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Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage
OBJECTIVES: Surgical treatment is expected to remove clot immediately in acute spontaneous intracerebral hemorrhage (SICH) patients. The aim of this study was to evaluate whether Naoxueshu could enhance the efficacy of clot removal surgery in acute SICH patients. METHODS: One hundred twenty patients...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821564/ https://www.ncbi.nlm.nih.gov/pubmed/33274855 http://dx.doi.org/10.1002/brb3.1957 |
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author | Song, Juexian Nie, Yuting Wang, Pingping Lu, Huiqiang Gao, Li |
author_facet | Song, Juexian Nie, Yuting Wang, Pingping Lu, Huiqiang Gao, Li |
author_sort | Song, Juexian |
collection | PubMed |
description | OBJECTIVES: Surgical treatment is expected to remove clot immediately in acute spontaneous intracerebral hemorrhage (SICH) patients. The aim of this study was to evaluate whether Naoxueshu could enhance the efficacy of clot removal surgery in acute SICH patients. METHODS: One hundred twenty patients who had been diagnosed as SICH according to neuroimaging were enrolled in this study. They received craniotomy, decompressive craniectomy, or minimally invasive surgical evacuation as appropriate and then were randomized into two groups: the Naoxueshu group (NXS group, n = 60) and the control group (n = 60). All the patients received standard medical management while patients in NXS group also took Naoxueshu oral liquid 10 ml with three times a day for seven consecutive days. The primary outcome was the 7‐day hematoma volume and secondary outcomes were 7‐day National Institutes of Health Stroke Scale (NIHSS) score and 7‐day cerebral edema score. RESULTS: After clot removal surgery, hematoma volume in NXS group (9.5 ± 8.0) was significantly decreased than that in Control group (21.3 ± 22.9, p < .0001) 7 days after surgery. Moreover, cerebral edema was also relieved after 7‐day's Naoxueshu treatment (2.5 ± 0.9 vs. 2.9 ± 0.7, p = .043). Since patients in NXS group had worse baseline NIHSS score (17.2 ± 8.1 vs. 13.7 ± 10.1, p = .039), it was reasonable to conclude that Naoxueshu treatment could improve patients’ neurological function because 7‐day NIHSS score of the two groups was similar. CONCLUSION: Naoxueshu oral liquid could relieve hematoma volume and cerebral edema after clot removal surgery in acute SICH patients. Moreover, it had the potential to improve patients’ short‐term neurological function. |
format | Online Article Text |
id | pubmed-7821564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78215642021-01-29 Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage Song, Juexian Nie, Yuting Wang, Pingping Lu, Huiqiang Gao, Li Brain Behav Original Research OBJECTIVES: Surgical treatment is expected to remove clot immediately in acute spontaneous intracerebral hemorrhage (SICH) patients. The aim of this study was to evaluate whether Naoxueshu could enhance the efficacy of clot removal surgery in acute SICH patients. METHODS: One hundred twenty patients who had been diagnosed as SICH according to neuroimaging were enrolled in this study. They received craniotomy, decompressive craniectomy, or minimally invasive surgical evacuation as appropriate and then were randomized into two groups: the Naoxueshu group (NXS group, n = 60) and the control group (n = 60). All the patients received standard medical management while patients in NXS group also took Naoxueshu oral liquid 10 ml with three times a day for seven consecutive days. The primary outcome was the 7‐day hematoma volume and secondary outcomes were 7‐day National Institutes of Health Stroke Scale (NIHSS) score and 7‐day cerebral edema score. RESULTS: After clot removal surgery, hematoma volume in NXS group (9.5 ± 8.0) was significantly decreased than that in Control group (21.3 ± 22.9, p < .0001) 7 days after surgery. Moreover, cerebral edema was also relieved after 7‐day's Naoxueshu treatment (2.5 ± 0.9 vs. 2.9 ± 0.7, p = .043). Since patients in NXS group had worse baseline NIHSS score (17.2 ± 8.1 vs. 13.7 ± 10.1, p = .039), it was reasonable to conclude that Naoxueshu treatment could improve patients’ neurological function because 7‐day NIHSS score of the two groups was similar. CONCLUSION: Naoxueshu oral liquid could relieve hematoma volume and cerebral edema after clot removal surgery in acute SICH patients. Moreover, it had the potential to improve patients’ short‐term neurological function. John Wiley and Sons Inc. 2020-12-04 /pmc/articles/PMC7821564/ /pubmed/33274855 http://dx.doi.org/10.1002/brb3.1957 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC 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 Nie, Yuting Wang, Pingping Lu, Huiqiang Gao, Li Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title | Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title_full | Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title_fullStr | Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title_full_unstemmed | Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title_short | Naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
title_sort | naoxueshu relieves hematoma after clot removal in acute spontaneous intracerebral hemorrhage |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821564/ https://www.ncbi.nlm.nih.gov/pubmed/33274855 http://dx.doi.org/10.1002/brb3.1957 |
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