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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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Epidemiology and Infectious Diseases</journal-id><journal-title-group><journal-title xml:lang="en">Epidemiology and Infectious Diseases</journal-title><trans-title-group xml:lang="ru"><trans-title>Эпидемиология и инфекционные болезни</trans-title></trans-title-group></journal-title-group><issn publication-format="print">3034-2007</issn><issn publication-format="electronic">3034-2015</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">109612</article-id><article-id pub-id-type="doi">10.17816/EID109612</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original study articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные исследования</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">A method for predicting the effectiveness of glucocorticoid therapy in patients with moderate COVID-19 based on simple clinical and laboratory data</article-title><trans-title-group xml:lang="ru"><trans-title>Способ прогнозирования эффективности глюкокортикоидной терапии у пациентов со среднетяжёлым течением COVID-19 на основе простых клинических и лабораторных данных</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7889-6052</contrib-id><contrib-id contrib-id-type="spin">7115-2713</contrib-id><name-alternatives><name xml:lang="en"><surname>Efremov</surname><given-names>Dmitry O.</given-names></name><name xml:lang="ru"><surname>Ефремов</surname><given-names>Дмитрий Олегович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>начальник инфекционного центра филиала №1 ФГБУ «Национальный медицинский исследовательский центр высоких медицинских технологий имени А. А. Вишневского» Минобороны России</p></bio><email>Efremov-d24@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0544-4167</contrib-id><contrib-id contrib-id-type="spin">4233-2046</contrib-id><name-alternatives><name xml:lang="en"><surname>Beloborodov</surname><given-names>Vladimir B.</given-names></name><name xml:lang="ru"><surname>Белобородов</surname><given-names>Владимир Борисович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Med.), Professor</p></bio><bio xml:lang="ru"><p>д.м.н., профессор</p></bio><email>belvb1070@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Branch No. 1 of the National Medical Research Center for High Medical Technologies</institution></aff><aff><institution xml:lang="ru">Филиал № 1 Национального медицинского исследовательского центра высоких медицинских технологий имени А.А. Вишневского</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Russian Medical Academy of Continuous Professional Education</institution></aff><aff><institution xml:lang="ru">Российская медицинская академия непрерывного профессионального образования</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2022-09-09" publication-format="electronic"><day>09</day><month>09</month><year>2022</year></pub-date><pub-date date-type="pub" iso-8601-date="2022-10-27" publication-format="electronic"><day>27</day><month>10</month><year>2022</year></pub-date><volume>27</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>75</fpage><lpage>88</lpage><history><date date-type="received" iso-8601-date="2022-08-04"><day>04</day><month>08</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-09-06"><day>06</day><month>09</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Eco-vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, ООО "Эко-вектор"</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Eco-vector</copyright-holder><copyright-holder xml:lang="ru">ООО "Эко-вектор"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2025-10-27"/></permissions><self-uri xlink:href="https://rjeid.com/1560-9529/article/view/109612">https://rjeid.com/1560-9529/article/view/109612</self-uri><abstract xml:lang="en"><p><italic>BACKGROUND:</italic> In patients hospitalized with coronavirus infection (COVID-19), methods for predicting the effectiveness of anti-inflammatory therapy have important practical implications for optimizing treatment and outcomes. To date, several indicators of COVID-19 patients (age, comorbidities, and laboratory criteria for the intensity of inflammation) have been identified to indicate a high probability of a severe course and a risk of an adverse outcome. However, the problem of predicting the effectiveness of anti-inflammatory therapy in patients with moderate COVID-19 is not well understood.