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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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">212</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2018-17-4-43-50</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Results of clinical application of pathogen-reduced red blood cell suspension in children with oncological and hematological diseases</article-title><trans-title-group xml:lang="ru"><trans-title>Результаты клинического применения патоген-редуцированной эритроцитной взвеси у детей с онкологическими и гематологическими заболеваниями</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9881-1041</contrib-id><name-alternatives><name xml:lang="en"><surname>Kumukova</surname><given-names>I. B.</given-names></name><name xml:lang="ru"><surname>Кумукова</surname><given-names>И. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>transfusiologist.</p><p>117997, Moscow, Samory Mashela st., 1. </p></bio><bio xml:lang="ru"><p>врач-трансфузиолог.</p><p> 117997, Москва, ГСП-7, ул. Саморы Машела, 1. </p></bio><email>irina_kumukova@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0231-1617</contrib-id><name-alternatives><name xml:lang="en"><surname>Trakhtman</surname><given-names>P. I.</given-names></name><name xml:lang="ru"><surname>Трахтман</surname><given-names>П. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1219-8654</contrib-id><name-alternatives><name xml:lang="en"><surname>Starostin</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Старостин</surname><given-names>Н. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8392-6209</contrib-id><name-alternatives><name xml:lang="en"><surname>Kadaeva</surname><given-names>L. J.</given-names></name><name xml:lang="ru"><surname>Кадаева</surname><given-names>Л. Ж.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7576-4836</contrib-id><name-alternatives><name xml:lang="en"><surname>Chaykina</surname><given-names>O. A.</given-names></name><name xml:lang="ru"><surname>Чайкина</surname><given-names>О. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation.</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России.</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-01-13" publication-format="electronic"><day>13</day><month>01</month><year>2019</year></pub-date><volume>17</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>43</fpage><lpage>50</lpage><history><date date-type="received" iso-8601-date="2019-01-12"><day>12</day><month>01</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-01-12"><day>12</day><month>01</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/212">https://hemoncim.com/jour/article/view/212</self-uri><abstract xml:lang="en"><p>The problem of blood-borne infections remains relevant in transfusion medicine. Pathogen reduction technologies (PRT) provide a preventive approach to a wide range of transfusion-transmitted infectious diseases. To date, PRT widely used for a number of blood components, however, the use of these technologies for the treatment of erythrocyte-containing components has not been studied. Objective: to conduct a comparative analysis of the clinical efficacy of transfusions of pathogen-reduced and gamma-irradiated erythrocyte suspension in pediatric patients with various oncological and hematological diseases. Seventy transfusions of red blood cell suspensions (RBC-S) (35 transfusions of pathogen-reduced RBC-S and 35 transfusions of gammairradiated RBC-S) in pediatric patients with oncological and hematological diseases were analized. Clinical efficacy parameters such as the hemoglobin and the hematocrit increment after transfusion, the interval between transfusions, the frequency and severity of transfusion reactions were estimated. We also evaluated the correlation between the hemoglobin and the hematocrit increment with age, patient’s body weight, the hemoglobin concentration and patient's hematocrit before transfusion, the volume of transfusion, the hemoglobin dose and the adjusted hemoglobin dose received for transfusion. We found that the clinical efficacy and safety of RBC-Ss of the compared groups did not differ: the hematocrit and the hemoglobin increment, the frequency and severity of transfusion reactions, and the interval between transfusions were comparable between groups. There was no evidence of immune elimination and allo-sensibilization caused by pathogen-reduced RBC-S. In the group of patients receiving pathogen-reduced RBC-S, a correlation was found between the increase in the hemoglobin and hematocrit values with some of the EV indices. According to our data, the spectrum of efficiency and safety indicators of pathogen-reduced RBC-S is no worse than that of gamma-irradiated RBC-S, provided that RBC-S is used for 14 days of storage.</p></abstract><trans-abstract xml:lang="ru"><p>Проблема гемотрансмиссивных инфекций сохраняет актуальность в практической трансфу- зиологии. Технологии редукции патогенов (ТРП) обеспечивают превентивный подход в отношении широкого спектра трансфузионно-опасных инфекций. ТРП нашли широкое применение при клиническом использовании ряда компонентов крови, однако возможности использования данных технологий для обработки эритроцитсодержащих компонентов не изучены. Целью работы был сравнительный анализ клинической эффективности трансфузий патоген-редуцированной и гамма-облученной эритроцитной взвеси у пациентов детского возраста с различными онкологическими и гематологическими заболеваниями. Проведен анализ 70 трансфузий эритроцитных взвесей (ЭВ) в двух группах пациентов детского возраста с онкологическими и гематологическими заболеваниями (35 трансфузий патоген-редуцированной ЭВ и 35 трансфузий гамма-облученной ЭВ). Исследованы параметры клинической эффективности: прирост гемоглобина и гематокрита после трансфузии, интервал между трансфузиями, частота и тяжесть посттрансфузионных реакций. Проведена оценка наличия корреляции между приростом гемоглобина и гематокрита с возрастом, массой тела пациента, концентрацией гемоглобина и гематокрита пациента до трансфузии, объемом трансфузии, дозой гемоглобина и скорректированной дозой гемоглобина, полученной за трансфузию. Исследование показало клиническую эффективность и безопасность сравниваемых ЭВ. Прирост гемоглобина, гематокрита, частота и тяжесть посттрансфузионных реакций, а также интервал между трансфузиями не отличались в двух группах пациентов. Использование патоген-редуцированной ЭВ не приводило к активации иммунного ответа. У пациентов, получавших патоген-редуцированную ЭВ, была обнаружена корреляционная связь между приростом гемоглобина и гематокрита с дозой и скорректированной дозой гемоглобина, полученной за трансфузию. Эффективность и безопасность патоген-редуцированной ЭВ представляются не хуже, чем гамма-облученной ЭВ, при условии использования ЭВ в течение 14 дней хранения.</p></trans-abstract><kwd-group xml:lang="en"><kwd>pathogen reduction technologies</kwd><kwd>transfusion support</kwd><kwd>pediatric transfusions</kwd><kwd>oncological diseases</kwd><kwd>hematological diseases</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>технологии редукции патогенов</kwd><kwd>трансфузионная поддержка</kwd><kwd>педиатрические трансфузии</kwd><kwd>онкологические заболевания</kwd><kwd>гематологические заболевания</kwd></kwd-group><funding-group><funding-statement xml:lang="en">Terumo, Caridian BCT Biotechnologies, Lakewood, CO, США.</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Stramer S.L., Dodd R.Y. Transfusiontransmitted emerging infectious diseases: 30 years of challenges and progress. 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