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Geç Neonatal Sepsiste, Trombosit ve Eritrosit İndeksleri ve Prognoza Etkisi

Year 2025, Volume: 22 Issue: 1, 97 - 103
https://doi.org/10.35440/hutfd.1562572

Abstract

Amaç: Yenidoğanların mortalite ve morbiditesinin en önemli nedenlerin biri yenidoğan sepsisidir. Tanı ve tedavisindeki tüm gelişmelere rağmen önemli bir halk sağlığı sorunu olarak karşımıza çıkmaktadır. Bu araştırmada, geç başlangıçlı sepsis tanısı ile yenidoğan yoğun bakım ünitesine (YYBÜ) yatışı yapılan yenidoğanların tedavinin başlangıcı ve 7.gündeki hemogram parametrelerinin değerlendirilmesi amaç-lanmaktadır.
Materyal ve Metod: Bu araştırma Ocak 2017-Şubat 2020 tarihleri arasında bir üniversite hastanesinin YYBÜ’sinde geç başlangıçlı yenidoğan sepsisi tanısıyla bakım ve tedavi almış yenidoğanlarla kesitsel tipte yürütülmüştür. Postnatal 72. saat ile 30. günler arasında olan ve kan veya idrar kültüründe üre-mesi olan yenidoğanlar araştırmaya dahil edildi. Araştırmanın verileri dijital ortamda retrospektif olarak sepsisin 1. ve 7. günlerinde alınan hemogram parametreleri, CRP düzeyleri, girişimsel işlem durumu, kültürün alındığı vücut sıvısı, kültür sonucu, başlangıçta uygulanan tedavi, takip ve tedaviler-de yapılan değişim, yatış nedeni ve mortalite gibi durumların taranması sonucunda elde edilmiştir.
Bulgular: Yenidoğanların %58.4’ünün erkek ve %50.6’sının term bebek olduğu belirlenmiştir. Yaşamını kaybeden yenidoğanların sepsisin 7. gününde RBC ve MCH düzeyleri, sepsisin 1. gününde MCV düzey-leri ile 1. ve 7. günlerinde HGB, HCT ve PLT düzeyleri yaşayan yenidoğanlara göre istatistiksel olarak anlamlı düzeyde daha düşük saptanmıştır. Ayrıca, yaşamını kaybeden yenidoğanların sepisinin 1. gü-nünde MPV düzeyleri ile 1. ve 7. günlerinde CRP düzeyleri yaşayan yenidoğanlara göre istatistiksel olarak anlamlı seviyede daha yüksek olarak tespit edilmiştir.
Sonuç: Sonuçlardan anlaşılacağı üzere geç başlangıçlı sepsis tanılı yenidoğanların takibinde sepisinin 7. günü RBC ve MCH düzeyleri, sepsisin 1. günü MCV düzeyleri ile sepsisin 1. günü ve 7. günü HGB, HCT ve PLT düzeylerinin düşüklüğünün ve sepsinin 1. günü ve 7. günü CRP düzeyleri ile sepsisin 1. gününde MPV düzeylerinin yüksekliğinin kötü prognostik faktör olarak değerlendirilmesi gerektiği ve mortalite ile ilişkili olduğu kanıtlanmıştır.

Anahtar Kelimeler: Geç başlangıçlı yenidoğan sepsisi; Prognoz; Trombosit; Eritrosit

