<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">russjcardiol</journal-id><journal-title-group><journal-title xml:lang="ru">Российский кардиологический журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Cardiology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1560-4071</issn><issn pub-type="epub">2618-7620</issn><publisher><publisher-name>«SILICEA-POLIGRAF» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15829/1560-4071-2014-4-ENG-22-27</article-id><article-id custom-type="elpub" pub-id-type="custom">russjcardiol-602</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL STUDIES</subject></subj-group></article-categories><title-group><article-title>БЕЗОПАСНОСТЬ ТИРОФИБАНА ДЛЯ ПАЦИЕНТОВ С ОСТРЫМ ИШЕМИЧЕСКИМ ИНСУЛЬТОМ В РУТИННОЙ КЛИНИЧЕСКОЙ ПРАКТИКЕ</article-title><trans-title-group xml:lang="en"><trans-title>SAFETY OF TIROFIBAN FOR PATIENTS WITH ACUTE ISCHEMIC STROKE IN ROUTINE CLINICAL PRACTICE</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Zhang</surname><given-names>Yan-Jun</given-names></name><name name-style="western" xml:lang="en"><surname>Zhang</surname><given-names>Yan-Jun</given-names></name></name-alternatives><bio xml:lang="en"><p>Department of Geriatrics, People’s Hospital of Zhengzhou, Zhengzhou 450003, China. Tel: 86–0371–67077323</p></bio><email xlink:type="simple">yjlqcn@163.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Liu</surname><given-names>Qing</given-names></name><name name-style="western" xml:lang="en"><surname>Liu</surname><given-names>Qing</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Zhan</surname><given-names>Qin</given-names></name><name name-style="western" xml:lang="en"><surname>Zhan</surname><given-names>Qin</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Li</surname><given-names>Qiong</given-names></name><name name-style="western" xml:lang="en"><surname>Li</surname><given-names>Qiong</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="en" id="aff-1"><institution>Department of Geriatrics, People’s Hospital of Zhengzhou, Zhengzhou, China</institution></aff><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>28</day><month>04</month><year>2014</year></pub-date><volume>0</volume><issue>4-ENG</issue><fpage>22</fpage><lpage>27</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Zhang Y., Liu Q., Zhan Q., Li Q., 2014</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="ru">Zhang Y., Liu Q., Zhan Q., Li Q.</copyright-holder><copyright-holder xml:lang="en">Zhang Y., Liu Q., Zhan Q., Li Q.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://russjcardiol.elpub.ru/jour/article/view/602">https://russjcardiol.elpub.ru/jour/article/view/602</self-uri><abstract><sec><title>Цель</title><p>Цель. Данная работа направлена на исследование безопасности применения одного тирофибана и в сочетании с различными препаратами в острый период ишемического инсульта (ОИИ).</p></sec><sec><title>Материал и методы</title><p>Материал и методы. 120 пациентов с ОИИ были включены в это исследование. Они были разделены на 3 группы: Группа А (тирофибан, n=68), группа б (тирофибан плюс тромболитическая терапия, n=26), и группа C (тирофибан плюс сопутствующее лечение, n=26). Факторы риска, степень тяжести инсульта, первичное обследование, схемы лечения, осложнений и долгосрочные результаты были проанализированы.</p></sec><sec><title>Результаты</title><p>Результаты. Восемь пациентов (6,7%) в группе, у 6 (23,1%) в группе B и 2 пациентов (7,7%) в группе C, были кровотечения во время или после лечения. Шестнадцать пациентов (6 в группе А, 8-в группе B и 2 в группе C) умерли во время госпитализации. Уровень смертности составил 13,3% (8,8% для группы А, 30,7% для группы B и 7,7% для группы C, соответственно) в фазе обострения. Благоприятный исход (mRS 0–2) в первые три месяца после инсульта наблюдался только в 43,3% пациентов (44,1% в группе А, 46,7% в группе В и 36,4% в группе C). Средний Barthel index был 72,3 в группе А, 84,4 в группе B и 56,8 группы C (Общая оценка: 71,0).