Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke

Abstract Aim The effectiveness of neuroprotective agents is still unclear. Here we analyzed the clinical outcomes of acute ischemic stroke (AIS) patients treated with human urinary kallidinogenase (HUK) or edaravone (Eda) combined with butylphthalide (NBP). Methods From January 2016 to December 2017...

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Main Authors: Yun Qian, Yi Lyu, Minhai Jiang, Bo Tang, Tian Nie, Shan Lu
Format: Article
Language:English
Published: Wiley 2019-12-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.1438
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author Yun Qian
Yi Lyu
Minhai Jiang
Bo Tang
Tian Nie
Shan Lu
author_facet Yun Qian
Yi Lyu
Minhai Jiang
Bo Tang
Tian Nie
Shan Lu
author_sort Yun Qian
collection DOAJ
description Abstract Aim The effectiveness of neuroprotective agents is still unclear. Here we analyzed the clinical outcomes of acute ischemic stroke (AIS) patients treated with human urinary kallidinogenase (HUK) or edaravone (Eda) combined with butylphthalide (NBP). Methods From January 2016 to December 2017, a total of 165 AIS patients were enrolled in this open‐label, randomized controlled clinical study. Patients were randomly allocated into HUK group and Eda group in a ratio of 2:1. All the patients received basic treatments and NBP (200 mg p.o. qid) while HUK group received 0.15 PNA unit of HUK injection (ivgtt. qd) and Eda group received 30 mg Eda (ivgtt. bid) for 14 consecutive days. Independency rate [12‐month modified Rankin Scale (mRS) score ≤ 1] and related factors were compared between the two groups. Results Twelve‐month mRS score of the HUK group (1, IQR 0~1) was significantly lower compared with Eda group (2, IQR 1~3, p < .0001). The HUK treatment achieved an independency rate of 79.1% while the Eda treatment only had 45.3% (p < .0001). Further binary logistic regression showed that recurrent stroke (RR: 0.1, 95% CI: 0.0~0.1, p = .038) and HUK treatment (RR: 4.2, 95% CI: 1.1~16.5, p = .041) could significantly affect patients' 12‐month outcomes. Conclusion Human urinary kallidinogenase combined with NBP can enhance AIS patients' long‐term independency rate, and the effectiveness of HUK combined therapy is better than Eda.
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spelling doaj.art-d1e33c1630004798aef917726d1b18d62022-12-22T01:20:37ZengWileyBrain and Behavior2162-32792019-12-01912n/an/a10.1002/brb3.1438Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic strokeYun Qian0Yi Lyu1Minhai Jiang2Bo Tang3Tian Nie4Shan Lu5Department of Neurology Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou ChinaDepartment of Anesthesiology Minhang Hospital Fudan University Shanghai ChinaDepartment of Neurology Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou ChinaDepartment of Neurology Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou ChinaDepartment of Neurology Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou ChinaDepartment of Neurology Affiliated Hangzhou First People's Hospital Zhejiang University School of Medicine Hangzhou ChinaAbstract Aim The effectiveness of neuroprotective agents is still unclear. Here we analyzed the clinical outcomes of acute ischemic stroke (AIS) patients treated with human urinary kallidinogenase (HUK) or edaravone (Eda) combined with butylphthalide (NBP). Methods From January 2016 to December 2017, a total of 165 AIS patients were enrolled in this open‐label, randomized controlled clinical study. Patients were randomly allocated into HUK group and Eda group in a ratio of 2:1. All the patients received basic treatments and NBP (200 mg p.o. qid) while HUK group received 0.15 PNA unit of HUK injection (ivgtt. qd) and Eda group received 30 mg Eda (ivgtt. bid) for 14 consecutive days. Independency rate [12‐month modified Rankin Scale (mRS) score ≤ 1] and related factors were compared between the two groups. Results Twelve‐month mRS score of the HUK group (1, IQR 0~1) was significantly lower compared with Eda group (2, IQR 1~3, p < .0001). The HUK treatment achieved an independency rate of 79.1% while the Eda treatment only had 45.3% (p < .0001). Further binary logistic regression showed that recurrent stroke (RR: 0.1, 95% CI: 0.0~0.1, p = .038) and HUK treatment (RR: 4.2, 95% CI: 1.1~16.5, p = .041) could significantly affect patients' 12‐month outcomes. Conclusion Human urinary kallidinogenase combined with NBP can enhance AIS patients' long‐term independency rate, and the effectiveness of HUK combined therapy is better than Eda.https://doi.org/10.1002/brb3.1438acute ischemic strokebutylphthalideedaravonehuman urinary kallidinogenase
spellingShingle Yun Qian
Yi Lyu
Minhai Jiang
Bo Tang
Tian Nie
Shan Lu
Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
Brain and Behavior
acute ischemic stroke
butylphthalide
edaravone
human urinary kallidinogenase
title Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
title_full Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
title_fullStr Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
title_full_unstemmed Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
title_short Human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
title_sort human urinary kallidinogenase or edaravone combined with butylphthalide in the treatment of acute ischemic stroke
topic acute ischemic stroke
butylphthalide
edaravone
human urinary kallidinogenase
url https://doi.org/10.1002/brb3.1438
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