<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">clinvest</journal-id><journal-title-group><journal-title xml:lang="ru">Качественная клиническая практика</journal-title><trans-title-group xml:lang="en"><trans-title>Kachestvennaya Klinicheskaya Praktika = Good Clinical Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2588-0519</issn><issn pub-type="epub">2618-8473</issn><publisher><publisher-name>ООО «Издательство ОКИ</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.37489/2588-0519-2022-2-13-20</article-id><article-id custom-type="elpub" pub-id-type="custom">clinvest-613</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>ИССЛЕДОВАНИЯ РЕАЛЬНОЙ КЛИНИЧЕСКОЙ ПРАКТИКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REAL-WORLD STUDIES</subject></subj-group></article-categories><title-group><article-title>Модель логистической регрессии для прогнозирования летальности в отделении интенсивной терапии: проблемы и решения</article-title><trans-title-group xml:lang="en"><trans-title>A logistic regression-based model to predict ICU mortality: problems and solutions</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5016-210X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лучинин</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Luchinin</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лучинин Александр Сергеевич - кандидат медицинских наук, старший научный сотрудник отдела организации и сопровождения научных исследований КНИИГиПК ФМБА России.</p><p>Киров.</p></bio><bio xml:lang="en"><p>Alexander S. Luchinin - PhD, Cand. Sci. Med., Senior Researcher of the Department of Organization and Support of Scientific Research, KRIHBT.</p><p>Kirov.</p></bio><email xlink:type="simple">luchinin@niigpk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5509-5308</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лянгузов</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Lyanguzov</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лянгузов Алексей В. - кандидат медицинских наук, КНИИГиПК ФМБА России.</p><p>Киров.</p></bio><bio xml:lang="en"><p>Alexey V. Lyanguzov - PhD, Cand. Sci. Med., KRIHBT.</p><p>Kirov.</p></bio><email xlink:type="simple">lyanguzov@niigpk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Кировский научно-исследовательский институт гематологии и переливания крови Федерального медико-биологического агентства</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Kirov Research Institute of Hematology and Blood Transfusion under the Federal Medical Biological Agency</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>02</day><month>08</month><year>2022</year></pub-date><volume>0</volume><issue>2</issue><fpage>13</fpage><lpage>20</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Лучинин А.С., Лянгузов А.В., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Лучинин А.С., Лянгузов А.В.</copyright-holder><copyright-holder xml:lang="en">Luchinin A.S., Lyanguzov A.V.</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.clinvest.ru/jour/article/view/613">https://www.clinvest.ru/jour/article/view/613</self-uri><abstract><p>Летальность в отделении интенсивной терапии является одной из важнейших метрик качества медицинской помощи. Цель исследования — создание модели прогноза летальности для пациентов с заболеваниями крови с использованием метода логистической регрессии и описание условий его применения при анализе данных. В исследование включили 202 пациента в возрасте от 19 до 82 лет (медиана — 57 лет), из них — 112 (55 %) мужчин и 90 (45 %) женщин. Статистический анализ проводился с использованием языка программирования R (версия 3.4.2). Вероятность смерти в отделении интенсивной терапии равнялась 33 % (67 из 202 пациентов), шансы — 0,496 (67/135). Согласно полученной модели снижение уровня тромбоцитов у пациента в 2 раза повышает шансы смерти в отделении интенсивной терапии на 31 %, или в 1,3 раза, снижение уровня общего белка в 2 раза — увеличивает шансы смерти в 11 раз, а любое нарушение сознания по шкале Глазго — почти в 20 раз при условии, что остальные переменные не изменяются. Чувствительность модели равнялась 82,3 %, специфичность — 80 %, точность — 81,6 % (95 % ДИ 67,9–91,2 %). Общая точность модели оказалась выше существующих шкал прогноза летальности qSOFA и MEWS, несмотря на простой метод анализа данных. Исследования в данной области необходимо продолжать.