Boned Sandra, Padroni Marina, Rubiera Marta, Tomasello Alejandro, Coscojuela Pilar, Romero Nicolás, Muchada Marián, Rodríguez-Luna David, Flores Alan, Rodríguez Noelia, Juega Jesús, Pagola Jorge, Alvarez-Sabin José, Molina Carlos A, Ribó Marc
Stroke Unit, Department of Neurology, Vall d'Hebron University Hospital, Vall d'Hebron Research Institute, Barcelona, Spain.
Departament de Medicina, Universitat Autónoma de Barcelona, Barcelona, Spain.
J Neurointerv Surg. 2017 Jan;9(1):66-69. doi: 10.1136/neurintsurg-2016-012494. Epub 2016 Aug 26.
Identifying infarct core on admission is essential to establish the amount of salvageable tissue and indicate reperfusion therapies. Infarct core is established on CT perfusion (CTP) as the severely hypoperfused area, however the correlation between hypoperfusion and infarct core may be time-dependent as it is not a direct indicator of tissue damage. This study aims to characterize those cases in which the admission core lesion on CTP does not reflect an infarct on follow-up imaging.
We studied patients with cerebral large vessel occlusion who underwent CTP on admission but received endovascular thrombectomy based on a non-contrast CT Alberta Stroke Program Early CT Score (ASPECTS) >6. Admission infarct core was measured on initial cerebral blood volume (CBV) CTP and final infarct on follow-up CT. We defined ghost infarct core (GIC) as initial core minus final infarct >10 mL.
79 patients were studied. Median National Institutes of Health Stroke Scale (NIHSS) score was 17 (11-20), median time from symptoms to CTP was 215 (87-327) min, and recanalization rate (TICI 2b-3) was 77%. Thirty patients (38%) presented with a GIC >10 mL. GIC >10 mL was associated with recanalization (TICI 2b-3: 90% vs 68%; p=0.026), admission glycemia (<185 mg/dL: 42% vs 0%; p=0.028), and time to CTP (<185 min: 51% vs >185 min: 26%; p=0.033). An adjusted logistic regression model identified time from symptom to CTP imaging <185 min as the only predictor of GIC >10 mL (OR 2.89, 95% CI 1.04 to 8.09). At 24 hours, clinical improvement was more frequent in patients with GIC >10 mL (66.6% vs 39%; p=0.017).
CT perfusion may overestimate final infarct core, especially in the early time window. Selecting patients for reperfusion therapies based on the CTP mismatch concept may deny treatment to patients who might still benefit from reperfusion.
入院时识别梗死核心对于确定可挽救组织的量及指导再灌注治疗至关重要。梗死核心在CT灌注成像(CTP)上被定义为严重灌注不足的区域,然而,灌注不足与梗死核心之间的相关性可能随时间变化,因为它并非组织损伤的直接指标。本研究旨在描述那些CTP上的入院核心病灶在随访成像时未显示为梗死的病例特征。
我们研究了大脑大血管闭塞患者,这些患者入院时接受了CTP检查,但基于非增强CT艾伯塔卒中项目早期CT评分(ASPECTS)>6接受了血管内血栓切除术。入院时梗死核心通过初始脑血容量(CBV)CTP测量,随访CT测量最终梗死灶。我们将幽灵梗死核心(GIC)定义为初始核心减去最终梗死灶>10 mL。
共研究了79例患者。美国国立卫生研究院卒中量表(NIHSS)评分中位数为17(11 - 20),症状出现至CTP的时间中位数为215(87 - 327)分钟,再通率(TICI 2b - 3)为77%。30例患者(38%)出现GIC>10 mL。GIC>10 mL与再通(TICI 2b - 3:90%对68%;p = 0.026)、入院时血糖水平(<185 mg/dL:42%对0%;p = 0.028)以及至CTP的时间(<I85分钟:51%对>185分钟:26%;p = 0.033)相关。校正后的逻辑回归模型确定症状至CTP成像时间<185分钟是GIC>10 mL的唯一预测因素(OR 2.89,95%CI 1.04至8.09)。在24小时时,GIC>10 mL的患者临床改善更常见(66.6%对39%;p = 0.017)。
CT灌注可能高估最终梗死核心,尤其是在早期时间窗内。基于CTP不匹配概念选择患者进行再灌注治疗可能会使仍可从再灌注中获益的患者得不到治疗。