Clinical and laboratory manifestations of congenital infectious and inflammatory diseases in extremely low and very low birth weight infants


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Objective. To study the clinical and laboratory manifestations of congenital infections in extremely low and very low birth weight (ELBW and VLBW) infants. Subject and methods. A prospective study included 129 ELBW and VLBW neonatal infants, 51 of whom were found to have congenital infection, 52 babies formed a group at high risk for congenital infection; the latter was excluded in 26 newborn infants. Clinical blood tests were carried out on day 1 of life and repeated on 3 of life; biochemical blood and hemostasiogram tests were done on day 3 of life; acid-base balance (ABB) and capillary blood lactate levels were estimated every 6-8 hours; C-reactive protein (CRP) and procalcitonin (PCT) were measured on day 3 of life; neurosonography, abdominal ultrasonography, echocardiography, and chest X-ray study were performed on day 1 of life. According to the babies’ status, neurosonography, echocardiography, and chest X-ray study were repeated on day 3 of life. Results. The characteristic manifestation of congenital infectious and inflammatory diseases in ELBW and VLBW infants in the first 72 hours of life is multiple organ dysfunction with the development of mainly respiratory and hemodynamic disorders and renal failure, which was accompanied by significant metabolic disturbances (hyperglycemia and persistent ABB disorders). Inflammatory changes in clinical blood tests have no sufficient sensitivity and specificity in verifying the diagnosis of congenital infection in ELBW and VLBW infants in the first 72 hours of life. The exception is the neutrophil index measured in the first 24 hours of life, which has moderate specificity, but low sensitivity. Conclusion. The isolated increase of one of the biochemical markers for systemic inflammation (CRP or PCT) in the absence of other clinical and laboratory signs may not be used as a significant sign of the diagnosis of congenital infection in ELBW and VLBW babies at least in the first 72 hours of life.

全文:

受限制的访问

作者简介

Olga Milaya

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation

Email: o_milaya@oparina4.ru
postgraduate of neonatal intensive care unit of the obstetric department

Oleg Ionov

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation

Email: o_ionov@oparina4.ru
Ph.D., Head of the intensive care department of neonatology and pediatrics

Anna Degtyareva

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation

Email: a_degtyareva@oparina4.ru
MD, Head of the Scientific Advisory Pediatrics Division of Neonatology and Pediatrics

Anna Levadnaya

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation

Email: a_levadnaya@oparina4.ru
PhD, researcher at the Department of Clinical Pharmacology

Dmtitry Degtyarev

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of the Russian Federation

Email: d_degtiarev@oparina4.ru
MD, PhD, DM, professor, Deputy Director for Science

参考

  1. Самсыгина Г.А. О предрасполагающих факторах и факторах риска развития неонатального сепсиса и о современных подходах его лечения. Педиатрия. Журнал имени Г.Н. Сперанского. 2012; 91(3): 32-7. [Samsygina G.A. About predisposing factors and risk factors for neonatal sepsis and modern approaches its treatment. Pediatrics. G.N. Speranskii Journal. 2012; 91 (3): 32-7.]
  2. Шабалов Н.П. Общебиологическая проблема: закономерности и последствия перинатального инфицирования. Педиатрия. Журнал имени Г.Н. Сперанского. 2012; 91(3): 26-31. [Shabalov N.P. General biological problem: the patterns and consequences of perinatal transmission. Pediatrics. G.N. Speranskii Journal. 2012; 91 (3): 26-31.]
  3. Голубцова Ю.М., Дегтярев Д.Н. Современные подходы к профилактике, диагностике и лечению раннего неонатального сепсиса. Неонатология. 2014; 2: 15-25. [Golubtsova Yu.M., Degtyarev D.N. Current approaches to prevention, diagnosis and treatment of early neonatal sepsis. Neonatology. 2014; 2: 15-25.]
  4. Антонов А.Г., Байбарина Е.Н. Внутриутробная пневмония (Критерии диагностики и стандарты лечения). Методические рекомендации. М.; 1997: 3-6. [Antonov A.G., Baibarina E.N. Intrauterine pneumonia (Criteria for diagnosis and treatment standards). Guidelines. M.; 1997: 3-6.]
  5. Ионов О.В., Мостовой А.В., Овсянников Д.Ю. Дыхательные расстройства у новорожденных. В кн.: Володин Н.Н., ред. Неонатология. Национальное руководство. Краткое издание. М.: ГЕОТАР-Медиа; 2013: 204-10. [Ionov O.V., Mostovoy A.V., Ovsyannikov D.Yu. Respiratory disorders in the newborn. In: Volodin N.N., eds. Neonatology. National guideline. Short Edition. M.: GEOTAR-Media; 2013: 204-10.]
  6. Самсыгина Г.А., Шабалов Н.П., Дегтярева М.В. Сепсис. В кн.: Володин Н.Н., ред. Неонатология. Национальное руководство. Краткое издание. М.: ГЕОТАР-Медиа; 2013: 766-70. [Samsygina G.A., Shabalov N.P., Degtyareva M.V. Sepsis. In: Volodin N., eds. Neonatology. National guideline. Short Edition. M .: GEOTAR-Media; 2013: 766-70.]
  7. Report on the expert meeting on neonatal and paediatric sepsis. 8 June 2010, EMA London.
  8. Janota J., Stranák Z., Statecá B., Dohnalová A., Šípek A., Šimák J. Characterization of multiple organ dysfunction syndrome in very low birthweight infants: a new sequential scoring system. Shock. 2001; 15(5): 348-52.
  9. Wojkowska-Mach J., Borszewska-Kornacka M., Domańska J., Gadzinowski J., Gulczyńska E., Helwich E. et al. Early-onset infections of very-low-birth-weight infants in Polish neonatal intensive care units. Pediatr. Infect. Dis. J. 2012; 31(7): 691-5.
  10. Cetinkaya M., Köksal N., Özkan H. A new scoring system for evaluation of multiple organ dysfunction syndrome in premature infants. Am. J. Crit. Care. 2012; 21(5): 328-37.
  11. Shah B.A., Padbury J.F. Neonatal sepsis: an old problem with new insights. Virulence. 2014; 5(1): 170-8.
  12. Decaro M.H., Vain N.E. Hyperglycaemia in preterm neonates: what to know, what to do. Early Hum. Dev. 2011; 87(Suppl.1): S19-22.
  13. Makkar M., Gupta C., Pathak R., Garg S., Mahajan N.C. Performance evaluation of hematologic scoring system in early diagnosis of neonatal sepsis. J. Clin. Neonatol. 2013; 2(1): 25-9.
  14. Arif S.A., Ehsan A., Arif M., Hussain J., Bano R. Early diagnosis of neonatal sepsis through haematological and biochemical markers. Gomal J. Med. Sci. 2013; 11(2): 178.
  15. Jiang Z., Ye G.Y. 1:4 matched case-control study on influential factor of early onset neonatal sepsis. Eur. Rev. Med. Pharmacol. Sci. 2013; 17(18): 2460-6.
  16. Hofer N., Zacharias E., Müller W., Resch B. An update on the use of C-reactive protein in early-onset neonatal sepsis: current insights and new tasks. Neonatology. 2012; 102(1): 25-36.
  17. Remington J.S., Klein J.O., eds. Infectious diseases of the fetus and newborn infant. 3rd ed. Philadelphia: Saunders; 1990.

补充文件

附件文件
动作
1. JATS XML

版权所有 © Bionika Media, 2014
##common.cookie##