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<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">ophthalmology</journal-id><journal-title-group><journal-title xml:lang="ru">Офтальмология</journal-title><trans-title-group xml:lang="en"><trans-title>Ophthalmology in Russia</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1816-5095</issn><issn pub-type="epub">2500-0845</issn><publisher><publisher-name>Ophthalmology</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18008/1816-5095-2016-3-197-204</article-id><article-id custom-type="elpub" pub-id-type="custom">ophthalmology-324</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>ОФТАЛЬМОФАРМАКОЛОГИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PHARMACOLOGY</subject></subj-group></article-categories><title-group><article-title>ОЦЕНКА ЭФФЕКТИВНОСТИ И БЕЗОПАСНОСТИ НОВОГО КОМБИНИРОВАННОГО ПРЕПАРАТА С РЕКОМБИНАНТНЫМ ИНТЕРФЕРОНОМ И БЕТАМЕТАЗОНОМ ПРИ ОБОСТРЕНИИ ПОЛЛИНОЗА</article-title><trans-title-group xml:lang="en"><trans-title>EFFICACY AND SAFETY OF A NEW COMBINED MEDICATION WITH RECOMBINANT INTERFERON AND BETAMETHASONE IN THE TREATMENT OF HAY FEVER DURING PERIODS OF EXACERBATION</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>Рябцева</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Ryabtseva</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>доктор медицинских наук, профессор, руководитель офтальмологического отделения</p></bio><bio xml:lang="en"><p>MD, prof., Head of Ophthalmology Department</p></bio><email xlink:type="simple">moniki_glaz@rambler.ru</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>Сотникова</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Sotnikova</surname><given-names>N. Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>доктор медицинских наук, профессор, заведующая лабораторией клинической иммунологии</p></bio><bio xml:lang="en"><p>MD, prof., Head of the Clinical Immunology Laboratory</p></bio><email xlink:type="simple">niimid.immune@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чумиков</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Chumikov</surname><given-names>O. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>главный врач</p></bio><bio xml:lang="en"><p>head doctor</p></bio><email xlink:type="simple">rgd_hospital@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ступакова</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Stupakova</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>младший научный сотрудник офтальмо‑ логического отделения </p></bio><bio xml:lang="en"><p>Research Assistant</p></bio><email xlink:type="simple">moniki_glaz@rambler.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ГБУЗ МО МОНИКИ им. М.Ф. Владимирского  &#13;
ул. Щепкина, 61/2, Москва,129110, Российская Федерация</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Regional Research and Clinical Institute (MONIKI). 61/2, Str. Shchepkin, Moscow, 129110, Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБУ «Ивановский научно-исследовательский институт материнства и детства им. В.Н. Городкова» Минздрава России ул. Победы, 20, г. Иваново, 153045, Российская Федерация</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Gorodkov Ivanovo Research Institute of Maternity and Childhood. 20, Str. Victory, Ivanovo, 153045, Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>НУЗ «Отделенческая больница на станции Иваново ОАО «РЖД» &#13;
ул. Полка Нормандия Неман, 106, г. Иваново,153043, Российская Федерация</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Ivanovo Russian Railway Hospital,106, Normandy-Neman Regiment st., Ivanovo, 153043, Russian Federation</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>29</day><month>09</month><year>2016</year></pub-date><volume>13</volume><issue>3</issue><fpage>197</fpage><lpage>204</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рябцева А.А., Сотникова Н.Ю., Чумиков О.В., Ступакова Н.А., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Рябцева А.А., Сотникова Н.Ю., Чумиков О.В., Ступакова Н.А.</copyright-holder><copyright-holder xml:lang="en">Ryabtseva A.A., Sotnikova N.Y., Chumikov O.V., Stupakova N.A.