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    Academic Journal

    Source: Mother and Baby in Kuzbass; № 3 (2025): сентябрь; 60-73 ; Мать и Дитя в Кузбассе; № 3 (2025): сентябрь; 60-73 ; 2542-0968 ; 1991-010X

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    Academic Journal

    Source: Current Pediatrics; Том 22, № 6 (2023); 498-505 ; Вопросы современной педиатрии; Том 22, № 6 (2023); 498-505 ; 1682-5535 ; 1682-5527

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    Relation: https://vsp.spr-journal.ru/jour/article/view/3351/1346; Шабалов Н.П., Софронова Л.Н. Неонатология: в 2 т.: учебное пособие. — 7-е изд., перераб. и доп. — М.: ГЭОТАР-Медиа; 2020. — 720 с.; Newman AJ, Gross S. Hyperbilirubinemia in Breast-Fed Infants. Pediatrics. 1963;32(6):995-1001. doi: https://doi.org/10.1542/peds.32.6.995; Schneider AP 2nd. Breast milk jaundice in the newborn. A real entity. JAMA. 1986;255(23):3270-3274. doi: https://doi.org/10.1001/jama.1986.03370230076034; Неонатология: клинические рекомендации / под ред. Н.Н. Володина, Д.Н. Дегтярева, Д.С. Крючко. — М.: ГЭОТАР-Медиа; 2019. — 320 с.; Kemper AR, Newman TB, Slaughter JL, et al. Clinical Practice Guideline Revision: Management of Hyperbilirubinemia in the Newborn Infant 35 or More Weeks of Gestation. Pediatrics. 2022;150(3): e2022058859. doi: https://doi.org/10.1542/peds.2022-058859; Preer GL, Philipp BL. Understanding and managing breast milk jaundice. Arch Dis Child Fetal Neonatal Ed. 2011;96(6):F461- F466. doi: https://doi.org/10.1136/adc.2010.184416; Ullah S, Rahman K, Hedayati M. Hyperbilirubinemia in Neonates: Types, Causes, Clinical Examinations, Preventive Measures and Treatments: A Narrative Review Article. Iran J Public Health. 2016; 45(5):558-568.; Bratton S, Cantu RM, Stern M. Breast Milk Jaundice. 2023 Jan 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023.; Ketsuwan S, Baiya N, Maelhacharoenporn K, Puapornpong P. The Association of Breastfeeding Practices with Neonatal Jaundice. J Med Assoc Thai. 2017;100(3):255-261.; Noel-Weiss J, Courant G, Woodend AK. Physiological weight loss in the breastfed neonate: a systematic review. Open Med. 2008;2(4):e99-e110.; Huang H, Huang J, Huang W, et al. Breast milk jaundice affects breastfeeding: From the perspective of intestinal flora and SCFAs-GPR41/43. Front Nutr. 2023;10:1121213. doi: https://doi.org/10.3389/fnut.2023.1121213; Prameela KK. Breastfeeding during breast milk jaundice — a pathophysiological perspective. Med J Malaysia. 2019;74(6):527-533.; Levitt DG, Levitt MD. Quantitative assessment of the multiple processes responsible for bilirubin homeostasis in health and disease. Clin Exp Gastroenterol. 2014;7:307-328. doi: https://doi.org/10.2147/CEG.S64283; Flaherman VJ, Maisels MJ. ABM Clinical Protocol #22: Guidelines for Management of Jaundice in the Breastfeeding Infant 35 Weeks or More of Gestation-Revised 2017. Breastfeed Med. 2017;12(5): 250-257. doi: https://doi.org/10.1089/bfm.2017.29042.vjf; Deshpande PG, Aslam M. Breast Milk Jaundice. In: Medscape. Updated: Nov 18, 2021. Available online: https://emedicine.medscape.com/article/973629-overview. Accessed on November 22, 2023.; Maisels MJ, Clune S, Coleman K, et al. The natural history of jaundice in predominantly breastfed infants. Pediatrics. 2014; 134(2):e340-e345. doi: https://doi.org/10.1542/peds.2013-4299; Bentz MG, Carmona N, Bhagwat MM, et al. Beyond “Asian”: Specific East and Southeast Asian Races or Ethnicities Associated With Jaundice Readmission. Hosp Pediatr. 