</p></sec><sec><title>Вывод</title><p>Вывод. Лечение инсультов с применением тирофибана безопасно при ОИИ. Большие рандомизированные контролируемые испытания будут необходимы в будущем для уменьшения незначительных кровотечений как осложнений терапии тирофибаном.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Aim</title><p>Aim. This work aims to study the safety of tirofiban alone and in combination with various treatments in acute ischemic stroke (AIS).</p></sec><sec><title>Material and methods</title><p>Material and methods. 120 AIS patients were included in this study. There were 3 groups as below: Group A (tirofiban alone, n=68), Group B (tirofiban plus thrombolytic therapy, n=26), and Group C (tirofiban plus bridging therapy, n=26). Risk factors, stroke severity, initial imaging, treatment regimens, complications and longterm outcomes were analyzed.</p></sec><sec><title>Results</title><p>Results. Eight patients (6,7%) in Group A, 6 patients (23,1%) in Group B and 2 patients (7,7%) in Group C had hemorrhage during or after treatment. Sixteen patients (6 in Group A, 8 in Group B and 2 in Group C) died during hospital admission. The mortality rate was 13,3% (8,8% for Group A, 30,7% for Group B and 7,7% for Group C, respectively) in the acute phase. A favorable outcome (mRS 0–2) at the first three months after stroke was only observed in 43,3% of patients (44,1% in Group A, 46,7% in Group B and 36,4% in Group C). The average Barthel index was 72,3 in Group A, 84,4 in Group B and 56,8 in Group C (total score: 71,0).</p></sec><sec><title>Conclusion</title><p>Conclusion. The stroke treatment with tirofiban is safe in AIS. A large randomized controlled trial in the future will be needed to decrease the minor bleeding complication of tirofiban therapy.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>тирофибан</kwd><kwd>острый ишемический инсульт</kwd><kwd>безопасность</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Tirofiban</kwd><kwd>acute ischemic stroke</kwd><kwd>safety</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Suwanwela NC, Phanthumchinda K, Likitjaroen Y. Thrombolytic therapy in acute ischemic stroke in Asia: The first prospective evaluation. Clin Neurol Neurosurg 2006; 108 (6):549– 52.</mixed-citation><mixed-citation xml:lang="en">Suwanwela NC, Phanthumchinda K, Likitjaroen Y. Thrombolytic therapy in acute ischemic stroke in Asia: The first prospective evaluation. Clin Neurol Neurosurg 2006; 108 (6):549– 52.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Nandigam K, Narayan SK, Elangovan S, et al. Feasibility of acute thrombolytic therapy for stroke. Neurol India 2003; 51 (4):470–3.</mixed-citation><mixed-citation xml:lang="en">Nandigam K, Narayan SK, Elangovan S, et al. Feasibility of acute thrombolytic therapy for stroke. Neurol India 2003; 51 (4):470–3.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar S, Rajshekher G, Prabhakar S. Platelet glycoprotein IIb/IIIa inhibitors in acute ischemic stroke. Neurol India 2008; 56 (4):399–404.</mixed-citation><mixed-citation xml:lang="en">Kumar S, Rajshekher G, Prabhakar S. Platelet glycoprotein IIb/IIIa inhibitors in acute ischemic stroke. Neurol India 2008; 56 (4):399–404.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Siebler M, Hennerici MG, Schneider D, et al. Safety of Tirofiban in acute Ischemic Stroke: the SaTIS trial. Stroke 2011; 42 (9):2388–92.</mixed-citation><mixed-citation xml:lang="en">Siebler M, Hennerici MG, Schneider D, et al. Safety of Tirofiban in acute Ischemic Stroke: the SaTIS trial. Stroke 2011; 42 (9):2388–92.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Ciccone A, Abraha I, Santilli I. Glycoprotein IIb-IIIa Inhibitors for Acute Ischemic Stroke. Stroke 2007. [Epub ahead of print].</mixed-citation><mixed-citation xml:lang="en">Ciccone A, Abraha I, Santilli I. Glycoprotein IIb-IIIa Inhibitors for Acute Ischemic Stroke. Stroke 2007. [Epub ahead of print].