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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">nid</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология и диализ</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology and Dialysis</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1680-4422</issn><issn pub-type="epub">2618-9801</issn><publisher><publisher-name>Российское диализное общество</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">nid-441</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>Гемолитико-уремический синдром у детей: эпидемиология, особенности клинико-лабораторного течения, лечение и исходы (Одноцентровое исследование)</article-title><trans-title-group xml:lang="en"><trans-title>Hemolytic uremic syndrome in children: epidemiology, clinical and laboratory findings, treatment and outcomes (Single center study)</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>Байко</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Baiko</surname><given-names>S. V.</given-names></name></name-alternatives><email xlink:type="simple">baiko@yandex.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>Сукало</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Sukalo</surname><given-names>A. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Судновская</surname><given-names>К. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Sudnovskaya</surname><given-names>K. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Белорусский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Belarusian State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Белорусский государственный медицинский университет; Национальная академия наук Беларуси</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Belarusian State Medical University; Belarusian National Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>УЗ «Минская областная детская клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Minsk Regional Children’s Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>19</day><month>08</month><year>2024</year></pub-date><volume>18</volume><issue>3</issue><fpage>282</fpage><lpage>299</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Байко С.В., Сукало А.В., Судновская К.А., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Байко С.В., Сукало А.В., Судновская К.А.</copyright-holder><copyright-holder xml:lang="en">Baiko S.V., Sukalo A.V., Sudnovskaya K.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://journal.nephro.ru/jour/article/view/441">https://journal.nephro.ru/jour/article/view/441</self-uri><abstract><p>Гемолитико-уремический синдром (ГУС) является наиболее частой причиной острой почечной недостаточности у детей раннего возраста. Цель исследования: оценить заболеваемость ГУС у детей в республике Беларусь, изучить возрастные и половые различия, сезонные колебания, распространенность различных вариантов ГУС, а также гематологические и биохимические изменения крови и их динамику в процессе восстановления функции почек, степень диагностической значимости маркеров острого повреждения почек, активации комплемента, тромбоза и воспаления. Материалы и методы: в проспективное, продольное, непрерывное исследование включено 218 детей, перенесших ГУС за период 2005-2014 г. в Беларуси. Результаты: ГУС наиболее часто развивается у детей в возрасте до 5 лет (89,9%), встречается с одинаковой частотой среди представителей обоих полов, чаще среди городского населения. Заболеваемость составила 3,9 случая на 100 000 детского населения в возрасте &lt;5 лет и 1,5 в возрасте &lt;15 лет. Наиболее частый вариант ГУС - диарея-ассоциированный (96,3%), связь с шига-токсином которого подтверждена в 49,5% случаев. Описаны особенности клинико-лабораторного течения заболевания и лечения у детей, получавших заместительную почечную терапию и без нее. Перитонеальный диализ был методом выбора у 77,9% пациентов, нуждавшихся в диализной терапии. Выводы: применение ряда организационных мероприятий, диагностических и лечебных рекомендаций позволило снизить летальность у детей с ГУС до 2,3%. Результаты лечения детей с атипичным ГУС остаются неудовлетворительными.</p></abstract><trans-abstract xml:lang="en"><p>Hemolytic uremic syndrome (HUS) is the most common cause of acute renal failure in children under 5. Aim: to assess the incidence of HUS in children in Belarus, to study its age and sex differences, seasonal variations, incidence of different variants of HUS, as well as hematological and biochemical blood changes and their dynamics in the process of recovery of renal function, the diagnostic significance of markers of acute kidney injury, complement activation, thrombosis and inflammation. Materials and methods: 218 children with HUS were included to a prospective, long-term, uninterrupted study for the 10 year period 2005-2014 in Belarus. Results: HUS more often develops in children under the age of 5 years (89.9%), occurs with equal frequency among both sexes, more often in the urban population. The incidence was 3.9 cases per 100 000 children population of age &lt;5 years and 1.5 at the age of &lt;15 years. The most common type of HUS is diarrhea-associated (96.3%), a link with Shiga-toxin was confirmed in 49.5% of cases. The clinical and laboratory changes of the disease and treatment in those who received renal replacement therapy and without it were described. Peritoneal dialysis has been the method of choice in 77.9% of patients requiring dialysis therapy. Conclusions: the use of a number of organizational, diagnostic and treatment recommendations allowed reducing mortality in children with HUS to 2.3%. The results of treatment of children with atypical HUS remain unsatisfactory.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гемолитико-уремический синдром</kwd><kwd>эпидемиология</kwd><kwd>заболеваемость</kwd><kwd>летальность</kwd><kwd>дети</kwd><kwd>клинические изменения</kwd><kwd>лабораторные показатели</kwd><kwd>NGAL</kwd><kwd>витамин Д</kwd><kwd>С3 фракция комплемента</kwd><kwd>hemolytic uremic syndrome</kwd><kwd>epidemiology</kwd><kwd>incidence</kwd><kwd>mortality</kwd><kwd>children</kwd><kwd>clinical changes</kwd><kwd>laboratory findings</kwd><kwd>NGAL</kwd><kwd>vitamin D</kwd><kwd>C3 complement</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">Байко С.В. Гемолитико-уремический синдром: эпидемиология, классификация, клиника, диагностика, лечение (Часть 1). Нефрология и диализ. 2007. 9(4): 370-377.</mixed-citation><mixed-citation xml:lang="en">Байко С.В. 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