2018;8(5):269-273. doi: https://doi.org/10.1542/hpeds.2017-0234; Gao C, Guo Y, Huang M, et al. Breast Milk Constituents and the Development of Breast Milk Jaundice in Neonates: A Systematic Review. Nutrients. 2023;15(10):2261. doi: https://doi.org/10.3390/nu15102261; Arias IM, Gartner LM, Seifter S, Furman M. Prolonged neonatal unconjugated hyperbilirubinemia associated with breast feeding and a steroid, pregnane-3(alpha), 20(beta)-diol, in maternal milk that inhibits glucuronide formation in vitro. J Clin Invest. 1964; 43(11):2037-2047. doi: https://doi.org/10.1172/jci105078; Guo Q, Cui M, Liu X, et al. Effect of Epidermal Growth Factor in Human Milk and Maternal Diet on Late-Onset Breast Milk Jaundice: A Case-Control Study in Beijing. Nutrients. 2022;14(21):4587. doi: https://doi.org/10.3390/nu14214587; Demirkol M, Bohles H. Breast milk taurine and its possible influence on the development of breast milk induced jaundice of the neonate — a hypothesis. Adv Exp Med Biol. 1994;359:405-410. doi: https://doi.org/10.1007/978-1-4899-1471-2_42; Amato M, Howald H, von Muralt G. Fat Content of Human Milk and Breast Milk Jaundice. Acta Paediatr Int J Paediatr. 1985;74(5):805-806. doi: https://doi.org/10.1111/j.1651-2227.1985.tb10039.x; Poland RL, Schultz GE, Garg G. High milk lipase activity associated with breast milk jaundice. Pediatr Res. 1980;14:1328-1331. doi: https://doi.org/10.1203/00006450-198012000-00011; Forsyth JS, Donnet L, Ross PE. A study of the relationship between bile salts, bile salt-stimulated lipase, and free fatty acids in breast milk: Normal infants and those with breast milk jaundice. J Pediatr Gastroenterol Nutr. 1990;11(2):205-210. doi: https://doi.org/10.1097/00005176-199008000-00009; Shibuya A, Itoh T, Tukey RH, Fujiwara R. Impact of fatty acids on human UDP-glucuronosyltransferase 1A1 activity and its expression in neonatal hyperbilirubinemia. Sci Rep. 2013;3:2903. doi: https://doi.org/10.1038/srep02903; Foliot A, Ploussard JP, Housset E, Christoforov. Breast milk jaundice: In vitro inhibition of rat liver bilirubin-uridine diphosphate glucuronyltransferase activity and Z protein-bromosulfophthalein binding by human breast milk. Pediatr Res. 1976;10(6):594-598. doi: https://doi.org/10.1203/00006450-197606000-00007; Gao C, Miller J, Middleton PF, et al. Changes to breast milk fatty acid composition during storage, handling and processing: A systematic review. Prostaglandins Leukot Essent Fatty Acids. 2019;146:1-10. doi: https://doi.org/10.1016/j.plefa.2019.04.008; Manganaro R, Marseglia L, Mami C, et al. Serum alphafetoprotein (AFP) levels in breastfed infants with prolonged indirect hyperbilirubinemia. Early Hum Dev. 2008;84:487-490. doi: https://doi.org/10.1016/j.earlhumdev.2008.01.005; Apaydin K, Ermis B, Arasli M, et al. Cytokines in human milk and late-onset breast milk jaundice. Pediatr Int. 2012;54(6):801-805. doi: https://doi.org/10.1111/j.1442-200X.2012.03680.x; Kumral A, Ozkan H, Duman N, et al. Breast milk jaundice correlates with high levels of epidermal growth factor. Pediatr Res. 2009;66(2):218-221. doi: https://doi.org/10.1203/PDR.0b013e3181ac4a30; Li Y, Shen N, Li J, et al. Changes in intestinal Flora and Metabolites in neonates with breast Milk jaundice. Front Pediatr. 2020;8:177. doi: https://doi.org/10.3389/fped.2020.00177; McCarville JL, Chen GY, Cuevas VD, et al. Microbiota metabolites in health and disease. Annu Rev Immunol. 