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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">ppharm</journal-id><journal-title-group><journal-title xml:lang="ru">Педиатрическая фармакология</journal-title><trans-title-group xml:lang="en"><trans-title>Pediatric pharmacology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1727-5776</issn><issn pub-type="epub">2500-3089</issn><publisher><publisher-name>Издательство «ПедиатрЪ»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">ppharm-1075</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 СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>ОСОБЕННОСТИ ПОРАЖЕНИЯ ОРГАНОВ ДЫХАНИЯ ПРИ МУКОВИСЦИДОЗЕ. КЛИНИЧЕСКАЯ ЭФФЕКТИВНОСТЬ ТЕРАПИИ ДОРНАЗОЙ АЛЬФА У ДЕТЕЙ</article-title><trans-title-group xml:lang="en"><trans-title>SPECIFIC DISORDERS OF THE RESPIRATORY SYSTEM IN CYSTIC FIBROSIS. CLINICAL EFFICACY OF THERAPY WITH DORNASE ALFA IN CHILDREN</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>Симанова</surname><given-names>Т.В.</given-names></name><name name-style="western" xml:lang="en"><surname>Simanova</surname><given-names>T.V.</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>Ожегов</surname><given-names>А.М.</given-names></name><name name-style="western" xml:lang="en"><surname>Ozhegov</surname><given-names>A.M.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Цыганок</surname><given-names>А.В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tsyganok</surname><given-names>A.V.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Республиканская детская клиническая больница Минздрава Удмуртской Республики</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Republican Children’s Clinical Hospital of the Healthcare Ministry of the Udmurtian Republic</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Ижевская государственная медицинская академия Росздрава</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Izhevsk State Medical Academy of the Russia’s Federal Healthcare Agency</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2010</year></pub-date><pub-date pub-type="epub"><day>04</day><month>12</month><year>2015</year></pub-date><volume>7</volume><issue>6</issue><issue-title>Педиатрическая фармакология</issue-title><fpage>44</fpage><lpage>48</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Симанова Т., Ожегов А., Цыганок А., 2010</copyright-statement><copyright-year>2010</copyright-year><copyright-holder xml:lang="ru">Симанова Т., Ожегов А., Цыганок А.</copyright-holder><copyright-holder xml:lang="en">Simanova T., Ozhegov A., Tsyganok 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.pedpharma.ru/jour/article/view/1075">https://www.pedpharma.ru/jour/article/view/1075</self-uri><abstract><p>Статья посвящена особенностям поражения органов дыхания при муковисцидозе. Было обследовано 64 больных муковисцидозом (МВ) в возрасте от 2 месяцев до 32 лет, жителей Удмуртской Республики. Изучены эпидемиологические и генетические особенности заболевания в указанном регионе РФ. Проведены клинические, рентгенологические, функциональные и микробиологические исследования дыхательной системы у больных МВ. Установлено более частое формирование тяжелых структурных изменений бронхолегочной системы при генотипе delF508 и хронической инфекции Pseudomonas aeruginosa, Staphylococcus aureus. Полученные данные указывают на целесообразность выделения наиболее уязвимых (по тяжелому поражению органов дыхания) групп пациентов с МВ для оптимизации терапевтических мероприятий. Представлены показатели клинической эффективности терапии дорназой альфа у детей с МВ. Ключевые слова: муковисцидоз, генотип, мутация delF508, органы дыхания, синегнойная инфекция, стафилококковая инфекция, функция внешнего дыхания, муколитическая терапия, дорназа альфа. </p><p>(Педиатрическая фармакология. – 2010; 7(6):44-48)</p></abstract><trans-abstract xml:lang="en"><p>The article is devoted to specific disorders of the respiratory system in cystic fibrosis. 64 patients with cystic fibrosis (CF) aged 2 months to 32 years and residing in the Udmurtian Republic were studied. Epidemiological and genetic specifics of this disease in the mentioned region of the RF were examined. Clinical, X-ray, functional and microbiological studies of the CF patients’ respiratory system were conducted. It was found that genotype delF508 and chronic infection Pseudomonas aeruginosa, Staphylococcus aureus cause severe structural changes to the bronchopulmonary system more often. The obtained data suggest the advisability of identifying the groups of CF patients at the highest risk of severe respiratory system disorders in order to optimise therapeutic efforts. The article provides indicators of clinical efficacy of a dornase alfa therapy in CF children.Key words: cystic fibrosis, genotype, delF508 mutation, respiratory organs, pseudomonas aeruginosa infection, staphylococcal infection, respiratory function, mucolytic function, dornase alfa. </p><p> (Pediatric Pharmacology. – 2010; 7(6):44-48)</p></trans-abstract></article-meta></front><back><ref-list><title>References</title></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>
