来源不明的栓塞性卒中患者卒中复发评分的独立外部验证。

Q2 Medicine
Thies Ingwersen, Manuel C Olma, Eckhard Schlemm, Carola Mayer, Bastian Cheng, Serdar Tütüncü, Paulus Kirchhof, Roland Veltkamp, Joachim Röther, Ulrich Laufs, Darius G Nabavi, George Ntaios, Matthias Endres, Karl Georg Haeusler, Götz Thomalla
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引用次数: 0

摘要

背景:不明来源栓塞性卒中(ESUS)在缺血性卒中中占很大比例。脑卒中复发评分已被证明可以根据临床和影像学特征预测ESUS患者脑卒中复发的风险。本研究旨在使用随机对照试验的数据从外部验证ESUS复发评分的性能。方法:验证数据集由MonDAFIS研究的PreDAFIS子研究中登记的具有可用磁共振成像(MRI)数据的合格中风患者组成。该评分使用三个变量计算:年龄(35岁后每十年1分)、白质高信号的存在(2分)和多区域缺血性卒中(3分)。按照原始出版物中的描述,将患者分为风险组。使用标准判别和校准方法对模型进行了评估。结果:1054例患者中,241例(22.9%)为ESUS。由于MRI质量不足,三名患者被排除在外,剩下238名患者(中位年龄65.5岁[IQR20.75],39%为女性)进行分析。其中,30名(13%)患者在383个患者年的随访期内经历了复发性缺血性中风或短暂性脑缺血发作(TIA),相应的发病率为7.8/100个患者年(95%CI 5.3-11.2) ≥ 7例患者的卒中复发风险是评分为0-4的患者的2.46倍(危险比(HR),95%CI 1.02-5.93)。低(0-4)、中(5-6)和高危组中风复发的累积概率(≥ 7) 分别为9%、13%和23%(log-rank检验,χ2 = 4.2,p = 0.1)。结论:已公布评分系统的外部验证支持阈值 ≥ 7用于识别脑卒中复发高危的ESUS患者。然而,可能需要进一步调整,以提高模型在独立队列中的性能。风险评分的使用可能有助于指导ESUS患者的扩展诊断和二级预防的进一步试验。试验注册:临床试验,NCT02204267。2014年7月30日注册,https://clinicaltrials.gov/ct2/show/NCT02204267。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Independent external validation of a stroke recurrence score in patients with embolic stroke of undetermined source.

Independent external validation of a stroke recurrence score in patients with embolic stroke of undetermined source.

Independent external validation of a stroke recurrence score in patients with embolic stroke of undetermined source.

Independent external validation of a stroke recurrence score in patients with embolic stroke of undetermined source.

Background: Embolic stroke of undetermined source (ESUS) accounts for a substantial proportion of ischaemic strokes. A stroke recurrence score has been shown to predict the risk of recurrent stroke in patients with ESUS based on a combination of clinical and imaging features. This study aimed to externally validate the performance of the ESUS recurrence score using data from a randomized controlled trial.

Methods: The validation dataset consisted of eligible stroke patients with available magnetic resonance imaging (MRI) data enrolled in the PreDAFIS sub-study of the MonDAFIS study. The score was calculated using three variables: age (1 point per decade after 35 years), presence of white matter hyperintensities (2 points), and multiterritorial ischaemic stroke (3 points). Patients were assigned to risk groups as described in the original publication. The model was evaluated using standard discrimination and calibration methods.

Results: Of the 1054 patients, 241 (22.9%) were classified as ESUS. Owing to insufficient MRI quality, three patients were excluded, leaving 238 patients (median age 65.5 years [IQR 20.75], 39% female) for analysis. Of these, 30 (13%) patients experienced recurrent ischaemic stroke or transient ischemic attack (TIA) during a follow-up period of 383 patient-years, corresponding to an incidence rate of 7.8 per 100 patient-years (95% CI 5.3-11.2). Patients with an ESUS recurrence score value of ≥ 7 had a 2.46 (hazard ratio (HR), 95% CI 1.02-5.93) times higher risk of stroke recurrence than patients with a score of 0-4. The cumulative probability of stroke recurrence in the low-(0-4), intermediate-(5-6), and high-risk group (≥ 7) was 9%, 13%, and 23%, respectively (log-rank test, χ2 = 4.2, p = 0.1).

Conclusions: This external validation of a published scoring system supports a threshold of ≥ 7 for identifying ESUS patients at high-risk of stroke recurrence. However, further adjustments may be required to improve the model's performance in independent cohorts. The use of risk scores may be helpful in guiding extended diagnostics and further trials on secondary prevention in patients with ESUS.

Trial registration: Clinical Trials, NCT02204267. Registered 30 July 2014, https://clinicaltrials.gov/ct2/show/NCT02204267 .

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