2020;38:147-170. doi: https://doi.org/10.1146/annurev-immunol-071219-125715; Agus A, Clément K, Sokol H. Gut microbiota-derived metabolites as central regulators in metabolic disorders. Gut. 2021;70(6): 1174-1182. doi: https://doi.org/10.1136/gutjnl-2020-323071; Gonçalves P, Araújo JR, Di Santo JP. A cross-talk between microbiota-derived short-chain fatty acids and the host mucosal immune system regulates intestinal homeostasis and inflammatory bowel disease. Inflamm Bowel Dis. 2018;24(3):558-572. doi: https://doi.org/10.1093/ibd/izx029; Kayama H, Okumura R, Takeda K. Interaction between the microbiota, epithelia, and immune cells in the intestine. Annu Rev Immunol. 2020;38:23-48. doi: https://doi.org/10.1146/annurev-immunol-070119-115104; Hansen TWR, Wong RJ, Stevenson DK. Molecular physiology and pathophysiology of bilirubin handling by the blood, liver, intestine, and brain in the newborn. Physiol Rev. 2020;100(3):1291-346. doi: https://doi.org/10.1152/physrev.00004.2019; Chen K, Yuan T. The role of microbiota in neonatal hyperbilirubinemia. Am J Transl Res. 2020;12:7459-7474.; Novák P Jackson AO, Zhao GJ, Yin K. Bilirubin in metabolic syndrome and associated inflammatory diseases: new perspectives. Life Sci. 2020;257:118032. doi: https://doi.org/10.1016/j.lfs.2020.118032; Ma J, Li Z, Zhang W, et al. Comparison of gut microbiota in exclusively breast-fed and formula-fed babies: a study of 91 term infants. Sci Rep. 2020;10:15792. doi: https://doi.org/10.1038/s41598-020-72635-x; Guo Q, Liu X, Cui M, et al. Characteristics of intestinal microbiota in infants with late-onset breast milk jaundice. Front Nutr. 2023;10: 1119768. doi: https://doi.org/10.3389/fnut.2023.1119768; Tukey RH, Strassburg CP. Human UDP-glucuronosyltransferases: metabolism, expression, and disease. Annu Rev Pharmacol Toxicol. 2000;40:581-616. doi: https://doi.org/10.1146/annurev.pharmtox.40.1.581.; Maisels MJ, Kring E. Rebound in serum bilirubin level following intensive phototherapy. Arch Pediatr Adolesc Med. 2002;156(7): 669-672. doi: https://doi.org/10.1001/archpedi.156.7.669; Fujiwara R, Maruo Y, Chen S, Tukey RH. Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia. Toxicol Appl Pharmacol. 2015;289(1):124-132. doi: https://doi.org/10.1016/j.taap.2015.08.018; Maruo Y, Nishizawa K, Sato H, et al. Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene. Pediatrics. 2000;106(5):E59. doi: https://doi.org/10.1542/peds.106.5.e59; Fujiwara R, Chen S, Karin M, Tukey RH. Reduced expression of UGT1A1 in intestines of humanized UGT1 mice via inactivation of NF-kB leads to hyperbilirubinemia. Gastroenterology. 2012;142(1): 109-118. doi: https://doi.org/10.1053/j.gastro.2011.09.045; Assenat E, Gerbal-Chaloin S, Larrey D, et al. Interleukin 1beta inhibits CAR-induced expression of hepatic genes involved in drug and bilirubin clearance. Hepatology. 2004;40(4):951-960. doi: https://doi.org/10.1002/hep.20387; Sumida K, Kawana M, Kouno E, et al. Importance of UDP-glucuronosyltransferase 1A1 expression in skin and its induction by UVB in neonatal hyperbilirubinemia. Mol Pharmacol. 2013;84(5): 679-686. doi: https://doi.org/10.1124/mol.113.088112; Ota Y Maruo Y Matsui K, et al. Inhibitory effect of 5e-pregnane-3a,20e-diol on transcriptional activity and enzyme activity of human bilirubin UDP-glucuronosyltransferase. Pediatr Res. 2011;70(5): 453-457. doi: https://doi.org/10.1203/PDR.0b013e31822f242e; Muchowski KE. Evaluation and treatment of neonatal hyperbilirubinemia. Am Fam Physician. 