Project Number

No

References

  • 1. WHO. Newborn Mortality. [updated 15 February 22]. Available from: https://www.who.int/news-room/fact-sheets/detail/levels-and-trends-in-child-mortality-report-2021
  • 2. Mussap M, Puxeddu E, Puddu M, Ottonello G, Coghe F, Comite P, et al. Soluble CD14 subtype (sCD14-ST) Presepsin in Prema-ture and Full Term Criticallyill New Borns With Sepsis and SIRS. Clin Chim Acta. 2015;451(Pt A):65-70.
  • 3. Silveira RDC, Giacomini C, Procianoy RS. Neonatal Sepsis and Septic Shock: Concepts Update and Review. RevBras Ter Inten-siva. 2010;22(3):280-90.
  • 4. Satar M, Arısoy AE, Celik IH. Turkish Neonatal Society Guideli-ne on Neonatal Infections-Diagnosis and Treatment. Turk Pedi-atri Ars. 2018;53(Suppl 1):88-100.
  • 5. Qazi SA, Stoll BJ. Neonatal Sepsis: A Major Global Public Health Challenge. Pediatr Infect Dis J. 2009;28(1 Suppl):1-2.
  • 6. Boghossian NS, Page GP, Bell EF, Stoll BJ, Murray JC, Cotten CM, et al. Late-onset Sepsis in Very Low Birth Weight Infants Fromsingleton and Multiple-Gestation Births. J Pediatr. 2013;162(6):1120-4.
  • 7. Vergnano S, Menson E, Kennea N, Embleton N, Russell AB, Watts T, et al. Neonatal Infections in England: The NeonIN Sur-veillance Network. Arch Dis Child Fetal Neonatal Ed. 2011;96(1):9-14.
  • 8. Gumus H, Kazanasmaz H. Investigation of Frequency, Isolated Microorganisms and Antibiotic Resistance in Culture-Proven Late Neonatal Sepsis Cases. KSÜ Med. J. 2018;13(3):81-84.
  • 9. Stoll BJ, Hansen NI, Sánchez PJ, Faix RG, Poindexter BB, Van Meurs KP, et al. Early Onset Neonatal Sepsis: The Burden of Group B Streptococcal and E.Coli Disease Continues. Pediat-rics. 2011;127(5):817-26.
  • 10. Dong Y, Speer CP. Late-onset Neonatal Sepsis: Recent Deve-lopments. Archives of Disease in Childhood-Fetaland Neonatal Edition. 2015;100(3):257-63.
  • 11. Tripathi S, Malik GK. Neonatal Sepsis: Past, Present And Futu-re; A Review Article. Internet Journal of Medical Update, 2010; 5(2):45-54.
  • 12. Manzoni P. Hematologic Aspects of Early and Late-Onset Sepsis in Preterm Infants. Clin Perinatol. 2015;42(3):587-95.
  • 13. European Medicines Agency (EMA). Report on the Expert Meeting on Neonatal and Paediatric Sepsis London; 2010 [up-dated 8 June 2010].
  • 14. Bateman RM, Sharpe MD, Singer M, Ellis CG. The Effect of Sepsis on the Erythrocyte. Int J MolSci. 2017;18(9):1932-3.
  • 15. Kliegman RM, St Geme JW, Blum NJ, Shah SS, MSCE, Tasker RC, Wilson KM. Nelson Textbook of Pediatrics (21th ed): Blood Di-sorders. Philadelphia: Elsevier, 2020; 961-74.
  • 16. Kling PJ. Iron Nutrition, Erythrocytes, and Erythropoietin in the NICU: Erythropoietic and Neuroprotective Effects. Neore-views. 2020;21(2):80-8
  • 17. Sadaka F, O’Brien J, Prakash S. Red Cell Distribution Widthand Outcome in Patients With Septicshock. J. Intensive Care Med. 2013; 28:307–13.
  • 18. Kim CH, Park JT, Kim EJ, Han JH, Han JS, Choi JY, et al. An Increase in Red Bloodcell Distribution with from Baseline Pre-dicts Mortality in Patients with Severe Sepsis or Septic Shock. Crit. Care. 2013.
  • 19. Garofoli F, Ciardelli L, Mazzucchelli I, Borghesi A, Angelini M, Bollani L, et al. The Red Cell Distribution Width (RDW): Value and role in Preterm, IUGR (intrauterine growth restricted), Full-Term Infants. Hematology. 2014; 19: 365-9.
  • 20. Yilmaz Z, Eralp O, Ilcol YO. Evaluation of Platelet Count and its Association with Plateletcrit, Mean Platelet Volume, and Pla-telet Size Distribution Width in a Canine Model of Endotoxe-mia. Vet Clin Pathol. 2008;37(2):159-3.
  • 21. Hanaganahalli SB, Sreeram S, Bompada M, Kuppannagari SK, Suresh PK, Philipose CS. Is MPV a Predictive Marker for Neona-tal Sepsis? A Pilot Study. J Pediatr Hematol Oncol. 2018;40(7):548-52.
  • 22. Ellahony DM, El-Mekkawy MS, Farag MM. A Study of Red Cell Distribution Width in Neonatal Sepsis. Pediatr Emerg Care. 2017;10.1097/PEC.0000000000001319.
  • 23. Shehab El-Din EM, El-Sokkary MM, Bassiouny MR, Hassan R. Epidemiology of Neonatal Sepsis and Implicated Pathogens: A Study from Egypt. Biomed Res Int. 2015; 2015: 509484.
  • 24. Giannoni E, Agyeman PKA, Stocker M, Posfay-Barbe KM, Hei-ninger U, Spycher BD, et al. Neonatal Sepsis of Early Onset, and Hospital-Acquired and Community-Acquired Late Onset: A Prospective Population-Based Cohort Study. J Pediatr. 2018; 201:106-14.
  • 25. Fanaroff A. Walsh MC. Fanar off and Martin′ s Neonatal-Perinatal Medicine Diseases of the Fetus and Infant. St. Louis, Missouri: Mosby. Elsevier; 2011
  • 26. Freitas FTM, Araujo AFOL, Melo MIS, Romero GAS. Late-onset Sepsis and Mortality Among Neonates in a Brazilian Intensive Care Unit: A Cohort Study and Survival Analysis. Epidemiol Infect. 2019; 147:208-9.
  • 27. El Manouni El Hassani S, Berkhout DJC, Niemarkt HJ, Mann S, De Boode WP, Cossey V, et al. Risk Factors for Late-Onset Sep-sis in Preterm Infants: A Multicenter Case-Control Study. Neo-natology. 2019;116(1):42-51.

