Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors

Abstract Introduction To evaluate effectiveness of human urinary kallindinogenase (HUK) in patients with acute ischemic stroke (AIS) according to Chinese ischemic stroke subclassification (CISS) and analyzed risk factors of clinical efficacy. Methods In this retrospective study, 134 patients receive...

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Main Authors: Si‐Qia Chen, Dong‐Yang Mao, Dun‐Can Wei, Wen‐Zhen He
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.1461
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author Si‐Qia Chen
Dong‐Yang Mao
Dun‐Can Wei
Wen‐Zhen He
author_facet Si‐Qia Chen
Dong‐Yang Mao
Dun‐Can Wei
Wen‐Zhen He
author_sort Si‐Qia Chen
collection DOAJ
description Abstract Introduction To evaluate effectiveness of human urinary kallindinogenase (HUK) in patients with acute ischemic stroke (AIS) according to Chinese ischemic stroke subclassification (CISS) and analyzed risk factors of clinical efficacy. Methods In this retrospective study, 134 patients received conventional therapy were enrolled to control group, and 132 patients received HUK treatment were enrolled to HUK group. National Institute of Health Stroke Scale (NIHSS) score was used to evaluate the clinical efficacy. Multivariate analysis of risk factors was performed by using logistic regression. Results After treatment, NIHSS score of HUK group was significant lower than that of control group (p = .009). Effectiveness rate was 71.2% in HUK group, and 53.7% in control group, respectively (p = .003). The NIHSS of patients with large artery atherosclerosis (LAA) subtype in HUK group was significantly lower than that in control group (p = .005). The absence of HUK (OR = 2.75), homocysteine (OR = 0.15), and CS subtype (OR = 0.18) were risk factors for HUK clinical efficacy. Conclusions Human urinary kallindinogenase is an effective therapeutic approach for treatment of patients with AIS, especially in patients with LAA subtype. The absence of HUK, elevated homocysteine, and cardiogenic stroke subtype were risk factor for clinical efficacy of HUK.
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spelling doaj.art-1e5a927a0ed24b7180bc280118d20e2a2022-12-22T00:52:56ZengWileyBrain and Behavior2162-32792020-01-01101n/an/a10.1002/brb3.1461Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factorsSi‐Qia Chen0Dong‐Yang Mao1Dun‐Can Wei2Wen‐Zhen He3Department of Neurology First Affiliated Hospital of Shantou University Medical College Shantou ChinaClinical Pharmacy First Affiliated Hospital of Shantou University Medical College Shantou ChinaDepartment of Pharmacy First Affiliated Hospital of Shantou University Medical College Shantou ChinaDepartment of Neurology First Affiliated Hospital of Shantou University Medical College Shantou ChinaAbstract Introduction To evaluate effectiveness of human urinary kallindinogenase (HUK) in patients with acute ischemic stroke (AIS) according to Chinese ischemic stroke subclassification (CISS) and analyzed risk factors of clinical efficacy. Methods In this retrospective study, 134 patients received conventional therapy were enrolled to control group, and 132 patients received HUK treatment were enrolled to HUK group. National Institute of Health Stroke Scale (NIHSS) score was used to evaluate the clinical efficacy. Multivariate analysis of risk factors was performed by using logistic regression. Results After treatment, NIHSS score of HUK group was significant lower than that of control group (p = .009). Effectiveness rate was 71.2% in HUK group, and 53.7% in control group, respectively (p = .003). The NIHSS of patients with large artery atherosclerosis (LAA) subtype in HUK group was significantly lower than that in control group (p = .005). The absence of HUK (OR = 2.75), homocysteine (OR = 0.15), and CS subtype (OR = 0.18) were risk factors for HUK clinical efficacy. Conclusions Human urinary kallindinogenase is an effective therapeutic approach for treatment of patients with AIS, especially in patients with LAA subtype. The absence of HUK, elevated homocysteine, and cardiogenic stroke subtype were risk factor for clinical efficacy of HUK.https://doi.org/10.1002/brb3.1461acute ischemic strokeChinese ischemic stroke subclassificationhomocysteinehuman urinary kallidinogenaselarge artery atherosclerosisrisk factor
spellingShingle Si‐Qia Chen
Dong‐Yang Mao
Dun‐Can Wei
Wen‐Zhen He
Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
Brain and Behavior
acute ischemic stroke
Chinese ischemic stroke subclassification
homocysteine
human urinary kallidinogenase
large artery atherosclerosis
risk factor
title Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
title_full Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
title_fullStr Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
title_full_unstemmed Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
title_short Human urinary kallindinogenase therapy for acute ischemic stroke according to Chinese ischemic stroke subclassification: Clinical efficacy and risk factors
title_sort human urinary kallindinogenase therapy for acute ischemic stroke according to chinese ischemic stroke subclassification clinical efficacy and risk factors
topic acute ischemic stroke
Chinese ischemic stroke subclassification
homocysteine
human urinary kallidinogenase
large artery atherosclerosis
risk factor
url https://doi.org/10.1002/brb3.1461
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