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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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pharmateca</journal-id><journal-title-group><journal-title xml:lang="en">Pharmateca</journal-title><trans-title-group xml:lang="ru"><trans-title>Фарматека</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2073-4034</issn><issn publication-format="electronic">2414-9128</issn><publisher><publisher-name xml:lang="en">Bionika Media</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">278823</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">EFFECACY AND SAFETY OF SANDOSTATIN® LAR IN HIGH DOSES: REVIEW OF RESEARCHES IN EUROPEAN CENTERS</article-title><trans-title-group xml:lang="ru"><trans-title>ЭФФЕКТИВНОСТЬ И БЕЗОПАСНОСТЬ ЛЕЧЕНИЯ САНДОСТАТИНОМ ЛАР В ВЫСОКИХ ДОЗАХ: ОБЗОР ИССЛЕДОВАНИЙ ЕВРОПЕЙСКИХ ЦЕНТРОВ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ilovayskaya</surname><given-names>Irena Adol'fovna</given-names></name><name xml:lang="ru"><surname>Иловайская</surname><given-names>Ирэна Адольфовна</given-names></name></name-alternatives><bio xml:lang="ru"><p>МОНИКИ им. М.Ф. Владимирского, Москва</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Ilovayskaya</surname><given-names>I A</given-names></name><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en"></institution></aff><aff><institution xml:lang="ru">МОНИКИ им. М.Ф. Владимирского, Москва</institution></aff></aff-alternatives><aff id="aff2"><institution></institution></aff><pub-date date-type="pub" iso-8601-date="2011-03-15" publication-format="electronic"><day>15</day><month>03</month><year>2011</year></pub-date><volume>18</volume><issue>5</issue><issue-title xml:lang="en">NO5 (2011)</issue-title><issue-title xml:lang="ru">№5 (2011)</issue-title><fpage>28</fpage><lpage>32</lpage><history><date date-type="received" iso-8601-date="2023-02-23"><day>23</day><month>02</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2011, Bionika Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, ООО «Бионика Медиа»</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="en">Bionika Media</copyright-holder><copyright-holder xml:lang="ru">ООО «Бионика Медиа»</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/2073-4034/article/view/278823">https://journals.eco-vector.com/2073-4034/article/view/278823</self-uri><abstract xml:lang="en"><p>Therapy of somatostatin analogues plays an important role in the treatment of acromegaly and is used as an additional treatment after neurosurgical intervention or as a primary therapy. Prolonged form of octreotide (Swiss, Sandostatin® LAR) is the most studied and widely used as somatostatin analog. The initial dose of Sandostatin® LAR is typically 20 mg, however, according to many studies, it was noted that after the first 3 months of treatment does not always achieved remission of acromegaly and to better control the disease should increase the dose of the drug in most patients. This review focuses on the use of Sandostatin® LAR at high (30 mg per month or more) doses in patients with active acromegaly. The use of Sandostatin® LAR at high (30 mg per month or more) doses, increases the efficiency of achieving biochemical control of active acromegaly, without compromising the safety profile of this drug.</p></abstract><trans-abstract xml:lang="ru"><p>Медикаментозная терапия аналогами соматостатина занимает важное место в лечении акромегалии, и применяется как дополнительное лечение после нейрохирургического вмешательства, или как первичная терапия. Пролонгированная форма октреотида швейцарского производства (Сандостатин ЛАР®) является наиболее изученным и широко применяемым аналогом соматостатина. Начальная доза сандостатина ЛАР обычно составляет 20 мг, однако по данным многих исследований было отмечено, что после первых 3х месяцев лечения не всегда достигается ремиссия акромегалия, и для улучшения контроля над заболеванием необходимо увеличивать дозу препарата у большей части пациентов. Данный обзор посвящен применению сандостатина ЛАР в высоких (30 мг в мес и более) дозах в лечении пациентов с активной акромегалией. Применение сандостатина ЛАР в высоких (30 мг в мес и более) дозах повышает эффективность достижения биохимического контроля над активной акромегалией, не ухудшая при этом профиль безопасности данного препарата.</p></trans-abstract><kwd-group xml:lang="en"><kwd>acromegaly</kwd><kwd>drug treatment</kwd><kwd>Sandostatin® LAR</kwd><kwd>efficiency</kwd><kwd>safety</kwd><kwd>high-dose</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>акромегалия</kwd><kwd>медикаментозное лечение</kwd><kwd>сандостатин ЛАР</kwd><kwd>эффективность</kwd><kwd>безопасность</kwd><kwd>высокие дозы</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Holdaway IM, Bolland MJ, Gamble GD. A meta-analysis of the effect of lowering serum levels of GH and IGF-I on mortality in acromegaly. Eur J Endocrinol 2008;159:89-95.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Ludecke DK, Abe T. 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