Platelet and Erythrocyte Indices and Their Impact on Prognosis in Late Neonatal Sepsis

Year 2025, Volume: 22 Issue: 1, 97 - 103
https://doi.org/10.35440/hutfd.1562572

Abstract

Background: One of the most significant causes of mortality and morbidity in newborns is neonatal sepsis. Despite all the advancements in its diagnosis and treatment, it remains a major public health issue. This study aims to evaluate the hemogram parameters of newborns admitted to the neonatal intensive care unit (NICU) with a diagnosis of late-onset neonatal sepsis, both at the start of treatment and on the 7th day.
Materials and Methods: This study was conducted in a cross-sectional manner with 89 newborns who received care and treatment for late-onset neonatal sepsis in the neonatal intensive care unit (NICU) of a university hospital between January 2017 and February 2020. Newborns between the postnatal 72nd hour and 30th day with positive blood or urine cultures were included in the study. The data of the study were obtained retrospectively in the digital environment by screening hemogram parame-ters, CRP levels, interventional procedure status, body fluid from which the culture was taken, culture result, initial treatment, follow-up and change in treatments, reason for hospitalization and mortality on the 1st and 7th days of sepsis.
Results: It was determined that 58.4% of the newborns were male and 50.6% were term newborns. RBC and MCH levels on the 7th day of sepsis, MCV levels on the 1st day of sepsis, HGB, HCT and PLT levels on the 1st and 7th days of sepsis were found to be statistically significantly lower in newborns who lost their lives compared to living newborns. In addition, MPV levels on the 1st day of sepsis and CRP levels on the 1st and 7th days of sepsis of newborns who died were found to be statistically signi-ficantly higher than those of living newborns.
Conclusions: As can be understood from the results, it has been proven that low RBC and MCH levels on the 7th day of sepsis, MCV levels on the 1st day of sepsis, HGB, HCT and PLT levels on the 1st day and 7th day of sepsis, and high CRP levels on the 1st day and 7th day of sepsis and MPV levels on the 1st day of sepsis should be considered as poor prognostic factors and are associated with mortality in the follow-up of newborns diagnosed with late-onset sepsis.

