Outcomes and Recurrence Rates Among Patients With Provoked and Cryptogenic Cerebral Venous Thrombosis: Analysis of the ACTION CVT.

IF 2.3 Q3 CLINICAL NEUROLOGY Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200381
Sami Al Kasab, Eyad Almallouhi, Liqi Shu, Kimberly P Kicielinski, Setareh Salehi Omran, David S Liebeskind, Adeel S Zubair, Maria C Vedovati, Maurizio Paciaroni, Kateryna Antonenko, Mirjam R Heldner, Adam de Havenon, Nils Henninger, Shadi Yaghi
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Abstract

Background and objectives: Cerebral venous thrombosis (CVT) is a rare cause of stroke. While the standard treatment is anticoagulation, the type and duration of anticoagulation depends on the underlying etiology. This study aims to identify prevalence, risk factors, and recurrent venous thromboembolism (VTE) rates among patients with idiopathic (cryptogenic) CVT and CVT provoked by transient (peripartum, hormonal treatment, infection, trauma) and persistent (cancer, thrombophilia) factors.

Methods: We used the ACTION-CVT retrospective database which included consecutive patients who were treated for CVT in 27 stroke centers in the United States, Europe, and New Zealand from January 2015 to December 2020. We compared baseline characteristics and outcomes of patients with cryptogenic, transient provoked (TP) and those with persistent provoked (PP) CVT. Baseline characteristics was compared between the groups using χ2 test, t test, or Mann-Whitney U test as appropriate, followed by multivariable regression. We used Kaplan-Meier survival analysis to assess outcome occurrence. We used interaction analysis and Cox regression to assess the risks of recurrent VTE in patients with CVT.

Results: Among 1,025 included participants with CVT, 510 (49.8%) had no identified risk factor (cryptogenic), 363 (35.4%) had at least one transient provoking factor, and 152 (14.8%) had a persistent provoking factor. Patients with TP CVT were younger (p = 0.003) and more likely to be female patients (p < 0.001). When compared with patients with TP CVT, the risk of recurrent VTE was greater in patients with PP CVT (HR 2.59, 95% CI 1.29-5.22, p = 0.008) and nonsignificantly elevated in patients with cryptogenic CVT (HR 1.85. 95% CI 0.98-3.59, p = 0.059). In the interaction analysis, there was a trend toward higher rate of recurrent VTE in female patients with cryptogenic CVT and male patients with PP CVT.

Discussion: In this multicenter study, we found that outcomes of CVT differed depending on the underlying etiology. The risk of recurrent VTE in the PP and cryptogenic CVTs may be influenced by sex.

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诱发性和隐源性脑静脉血栓患者的预后和复发率:ACTION CVT分析。
背景和目的:脑静脉血栓(CVT)是中风的罕见病因。虽然标准治疗是抗凝,但抗凝的类型和持续时间取决于潜在的病因。本研究旨在确定特发性(隐源性)CVT 患者以及一过性(围产期、激素治疗、感染、创伤)和持续性(癌症、血栓性疾病)因素引起的 CVT 患者的患病率、风险因素和复发性静脉血栓栓塞(VTE)率:我们使用了 ACTION-CVT 回顾性数据库,其中包括 2015 年 1 月至 2020 年 12 月期间在美国、欧洲和新西兰 27 个卒中中心接受 CVT 治疗的连续患者。我们比较了隐源性、一过性诱发(TP)和持续性诱发(PP)CVT 患者的基线特征和预后。我们采用χ2检验、t检验或Mann-Whitney U检验对两组患者的基线特征进行比较,然后进行多变量回归。我们使用 Kaplan-Meier 生存分析来评估结果发生率。我们采用交互分析和 Cox 回归评估 CVT 患者复发 VTE 的风险:在 1025 名 CVT 患者中,510 人(49.8%)没有确定的风险因素(隐源性),363 人(35.4%)至少有一个短暂的诱发因素,152 人(14.8%)有一个持续的诱发因素。TP CVT 患者更年轻(p = 0.003),更可能是女性患者(p < 0.001)。与 TP CVT 患者相比,PP CVT 患者复发 VTE 的风险更高(HR 2.59,95% CI 1.29-5.22,p = 0.008),而隐源性 CVT 患者复发 VTE 的风险无显著升高(HR 1.85,95% CI 0.98-3.59,p = 0.059)。在交互分析中,女性隐源性 CVT 患者和男性 PP CVT 患者的复发性 VTE 发生率呈上升趋势:在这项多中心研究中,我们发现CVT的预后因病因而异。在 PP 型和隐源性 CVT 中,复发性 VTE 的风险可能受性别影响。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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