</p></abstract><trans-abstract xml:lang="en"><p>The ICU department’s mortality rate is one of the most important indicators of quality of care. Based on real clinical data, we attempted to build a prognostic model for patients with blood diseases in the ICU with using of the logistic regression method. The study included 202 patients in total. The median age was 57 (19–82) years. There were 112 (55 %) males and 90 (45 %) females. The statistical analysis was performed by using R software, version 3.4.2. The absolute risk of death (mortality rate) was 67 from 202 (33 %), odds — 0.496. The odds of death in ICU grow up to ~20 times if the patient has a Glasgow score of less than 15. Also, the odds of death increase by 1.3 and 11 times of PLT, or serum total protein level decreases by 2 times accordingly. Our model for “high-risk of death” detection classified patients in the test dataset with 0.816 accuracy (95 % CI 0.679–0.912), with sensitivity 0.823, and specificity 0.80. Despite the simple method for data analysis, we got a pretty accurate model of mortality prognosis with efficacy more than qSOFA and MEWS scales. Research in this area should continue.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>летальность</kwd><kwd>прогноз</kwd><kwd>логистическая регрессия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>mortality</kwd><kwd>prognosis</kwd><kwd>logistic regression</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">Lee J, Dubin JA, Maslove DM. Mortality Prediction in the ICU // Secondary Analysis of Electronic Health Records / ed. MIT Critical Data. Cham: Springer International Publishing, 2016. P. 315–324.</mixed-citation><mixed-citation xml:lang="en">Lee J, Dubin JA, Maslove DM. Mortality Prediction in the ICU // Secondary Analysis of Electronic Health Records / ed. MIT Critical Data. Cham: Springer International Publishing, 2016. P. 315–324.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Pirracchio R, Petersen ML, Carone M, et al. Mortality prediction in the ICU: can we do better? Results from the Super ICU Learner Algorithm (SICULA) project, a population-based study. Lancet Respir Med. 2015;3(1):42– 52. doi: 10.1016/S2213-2600(14)70239-5</mixed-citation><mixed-citation xml:lang="en">Pirracchio R, Petersen ML, Carone M, et al. Mortality prediction in the ICU: can we do better? Results from the Super ICU Learner Algorithm (SICULA) project, a population-based study. Lancet Respir Med. 2015;3(1):42– 52. doi: 10.1016/S2213-2600(14)70239-5</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Awad A, Bader-El-Den M, McNicholas J, et al. Predicting hospital mortality for intensive care unit patients: Time-series analysis. Health Informatics J. SAGE Publications Ltd, 2020;26(2):1043–59. doi: 10.1177/1460458219850323</mixed-citation><mixed-citation xml:lang="en">Awad A, Bader-El-Den M, McNicholas J, et al. Predicting hospital mortality for intensive care unit patients: Time-series analysis. Health Informatics J. SAGE Publications Ltd, 2020;26(2):1043–59. doi: 10.1177/1460458219850323</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Schober P, Vetter TR. Logistic Regression in Medical Research. Anesth Analg. 2021;132(2):365–6. doi: 10.1213/ANE.0000000000005247</mixed-citation><mixed-citation xml:lang="en">Schober P, Vetter TR. Logistic Regression in Medical Research. Anesth Analg. 2021;132(2):365–6. doi: 10.1213/ANE.0000000000005247</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Ahmed SN, Jhaj R, Sadasivam B, et al. Reversal of hypertensive heart disease: a multiple linear regression model. Discoveries (Craiova). 2021;9(4):e138.</mixed-citation><mixed-citation xml:lang="en">Ahmed SN, Jhaj R, Sadasivam B, et al. Reversal of hypertensive heart disease: a multiple linear regression model. Discoveries (Craiova). 2021;9(4):e138.