</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Haerten K, Krabbe C, Raiber M. Efficacy and safety of treatment of acute ischemic stroke with glycoprotein IIb/IIIa receptor blocker in routine clinical practice. Dtsch Med Wochenschr 2004; 129 (12):607–10.</mixed-citation><mixed-citation xml:lang="en">Haerten K, Krabbe C, Raiber M. Efficacy and safety of treatment of acute ischemic stroke with glycoprotein IIb/IIIa receptor blocker in routine clinical practice. Dtsch Med Wochenschr 2004; 129 (12):607–10.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Bogousslavsky J, Leclerc JR. Platelet glycoprotein IIb/IIIa antagonists for acute ischemic stroke. Neurology 2001; 57 (5 Suppl 2): S53–7.</mixed-citation><mixed-citation xml:lang="en">Bogousslavsky J, Leclerc JR. Platelet glycoprotein IIb/IIIa antagonists for acute ischemic stroke. Neurology 2001; 57 (5 Suppl 2): S53–7.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Hacke W, Kaste M, Fieschi C, et al. Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Lancet 1998; 352 (9136): 1245–51.</mixed-citation><mixed-citation xml:lang="en">Hacke W, Kaste M, Fieschi C, et al. Randomised double-blind placebo-controlled trial of thrombolytic therapy with intravenous alteplase in acute ischaemic stroke (ECASS II). Lancet 1998; 352 (9136): 1245–51.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Pancioli AM, Broderick T, Brott T, et al. The Combined Approch to Lysis Utilizing Eptifibatide and rt-PA in Acute ischemic stroke: the CLEAR Stroke Trial. Stroke 2008; 39 (12): 3268–76.</mixed-citation><mixed-citation xml:lang="en">Pancioli AM, Broderick T, Brott T, et al. The Combined Approch to Lysis Utilizing Eptifibatide and rt-PA in Acute ischemic stroke: the CLEAR Stroke Trial. Stroke 2008; 39 (12): 3268–76.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Kleinschnitz C, Pozgajova M, Pham M, et al. Targeting platelets in acute experimental stroke: Impact of glycoprotein ib, vi, and iib/iiia blockade on infarct size, functional outcome, and intracranial bleeding. Circulation 2007; 115 (17): 2323–30.</mixed-citation><mixed-citation xml:lang="en">Kleinschnitz C, Pozgajova M, Pham M, et al. Targeting platelets in acute experimental stroke: Impact of glycoprotein ib, vi, and iib/iiia blockade on infarct size, functional outcome, and intracranial bleeding. Circulation 2007; 115 (17): 2323–30.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Choudhri TF, Hoh BL, Zerwes HG, et al. Reduced microvascular thrombosis and improved outcome in acute murine stroke by inhibiting gp iib/iiia receptor-mediated platelet aggregation. J Clin Invest 1998; 102 (7): 1301–10.</mixed-citation><mixed-citation xml:lang="en">Choudhri TF, Hoh BL, Zerwes HG, et al. Reduced microvascular thrombosis and improved outcome in acute murine stroke by inhibiting gp iib/iiia receptor-mediated platelet aggregation. J Clin Invest 1998; 102 (7): 1301–10.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Moriguchi A, Maeda M, Mihara K, et al. Fk419, a novel nonpeptide gpiib/iiia antagonist, restores microvascular patency and improves outcome in the guinea-pig middle cerebral artery thrombotic occlusion model: Comparison with tirofiban. J Cereb Blood Flow Metab 2005; 25 (1): 75–86.</mixed-citation><mixed-citation xml:lang="en">Moriguchi A, Maeda M, Mihara K, et al. Fk419, a novel nonpeptide gpiib/iiia antagonist, restores microvascular patency and improves outcome in the guinea-pig middle cerebral artery thrombotic occlusion model: Comparison with tirofiban. J Cereb Blood Flow Metab 2005; 25 (1): 75–86.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Maeda M, Moriguchi A, Mihara K, et al. Fk419, a nonpeptide platelet glycoprotein iib/iiia antagonist, ameliorates brain infarction associated with thrombotic focal cerebral ischemia in monkeys: Comparison with tissue plasminogen activator. J Cereb Blood Flow Metab 2005; 25 (1):108–18.