Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99656
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorXiong, Len_US
dc.creatorChen, Xen_US
dc.creatorLiu, Jen_US
dc.creatorWong, LKSen_US
dc.creatorLeung, TWen_US
dc.date.accessioned2023-07-18T03:12:36Z-
dc.date.available2023-07-18T03:12:36Z-
dc.identifier.urihttp://hdl.handle.net/10397/99656-
dc.language.isoenen_US
dc.publisherFrontiers Media S.A.en_US
dc.rights© 2022 Xiong, Chen, Liu, Wong and Leung.en_US
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.en_US
dc.rightsThe following publication Xiong L, Chen X, Liu J, Wong LKS and Leung TW (2022) Cerebral Augmentation Effect Induced by External Counterpulsation Is Not Related to Impaired Dynamic Cerebral Autoregulation in Ischemic Stroke. Front. Neurol. 13:784836 is available at https://doi.org/10.3389/fneur.2022.784836.en_US
dc.subjectCerebral blood flowen_US
dc.subjectExternal counterpulsation|Dynamic cerebral autoregulation|Transfer functionanalysisen_US
dc.subjectIschemic strokeen_US
dc.titleCerebral augmentation effect induced by external counterpulsation is not related to impaired dynamic cerebral autoregulation in ischemic strokeen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume13en_US
dc.identifier.doi10.3389/fneur.2022.784836en_US
dcterms.abstractBackground and Purpose: Dynamic cerebral autoregulation is impaired after ischemic stroke. External counterpulsation (ECP) augments the cerebral blood flow of patients with ischemic stroke by elevation of blood pressure (BP). We aimed to investigate if cerebral augmentation effects during ECP were associated with impaired dynamic cerebral autoregulation in patients after acute ischemic stroke.-
dcterms.abstractMethods: Forty patients with unilateral ischemic stroke and large artery atherosclerosis in the anterior circulation territory within 7 days from symptom onset and eighteen healthy controls were recruited. We monitored changes in mean flow velocity over both middle cerebral arteries (MCA) by transcranial Doppler (TCD) before, during, and immediately after ECP. Cerebral augmentation index was MCA mean flow velocity increase in percentage during ECP compared with baseline to evaluate the augmentation effects of ECP. Spontaneous arterial BP and cerebral blood flow velocity in both bilateral MCAs were recorded using a servo-controlled plethysmograph and TCD, respectively. Transfer function analysis was used to derive the autoregulatory parameters, including phase difference (PD), and gain.-
dcterms.abstractResults: The cerebral augmentation index in patients with stroke was significantly higher on both the ipsilateral and contralateral sides than that in controls, while the PD in patients with stroke was significantly lower on both sides than those in controls (all P < 0.05). The cerebral augmentation index did not correlate with PD and gain on either the ipsilateral or contralateral side of patients with stroke or in controls (all P > 0.05). The cerebral augmentation index of patients with stroke was significantly related to mean BP change on the ipsilateral side (R2 = 0.108, P = 0.038).-
dcterms.abstractConclusion: The degree of ECP-induced cerebral augmentation effects as measured by the cerebral augmentation index did not correlate with the magnitude of impaired dynamic cerebral autoregulation.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationFrontiers in neurology, 2022, v. 13, 784836en_US
dcterms.isPartOfFrontiers in neurologyen_US
dcterms.issued2022-
dc.identifier.scopus2-s2.0-85130359340-
dc.identifier.eissn1664-2295en_US
dc.identifier.artn784836en_US
dc.description.validate202307 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; National Key Research and Development Program of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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