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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">gastro-j</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал гастроэнтерологии, гепатологии, колопроктологии</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Gastroenterology, Hepatology, Coloproctology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1382-4376</issn><issn pub-type="epub">2658-6673</issn><publisher><publisher-name>«Gastro» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.22416/1382-4376-2023-33-1-68-76</article-id><article-id custom-type="elpub" pub-id-type="custom">gastro-j-770</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>НАЦИОНАЛЬНАЯ ШКОЛА ГАСТРОЭНТЕРОЛОГИИ, ГЕПАТОЛОГИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>NATIONAL COLLEGE OF GASTROENTEROLOGY, HEPATOLOGY</subject></subj-group></article-categories><title-group><article-title>Как безошибочно выбрать ингибитор протонной помпы у пациента с гастроэзофагеальной рефлюксной болезнью?</article-title><trans-title-group xml:lang="en"><trans-title>How to Make the Right Choice of Proton Pump Inhibitor for Patients with Gastroesophageal Reflux Disease?</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0139-9773</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Евсютина</surname><given-names>Ю. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Evsyutina</surname><given-names>Yu. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Евсютина Юлия Викторовна — кандидат медицинских наук, магистр медицины, врач </p><p>ул. Буньон 46, 1011, Швейцария, Лозанна</p></bio><bio xml:lang="en"><p>Yulia V. Evsyutina — Cand. Sci. (Med), master of medicine, physician of Centre hospitalier universitaire vaudois (CHUV)</p><p>Rue du Bugnon 46, 1011, Lausanne, Switzerland</p></bio><email xlink:type="simple">evsyutina.yulia@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Университетский кантональный госпиталь</institution><country>Швейцария</country></aff><aff xml:lang="en"><institution>Centre hospitalier universitaire vaudois</institution><country>Switzerland</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>23</day><month>04</month><year>2023</year></pub-date><volume>33</volume><issue>1</issue><fpage>68</fpage><lpage>76</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Евсютина Ю.В., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Евсютина Ю.В.</copyright-holder><copyright-holder xml:lang="en">Evsyutina Y.V.</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.gastro-j.ru/jour/article/view/770">https://www.gastro-j.ru/jour/article/view/770</self-uri><abstract><sec><title>Цель исследования</title><p>Цель исследования: провести анализ основных фармакокинетических свойств ингибиторов протонной помпы (ИПП) и их значение в лечении гастроэзофагеальной рефлюксной болезни (ГЭРБ).</p></sec><sec><title>Основные положения</title><p>Основные положения. Пантопразол обладает высокой биодоступностью, абсолютная биодоступность пантопразола в дозе 40 мг составляет 77 % начиная с первого приема и не изменяется при повторном применении. Пантопразол демонстрирует более быстрое начало действия в сравнении с омепразолом. Одновременный прием пищи не изменяет биодоступность пантопразола. Подавление продукции соляной кислоты на фоне приема пантопразола сопровождается достижением эндоскопической ремиссии ГЭРБ к 28-му дню у 91 % пациентов с рефлюкс-эзофагитом и к 56-му дню — у всех пациентов в исследованиях «PANSTAR». Пантопразол в сравнении с другими ИПП оказывает незначительное влияние на CYP2C19, что минимизирует риск межлекарственных взаимодействий. Пантопразол — наиболее рН-селективный ИПП, что обусловливает специфичность действия только в париетальных клетках желудка и наибольшую безопасность длительного приема у пациентов с коморбидной патологией.</p></sec><sec><title>Заключение</title><p>Заключение. ИПП составляют основу терапии кислотозависимых заболеваний и, в частности, гастроэзофагеальной рефлюксной болезни. От других ИПП пантопразол отличает стойкая высокая биодоступность, продолжительный антисекреторный эффект, очень низкое сродство с цитохромом Р450.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Аim</title><p>Аim: to analyze the main pharmacokinetic properties of proton pump inhibitors (PPIs) and their significance in the treatment of gastroesophageal reflux disease (GERD).</p></sec><sec><title>Key points</title><p>Key points. Pantoprazole has a high bioavailability, the absolute bioavailability of pantoprazole at a dose of 40 mg is 77 % from the first dose and does not change with repeated use. Pantoprazole shows a faster onset of action than omeprazole. Simultaneous food intake does not change the bioavailability of pantoprazole. Suppression of hydrochloric acid production while taking pantoprazole accompanies by the achievement of endoscopic remission of GERD by day 28 in 91 % of patients with reflux esophagitis and by day 56 in all patients in the PANSTAR studies. Pantoprazole has little effect on CYP2C19 compared to other PPIs, minimizing the risk of drug-drug interactions. Pantoprazole is the most pH-selective PPI, which determines the specificity of action only in the parietal cells of the stomach and the greatest safety of long-term use in patients with comorbid pathology.</p></sec><sec><title>Conclusion</title><p>Conclusion. PPIs form the basis of the therapy of acid-dependent diseases, and, in particular, gastroesophageal reflux disease. Pantoprazole is distinguished from other PPIs by its persistent high bioavailability, long-term antisecretory effect, and very low affinity for cytochrome P450.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>гастроэзофагеальная рефлюксная болезнь</kwd><kwd>париетальная клетка</kwd><kwd>ингибиторы протонной помпы</kwd><kwd>пантопразол</kwd><kwd>биодоступность</kwd><kwd>межлекарственные взаимодействия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>gastroesophageal reflux disease</kwd><kwd>parietal cell</kwd><kwd>proton pump inhibitors</kwd><kwd>pantoprazole</kwd><kwd>bioavailability</kwd><kwd>drug-drug interactions</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">опубликована при поддержке КРКА.</funding-statement><funding-statement xml:lang="en">published with the support of Krka.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Ивашкин В.Т., Маев И.В., Трухманов А.С., Лапина Т.Л., Сторонова О.А., Зайратьянц О.В. и др. 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