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Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke
OBJECTIVES: To explore the efficiency and safety of Sanhuang Xiexin decoction in the treatment of acute ischemic stroke (AIS) patients after endovascular intervention examination. METHODS: In this prospective observational study, 121 AIS patients admitted in our hospital were enrolled from January 2...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346639/ https://www.ncbi.nlm.nih.gov/pubmed/30569662 http://dx.doi.org/10.1002/brb3.1185 |
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author | Song, Juexian Chen, Xin Lyu, Yi Zhuang, Wei Zhang, Jing Gao, Li Tong, Xiaolin |
author_facet | Song, Juexian Chen, Xin Lyu, Yi Zhuang, Wei Zhang, Jing Gao, Li Tong, Xiaolin |
author_sort | Song, Juexian |
collection | PubMed |
description | OBJECTIVES: To explore the efficiency and safety of Sanhuang Xiexin decoction in the treatment of acute ischemic stroke (AIS) patients after endovascular intervention examination. METHODS: In this prospective observational study, 121 AIS patients admitted in our hospital were enrolled from January 2012 to December 2015. They were randomly divided into two groups, 61 patients received Sanhuang Xiexin decoction + basic treatment (SX group) and 60 patients received basic treatment (control group). The prescription of Sanhuang Xiexin decoction was taken in the SX group, with one dose (100 ml), twice a day for 7 days orally. For all patients, blood samples were drawn on the first morning and sixth morning after endovascular intervention examination under fasting state for Fib (fibrinogen), PAgT (platelet aggregation test), CRP (C‐reactive protein), and TMAO (trimethylamine oxide) tested. Estimate the changes in plasma Fib, PAgT, CRP, and TMAO levels and the syndrome of fire‐heat scores. RESULTS: The plasma Fib, PAgT, CRP, and TMAO levels in the SX group were significantly lower than those in the control group (P(Fib) < 0.01, P(PAgT) < 0.01, P(CRP) = 0.02, P(TMAO) < 0.01). The syndrome of fire‐heat scores in the SX group was significantly lower than that in the control group (p < 0.01). The incidences of ischemic cerebrovascular events within 3 and 6 months after endovascular intervention treatment in the SX group were lower than those in the control group (P(3 month) = 0.04, P(6month) = 0.03). CONCLUSIONS: The prescription of Sanhuang Xiexin is efficient and safe in the treatment of AIS patients after endovascular intervention examination through reducing the inflammatory factors. |
format | Online Article Text |
id | pubmed-6346639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63466392019-01-29 Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke Song, Juexian Chen, Xin Lyu, Yi Zhuang, Wei Zhang, Jing Gao, Li Tong, Xiaolin Brain Behav Original Research OBJECTIVES: To explore the efficiency and safety of Sanhuang Xiexin decoction in the treatment of acute ischemic stroke (AIS) patients after endovascular intervention examination. METHODS: In this prospective observational study, 121 AIS patients admitted in our hospital were enrolled from January 2012 to December 2015. They were randomly divided into two groups, 61 patients received Sanhuang Xiexin decoction + basic treatment (SX group) and 60 patients received basic treatment (control group). The prescription of Sanhuang Xiexin decoction was taken in the SX group, with one dose (100 ml), twice a day for 7 days orally. For all patients, blood samples were drawn on the first morning and sixth morning after endovascular intervention examination under fasting state for Fib (fibrinogen), PAgT (platelet aggregation test), CRP (C‐reactive protein), and TMAO (trimethylamine oxide) tested. Estimate the changes in plasma Fib, PAgT, CRP, and TMAO levels and the syndrome of fire‐heat scores. RESULTS: The plasma Fib, PAgT, CRP, and TMAO levels in the SX group were significantly lower than those in the control group (P(Fib) < 0.01, P(PAgT) < 0.01, P(CRP) = 0.02, P(TMAO) < 0.01). The syndrome of fire‐heat scores in the SX group was significantly lower than that in the control group (p < 0.01). The incidences of ischemic cerebrovascular events within 3 and 6 months after endovascular intervention treatment in the SX group were lower than those in the control group (P(3 month) = 0.04, P(6month) = 0.03). CONCLUSIONS: The prescription of Sanhuang Xiexin is efficient and safe in the treatment of AIS patients after endovascular intervention examination through reducing the inflammatory factors. John Wiley and Sons Inc. 2018-12-19 /pmc/articles/PMC6346639/ /pubmed/30569662 http://dx.doi.org/10.1002/brb3.1185 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Song, Juexian Chen, Xin Lyu, Yi Zhuang, Wei Zhang, Jing Gao, Li Tong, Xiaolin Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title | Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title_full | Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title_fullStr | Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title_full_unstemmed | Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title_short | Sanhuang Xiexin decoction promotes good functional outcome in acute ischemic stroke |
title_sort | sanhuang xiexin decoction promotes good functional outcome in acute ischemic stroke |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346639/ https://www.ncbi.nlm.nih.gov/pubmed/30569662 http://dx.doi.org/10.1002/brb3.1185 |
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