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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">clinvest</journal-id><journal-title-group><journal-title xml:lang="ru">Качественная клиническая практика</journal-title><trans-title-group xml:lang="en"><trans-title>Kachestvennaya Klinicheskaya Praktika = Good Clinical Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2588-0519</issn><issn pub-type="epub">2618-8473</issn><publisher><publisher-name>ООО «Издательство ОКИ</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.37489/2588-0519-2021-2-4-15</article-id><article-id custom-type="elpub" pub-id-type="custom">clinvest-570</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>ФАРМАКОЭКОНОМИКА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PHARMACOECONOMICS</subject></subj-group></article-categories><title-group><article-title>Фармакоэкономические характеристики агонистов рецепторов глюкагоноподобного пептида-1 и препаратов на их основе</article-title><trans-title-group xml:lang="en"><trans-title>Pharmacoeconomic characteristics of agonists of receptors for glucagon-like peptide-1 and medicines on their base</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>Дьяков</surname><given-names>И. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Dyakov</surname><given-names>I. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дьяков Илья Николаевич, к. б. н., генеральный директор. SPIN-код: 1854-0958</p><p>Москва</p></bio><bio xml:lang="en"><p>Dyakov Ilya, Cand. Sci. Biology, General Director. SPIN code: 1854-0958</p><p>Moscow</p></bio><email xlink:type="simple">dyakov.ilya@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6348-6867</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зырянов</surname><given-names>С. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Zyryanov</surname><given-names>S. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Зырянов Сергей Кенсаринович, д. м. н., профессор, зав. кафедрой общей и клинической фармакологии. SPIN-код: 2725-9981</p><p>Москва</p></bio><bio xml:lang="en"><p>Zyryanov Sergey, Dr. Sci. (Med.), professor, Head of the Department of General and Clinical Pharmacology. SPIN code: 2725-9981</p><p>Moscow</p></bio><email xlink:type="simple">sergey.k.zyryanov@gmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>АНО «Научно-практический центр исследования проблем рациональной фармакотерапии и фармакоэкономики»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Non-proft organization “Scientifc and Practical Centre for rational pharmaceutical management and pharmacoeconomics problems”</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГАОУ ВО «Российский университет дружбы народов»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>RUDN University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>06</day><month>08</month><year>2021</year></pub-date><volume>0</volume><issue>2</issue><fpage>4</fpage><lpage>15</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Дьяков И.Н., Зырянов С.К., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Дьяков И.Н., Зырянов С.К.</copyright-holder><copyright-holder xml:lang="en">Dyakov I.N., Zyryanov S.K.</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.clinvest.ru/jour/article/view/570">https://www.clinvest.ru/jour/article/view/570</self-uri><abstract><p>Проблема эффективного контроля сахарного диабета является актуальной в том числе и с точки зрения оптимального расходования ресурсов здравоохранения. Агонисты рецепторов глюкагоноподобного пептида-1 (арГПП-1) являются одной из наиболее современных опций для контроля гликемии при сахарном диабете 2 типа (СД 2) и входят во все современные рекомендации по управлению заболеванием. Экономические сравнительные аспекты применения этих препаратов в отечественных условиях не изучались. Материал и методы. На основе опубликованных данных клинических исследований проведена сравнительная экономическая оценка применения инсулина гларгин + ликсисенатид (иГлаЛикси), Эксенатида (Экс), дулаглутида (Дула), лираглутида (Лира) и комбинаций этих арГПП-1 с иГла 100 ЕД/мл. Критерием эффективности выбрано число больных (в %), достигших целевого уровня компенсации СД по гликированному гемоглобину (HbA1c) менее 7 %. Проведено непрямое сравнение с расчётом отношения шансов (OR) получения клинического эффекта. С помощью моделирования определены прямые (расходы на лекарства и лечение сердечно-сосудистых осложнений) и непрямые медицинские (оплата листков нетрудоспособности), а также непрямые немедицинские (потери ВВП) затраты. Проведён анализ чувствительности полученных результатов. Результаты. Фармакоэкономический анализ, основанный на непрямых сравнениях эффективности иГлаЛикси и Дула (оба препарата входят в Перечень ЖНВЛП), а также Лира и Экс (не входят в Перечень ЖНВЛП), показал экономические преимущества эффективного контроля СД 2. иГлаЛикси продемонстрировал существенные экономические преимущества как при сравнении с применением только арГПП-1 (снижение прямых затрат в сравнении с Экс на 23,8 %, с Дула — на 15,6 %, с Лира — на 54,4 %), так и их комбинаций с инсулином гларгин 100 ЕД/мл (снижение прямых затрат в сравнении с иГла + Экс на 16,2 %, с иГла + Дула — на 15,2 %). Общие расходы (прямые + непрямые) иГла Ликси снижал в большей степени в сравнении с Экс, Дула и Лира (на 19,9, 9,3 и 45,2 %, соответственно). Заключение. Эффективный контроль СД 2 с помощью современных арГПП-1 и препаратов на их основе является экономически выгодным с позиции государства вследствие уменьшения расходов на предупреждаемые осложнения заболевания.</p></abstract><trans-abstract xml:lang="en"><p>The effective control of Diabetes Mellitus (DM) is an actual problem from optimal expenditures of health care system point of view. Agonists of receptors for glucagon like peptide-1 (aGLP-1) are one of the modern option for glycemia control in DM Type 2 and included in all current guidelines for the treatment control. The economic comparative aspects of the use of these drugs in the local conditions have not been studied. Materials and methods. Comparative economic evaluation of insulin glargine + lixisenatide (iGlaLixi), exenatide (Exe), dulaglutide (Dula), liraglutide (Lira) and combinations of their aGLP-1 with iGla 100 U has been performed base on published clinical data of efficacy. Number of patients with HbA1c &lt;7 % was chosen as efficacy criterion. Non-direct comparison with Odds Ratio (OR) calculation was prepared. Direct and indirect costs (medications, treatment of CV-complications, GDP loses etc.) were indicated and calculated based on constructed model. Sensitivity analysis has been provided for validation of results. Results. Pharmacoeconomic analysis based on non-direct efficacy comparisons of iGlaLixi, Exe, Lira and Dula has shown of economic advantages of effective DM2T control. iGlaLixi has demonstrated economic advantages as well usage aGLP-1 only (direct costs decreasing vs Exe on 23,8 %, vs Dula on 15,6 %, vs Lira on 54,4 %) as their combinations with iGla 100 U (direct costs decreasing vs iGla 100 U + Exe on 23,8 %, vs iGla 100 U + Dula on 15,2 %). iGlaLixi decreased a total cost (direct and non-direct) better than Exe, Dula and Lira (on 19,9, 9,3 и 45,2 % accordingly). Conclusion. An effective control of DM2T with aGLP-1 and medicines on their base has an economic value because lead to expenditures for complications decreasing from government position.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>сахарный диабет 2 типа</kwd><kwd>фармакоэкономика</kwd><kwd>инсулин гларгин + ликсисенатид</kwd><kwd>лираглутид</kwd><kwd>Эксенатид</kwd><kwd>дулаглутид</kwd></kwd-group><kwd-group xml:lang="en"><kwd>diabetes mellitus type 2</kwd><kwd>pharmacoeconomics</kwd><kwd>insulin glargine + lixisenatide</kwd><kwd>liraglutide</kwd><kwd>exenatide</kwd><kwd>dulaglutide</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">Клинические рекомендации «Сахарный диабет 2 типа у взрослых» Утверждены Минздравом России. 2019. 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