</p> <p><italic>AIM</italic>: This study aimed to develop a predictive model to determine the effectiveness/failure of anti-inflammatory therapy with glucocorticosteroids (GCS) in patients with moderate COVID-19 to improve the treatment outcomes of hospitalized patients.</p> <p><italic>MATERIALS AND METHODS:</italic> This study retrospectively analyzed electronic medical record data of all patients admitted consecutively from October 1, 2020, to January 31, 2021. The study included 71 patients with probable (clinically confirmed) and confirmed (laboratory) COVID-19 of moderate course, with characteristic changes in the lungs according to computed tomography of the chest organs (CT-CCT). Given the severity of the course, all study patients were prescribed GCS in accordance with the current version of the Interim Guidelines of the Ministry of Health of the Russian Federation.</p> <p><italic>RESULTS:</italic> A total of 71 patients were studied, and 53 (74.7%) of them did not require an escalation of anti-inflammatory therapy, which is regarded as an effective use of corticosteroids as an anti-inflammatory therapy (group 1). In the remaining 18 patients, the use of corticosteroids for an average of 5.5 (3–6) days did not have a definite clinical effect and required the additional use of monoclonal antibodies (MCA) to interleukin-6 (IL-6) or to its receptor (group 2). Using logistic regression analysis and receiver operating characteristic analysis, a mathematical model was developed and evaluated to predict the outcome of anti-inflammatory corticosteroid therapy in patients with moderate COVID-19. As risk factors, indicators that had significant differences in the studied groups before GCS initiation were selected: number of lymphocytes, platelets, and body temperature. The quality of the constructed model is assessed as very good, and the optimal cutoff point is 0.697. The sensitivity index of the model is 81.1%, and the specificity index is 72.2%.</p> <p><italic>CONCLUSIONS:</italic> The mathematical model makes it possible to predict the effectiveness of GCS therapy according to the number of lymphocytes, platelets, and body temperature. The mathematical model is adequate and has a high sensitivity and specificity.</p></abstract><trans-abstract xml:lang="ru"><p><italic>Обоснование.</italic> У пациентов, госпитализированных с коронавирусной инфекцией (COVID-19), способы прогнозирования эффективности противовоспалительной терапии имеют важное практическое значение для оптимизации лечения и исходов. К настоящему времени выявлен ряд показателей у пациентов с COVID-19 (возраст, сопутствующая патология, лабораторные критерии интенсивности воспаления), указывающих на высокую вероятность тяжёлого течения и риска неблагоприятного исхода. Однако проблема прогнозирования эффективности противовоспалительной терапии у пациентов со среднетяжёлым течением COVID-19 изучена недостаточно.</p> <p><italic>Цель исследования</italic> — разработать прогностическую модель для определения эффективности/неэффективности противовоспалительной терапии глюкокортикоидами (ГКС) у пациентов со среднетяжёлым течением COVID-19 для улучшения результатов лечения госпитализированных пациентов.</p> <p><italic>Материалы и методы.</italic> Проведён ретроспективный анализ данных электронных историй болезни всех пациентов, поступивших в инфекционный центр последовательно с 1 октября 2020 г. по 31 января 2021 г. В исследование включён 71 пациент с вероятным (клинически подтверждённым) и подтверждённым (лабораторно) случаем COVID-19 среднетяжёлого течения с характерными изменениями в лёгких по данным компьютерной томографии органов грудной клетки. С учётом тяжести течения заболевания всем пациентам выборки назначены ГКС в соответствии с актуальной версией временных методических рекомендаций Министерства здравоохранения Российской Федерации.