2014;89(11):873-878.; Xiao LL, Zhang XF, Wang XY. Changes in epidermal growth factor concentrations in neonates with late-onset breast milk jaundice after stopping breast feeding. Zhongguo Dang Dai Er Ke Za Zhi. 2013;15(12):1079-1081.; Fawaz R, Baumann U, Ekong U, et al. Guideline for the Evaluation of Cholestatic Jaundice in Infants: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition. J Pediatr Gastroenterol Nutr. 2017;64(1):154-168. doi: https://doi.org/10.1097/MPG.0000000000001334; Banakar MK, Subbarayan A. A study of prolonged jaundice screen in healthy term babies. Indian J Clin Biochem. 2008;23(3):286-289. doi: https://doi.org/10.1007/s12291-008-0064-9; Kaplan M, Kaplan E, Hammerman C, et al. Post-phototherapy neonatal bilirubin rebound: a potential cause of significant hyperbilirubinaemia. Arch Dis Child. 2006;91(1):31-34. https://doi.org/doi:10.1136/adc.2005.081224; Chang PW, Kuzniewicz MW, McCulloch CE, Newman TB. A Clinical Prediction Rule for Rebound Hyperbilirubinemia Following Inpatient Phototherapy. Pediatrics. 2017;139(3):e20162896. doi: https://doi.org/10.1542/peds.2016-2896; So V, Coo H, Khurshid F. Validation of published rebound hyperbilirubinemia risk prediction scores during birth hospitalization after initial phototherapy: a retrospective chart review. Pediatr Res. 2022; 91(4):888-895. doi: https://doi.org/10.1038/s41390-021-01478-7; Sachdeva M, Murki S, Oleti TP, Kandraju H. Intermittent versus continuous phototherapy for the treatment of neonatal non-hemolytic moderate hyperbilirubinemia in infants more than 34 weeks of gestational age: a randomized controlled trial. Eur J Pediatr. 2015; 174(2):177-181. doi: https://doi.org/10.1007/s00431-014-2373-8; Pettersson M, Eriksson M, Odlind A, Ohlin A. Home phototherapy of term neonates improves parental bonding and stress: findings from a randomized controlled trial. Acta Paediatr. 2022;111(4): 760-766. doi: https://doi.org/10.1111/apa.16231; Awad MH, Amer S, Hafez M, et al. Fenofibrate as an adjuvant to phototherapy in pathological unconjugated hyperbilirubinemia in neonates: a randomized control trial. J Perinatol. 2021;41(4): 865-872. doi: https://doi.org/10.1038/s41372-020-00861-2; Lazarus G, Francie J, Roeslani RD, et al. Role of ursodeoxycholic acid in neonatal indirect hyperbilirubinemia: a systematic review and meta-analysis of randomized controlled trials. Ital J Pediatr. 2022; 48(1):179. doi: https://doi.org/10.1186/s13052-022-01372-w; Mutlu M, Aslan Y, Kader Ş, Aktürk Acar F. Preventive Effects of Probiotic Supplementation on Neonatal Hyperbilirubinemia Caused by Isoimmunization. Am J Perinatol. 2020;37(11):1173-1176. doi: https://doi.org/10.1055/s-0039-1692690; Nuzzi G, Trambusti I, DI Cicco ME, Peroni DG. Breast milk: more than just nutrition! Minerva Pediatr (Torino). 2021;73(2):111-114. doi: https://doi.org/10.23736/S2724-5276.21.06223-X; Geddes DT, Gridneva Z, Perrella SL, et al. 25 Years of Research in Human Lactation: From Discovery to Translation. Nutrients. 2021;13(9):3071. doi: https://doi.org/10.3390/nu13093071; Rahkonen P, Heinonen K, Pesonen AK, et al. Mother-child interaction is associated with neurocognitive outcome in extremely low gestational age children. Scand J Psychol. 2014;55(4): 311-318. doi: https://doi.org/10.1111/sjop.12133; Liu J, Leung P, Yang A. Breastfeeding and active bonding protects against children's internalizing behavior problems. Nutrients. 