</mixed-citation><mixed-citation xml:lang="en">Maeda M, Moriguchi A, Mihara K, et al. Fk419, a nonpeptide platelet glycoprotein iib/iiia antagonist, ameliorates brain infarction associated with thrombotic focal cerebral ischemia in monkeys: Comparison with tissue plasminogen activator. J Cereb Blood Flow Metab 2005; 25 (1):108–18.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Coller BS. Binding of abciximab to alpha v beta 3 and activated alpha m beta 2 receptors: With a review of platelet-leukocyte interactions. Thromb Haemost. 1999; 82 (2): 326–36.</mixed-citation><mixed-citation xml:lang="en">Coller BS. Binding of abciximab to alpha v beta 3 and activated alpha m beta 2 receptors: With a review of platelet-leukocyte interactions. Thromb Haemost. 1999; 82 (2): 326–36.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Murphy JF, Bourdet JC, Wyler B, et al. The vitronectin receptor (alpha v beta 3) is implicated, in coorperation with p-selectin and platelet-activating facotr, in the adhesion of monocytes to activated endothelial cells. Biochem J 1994; 304 (Pt2): 537–42.</mixed-citation><mixed-citation xml:lang="en">Murphy JF, Bourdet JC, Wyler B, et al. The vitronectin receptor (alpha v beta 3) is implicated, in coorperation with p-selectin and platelet-activating facotr, in the adhesion of monocytes to activated endothelial cells. Biochem J 1994; 304 (Pt2): 537–42.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Molina CA, Alvarez-Sabin J, Montaner J, et al. Thrombolysis-related hemorrhagic infarction: a marker of early reperfusion, reduced infarct size, and improved outcome in patients with proximal middle cerebral artery occlusion. Stroke 2002; 33 (6): 1551–6.</mixed-citation><mixed-citation xml:lang="en">Molina CA, Alvarez-Sabin J, Montaner J, et al. Thrombolysis-related hemorrhagic infarction: a marker of early reperfusion, reduced infarct size, and improved outcome in patients with proximal middle cerebral artery occlusion. Stroke 2002; 33 (6): 1551–6.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Montaner J, Molina CA, Monasterio J, et al. Matrix metalloproteinase-9 pretreatment level predicts intracranial hemorrhagic complications after thrombolysis in human stroke. Circulation 2003; 107 (4):598–603.</mixed-citation><mixed-citation xml:lang="en">Montaner J, Molina CA, Monasterio J, et al. Matrix metalloproteinase-9 pretreatment level predicts intracranial hemorrhagic complications after thrombolysis in human stroke. Circulation 2003; 107 (4):598–603.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mangiafico S, Cellerini M, Nencini P, et al. Intravenous glycoprotein iib/iiia inhibitor (tirofiban) followed by intra-arterial urokinase and mechanical thrombolysis in stroke. AJNR Am J Neuroradiol 2005; 26 (10): 2595–601.</mixed-citation><mixed-citation xml:lang="en">Mangiafico S, Cellerini M, Nencini P, et al. Intravenous glycoprotein iib/iiia inhibitor (tirofiban) followed by intra-arterial urokinase and mechanical thrombolysis in stroke. AJNR Am J Neuroradiol 2005; 26 (10): 2595–601.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Junghans U, Seitz RJ, Aulich A, et al. Bleeding risk of tirofiban, a nonpeptide GPIIb/IIIa platelet receptor antagonist in progressive stroke: an open pilot study. Cerebrovasc Dis 2001; 12 (4):308–12.</mixed-citation><mixed-citation xml:lang="en">Junghans U, Seitz RJ, Aulich A, et al. Bleeding risk of tirofiban, a nonpeptide GPIIb/IIIa platelet receptor antagonist in progressive stroke: an open pilot study. Cerebrovasc Dis 2001; 12 (4):308–12.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Alexandrov AV, Grotta JC. Arterial reocclusion in stroke patients treated with intravenous tissue plasminogen activator. Neurology 2002; 59 (6): 862–7.</mixed-citation><mixed-citation xml:lang="en">Alexandrov AV, Grotta JC. Arterial reocclusion in stroke patients treated with intravenous tissue plasminogen activator. Neurology 2002; 59 (6): 862–7.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
