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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 pub-id-type="doi">10.28996/1680-4422-2017-2-271-279</article-id><article-id custom-type="elpub" pub-id-type="custom">nid-369</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>Артериальная гипертензия у детей, перенесших гемолитико-уремический синдром</article-title><trans-title-group xml:lang="en"><trans-title>Arterial hypertension in children after hemolytic uremic syndrome</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>Абросимова</surname><given-names>Н. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Abrosimova</surname><given-names>N. N.</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 «2-я городская детская клиническая больница»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>2nd Children's Hospital</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>15</day><month>08</month><year>2024</year></pub-date><volume>19</volume><issue>2</issue><fpage>271</fpage><lpage>279</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Байко С.В., Сукало А.В., Абросимова Н.Н., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Байко С.В., Сукало А.В., Абросимова Н.Н.</copyright-holder><copyright-holder xml:lang="en">Baiko S.V., Sukalo A.V., Abrosimova N.N.</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/369">https://journal.nephro.ru/jour/article/view/369</self-uri><abstract><p>Ртериальная гипертензия (АГ) является одним из наиболее частых осложнений, сохраняющихся или развивающихся вновь после перенесенного гемолитико-уремического синдрома (ГУС). АГ, выявленная в детском возрасте, представляет высокий риск развития сердечно-сосудистой и почечной патологии во взрослой жизни. Цель исследования: определить частоту встречаемости и характеристики АГ у детей после перенесенного ГУС, оценить суточный ритм, вариабельность артериального давления (АД) и взаимосвязи между уровнями АД и другими факторами неблагоприятного исхода ГУС. Материалы и методы: в исследование включено 59 детей в возрасте 7 лет (5,9; 8,3) и катамнезом ГУС 5,12±2,07 лет. Всем пациентам проведено суточное мониторирование АД (СМАД), выполнены антропометрические измерения, определены суточные потери белка и альбумина с мочой, рассчитана скорость клубочковой фильтрации. Результаты: по данным СМАД установлена частота различных форм АГ у детей в катамнезе ГУС: прегипертензия у 10,2% пациентов, АГ «белого халата» у 13,6% и скрытая АГ у 6,8%. АГ выявлялась с высокой частотой как у получавших диализ в остром периоде ГУС, так из без него (29,6% и 20%, соответственно). Повышенное АД определялось преимущественно в ночное время за счет систолического и сопровождалось его повышенной нагрузкой и недостаточным ночным снижением. У ряда пациентов ожирение утяжеляло течение систолической АГ, которая сохранялась на протяжении суток. Микроальбуминурия (МАУ) встречалась у 50% детей c АГ и тесно коррелировала с тяжестью почечного повреждения в остром периоде ГУС (rs=0,4, p&lt;0,05). Выводы: учитывая преимущественно ночную АГ у детей после ГУС, суточному мониторированию АД отводится ключевое место в ее диагностике. Выявление патологической МАУ у этой категории пациентов является показанием для проведения СМАД, даже если АД не превышает возрастные нормы на визите у врача.</p></abstract><trans-abstract xml:lang="en"><p>Arterial hypertension (AH) is one of the most common complications which remains or redevelops after hemolytic uremic syndrome (HUS). AH that diagnosed in childhood represents a high risk of developing cardiovascular and renal disease in adult age. Aim: to determine the incidence and characteristics of AH in children after HUS; to assess circadian rhythm, blood pressure (BP) variability and the relationship between BP levels and other risk factors of unfavourable outcome of HUS. Materials and methods: the study included 59 children, aged 7 years (5.9; 8.3) and fol-low-up of HUS 5.12±2.07 years. All patients underwent daily blood pressure monitoring (ABPM), anthropometric measurements were performed, losses of protein and albumin in the urine were determined daily, glomerular filtration rate was calculated. Results: According to ABPM the prevalence of different forms of arterial hypertension in children after HUS was established: prehypertension was found in 10.2% of patients, white coat and masked AH were found in 13.6% and in 6.8% of patients. AH was detected more frequently in those patients who receiving dialysis in the acute period of HUS than without it (29.6% vs. 20%). High blood pressure was observed mainly at night time. In some patients obesity worsened systolic hypertension, which persisted throughout the day. Microalbuminuria was found in 50% of children with AH closely correlated with the severity of renal damage in the acute period of HUS (rs=0.4; p&lt;0.05). Conclusions: Considering that AH in children after HUS is the predominantly nocturnal, 24h monitoring of blood pressure play a key role in its diagnosis. The detection of pathological microalbuminuria in this category of patients is the indication for ABPM, even at normal office BP.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>артериальная гипертензия</kwd><kwd>гемолитико-уремический синдром (ГУС)</kwd><kwd>дети</kwd><kwd>микроальбуминурия</kwd><kwd>суточное мониторирование артериального давления (СМАД)</kwd><kwd>arterial hypertension</kwd><kwd>hemolytic uremic syndrome (HUS)</kwd><kwd>children</kwd><kwd>microalbuminuria</kwd><kwd>24 h ambulatory blood pressure monitoring (ABPM)</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., Сукало А.В., Судновская К.А. Гемолитико-уремический синдром у детей: эпидемиология, особенности клинико-лабораторного течения, лечение и исходы (одноцентровое исследование). 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