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Lunt M. Introduction to statistical modelling 2: categorical variables and interactions in linear regression. Rheumatology (Oxford). 2015;54(7):1141–4. doi: 10.1093/rheumatology/ket172</mixed-citation><mixed-citation xml:lang="en">Lunt M. Introduction to statistical modelling 2: categorical variables and interactions in linear regression. Rheumatology (Oxford). 2015;54(7):1141–4. doi: 10.1093/rheumatology/ket172</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Serdar CC, Cihan M, Yücel D, et al. Sample size, power and effect size revisited: simplified and practical approaches in pre-clinical, clinical and laboratory studies. Biochem Med (Zagreb). 2021;31(1):010502. doi: 10.11613/BM.2021.010502</mixed-citation><mixed-citation xml:lang="en">Serdar CC, Cihan M, Yücel D, et al. Sample size, power and effect size revisited: simplified and practical approaches in pre-clinical, clinical and laboratory studies. Biochem Med (Zagreb). 2021;31(1):010502. doi: 10.11613/BM.2021.010502</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Jenkins DG, Quintana-Ascencio PF. A solution to minimum sample size for regressions. PLoS One. 2020;15(2):e0229345. doi: 10.1371/journal.pone.0229345</mixed-citation><mixed-citation xml:lang="en">Jenkins DG, Quintana-Ascencio PF. A solution to minimum sample size for regressions. PLoS One. 2020;15(2):e0229345. doi: 10.1371/journal.pone.0229345</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Wilson Van Voorhis CR, Morgan BL. Understanding Power and Rules of Thumb for Determining Sample Size. TQMP. 2007;3(2):43–50. doi: 10.20982/tqmp.03.2.p043</mixed-citation><mixed-citation xml:lang="en">Wilson Van Voorhis CR, Morgan BL. Understanding Power and Rules of Thumb for Determining Sample Size. TQMP. 2007;3(2):43–50. doi: 10.20982/tqmp.03.2.p043</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Peduzzi P, Concato J, Kemper E, et al. A simulation study of the number of events per variable in logistic regression analysis. J Clin Epidemiol. 1996;49(12):1373–9. doi: 10.1016/s0895-4356(96)00236-3</mixed-citation><mixed-citation xml:lang="en">Peduzzi P, Concato J, Kemper E, et al. A simulation study of the number of events per variable in logistic regression analysis. J Clin Epidemiol. 1996;49(12):1373–9. doi: 10.1016/s0895-4356(96)00236-3</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Bujang MA, Sa’at N, Sidik TMITAB, Joo LC. Sample Size Guidelines for Logistic Regression from Observational Studies with Large Population: Emphasis on the Accuracy Between Statistics and Parameters Based on Real Life Clinical Data. Malays J Med Sci. 2018;25(4):122–30. doi: 10.21315/mjms2018.25.4.12</mixed-citation><mixed-citation xml:lang="en">Bujang MA, Sa’at N, Sidik TMITAB, Joo LC. Sample Size Guidelines for Logistic Regression from Observational Studies with Large Population: Emphasis on the Accuracy Between Statistics and Parameters Based on Real Life Clinical Data. Malays J Med Sci. 2018;25(4):122–30. doi: 10.21315/mjms2018.25.4.12</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Ajana S, Acar N, Bretillon L, et al. Benefits of dimension reduction in penalized regression methods for high-dimensional grouped data: a case study in low sample size. Bioinformatics. 2019;35(19):3628–34. doi: 10.1093/bioinformatics/btz135</mixed-citation><mixed-citation xml:lang="en">Ajana S, Acar N, Bretillon L, et al. Benefits of dimension reduction in penalized regression methods for high-dimensional grouped data: a case study in low sample size. Bioinformatics. 2019;35(19):3628–34. doi: 10.1093/bioinformatics/btz135</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Santana AC, Barbosa AV, Yehia HC, et al. A dimension reduction technique applied to regression on high dimension, low sample size neurophysiological data sets. BMC Neurosci. 2021;22(1):1. doi: 10.1186/s12868-020-00605-0</mixed-citation><mixed-citation xml:lang="en">Santana AC, Barbosa AV, Yehia HC, et al. A dimension reduction technique applied to regression on high dimension, low sample size neurophysiological data sets. BMC Neurosci. 