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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Neurovascular Research</journal-id><journal-title-group><journal-title xml:lang="en">Current Neurovascular Research</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Neurovascular Research</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1567-2026</issn><issn publication-format="electronic">1875-5739</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">644249</article-id><article-id pub-id-type="doi">10.2174/0115672026287986240104074006</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Medicine</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Risk Factors and Prognosis of Early Neurological Deterioration after Bridging Therapy</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Xie</surname><given-names>Yiju</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Li</surname><given-names>Shengyu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Liuyu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Tang</surname><given-names>Shiting</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Yayuan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Tan</surname><given-names>Shuangquan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Liang</surname><given-names>Zhijian</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff id="aff1"><institution>Department of Neurology, The First Affiliated Hospital of Guangxi Medical University</institution></aff><aff id="aff2"><institution>Department of Neurology, Wuming Hospital of Guangxi Medical University</institution></aff><aff id="aff3"><institution>Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University</institution></aff><pub-date date-type="pub" iso-8601-date="2024-01-01" publication-format="electronic"><day>01</day><month>01</month><year>2024</year></pub-date><volume>21</volume><issue>1</issue><fpage>25</fpage><lpage>31</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/1567-2026/article/view/644249">https://journals.eco-vector.com/1567-2026/article/view/644249</self-uri><abstract xml:lang="en"><p id="idm46041443791056">Background:Early neurological deterioration (END) after bridging therapy (BT) of acute ischemic stroke (AIS) patients is associated with poor outcomes.</p><p id="idm46041443795056">Objective:We aimed to study the incidence, risk factors and prognosis of END after BT.</p><p id="idm46041443799024">Methods:From January to December 2021, the clinical data of AIS patients treated by BT (intravenous thrombolysis with alteplase prior to mechanical thrombectomy) from three comprehensive stroke centers were analyzed. Patients were divided into non-END group and END group according to whether they developed END within 72 hours of symptom onset. Modified Rankin scale (mRS) was used to assess the patients prognosis at 90 days, and favorable outcomes were defined as mRS≤2. The incidence of END was investigated, and binary logistic regression analysis was used to explore its associated factors.</p><p id="idm46041443804080">Results:The incidence of END after BT was 33.67%. The eligible 90 patients included 29 cases in the END group and 61 cases in the non-END group. Multivariate Logistic regression analysis showed that increase of systolic blood pressure (SBP) (OR=1.026, 95%CI:1.001-1.051, p =0.043), higher level of blood glucose at admission (OR=1.389, 95%CI:1.092-1.176, p =0.007) and large artery atherosclerosis (LAA) subtype (OR=8.009, 95%CI:2.357-27.223, p =0.001) were independent risk factors of END. Compared with the non-END group, the END group had significantly lower rates of good outcomes (6.90% versus 65.57%, p =0.001) while higher rates of mortality (44.83% versus 4.92%, p =0.001).</p><p id="idm46041443813456">Conclusion:It was found that the incidence of END after BT in AIS patients was 33.67%. An increase in SBP, higher glucose levels at admission, and LAA were independent risk factors of END that predicted a poor prognosis.</p></abstract><kwd-group xml:lang="en"><kwd>Early neurological deterioration</kwd><kwd>acute ischemic stroke</kwd><kwd>bridging therapy</kwd><kwd>risk factors</kwd><kwd>prognosis</kwd><kwd>systolic blood pressure.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Ois A, Martinez-Rodriguez JE, Munteis E, et al. Steno-occlusive arterial disease and early neurological deterioration in acute ischemic stroke. 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