2013;6(1):76-89. doi: https://doi.org/10.3390/nu6010076; Vidavalur R, Devapatla S. Trends in hospitalizations of newborns with hyperbilirubinemia and kernicterus in United States: an epidemiological study. J Matern Fetal Neonatal Med. 2022;35(25):7701-7706. doi: https://doi.org/10.1080/14767058.2021.1960970; Alkén J, Håkansson S, Ekéus C, et al. Rates of Extreme Neonatal Hyperbilirubinemia and Kernicterus in Children and Adherence to National Guidelines for Screening, Diagnosis, and Treatment in Sweden. JAMA Netw Open. 2019;2(3):e190858. doi: https://doi.org/10.1001/jamanetworkopen.2019.0858; McNamara RK, Vannest JJ, Valentine CJ. Role of perinatal long-chain omega-3 fatty acids in cortical circuit maturation: Mechanisms and implications for psychopathology. World J Psychiatry. 2015;5(1):15-34. doi: https://doi.org/10.5498/wjp.v5.i1.15; Anderson JW, Johnstone BM, Remley DT. Breast feeding and cognitive development: a meta-analysis. Am J Clin Nutr. 1999; 70(4):525-535. doi: https://doi.org/10.1093/ajcn/70.4.525; Kramer MS, Aboud F, Mironova E, et al. Breastfeeding and child cognitive development: new evidence from a large randomized trial. Arch Gen Psychiatry. 2008;65(5):578-584. doi: https://doi.org/10.1001/archpsyc.65.5.578; Horta BL, Loret de Mola C, Victora CG. Breastfeeding and intelligence: a systematic review and meta-analysis. Acta Paediatr. 2015;104(467):14-19. doi: https://doi.org/10.1111/apa.13139; Deoni SCL, Dean DC, Piryatinsky I, et al. Breastfeeding and early white matter development: A cross-sectional study. Neuroimage. 2013;82:77-86. doi: https://doi.org/10.1016/j.neuroimage.2013.05.090; Schött U, Solomon C, Fries D, Bentzer P The endothelial glycocalyx and its disruption, protection and regeneration: a narrative review. Scand J Trauma Resusc Emerg Med. 2016; 24:48. doi: https://doi.org/10.1186/s13049-016-0239-y; Kutuzov N, Flyvbjerg H, Lauritzen M. Contributions of the glycocalyx, endothelium, and extravascular compartment to the blood-brain barrier. Proc Natl Acad Sci USA. 2018;115(40): E9429-E9438. doi: https://doi.org/10.1073/pnas.1802155115; Liu B, Newburg DS. Human milk glycoproteins protect infants against human pathogens. Breastfeed Med. 2013;8(4):354-362. doi: https://doi.org/10.1089/bfm.2013.0016; Hassiotou F, Beltran A, Chetwynd E, et al. Breastmilk is a novel source of stem cells with multilineage differentiation potential. Stem Cells. 2012;30(10):2164-2174. doi: https://doi.org/10.1002/stem.1188; Velasco I, Santos C, Limon J, et al. Bioactive components in human milk along the first month of life: effects of iodine supplementation during pregnancy. Ann Nutr Metab. 2016;68(2):130-136. doi: https://doi.org/10.1159/000443800; Aydin MS, Yiğit EN, Vatandaşlar E, et al. Transfer and integration of breast milk stem cells to the brain of suckling pups. Sci Rep. 2018; 8(1):4289. doi: https://doi.org/10.1038/s41598-018-32715-5; Irmak MK, Oztas Y, Oztas E. Integration of maternal genome into the neonate genome through breast milk mRNA transcripts and reverse transcriptase. Theor Biol Med Model. 2012;9:20. doi: https://doi.org/10.1186/1742-4682-9-20; Păduraru L, Dimitriu DC, Avasiloaiei AL, et al. Total antioxidant status in fresh and stored human milk from mothers of term and preterm neonates. Pediatr Neonatol. 2018;59(6):600-605. doi: https://doi.org/10.1016/j.pedneo.2018.02.004; DiNicolantonio JJ, McCarty MF, O'Keefe JH. Antioxidant bilirubin works in multiple ways to reduce risk for obesity and its health complications. Open Heart. 