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血管内卒中治疗期间白质病变对阿司匹林和普通肝素的效应修饰作用。

White matter lesion effect modification of aspirin and unfractionated heparin during endovascular stroke treatment.

作者信息

van Poppel Laura M, de Vries Lucas, Mojtahedi Mahsa, van Voorst Henk, Konduri Praneeta R, van de Graaf Rob A, van der Steen Wouter, Martou Laura, Bentley Paul, Marquering Henk A, Emmer Bart J, Majoie Charles B L M

机构信息

Department of Radiology and Nuclear Medicine, Amsterdam UMC, Amsterdam, The Netherlands.

Department of Biomedical Engineering and Physics, Amsterdam UMC, Amsterdam, The Netherlands.

出版信息

Insights Imaging. 2025 Oct 22;16(1):224. doi: 10.1186/s13244-025-02095-2.

Abstract

OBJECTIVES

Periprocedural aspirin or unfractionated heparin during endovascular treatment in acute ischemic stroke increases symptomatic intracranial hemorrhage (sICH) risk without improving functional outcome. White matter lesions (WMLs) are associated with higher sICH risk and poor functional outcome following stroke. We aimed to assess whether WML volume modifies the effect of aspirin or heparin.

MATERIALS AND METHODS

In this post-hoc analysis of the MR CLEAN-MED trial, WML volume was automatically determined using deep learning-based segmentation on baseline non-contrast CT scans. Outcomes included good functional outcome (modified Rankin Scale 0-2 at 90 days), any ICH, asymptomatic ICH (aICH), and sICH. Patients received either aspirin or not, and either heparin or not. Multivariable logistic regression evaluated treatment effect and effect modification.

RESULTS

Of 628 patients, 614 with baseline CT were included. Median WML volume was 0.59 mL without significant differences between treatment arms. WML volume significantly modified the effect of aspirin on sICH (p = 0.01), but not on functional outcome (p = 0.95), any ICH (p = 0.52), or aICH (p = 0.30). Aspirin was associated with increased sICH risk, which decreased with increasing WML volume (aOR 0.96 [95% CI: 0.93-0.99] per 1 mL). For patients with large WML volumes, aspirin showed no significant effect on sICH risk. The effect of heparin on functional outcome, any ICH, aICH, and sICH was not modified by WML volume (p = 0.53, p = 0.26, p = 0.08, p = 0.63, respectively).

CONCLUSIONS

WML volume significantly modified the effect of aspirin on sICH risk, with aspirin-associated risk decreasing as WML volume increased. WML volume did not modify the effect of aspirin or heparin on other outcomes.

CRITICAL RELEVANCE STATEMENT

WML volume on non-contrast CT modifies the effect of aspirin during endovascular thrombectomy on sICH risk, yet no WML-based patient subgroup showed save benefits from periprocedural aspirin or heparin treatment.

KEY POINTS

Periprocedural aspirin and unfractionated heparin during endovascular treatment cause a higher hemorrhage risk. WML volume is associated with worse functional outcome and WML volume significantly modifies the effect of aspirin on symptomatic hemorrhage risk, with aspirin-associated risk decreasing with increasing WML volume. No WML-volume-based patient subgroup was identified where aspirin or heparin treatment demonstrated safe clinical benefit.

摘要

目的

急性缺血性卒中血管内治疗期间使用围手术期阿司匹林或普通肝素会增加症状性颅内出血(sICH)风险,且无法改善功能结局。白质病变(WMLs)与卒中后较高的sICH风险及不良功能结局相关。我们旨在评估WML体积是否会改变阿司匹林或肝素的作用。

材料与方法

在这项对MR CLEAN-MED试验的事后分析中,利用基于深度学习的分割方法在基线非增强CT扫描上自动测定WML体积。结局包括良好功能结局(90天时改良Rankin量表评分为0-2)、任何颅内出血(ICH)、无症状ICH(aICH)和sICH。患者接受了阿司匹林或未接受阿司匹林治疗,以及肝素或未接受肝素治疗。多变量逻辑回归评估治疗效果及效应修正。

结果

628例患者中,纳入了614例有基线CT的患者。WML体积中位数为0.59 mL,各治疗组之间无显著差异。WML体积显著改变了阿司匹林对sICH的作用(p = 0.01),但对功能结局(p = 0.95)、任何ICH(p = 0.52)或aICH(p = 0.30)无影响。阿司匹林与sICH风险增加相关,该风险随WML体积增加而降低(每1 mL的调整后比值比为0.96 [95%可信区间:0.93-0.99])。对于WML体积大的患者,阿司匹林对sICH风险无显著影响。肝素对功能结局、任何ICH、aICH和sICH的作用未被WML体积改变(分别为p = 0.53、p = 0.26、p = 0.08、p = 0.63)。

结论

WML体积显著改变了阿司匹林对sICH风险的作用,随着WML体积增加,阿司匹林相关风险降低。WML体积未改变阿司匹林或肝素对其他结局的作用。

关键相关性声明

非增强CT上的WML体积改变了血管内血栓切除术期间阿司匹林对sICH风险的作用,但没有基于WML的患者亚组显示围手术期阿司匹林或肝素治疗有安全益处。

要点

血管内治疗期间围手术期使用阿司匹林和普通肝素会导致更高的出血风险。WML体积与更差的功能结局相关,且WML体积显著改变了阿司匹林对症状性出血风险的作用,随着WML体积增加,阿司匹林相关风险降低。未识别出阿司匹林或肝素治疗显示有安全临床益处的基于WML体积的患者亚组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19af/12546164/4463321c3eb7/13244_2025_2095_Fig1_HTML.jpg

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