</p> <p><italic>Результаты.</italic> Всего изучен 71 пациент, у 53 (74,7%) эскалация противовоспалительной терапии не потребовалась, что расценено как эффективное применение ГКС в качестве противовоспалительной терапии (группа 1). У остальных 18 пациентов применение ГКС в течение в среднем 5,5 (от 3 до 6) суток не имело определённого клинического эффекта и потребовало дополнительного применения моноклональных антител к интерлейкину-6 или его рецептору (группа 2). С помощью логистического регрессионного анализа и ROC-анализа проведена разработка и оценка математической модели, позволяющей прогнозировать исход противовоспалительной терапии ГКС у пациентов со среднетяжёлым течением COVID-19. В качестве факторов риска были выбраны показатели, имевшие достоверные различия в изученных группах перед назначением ГКС: количество лимфоцитов, тромбоцитов и температура тела. Качество построенной модели оценивается как очень хорошее, оптимальная точка отсечения — 0,697. Показатель чувствительности модели — 81,1%, специфичности — 72,2%.</p> <p><italic>Заключение.</italic> Математическая модель позволяет прогнозировать эффективность терапии ГКС по количеству лимфоцитов, тромбоцитов и уровню температуры тела. Математическая модель адекватна, имеет высокий показатель чувствительности и специфичности.</p></trans-abstract><kwd-group xml:lang="en"><kwd>COVID-19</kwd><kwd>glucocorticoids hormones</kwd><kwd>treatment efficacy</kwd><kwd>risk factors</kwd><kwd>predictive model</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>COVID-19</kwd><kwd>глюкокортикоидные гормоны</kwd><kwd>эффективность лечения</kwd><kwd>факторы риска</kwd><kwd>прогностическая модель</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Drapkina OM, Maev IV, Bakulin IG, et al. Interim guidelines: Diseases of the digestive organs in the context of a new coronavirus infection pandemic (COVID-19). Profilakticheskaya Meditsina. 2020;23(3):2120–2152. (In Russ). doi: 10.17116/profmed202023032120</mixed-citation><mixed-citation xml:lang="ru">Драпкина О.М., Маев И.В., Бакулин И.Г., и др. Временные методические рекомендации: «Болезни органов пищеварения в условиях пандемии новой коронавирусной инфекции (COVID-19)» // Профилактическая медицина. 2020. Т. 23, № 3. С. 2120–2152. doi: 10.17116/profmed202023032120</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Fang J, Wu Q, Ye F, et al. Network-Based Identification and Experimental Validation of Drug Candidates Toward SARS-CoV-2 via Targeting Virus-Host Interactome. Front Genet. 2021;12:728960. doi: 10.3389/fgene.2021.728960</mixed-citation><mixed-citation xml:lang="ru">Fang J., Wu Q., Ye F., et al. Network-Based Identification and Experimental Validation of Drug Candidates Toward SARS-CoV-2 via Targeting Virus-Host Interactome // Front Genet. 2021. Vol. 12. P. 728960. doi: 10.3389/fgene.2021.728960</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Aprajita, Choudhary M. Design, synthesis and characterization of novel Ni(II) and Cu(II) complexes as antivirus drug candidates against SARS-CoV-2 and HIV virus. J Mol Struct. 2022;1263:133114. doi: 10.1016/j.molstruc.2022.133114</mixed-citation><mixed-citation xml:lang="ru">Aprajita, Choudhary M. Design, synthesis and characterization of novel Ni(II) and Cu(II) complexes as antivirus drug candidates against SARS-CoV-2 and HIV virus // J Mol Struct. 