</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://www.ophthalmojournal.com/opht/article/view/324">https://www.ophthalmojournal.com/opht/article/view/324</self-uri><abstract><p>Цель работы. Оценить эффективность, безопасность и переносимость нового комбинированного лекарственного препарата Аллергоферон® бета при лечении пациентов с обострением поллиноза (сезонного аллергического ринита и конъюнктивита) среднетяжелого течения. Пациенты и методы. Объектом исследования являлся лекарственный препарат Аллергоферон® бета (лекарственная форма — капли глазные и назальные), содержащий в качестве активных компонентов интерферон человеческий рекомбинантный альфа-2b не менее 5 000 МЕ/мл и бетаметазон натрия фосфат 1,0 мг/мл. В клиническом исследовании участвовало 120 пациентов с длительностью поллиноза не менее двух лет, в возрасте от 18 до 65 лет: 76 женщин и 44 мужчины. Все обследуемые имели клиническую картину обострения поллиноза среднетяжелого течения. Пациентов с основным заболеванием распределили на две равные группы. Участники опытной группы получали исследуемый лекарственный препарат Аллергоферон® бета, в группе сравнения использовали Офтан® Дексаметазон и Насобек. По дизайну исследование было открытое, многоцентровое, параллельное, сравнительное, контролируемое, рандомизированное. результаты. Новый комбинированный лекарственный препарат Аллергоферон® бета оказывал выраженный терапевтический эффект в процессе купирования основных клинических проявлений при обострении поллиноза. Межгрупповое сравнение одноименных симптомов показало, что купирование клинической симптоматики обострения поллиноза у пациентов, получавших изучаемый препарат, имело место в более ранние сроки от начала лечения (5-й день терапии по сравнению с 10-м днем в контрольной группе), а само заболевание протекало в более легкой форме по сравнению с группой контроля. Лечебная эффективность исследуемого лекарственного препарата составила 85,96% (для контрольной группы — 74,73%; р&lt;0,05). В ходе клинического исследования не отмечено случаев нежелательных явлений, общей или местной токсико-аллергической реакции. Переносимость пациентами данного препарата оценена как «хорошая». Заключение. По результатам клинического исследования препарат Аллергоферон® бета рекомендован к государственной регистрации и медицинскому применению при лечении поллиноза (сезонного аллергического ринита и конъюнктивита) среднетяжелого течения в стадии обострения.</p></abstract><trans-abstract xml:lang="en"><sec><title>Objective</title><p>Objective: to assess the efficacy, safety and tolerability of the new combined medication Allergoferon® beta in patients with moderate-to-severe hay fever (seasonal allergic rhinitis and conjunctivitis) during periods of exacerbation. patients and methods: the object of our study was medication Allergoferon® beta (recombinant human interferon alpha-2b, not less than 5000 IU/ml + betamethasone sodium phosphate, 1.0 mg/ml) in the form of eye and nasal drops. Total of 120 patients aged 18-65 years with hay fever for at least two years were enrolled in the clinical trial, including 76 women and 44 men. All patients had a clinical picture of moderate-to-severe hay fever during periods of exacerbation. Patients were divided into two equal groups. The main group received Allergoferon® beta, the control group was treated with Oftan® Dexamethasone and Nasobek medications. This trial used a randomized, open-label, multicenter, parallel, comparative, controlled study design. results: we found that new combined medication Allergoferon® beta had a significant therapeutic effect in relieving main clinical manifestations of acute hay fever and showed a higher efficacy, than the comparison remedies. By comparing similar symptoms in both groups, we observed that in patients treated with Allergoferon® beta clinical symptoms of acute hay fever were relieved earlier (on the 5th day of treatment), than in the control group (on the 10th day of treatment) and the disease itself proceeded milder. Therapeutic efficacy of Allergoferon® beta was 85,96% (in the control group — 74,73%, p&lt;0.05). During clinical trial we have not observed any adverse effects; general or local toxic and allergic reactions were also not discovered. The medication tolerability was rated as “good” for patients. Conclusion: according to the clinical study results, the medication Allergoferon® beta (eye and nasal drops) is recommended for the state registration and can be used by medical professionals in the treatment of moderate-to-severe hay fever (seasonal allergic rhinitis and conjunctivitis), including periods of exacerbation.</p></sec><sec><title> </title><p> </p></sec><sec><title> </title><p> </p></sec><sec><title> </title><p> </p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>поллиноз</kwd><kwd>эффективность</kwd><kwd>безопасность</kwd><kwd>рекомбинантный интерферон</kwd><kwd>бетаметазон</kwd><kwd>Аллергоферон® бета</kwd></kwd-group><kwd-group xml:lang="en"><kwd>hay fever</kwd><kwd>efficacy</kwd><kwd>safety</kwd><kwd>recombinant interferon</kwd><kwd>betamethasone</kwd><kwd>Allergoferon® beta</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">Khaitov R.M. ed. 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