Ethical Statement

Before starting the study, approval from the clinical research ethics committee of a university was obtained with the decision numbered 19/09/15 dated 22.10.2019 and institutional permission from the hospital where the study was conducted. The study was conducted in accordance with the principles of the Declaration of Helsinki.

Supporting Institution

This study has not been supported by any funding.

Project Number

No

References

  • 1. WHO. Newborn Mortality. [updated 15 February 22]. Available from: https://www.who.int/news-room/fact-sheets/detail/levels-and-trends-in-child-mortality-report-2021
  • 2. Mussap M, Puxeddu E, Puddu M, Ottonello G, Coghe F, Comite P, et al. Soluble CD14 subtype (sCD14-ST) Presepsin in Prema-ture and Full Term Criticallyill New Borns With Sepsis and SIRS. Clin Chim Acta. 2015;451(Pt A):65-70.
  • 3. Silveira RDC, Giacomini C, Procianoy RS. Neonatal Sepsis and Septic Shock: Concepts Update and Review. RevBras Ter Inten-siva. 2010;22(3):280-90.
  • 4. Satar M, Arısoy AE, Celik IH. Turkish Neonatal Society Guideli-ne on Neonatal Infections-Diagnosis and Treatment. Turk Pedi-atri Ars. 2018;53(Suppl 1):88-100.
  • 5. Qazi SA, Stoll BJ. Neonatal Sepsis: A Major Global Public Health Challenge. Pediatr Infect Dis J. 2009;28(1 Suppl):1-2.
  • 6. Boghossian NS, Page GP, Bell EF, Stoll BJ, Murray JC, Cotten CM, et al. Late-onset Sepsis in Very Low Birth Weight Infants Fromsingleton and Multiple-Gestation Births. J Pediatr. 2013;162(6):1120-4.
  • 7. Vergnano S, Menson E, Kennea N, Embleton N, Russell AB, Watts T, et al. Neonatal Infections in England: The NeonIN Sur-veillance Network. Arch Dis Child Fetal Neonatal Ed. 2011;96(1):9-14.
  • 8. Gumus H, Kazanasmaz H. Investigation of Frequency, Isolated Microorganisms and Antibiotic Resistance in Culture-Proven Late Neonatal Sepsis Cases. KSÜ Med. J. 2018;13(3):81-84.
  • 9. Stoll BJ, Hansen NI, Sánchez PJ, Faix RG, Poindexter BB, Van Meurs KP, et al. Early Onset Neonatal Sepsis: The Burden of Group B Streptococcal and E.Coli Disease Continues. Pediat-rics. 2011;127(5):817-26.
  • 10. Dong Y, Speer CP. Late-onset Neonatal Sepsis: Recent Deve-lopments. Archives of Disease in Childhood-Fetaland Neonatal Edition. 2015;100(3):257-63.
  • 11. Tripathi S, Malik GK. Neonatal Sepsis: Past, Present And Futu-re; A Review Article. Internet Journal of Medical Update, 2010; 5(2):45-54.
  • 12. Manzoni P. Hematologic Aspects of Early and Late-Onset Sepsis in Preterm Infants. Clin Perinatol. 2015;42(3):587-95.
  • 13. European Medicines Agency (EMA). Report on the Expert Meeting on Neonatal and Paediatric Sepsis London; 2010 [up-dated 8 June 2010].
  • 14. Bateman RM, Sharpe MD, Singer M, Ellis CG. The Effect of Sepsis on the Erythrocyte. Int J MolSci. 2017;18(9):1932-3.
  • 15. Kliegman RM, St Geme JW, Blum NJ, Shah SS, MSCE, Tasker RC, Wilson KM. Nelson Textbook of Pediatrics (21th ed): Blood Di-sorders. Philadelphia: Elsevier, 2020; 961-74.