2022. Vol. 1263. P. 133114. doi: 10.1016/j.molstruc.2022.133114</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Ren PX, Shang WJ, Yin WC, et al. A multi-targeting drug design strategy for identifying potent anti-SARS-CoV-2 inhibitors. Acta Pharmacol Sin. 2022;43(2):483–493. doi: 10.1038/s41401-021-00668-7</mixed-citation><mixed-citation xml:lang="ru">Ren P.X., Shang W.J., Yin W.C., et al. A multi-targeting drug design strategy for identifying potent anti-SARS-CoV-2 inhibitors // Acta Pharmacol Sin. 2022. Vol. 43, N 2. P. 483–493. doi: 10.1038/s41401-021-00668-7</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Horby P, Lim WS, Emberson JR, et al.; RECOVERY Collaborative Group. Dexamethasone in Hospitalized Patients with Covid-19. N Engl J Med. 2021;384(8):693–704. doi: 10.1056/NEJMoa2021436</mixed-citation><mixed-citation xml:lang="ru">Horby P., Lim W.S., Emberson J.R., et al.; RECOVERY Collaborative Group. Dexamethasone in Hospitalized Patients with Covid-19 // N Engl J Med. 2021. Vol. 384, N 8. P. 693–704. doi: 10.1056/NEJMoa2021436</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Li Y, Zhou X, Li T, et al. Corticosteroid prevents COVID-19 progression within its therapeutic window: a multicentre, proof-of-concept, observational study. Emerg Microbes Infect. 2020;9(1): 1869–1877. doi: 10.1080/22221751.2020.1807885</mixed-citation><mixed-citation xml:lang="ru">Li Y., Zhou X., Li T., et al. Corticosteroid prevents COVID-19 progression within its therapeutic window: a multicentre, proof-of-concept, observational study // Emerg Microbes Infect. 2020. Vol. 9, N 1. P. 1869–1877. doi: 10.1080/22221751.2020.1807885</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Fadel R, Morrison AR, Vahia A, et al.; Henry Ford COVID-19 Management Task Force. Early Short-Course Corticosteroids in Hospitalized Patients With COVID-19. Clin Infect Dis. 2020;71(16): 2114–2120. doi: 10.1093/cid/ciaa601</mixed-citation><mixed-citation xml:lang="ru">Fadel R., Morrison A.R., Vahia A., et al.; Henry Ford COVID-19 Management Task Force. Early Short-Course Corticosteroids in Hospitalized Patients With COVID-19 // Clin Infect Dis. 2020. Vol. 71, N 16. P. 2114–2120. doi: 10.1093/cid/ciaa601</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Chalmers JD, Crichton ML, Goeminne PC, et al. Management of hospitalised adults with coronavirus disease 2019 (COVID-19): a European Respiratory Society living guideline. Eur Respir J. 2021; 57(4):2100048. doi: 10.1183/13993003.00048-2021. Erratum in: Eur Respir J. 2022;60(2).</mixed-citation><mixed-citation xml:lang="ru">Chalmers J.D., Crichton M.L., Goeminne P.C., et al. Management of hospitalised adults with coronavirus disease 2019 (COVID-19): a European Respiratory Society living guideline // Eur Respir J. 2021. Vol. 57, N 4. P. 2100048. doi: 10.1183/13993003.00048-2021. Erratum in: Eur Respir J. 2022. Vol. 60, N 2.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Huang I, Pranata R, Lim MA, et al. C-reactive protein, procalcitonin, D-dimer, and ferritin in severe coronavirus disease-2019: a meta-analysis. Ther Adv Respir Dis. 2020;14:1753466620937175. doi: 10.1177/1753466620937175</mixed-citation><mixed-citation xml:lang="ru">Huang I., Pranata R., Lim M.A., et al. C-reactive protein, procalcitonin, D-dimer, and ferritin in severe coronavirus disease-2019: a meta-analysis // Ther Adv Respir Dis. 2020. Vol. 14. P. 1753466620937175. doi: 10.1177/1753466620937175</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Choron RL, Butts CA, Bargoud C, et al. Fever in the ICU: A Predictor of Mortality in Mechanically Ventilated COVID-19 Patients. J Intensive Care Med. 2021;36(4):484–493. doi: 10.1177/0885066620979622</mixed-citation><mixed-citation xml:lang="ru">Choron R.L., Butts C.A., Bargoud C., et al. Fever in the ICU: A Predictor of Mortality in Mechanically Ventilated COVID-19 Patients // J Intensive Care Med. 2021. Vol. 36, N 4. P. 484–493. doi: 10.1177/0885066620979622</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Da Rosa Mesquita R, Francelino Silva Junior LC, Santos Santana FM, et al. Clinical manifestations of COVID-19 in the general population: systematic review. Wien Klin Wochenschr. 2021; 133(7-8):377–382. doi: 10.1007/s00508-020-01760-4</mixed-citation><mixed-citation xml:lang="ru">Da Rosa Mesquita R., Francelino Silva Junior L.C., Santos Santana F.M., et al. Clinical manifestations of COVID-19 in the general population: systematic review // Wien Klin Wochenschr. 2021. Vol. 133, N 7-8. P. 377–382. doi: 10.1007/s00508-020-01760-4</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">He X, Cheng X, Feng X, et al. Clinical Symptom Differences Between Mild and Severe COVID-19 Patients in China: A Meta-Analysis. Front Public Health. 