods: A single-center prospective study was carried out for four non-consecutive months between December 2018 and July 2019 in one of the two comprehensive stroke centers in Eastern Lithuania. A telephone-based follow-up was conveyed at 90 days using the modified Rankin Scale (mRS) and EuroQoL five-dimensional three-level descriptive system (EQ-5D-3L) with a self-rated visual analog scale (EQ-VAS). One-year case fatality was investigated. Results: We included 238 AIS patients with a mean age of 71.4 ± 11.9 years of whom 45.0% were female. A striking 97 (40.8%) AIS patients had a concomitant AF, in 68 (70.1%) of whom the AF was pre-existing. The AIS patients with AF were at a significantly higher risk for a large vessel occlusion (LVO; odds ratio 2.72 [95% CI 1.38−5.49], p = 0.004), and had a more severe neurological impairment at presentation (median NIHSS score (interquartile range): 9 (6−16) vs. 6 (3−9), p < 0.001). The LVO status was only detected in those who had received computed tomography angiography. Fifty-five (80.9%) patients with pre-existing AF received insufficient anticoagulation at stroke onset. All patients received a 12-lead ECG, however, in-hospital 24-h Holter monitoring was only performed in 3.4% of AIS patients without pre-existing AF. Although multivariate analyses found no statistically significant difference in one-year stroke patient survival and favorable functional status (mRS 0−2) at 90 days, when adjusted for age, gender, reperfusion treatment, baseline functional status, and baseline NIHSS, stroke patients with AF had a significantly poorer self-perceived HRQoL, indicated by a lower EQ-VAS score (regression coefficient ± standard error: β = −11.776 ± 4.850, p = 0.017). Conclusions: In our single-center prospective observational study in Lithuania, we found that 40.8% of AIS patients had a concomitant AF, were at a higher risk for an LVO, and had a significantly poorer self-perceived HRQoL at 90 days. Despite the high AF prevalence, diagnostic tools for subclinical AF were greatly underutilized.

摘要

背景与目的

心房颤动(AF)是最常见的心律失常,发生急性缺血性卒中(AIS)的风险增加 5 倍。我们旨在评估立陶宛卒中患者队列中 AF 的患病率,并评估其对患者病死率、功能结局和 90 天健康相关生活质量(HRQoL)的影响。

材料与方法

2018 年 12 月至 2019 年 7 月,在立陶宛东部的 2 个综合卒中中心之一进行了一项为期 4 个月的单中心前瞻性研究。通过改良 Rankin 量表(mRS)和 EuroQoL 五维三水平描述性系统(EQ-5D-3L)与自我评定视觉模拟量表(EQ-VAS)进行了 90 天的电话随访。调查了 1 年的病死率。

结果

我们纳入了 238 例平均年龄为 71.4±11.9 岁的 AIS 患者,其中 45.0%为女性。令人惊讶的是,97(40.8%)例 AIS 患者同时存在 AF,其中 68(70.1%)例患者的 AF 是预先存在的。AF 合并 AIS 的 AIS 患者发生大血管闭塞(LVO)的风险显著增加(比值比 2.72[95%可信区间 1.38-5.49],p=0.004),且入院时神经功能损伤更严重(中位数 NIHSS 评分[四分位距]:9[6-16] vs. 6[3-9],p<0.001)。LVO 状态仅在接受 CT 血管造影的患者中被发现。55(80.9%)例预先存在 AF 的患者在卒中发作时未接受充分抗凝治疗。所有患者均接受了 12 导联心电图检查,但只有 3.4%的无预先存在 AF 的 AIS 患者进行了院内 24 小时动态心电图监测。尽管多变量分析发现,在 90 天时,AF 对卒中患者的 1 年生存率和良好的功能状态(mRS 0-2)没有统计学意义上的差异,但在调整年龄、性别、再灌注治疗、基线功能状态和基线 NIHSS 后,AF 合并卒中患者的自我感知 HRQoL 显著更差,表现为 EQ-VAS 评分较低(回归系数±标准误差:β=-11.776±4.850,p=0.017)。

结论

在我们立陶宛的单中心前瞻性观察性研究中,我们发现 40.8%的 AIS 患者存在合并性 AF,发生 LVO 的风险更高,且在 90 天时自我感知 HRQoL 显著更差。尽管 AF 的患病率很高,但亚临床 AF 的诊断工具的利用率却大大降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e90/9230037/896217ce454d/medicina-58-00800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e90/9230037/b8f064ad2fb8/medicina-58-00800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e90/9230037/896217ce454d/medicina-58-00800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e90/9230037/b8f064ad2fb8/medicina-58-00800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e90/9230037/896217ce454d/medicina-58-00800-g002.jpg

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