2021;22(1):1. doi: 10.1186/s12868-020-00605-0</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Ishwaran H, O’Brien R. Commentary: The problem of class imbalance in biomedical data. J Thorac Cardiovasc Surg. 2021;161(6):1940–1. doi: 10.1016/j.jtcvs.2020.06.052</mixed-citation><mixed-citation xml:lang="en">Ishwaran H, O’Brien R. Commentary: The problem of class imbalance in biomedical data. J Thorac Cardiovasc Surg. 2021;161(6):1940–1. doi: 10.1016/j.jtcvs.2020.06.052</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Ameringer S, Serlin RC, Ward S. Simpson’s Paradox and Experimental Research. Nurs Res. 2009;58(2):123–7. doi: 10.1097/NNR.0b013e318199b517</mixed-citation><mixed-citation xml:lang="en">Ameringer S, Serlin RC, Ward S. Simpson’s Paradox and Experimental Research. Nurs Res. 2009;58(2):123–7. doi: 10.1097/NNR.0b013e318199b517</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Senaviratna NaMR, Cooray TMJA. Diagnosing Multicollinearity of Logistic Regression Model. Asian Journal of Probability and Statistics. 2019;1– 9. doi: 10.9734/ajpas/2019/v5i230132</mixed-citation><mixed-citation xml:lang="en">Senaviratna NaMR, Cooray TMJA. Diagnosing Multicollinearity of Logistic Regression Model. Asian Journal of Probability and Statistics. 2019;1– 9. doi: 10.9734/ajpas/2019/v5i230132</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Cutanda Henríquez F. [Outliers and robust logistic regression in Health Sciences]. Rev Esp Salud Publica. 2008;82(6):617–25. doi: 10.1590/s1135-57272008000600003</mixed-citation><mixed-citation xml:lang="en">Cutanda Henríquez F. [Outliers and robust logistic regression in Health Sciences]. Rev Esp Salud Publica. 2008;82(6):617–25. doi: 10.1590/s1135-57272008000600003</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang Y, Zhou X, Wang Q, et al. Quality of reporting of multivariable logistic regression models in Chinese clinical medical journals. Medicine (Baltimore). 2017;96(21):e6972. doi: 10.1097/MD.0000000000006972</mixed-citation><mixed-citation xml:lang="en">Zhang Y, Zhou X, Wang Q, et al. Quality of reporting of multivariable logistic regression models in Chinese clinical medical journals. Medicine (Baltimore). 2017;96(21):e6972. doi: 10.1097/MD.0000000000006972</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Altman DG, Vergouwe Y, Royston P, et al. Prognosis and prognostic research: validating a prognostic model. BMJ. 2009;338:b605. doi: 10.1136/bmj.b605</mixed-citation><mixed-citation xml:lang="en">Altman DG, Vergouwe Y, Royston P, et al. Prognosis and prognostic research: validating a prognostic model. BMJ. 2009;338:b605. doi: 10.1136/bmj.b605</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Sun GW, Shook TL, Kay GL. Inappropriate use of bivariable analysis to screen risk factors for use in multivariable analysis. J Clin Epidemiol. 1996;49(8):907–16. doi: 10.1016/0895-4356(96)00025-x</mixed-citation><mixed-citation xml:lang="en">Sun GW, Shook TL, Kay GL. Inappropriate use of bivariable analysis to screen risk factors for use in multivariable analysis. J Clin Epidemiol. 1996;49(8):907–16. doi: 10.1016/0895-4356(96)00025-x</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang Z. Variable selection with stepwise and best subset approaches. Ann Transl Med. 2016;4(7):136. doi: 10.21037/atm.2016.03.35</mixed-citation><mixed-citation xml:lang="en">Zhang Z. Variable selection with stepwise and best subset approaches. Ann Transl Med. 2016;4(7):136. doi: 10.21037/atm.2016.03.35</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Tibshirani R. The lasso method for variable selection in the Cox model. Stat Med. 1997;16(4):385–95. doi: 10.1002/(sici)1097-0258(19970228)16:4&gt;385::aid-sim380&lt;3.0.co;2-3</mixed-citation><mixed-citation xml:lang="en">Tibshirani R. The lasso method for variable selection in the Cox model. Stat Med. 1997;16(4):385–95. doi: 10.1002/(sici)1097-0258(19970228)16:4&gt;385::aid-sim380&lt;3.0.co;2-3</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Musoro JZ, Zwinderman AH, Puhan MA, et al. Validation of prediction models based on lasso regression with multiply imputed data. BMC Med Res Methodol. 