2021;8:561264. doi: 10.3389/fpubh.2020.561264</mixed-citation><mixed-citation xml:lang="ru">He X., Cheng X., Feng X., et al. Clinical Symptom Differences Between Mild and Severe COVID-19 Patients in China: A Meta-Analysis // Front Public Health. 2021. Vol. 8. P. 561264. doi: 10.3389/fpubh.2020.561264</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Xu P, Zhou Q, Xu J. Mechanism of thrombocytopenia in COVID-19 patients. Ann Hematol. 2020;99(6):1205–1208. doi: 10.1007/s00277-020-04019-0</mixed-citation><mixed-citation xml:lang="ru">Xu P., Zhou Q., Xu J. Mechanism of thrombocytopenia in COVID-19 patients // Ann Hematol. 2020. Vol. 99, N 6. P. 1205–1208. doi: 10.1007/s00277-020-04019-0</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Huang I, Pranata R. Lymphopenia in severe coronavirus disease-2019 (COVID-19): systematic review and meta-analysis. J Intensive Care. 2020;8:36. doi: 10.1186/s40560-020-00453-4</mixed-citation><mixed-citation xml:lang="ru">Huang I., Pranata R. Lymphopenia in severe coronavirus disease-2019 (COVID-19): systematic review and meta-analysis // J Intensive Care. 2020. Vol. 8. P. 36. doi: 10.1186/s40560-020-00453-4</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Chew NW, Ngiam JN, Tham SM, et al. Fever as a predictor of adverse outcomes in COVID-19. QJM. 2021;114(10):706–714. doi: 10.1093/qjmed/hcab023</mixed-citation><mixed-citation xml:lang="ru">Chew N.W., Ngiam J.N., Tham S.M., et al. Fever as a predictor of adverse outcomes in COVID-19 // QJM. 2021. Vol. 114, N 10. P. 706–714. doi: 10.1093/qjmed/hcab023</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Sterne JAC, Murthy S, Diaz JV, et al.; WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group. Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19: A Meta-analysis. JAMA. 2020;324(13):1330–1341. doi: 10.1001/jama.2020.17023</mixed-citation><mixed-citation xml:lang="ru">Sterne J.A.C., Murthy S., Diaz J.V., et al.; WHO Rapid Evidence Appraisal for COVID-19 Therapies (REACT) Working Group. Association Between Administration of Systemic Corticosteroids and Mortality Among Critically Ill Patients With COVID-19: A Meta-analysis // JAMA. 2020. Vol. 324, N 13. P. 1330–1341. doi: 10.1001/jama.2020.17023</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Avdeev SN, Adamyan LV, Alekseeva EI, et al. Prevention, diagnosis and treatment of novel coronavirus infection (COVID-19): interim guidelines. Version 8 (09/03/2020). Moscow; 2020. 227 p. (In Russ).</mixed-citation><mixed-citation xml:lang="ru">Авдеев С.Н., Адамян Л.В., Алексеева Е.И., и др. Профилактика, диагностика и лечение новой коронавирусной инфекции (COVID-19): временные методические рекомендации. Версия 8 (03.09.2020). Москва, 2020. 227 с.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Avdeev SN, Adamyan LV, Alekseeva EI, et al. Prevention, diagnosis and treatment of novel coronavirus infection (COVID-19): interim guidelines. Version 8 (10/26/2020). Moscow; 2020. 236 p. (In Russ).</mixed-citation><mixed-citation xml:lang="ru">Авдеев С.Н., Адамян Л.В., Алексеева Е.И., и др. Профилактика, диагностика и лечение новой коронавирусной инфекции (COVID-19): временные методические рекомендации. Версия 9 (26.10.2020). Москва, 2020. 236 с.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Trukhacheva NV. Mathematical statistics in biomedical research using the Statistica package. Moscow: GEOTAR-Media; 2013. 384 p. (In Russ).</mixed-citation><mixed-citation xml:lang="ru">Трухачева Н.В. Математическая статистика в медико-биологических исследованиях с применением пакета Statistica. Москва: ГЭОТАР-Медиа, 2013. 384 с.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Grigoryev SG, Lobzin YuV, Skripchenko NV. the Role and place of logistic regression and ROC analysis in solving medical diagnostic task. Journal Infectology. 2016;8(4):36–45. (In Russ). doi: 10.22625/2072-6732-2016-8-4-36-45</mixed-citation><mixed-citation xml:lang="ru">Григорьев С.Г., Лобзин Ю.В., Скрипченко Н.В. Роль и место логистической регрессии и ROC-анализа в решении медицинских диагностических задач // Журнал инфектологии. 