2018;5(2):e000914. doi: https://doi.org/10.1136/openhrt-2018-000914; Hansen R, Gibson S, De Paiva Alves E, et al. Adaptive response of neonatal sepsis-derived Group B Streptococcus to bilirubin. Sci Rep. 2018;8(1):6470. doi: https://doi.org/10.1038/s41598-018-24811-3; Altuntaş N. Is There Any Effect of Hyperbilirubinemia on Breastfeeding? If Any, at Which Level? Breastfeed Med. 2020;15(1):29-34. doi: https://doi.org/10.1089/bfm.2019.0176; Huang Y, Chen L, Wang X, et al. Maternal knowledge, attitudes and practices related to neonatal jaundice and associated factors in Shenzhen, China: a facility-based cross-sectional study. BMJ Open. 2022;12(8):e057981. doi: https://doi.org/10.1136/bmjopen-2021-057981; Chu KH, Teng SW, Tai CJ, et al. Does Jaundice in Newborn Infants Affect Exclusivity and Duration of Breastfeeding in Taiwan? J Nurs Res. 2021;29(2):e145. doi: https://doi.org/10.1097/jnr.0000000000000420; Hokkanen L, Launes J, Michelsson K. Adult neurobehavioral outcome of hyperbilirubinemia in full term neonates — A 30 year prospective follow-up study. PeerJ. 2014;2:e294. doi: https://doi.org/10.7717/peerj.294; Tsao PC, Yeh HL, Shiau YS, et al. Long-term neurodevelopmental outcomes of significant neonatal jaundice in Taiwan from 20002003: A nationwide, population-based cohort study. Sci Rep. 2020; 10(1):11374. doi: https://doi.org/10.1038/s41598-020-68186-w; Chiu YW, Cheng SW, Yang CY, Weng YH. Breastfeeding in Relation to Neonatal Jaundice in the First Week After Birth: Parents' Perceptions and Clinical Measurements. Breastfeed Med. 2021; 16(4):292-299. doi: https://doi.org/10.1089/bfm.2020.0293

  8. 8
    Academic Journal

    Contributors: Not specified., Отсутствует.

    Source: Pediatric pharmacology; Том 21, № 2 (2024); 102-110 ; Педиатрическая фармакология; Том 21, № 2 (2024); 102-110 ; 2500-3089 ; 1727-5776

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    Relation: https://www.pedpharma.ru/jour/article/view/2436/1580; Newman TB, Wu YW, Kuzniewicz MW, et al. Childhood Seizures After Phototherapy. Pediatrics. 2018;142(4):e20180648. doi: https://doi.org/10.1542/peds.2018-0648; Maimburg R, Olsen J, Sun Y. Neonatal hyperbilirubinemia and the risk of febrile seizures and childhood epilepsy. Women and Birth. 2013;26:S33. doi: https://doi.org/10.1016/j.wombi.2013.08.196; Abdellatif M, Tawfik GM, Makram AM, et al. Association between neonatal phototherapy and future cancer: an updated systematic review and meta-analysis. Eur J Pediatr. 2023;182(1):329–341. doi: https://doi.org/10.1007/s00431-022-04675-6; Nouri SAH, Zarkesh M. Recent Advances in Adjuvant Pharmacotherapy for Neonatal Indirect Hyperbilirubinemia: A Narrative Review. J Compr Ped. 2023;14(3):e136461. doi: https://doi.org/10.5812/compreped-136461; Володин Н.Н., Дегтярев Д.Н., Дегтярева А.В. и др. Тактика ведения доношенных и недоношенных новорожденных с непрямой гипербилирубинемией (клинические рекомендации) // Неонатология: Новости. Мнения. Обучение. — 2017. — № 2. — С. 113–126. — doi: https://doi.org/10.24411/2308-2402-2017-00035; Hoffmann F, Allers K, Rombey T, et al. Nearly 80 systematic reviews were published each day: Observational study on trends in epidemiology and reporting over the years 2000–2019. J Clin Epidemiol. 2021;138:1–11. doi: https://doi.org/10.1016/j.jclinepi.2021.05.022; Ioannidis JP. The Mass Production of Redundant, Misleading, and Conflicted Systematic Reviews and Meta-analyses. Milbank Q. 2016;94(3):485–514. doi: https://doi.org/10.1111/1468-0009.12210; Pieper D, Hoffmann F. Retrieving Cochrane reviews is sometimes challenging and their reporting is not always optimal. Res Synth Methods. 