2014;14:116. doi: 10.1186/1471-2288-14-116</mixed-citation><mixed-citation xml:lang="en">Musoro JZ, Zwinderman AH, Puhan MA, et al. Validation of prediction models based on lasso regression with multiply imputed data. BMC Med Res Methodol. 2014;14:116. doi: 10.1186/1471-2288-14-116</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Dziak JJ, Coffman DL, Lanza ST, et al. Sensitivity and specificity of information criteria. Brief Bioinform. 2020;21(2):553–65. doi: 10.1093/bib/bbz016</mixed-citation><mixed-citation xml:lang="en">Dziak JJ, Coffman DL, Lanza ST, et al. Sensitivity and specificity of information criteria. Brief Bioinform. 2020;21(2):553–65. doi: 10.1093/bib/bbz016</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Kim JH. Multicollinearity and misleading statistical results. Korean J Anesthesiol. 2019;72(6):558–69. doi: 10.4097/kja.19087</mixed-citation><mixed-citation xml:lang="en">Kim JH. Multicollinearity and misleading statistical results. Korean J Anesthesiol. 2019;72(6):558–69. doi: 10.4097/kja.19087</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Li B, Martin EB, Morris AJ. Box–Tidwell transformation based partial least squares regression. Computers &amp; Chemical Engineering. 2001;25(9):1219–33.</mixed-citation><mixed-citation xml:lang="en">Li B, Martin EB, Morris AJ. Box–Tidwell transformation based partial least squares regression. Computers &amp; Chemical Engineering. 2001;25(9):1219–33.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Nattino G, Pennell ML, Lemeshow S. Assessing the goodness of fit of logistic regression models in large samples: A modification of the Hosmer-Lemeshow test. Biometrics. 2020;76(2):549–60. doi: 10.1111/biom.13249</mixed-citation><mixed-citation xml:lang="en">Nattino G, Pennell ML, Lemeshow S. Assessing the goodness of fit of logistic regression models in large samples: A modification of the Hosmer-Lemeshow test. Biometrics. 2020;76(2):549–60. doi: 10.1111/biom.13249</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Fluss R, Faraggi D, Reiser B. Estimation of the Youden Index and its associated cutoff point. Biom J. 2005;47(4):458–72. doi: 10.1002/bimj.200410135</mixed-citation><mixed-citation xml:lang="en">Fluss R, Faraggi D, Reiser B. Estimation of the Youden Index and its associated cutoff point. Biom J. 2005;47(4):458–72. doi: 10.1002/bimj.200410135</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Abdullah SMOB, Grand J, Sijapati A, et al. qSOFA is a useful prognostic factor for 30-day mortality in infected patients fulfilling the SIRS criteria for sepsis. Am J Emerg Med. 2020;38(3):512–6. doi: 10.1016/j.ajem.2019.05.037</mixed-citation><mixed-citation xml:lang="en">Abdullah SMOB, Grand J, Sijapati A, et al. qSOFA is a useful prognostic factor for 30-day mortality in infected patients fulfilling the SIRS criteria for sepsis. Am J Emerg Med. 2020;38(3):512–6. doi: 10.1016/j.ajem.2019.05.037</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Roney JK, Whitley BE, Maples JC, et al. Modified early warning scoring (MEWS): evaluating the evidence for tool inclusion of sepsis screening criteria and impact on mortality and failure to rescue. J Clin Nurs. 2015;24(23–24):3343– 54. doi: 10.1111/jocn.12952</mixed-citation><mixed-citation xml:lang="en">Roney JK, Whitley BE, Maples JC, et al. Modified early warning scoring (MEWS): evaluating the evidence for tool inclusion of sepsis screening criteria and impact on mortality and failure to rescue. J Clin Nurs. 2015;24(23–24):3343– 54. doi: 10.1111/jocn.12952</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Лучинин А. С. Искусственный интеллект в гематологии. Клиническая онкогематология. 2022;15(1):16–27. doi: 10.21320/2500-2139-2022-15-1-16-27</mixed-citation><mixed-citation xml:lang="en">Luchinin AS. Artificial Intelligence in Hematology. Clinical oncohematology. 2022;15(1):16–2. (In Russ). doi: 10.21320/2500-2139-2022-15-1-16-27</mixed-citation></citation-alternatives></ref></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>
