Hypoperfusion Index Ratio is Associated with Early Neurological Deficit Severity and Decline after Mechanical Thrombectomy in Large Vessel Occlusion Ischemic Stroke (P2-5.004)

医学 心脏病学 缺血性中风 闭塞 冲程(发动机) 神经功能缺损 内科学 灌注 缺血 麻醉 机械工程 工程类
作者
Małgorzata Miller,Brian Wideman,Muhib Khan,Nils Henninger
出处
期刊:Neurology [Lippincott Williams & Wilkins]
卷期号:102 (17_supplement_1)
标识
DOI:10.1212/wnl.0000000000206386
摘要

To determine whether a hypoperfusion index ratio (HIR) >0.5 is associated with a worse NIHSS score at 24h post-mechanical thrombectomy (MT) and early neurologic decline (END) in large vessel (LVO) versus distal and medium vessel occlusions (DMVO) acute ischemic stroke (AIS). HIR is a surrogate marker for collateral status and a predictor of infarct growth, malignant cerebral edema, and hemorrhagic transformation. Its utility to predict a poor NIHSS and END after MT for LVO versus DMVO has not been investigated. This is a retrospective study of 231 AIS patients with LVO or DMVO amenable for MT, and available CT-perfusion for HIR assessment pre-MT. Clinical and imaging characteristics were abstracted from medical records. The primary outcome was NIHSS at 24h post-MT. The secondary outcome was END, defined as >4-point increase in NIHSS between initial assessment and 24h post-MT. HIR>0.5 was more frequently present in LVO as compared to DMVO group (n=41 [66.1%] vs. n=21 [33.9%]; p=0.037). On multivariable linear regression, HIR>0.5 was independently associated with a worse NIHSS score at 24h post-MT in the entire cohort (Beta=0.132; p=0.014) and LVO (Beta=0.225, p=0.004), but not in DMVO group. END occurred in 26 (11.3%) subjects. On multivariable logistic regression, there was no association of HIR >0.5 with END in the entire cohort after adjustment. When analyzed separately, HIR>0.5 significantly increased the odds for END in LVO subjects (OR=5.787, 95%CI 1.179-28.515, p=0.031) but not in the DMVO group (OR=0.249, 95%CI 0.009-6.517-28.515, p=0.404). HIR >0.5 was independently associated with worse 24h post-MT NIHSS and END in LVO, but not DMVO AIS. Further studies are needed to determine whether distinct CTP parameters should be used for outcome prediction and patient selection for endovascular treatment in DMVO. Disclosure: Dr. Miller has nothing to disclose. Dr. Wideman has nothing to disclose. The institution of Dr. Khan has received research support from NINDS. The institution of Dr. Khan has received research support from Genentech. The institution of Dr. Khan has received research support from Spectrum Health-MSU alliance. Dr. Khan has received research support from NIH. Dr. Henninger has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Astrocyte Pharmaceuticals, Inc.. The institution of Dr. Henninger has received research support from DoD. The institution of Dr. Henninger has received research support from NIH.

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