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Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients

BACKGROUND: Since venous drainage in acute arterial ischemic stroke has not been thoroughly researched, we evaluate the effect of argatroban, a selective direct thrombin inhibitor, as a therapy to increase the rate of basal vein Rosenthal (BVR) drainage and improve patients’ post-stroke outcomes. MA...

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Autores principales: Liu, Shoufeng, Liu, Peipei, Wang, Po, Zhang, Fang, Wang, Lijun, Wang, Yu, Lu, Hao, Ma, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382300/
https://www.ncbi.nlm.nih.gov/pubmed/32667287
http://dx.doi.org/10.12659/MSM.924593
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author Liu, Shoufeng
Liu, Peipei
Wang, Po
Zhang, Fang
Wang, Lijun
Wang, Yu
Lu, Hao
Ma, Xiaofeng
author_facet Liu, Shoufeng
Liu, Peipei
Wang, Po
Zhang, Fang
Wang, Lijun
Wang, Yu
Lu, Hao
Ma, Xiaofeng
author_sort Liu, Shoufeng
collection PubMed
description BACKGROUND: Since venous drainage in acute arterial ischemic stroke has not been thoroughly researched, we evaluate the effect of argatroban, a selective direct thrombin inhibitor, as a therapy to increase the rate of basal vein Rosenthal (BVR) drainage and improve patients’ post-stroke outcomes. MATERIAL/METHODS: In this multicenter clinical trial, 60 eligible patients at 4.5 to 48 hours after the stroke onset were recruited. After being randomly allocated into 2 groups, they were treated with standard therapy either alone or with argatroban. RESULTS: Compared to the contralateral brain hemisphere, the mean flow velocity (MFV) in BVR drainage was significantly reduced in the stroke-afflicted ipsilateral hemisphere. After treatment with argatroban for 7 days, the MFV from BVR of the ipsilateral hemisphere in the argatroban treated group was significantly increased when compared to the control group. At 90 days after the onset of stroke, the MFV of BVR in the ipsilateral hemisphere was similar in both groups. Compared with controls, the argatroban-treated patients had smaller lesions from baseline to 7 days. Argatroban also improved National Institutes of Health Stroke Scale (NIHSS) scores on day 7 after the onset of stroke. Furthermore, the argatroban group’s neurological functions were superior to those of their untreated counterparts after 90 days. No difference was found in the incidence of adverse reactions between the 2 groups. CONCLUSIONS: These observations indicate that vein drainage change may contribute to the acute phase of brain edema and the outcomes of ischemic stroke patients. CLINICAL TRIAL REGISTRATION: URL-http://www.chictr.org Unique identifier: ChiCTR-IPR-16008663
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spelling pubmed-73823002020-08-03 Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients Liu, Shoufeng Liu, Peipei Wang, Po Zhang, Fang Wang, Lijun Wang, Yu Lu, Hao Ma, Xiaofeng Med Sci Monit Clinical Research BACKGROUND: Since venous drainage in acute arterial ischemic stroke has not been thoroughly researched, we evaluate the effect of argatroban, a selective direct thrombin inhibitor, as a therapy to increase the rate of basal vein Rosenthal (BVR) drainage and improve patients’ post-stroke outcomes. MATERIAL/METHODS: In this multicenter clinical trial, 60 eligible patients at 4.5 to 48 hours after the stroke onset were recruited. After being randomly allocated into 2 groups, they were treated with standard therapy either alone or with argatroban. RESULTS: Compared to the contralateral brain hemisphere, the mean flow velocity (MFV) in BVR drainage was significantly reduced in the stroke-afflicted ipsilateral hemisphere. After treatment with argatroban for 7 days, the MFV from BVR of the ipsilateral hemisphere in the argatroban treated group was significantly increased when compared to the control group. At 90 days after the onset of stroke, the MFV of BVR in the ipsilateral hemisphere was similar in both groups. Compared with controls, the argatroban-treated patients had smaller lesions from baseline to 7 days. Argatroban also improved National Institutes of Health Stroke Scale (NIHSS) scores on day 7 after the onset of stroke. Furthermore, the argatroban group’s neurological functions were superior to those of their untreated counterparts after 90 days. No difference was found in the incidence of adverse reactions between the 2 groups. CONCLUSIONS: These observations indicate that vein drainage change may contribute to the acute phase of brain edema and the outcomes of ischemic stroke patients. CLINICAL TRIAL REGISTRATION: URL-http://www.chictr.org Unique identifier: ChiCTR-IPR-16008663 International Scientific Literature, Inc. 2020-07-15 /pmc/articles/PMC7382300/ /pubmed/32667287 http://dx.doi.org/10.12659/MSM.924593 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Liu, Shoufeng
Liu, Peipei
Wang, Po
Zhang, Fang
Wang, Lijun
Wang, Yu
Lu, Hao
Ma, Xiaofeng
Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title_full Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title_fullStr Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title_full_unstemmed Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title_short Argatroban Increased the Basal Vein Drainage and Improved Outcomes in Acute Paraventricular Ischemic Stroke Patients
title_sort argatroban increased the basal vein drainage and improved outcomes in acute paraventricular ischemic stroke patients
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382300/
https://www.ncbi.nlm.nih.gov/pubmed/32667287
http://dx.doi.org/10.12659/MSM.924593
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