  • 16. Kling PJ. Iron Nutrition, Erythrocytes, and Erythropoietin in the NICU: Erythropoietic and Neuroprotective Effects. Neore-views. 2020;21(2):80-8
  • 17. Sadaka F, O’Brien J, Prakash S. Red Cell Distribution Widthand Outcome in Patients With Septicshock. J. Intensive Care Med. 2013; 28:307–13.
  • 18. Kim CH, Park JT, Kim EJ, Han JH, Han JS, Choi JY, et al. An Increase in Red Bloodcell Distribution with from Baseline Pre-dicts Mortality in Patients with Severe Sepsis or Septic Shock. Crit. Care. 2013.
  • 19. Garofoli F, Ciardelli L, Mazzucchelli I, Borghesi A, Angelini M, Bollani L, et al. The Red Cell Distribution Width (RDW): Value and role in Preterm, IUGR (intrauterine growth restricted), Full-Term Infants. Hematology. 2014; 19: 365-9.
  • 20. Yilmaz Z, Eralp O, Ilcol YO. Evaluation of Platelet Count and its Association with Plateletcrit, Mean Platelet Volume, and Pla-telet Size Distribution Width in a Canine Model of Endotoxe-mia. Vet Clin Pathol. 2008;37(2):159-3.
  • 21. Hanaganahalli SB, Sreeram S, Bompada M, Kuppannagari SK, Suresh PK, Philipose CS. Is MPV a Predictive Marker for Neona-tal Sepsis? A Pilot Study. J Pediatr Hematol Oncol. 2018;40(7):548-52.
  • 22. Ellahony DM, El-Mekkawy MS, Farag MM. A Study of Red Cell Distribution Width in Neonatal Sepsis. Pediatr Emerg Care. 2017;10.1097/PEC.0000000000001319.
  • 23. Shehab El-Din EM, El-Sokkary MM, Bassiouny MR, Hassan R. Epidemiology of Neonatal Sepsis and Implicated Pathogens: A Study from Egypt. Biomed Res Int. 2015; 2015: 509484.
  • 24. Giannoni E, Agyeman PKA, Stocker M, Posfay-Barbe KM, Hei-ninger U, Spycher BD, et al. Neonatal Sepsis of Early Onset, and Hospital-Acquired and Community-Acquired Late Onset: A Prospective Population-Based Cohort Study. J Pediatr. 2018; 201:106-14.
  • 25. Fanaroff A. Walsh MC. Fanar off and Martin′ s Neonatal-Perinatal Medicine Diseases of the Fetus and Infant. St. Louis, Missouri: Mosby. Elsevier; 2011
  • 26. Freitas FTM, Araujo AFOL, Melo MIS, Romero GAS. Late-onset Sepsis and Mortality Among Neonates in a Brazilian Intensive Care Unit: A Cohort Study and Survival Analysis. Epidemiol Infect. 2019; 147:208-9.
  • 27. El Manouni El Hassani S, Berkhout DJC, Niemarkt HJ, Mann S, De Boode WP, Cossey V, et al. Risk Factors for Late-Onset Sep-sis in Preterm Infants: A Multicenter Case-Control Study. Neo-natology. 2019;116(1):42-51.
There are 27 citations in total.

Details

Primary Language English
Subjects Pediatric Hematology and Oncology
Journal Section Research Article
Authors

Halil Dolap 0000-0003-2808-3533

Doğan Köse 0000-0002-2903-2976

Project Number No
Early Pub Date March 12, 2025
Publication Date
Submission Date October 8, 2024
Acceptance Date February 26, 2025
Published in Issue Year 2025 Volume: 22 Issue: 1

Cite

Vancouver Dolap H, Köse D. Platelet and Erythrocyte Indices and Their Impact on Prognosis in Late Neonatal Sepsis. Harran Üniversitesi Tıp Fakültesi Dergisi. 2025;22(1):97-103.

Harran Üniversitesi Tıp Fakültesi Dergisi  / Journal of Harran University Medical Faculty