Perfusion Abnormalities on 24-Hour Perfusion Imaging in Patients With Complete Endovascular Reperfusion.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Stroke Pub Date : 2024-09-01 Epub Date: 2024-08-15 DOI:10.1161/STROKEAHA.124.047441
Adnan Mujanovic, Anick Imhof, Shaokai Zheng, Eike I Piechowiak, Bettina L Serrallach, Thomas R Meinel, Tomas Dobrocky, Yasmin N Aziz, David J Seiffge, Martina Goeldlin, Marcel Arnold, Arsany Hakim, Roland Wiest, Jan Gralla, Eva A Mistry, Urs Fischer, Susanne Wegener, Johannes Kaesmacher
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引用次数: 0

Abstract

Background: Perfusion abnormalities in the infarct and salvaged penumbra have been proposed as a potential reason for poor clinical outcome (modified Rankin Scale score >2) despite complete angiographic reperfusion (Thrombolysis in Cerebral Infarction [TICI3]). In this study, we aimed to identify different microvascular perfusion patterns and their association with clinical outcomes among TICI3 patients.

Methods: University Hospital Bern's stroke registry of all patients between February 2015 and December 2021. Macrovascular reperfusion was graded using the TICI scale. Microvascular reperfusion status was evaluated within the infarct area on cerebral blood volume and cerebral blood flow perfusion maps obtained 24-hour postintervention. Primary outcome was functional independence (90-day modified Rankin Scale score 0-2) evaluated with the logistic regression analysis adjusted for age, sex, and 24-hour infarct volume from follow-up imaging.

Results: Based on microvascular perfusion findings, the entire cohort (N=248) was stratified into one of the 4 clusters: (1) normoperfusion (no perfusion abnormalities; n=143/248); (2) hyperperfusion (hyperperfusion on both cerebral blood volume and cerebral blood flow; n=54/248); (3) hypoperfusion (hypoperfusion on both cerebral blood volume and cerebral blood flow; n=14/248); and (4) mixed (discrepant findings, eg, cerebral blood volume hypoperfusion and cerebral blood flow hyperperfusion; n=37/248). Compared with the normoperfusion cluster, patients in the hypoperfusion cluster were less likely to achieve functional independence (adjusted odds ratio, 0.3 [95% CI, 0.1-0.9]), while patients in the hyperperfusion cluster tended to have better outcomes (adjusted odds ratio, 3.3 [95% CI, 1.3-8.8]).

Conclusions: In around half of TICI3 patients, perfusion abnormalities on the microvascular level can be observed. Microvascular hypoperfusion, despite complete macrovascular reperfusion, is rare but may explain the poor clinical course among some TICI3 patients, while a detrimental effect of hyperperfusion after reperfusion could not be confirmed.

完全血管内再灌注患者的 24 小时灌注成像异常。
背景:有人认为,尽管血管完全再灌注(脑梗塞溶栓治疗[TICI3]),但脑梗塞和救治后半影的灌注异常是临床预后不佳(改良Rankin量表评分>2)的潜在原因。本研究旨在确定不同的微血管灌注模式及其与 TICI3 患者临床预后的关系:方法:伯尔尼大学医院卒中登记处对 2015 年 2 月至 2021 年 12 月间的所有患者进行登记。采用TICI量表对大血管再灌注进行分级。根据干预后 24 小时获得的脑血容量和脑血流灌注图评估梗死区内的微血管再灌注状况。主要结果是功能独立性(90 天改良兰金量表评分 0-2 分),根据年龄、性别和 24 小时随访成像的梗死体积进行调整后,用逻辑回归分析进行评估:根据微血管灌注结果,整个组群(N=248)被分为 4 组:(1)正常灌注(无灌注异常;人数=143/248);(2)高灌注(脑血容量和脑血流量均高灌注;人数=54/248);(3)低灌注(脑血容量和脑血流量均低灌注;人数=14/248);(4)混合型(结果不一致,如脑血容量低灌注和脑血流量高灌注;人数=37/248)。与正常灌注组相比,低灌注组患者不太可能实现功能独立(调整后的几率比为0.3 [95% CI, 0.1-0.9]),而高灌注组患者的预后往往更好(调整后的几率比为3.3 [95% CI, 1.3-8.8]):结论:约有一半的 TICI3 患者可观察到微血管灌注异常。尽管大血管完全再灌注,但微血管灌注不足的情况并不多见,这可能是一些 TICI3 患者临床病程不佳的原因,而再灌注后过度灌注的有害影响则无法证实。
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来源期刊
Stroke
Stroke 医学-临床神经学
CiteScore
13.40
自引率
6.00%
发文量
2021
审稿时长
3 months
期刊介绍: Stroke is a monthly publication that collates reports of clinical and basic investigation of any aspect of the cerebral circulation and its diseases. The publication covers a wide range of disciplines including anesthesiology, critical care medicine, epidemiology, internal medicine, neurology, neuro-ophthalmology, neuropathology, neuropsychology, neurosurgery, nuclear medicine, nursing, radiology, rehabilitation, speech pathology, vascular physiology, and vascular surgery. The audience of Stroke includes neurologists, basic scientists, cardiologists, vascular surgeons, internists, interventionalists, neurosurgeons, nurses, and physiatrists. Stroke is indexed in Biological Abstracts, BIOSIS, CAB Abstracts, Chemical Abstracts, CINAHL, Current Contents, Embase, MEDLINE, and Science Citation Index Expanded.
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