Impact of flat-panel detector CT distal occlusion tracker (DOT) sign on early neurological deterioration after endovascular thrombectomy

医学 放射科 符号(数学) 闭塞 危险分层 探测器 核医学 计算机断层摄影术 中风风险 选择(遗传算法) 冲程(发动机) 工件(错误) 磁共振成像 风险评估
作者
Valentina Tudisco,Michele Romoli,Francesca Giannini,Beatrice Severi,Alessandro Polimene,F. Biondi,Davide Vicari,Ludovica Ferraù,Francesco Cordici,Federica Nicoletta Sepe,Sebastiano Giacomozzi,Giuseppe Borzì,Cristina Dell’Aera,Alberto Di Ruzza,Elvis Lafe,Fabrizio Giammello,António Toscano,Marco Longoni,Maria Ruggiero
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:97 (3): jnnp-2025
标识
DOI:10.1136/jnnp-2025-336783
摘要

BACKGROUND: A relevant proportion of patients experience early neurological deterioration (END) despite technically successful recanalisation for acute ischaemic stroke. We prospectively assessed the distal occlusion tracker (DOT) sign, detectable on flat-panel detector CT (FPDCT) immediately after mechanical thrombectomy (MT), to identify distal embolisation or incomplete microvascular reperfusion associated with END. METHODS: Our prospective multicentre observational study included consecutive patients with anterior circulation stroke treated with MT between January 2022 and December 2023 at two large comprehensive stroke centres. Post-procedural FPDCT was used to assess the presence of the DOT sign. The primary outcome was END. Secondary outcomes included 3 month functional outcome, 24 hour Alberta Stroke Program Early CT Score (ASPECTS) and haemorrhagic complications. Associations between the DOT sign and clinical-radiological variables, including Thrombolysis in Cerebral Infarction recanalization score (TICI), were evaluated through univariate and multivariate logistic regression. RESULTS: The DOT sign was present in 31% of cases and was associated with higher rates of END (25% vs 12.8%, p=0.003), lower recanalisation success (79.3% vs 91.1%, p<0.001) and greater prevalence of cortical hyperattenuation. On multivariate analysis, independent predictors of END included the DOT sign (aOR=2.07, p=0.040), cardioembolic aetiology, baseline National Institutes of Health Stroke Scale, FPDCT ASPECTS and unsuccessful reperfusion. The DOT sign led to reclassification of half of TICI 3 cases to lower grades. No significant difference in symptomatic intracranial haemorrhage was observed between groups. CONCLUSIONS: The DOT sign is a practical post-thrombectomy imaging marker helping in the prediction of END. Integrating the DOT sign assessment may help in the stratification of tissues at risk and risk of END, adding to the selection of patients for adjunctive intra-arterial medications.

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