2016. Т. 8, № 4. С. 36–45. doi: 10.22625/2072-6732-2016-8-4-36-45</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Li J, He X, Yuan Yuan, et al. Meta-analysis investigating the relationship between clinical features, outcomes, and severity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia. Am J Infect Control. 2021;49(1):82–89. doi: 10.1016/j.ajic.2020.06.008</mixed-citation><mixed-citation xml:lang="ru">Li J., He X., Yuan Yuan, et al. Meta-analysis investigating the relationship between clinical features, outcomes, and severity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia // Am J Infect Control. 2021. Vol. 49, N 1. P. 82–89. doi: 10.1016/j.ajic.2020.06.008</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Guo L, Wei D, Zhang X, et al. Clinical Features Predicting Mortality Risk in Patients With Viral Pneumonia: The MuLBSTA Score. Front Microbiol. 2019;10:2752. doi: 10.3389/fmicb.2019.02752. Erratum in: Front Microbiol. 2020 Jun 09;11:1304.</mixed-citation><mixed-citation xml:lang="ru">Guo L., Wei D., Zhang X., et al. Clinical Features Predicting Mortality Risk in Patients With Viral Pneumonia: The MuLBSTA Score // Front Microbiol. 2019. Vol. 10. P. 2752. doi: 10.3389/fmicb.2019.02752. Erratum in: Front Microbiol. 2020. Vol. 11. P. 1304.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Burian E, Jungmann F, Kaissis GA, et al. Intensive Care Risk Estimation in COVID-19 Pneumonia Based on Clinical and Imaging Parameters: Experiences from the Munich Cohort. J Clin Med. 2020;9(5):1514. doi: 10.3390/jcm9051514</mixed-citation><mixed-citation xml:lang="ru">Burian E., Jungmann F., Kaissis G.A., et al. Intensive Care Risk Estimation in COVID-19 Pneumonia Based on Clinical and Imaging Parameters: Experiences from the Munich Cohort // J Clin Med. 2020. Vol. 9, N 5. P. 1514. doi: 10.3390/jcm9051514</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Assaf D, Gutman Y, Neuman Y, et al. Utilization of machine-learning models to accurately predict the risk for critical COVID-19. Intern Emerg Med. 2020;15(8):1435–1443. doi: 10.1007/s11739-020-02475-0</mixed-citation><mixed-citation xml:lang="ru">Assaf D., Gutman Y., Neuman Y., et al. Utilization of machine-learning models to accurately predict the risk for critical COVID-19 // Intern Emerg Med. 2020. Vol. 15, N 8. P. 1435–1443. doi: 10.1007/s11739-020-02475-0</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Liu J, Liu Y, Xiang P, et al. Neutrophil-to-lymphocyte ratio predicts critical illness patients with 2019 coronavirus disease in the early stage. J Transl Med. 2020;18(1):206. doi: 10.1186/s12967-020-02374-0</mixed-citation><mixed-citation xml:lang="ru">Liu J., Liu Y., Xiang P., et al. Neutrophil-to-lymphocyte ratio predicts critical illness patients with 2019 coronavirus disease in the early stage // J Transl Med. 2020. Vol. 18, N 1. P. 206. doi: 10.1186/s12967-020-02374-0</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Yang X, Yang Q, Wang Y, et al. Thrombocytopenia and its association with mortality in patients with COVID-19. J Thromb Haemost. 2020;18(6):1469–1472. doi: 10.1111/jth.14848</mixed-citation><mixed-citation xml:lang="ru">Yang X., Yang Q., Wang Y., et al. Thrombocytopenia and its association with mortality in patients with COVID-19 // J Thromb Haemost. 2020. Vol. 18, N 6. P. 1469–1472. doi: 10.1111/jth.14848</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Wynants L, Van Calster B, Collins GS, et al. Prediction models for diagnosis and prognosis of covid-19: systematic review and critical appraisal. BMJ. 2020;369:m1328. doi: 10.1136/bmj.m1328. Update in: BMJ. 2021;372:n236. Erratum in: BMJ. 2020;369:m2204.</mixed-citation><mixed-citation xml:lang="ru">Wynants L., Van Calster B., Collins G.S., et al. Prediction models for diagnosis and prognosis of covid-19: systematic review and critical appraisal // BMJ. 2020. Vol. 369. P. m1328. doi: 10.1136/bmj.m1328. Update in: BMJ. 2021. Vol. 372. P. n236. Erratum in: BMJ. 2020. Vol. 369. P. m2204.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