2022;13(5):554–557. doi: https://doi.org/10.1002/jrsm.1564; Murad MH, Wang Z. Guidelines for reporting meta-epidemiological methodology research. Evid Based Med. 2017;22(4):139–142. doi: https://doi.org/10.1136/ebmed-2017-110713; Lefebvre C, Glanville J, Briscoe S, et al. Technical Supplement to Chapter 4: Searching for and selecting studies. In: Cochrane Handbook for Systematic Reviews of Interventions. Higgins JPT, Thomas J, Chandler J, et al., eds. Version 6.3 (updated October 2023). Cochrane, 2023.; R Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing; 2022. Available online: https://www.R-project.org. Accessed on February 23, 2024.; Grames EM, Stillman AN, Tingley MW, et al. litsearcher: An automated approach to identifying search terms for systematic reviews using keyword co-occurrence networks. Methods in Ecology and Evolution. 2019;10(10):1645–1654. doi: https://doi.org/10.1111/2041-210X.13268; Synnot A, Bragge P, Lunny C, et al. The currency, completeness and quality of systematic reviews of acute management of moderate to severe traumatic brain injury: A comprehensive evidence map. PLoS One. 2018;13(6):e0198676. doi: https://doi.org/10.1371/journal.pone.0198676; Shea BJ, Reeves BC, Wells G, et al. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;358:j4008. doi: https://doi.org/10.1136/bmj.j4008; Квашнина Д.В., Полибин Р.В., Саперкин Н.В. и др. AMSTAR 2 — инструмент оценки качества систематических обзоров // Эпидемиология и Вакцинопрофилактика. — 2022. — Т. 21. — № 3. — С. 80–89. — doi: https://doi:10.31631/2073-3046-2022-21-3-80-89; Kuitunen I, Kiviranta P, Sankilampi U, et al. Ursodeoxycholic acid as adjuvant treatment to phototherapy for neonatal hyperbilirubinemia: a systematic review and meta-analysis. 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    Relation: Актуальные вопросы современной медицинской науки и здравоохранения: сборник статей VIII Международной научно-практической конференции молодых учёных и студентов, Екатеринбург, 19-20 апреля 2023 г.; http://elib.usma.ru/handle/usma/14359

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    Contributors: The study was carried out with the financial support of the Government of the Novosibirsk region within the framework of the State Budget No. 122031700094-5 of Research Institutе of Internal and Preventive Medicine – Branch of the Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences., Исследование выполнено при финансовой поддержке Правительства Новосибирской области в рамках ГЗ № 122031700094-5.

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    Source: Неонатологія, хірургія та перинатальна медицина, Vol 8, Iss 4(30) (2018)
    Neonatology, surgery and perinatal medicine; Том 8, № 4(30) (2018): NEONATOLOGY, SURGERY AND PERINATAL MEDICINE; 71-78
    Неонатологія, хірургія та перинатальна медицина; Том 8, № 4(30) (2018): НЕОНАТОЛОГІЯ, ХІРУРГІЯ ТА ПЕРИНАТАЛЬНА МЕДИЦИНА; 71-78
    Неонатология, хирургия и перинатальная медицина; Том 8, № 4(30) (2018): НЕОНАТОЛОГИЯ, ХИРУРГИЯ И ПЕРИНАТАЛЬНАЯ МЕДИЦИНА; 71-78

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    Source: Сучасна педіатрія; № 2(90) (2018): Сучасна педіатрія; 66-70
    Современная педиатрия; № 2(90) (2018): Современная педиатрия; 66-70
    Sovremennaya pediatriya; № 2(90) (2018): Sovremennaya pediatriya; 66-70

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