Sepsis

Yazarlar

Gözde Atasever Yıldırım
https://orcid.org/0000-0002-6132-7096

Özet

Sepsis, sistemik inflamatuvar yanıt sendromu, immün disregülasyon, mikro dolaşım bozuklukları ve uç organ fonksiyon bozukluğu ile karakterize ciddi klinik bir sendromdur. Sepsiste erken tanı ve tedavi mortalitenin azaltılmasında oldukça önemlidir. Hastanın klinik durumunun tanınması ardından en kısa sürede yeterli sıvı ve geniş spektrumlu antibiyotik tedavisine başlamak gerekmektedir.  Ayrıca klinisyenler, klinik bulguların hastanın altta yatan patofizyolojisini doğru bir şekilde yansıtmayabileceğinin farkında olmalı, daha ileri monitörizasyon yöntemlerinin (ekokardiyografi, arteriyel kateter vb.) gerekebileceğini göz önünde bulundurmalıdır.

Sepsis is a serious clinical syndrome characterised by systemic inflammatory response syndrome, immune dysregulation, microcirculatory disorders and end organ dysfunction. Early diagnosis and treatment in sepsis is very important in reducing mortality. Adequate fluid and broad-spectrum antibiotic treatment should be started as soon as possible following the recognition of the patient’s clinical condition. In addition, clinicians should be aware that clinical findings may not accurately reflect the underlying pathophysiology of the patient and it should be considered that further monitoring methods (echocardiography, arterial catheter etc.) may be required.

Referanslar

Pomerantz W. Systemic Inflamatory Response Syndrome (SIRS) and Sepsis in Children: Definitions, Epidemiology, Clinical Manifestations, and Diagnosis.2022; Available from: https://www.uptodate.com/contents/systemic-inflammatory-response-syndrome-sirs-and-sepsis-in-children-definitions-epidemiology-clinical-manifestations-and-diagnosis?search=SEPS%C4%B0S&source=search_result&selectedTitle=1~150&usage_type=default&display_rank=1#H1

Goldstein B, Giroir B, Randolph A. International Consensus Conference on Pediatric Sepsis. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6:2.

Davis AL, Carcillo JA, Aneja RK, et al. American College of Critical Care Medicine Clinical Practice Parameters for Hemodynamic Support of Pediatric and Neonatal Septic Shock. Crit Care Med. 2017; 45: 1061.

Duman M, Şevketoğlu E, Arslanköylü AE, ve ark. Çocuklarda Sepsis ve Septik Şok Protokolü. J Pediatr Emerg Intensive Care Med 2020; 7(Suppl1): 45-58.

Graciano AL, Balko JA, Rahn DS, et al. The Pediatric Multiple Organ Dysfunction Score (P-MODS): development and validation of an abjective scale to measure the severity of multiple organ dysfuncion in critically ill children. Crit Care Med. 2005; 33:1484.

Butt W. Septic shock. Pediatr Clin North Am. 2001; 48:601.

Gaines NN, Patel B, Williams EA, Cruz AT. Etiologies of septic shock in a pediatric emergency department population. Pediatr Infect Dis J. 2012; 31: 1203.

Watsons RS, Carcillo JA, Linde-Zwirble WT, et al. The epidemiology of severe sepsis in children in the United Stataes. Am J Respir Crit Care Med. 2003; 167:695.

Lee CY, Chen PY, Huang FL, Lin CF. Microbiologic spectrum and susceptibility pattem of clinical isolates from the pediatric intensive care unit in a single medical center- 6 years’ experience. J Microbiol Immunol Inect. 2009; 42:160.

Weiss SL, Ftizgerald JC, Pappachan J, et al. Global epidemiology of pediatric sevre sepsis: the sepsis prevelance, outcomes, and therapies study. Am J Respir Crit Care Med. 2015; 191: 1147.

Zaoutis TE, Prasad PA, Localio AR, et al. Risk factors and predictors for candidemia in pediatric intensive care unit patients: implications for preventtion. Clin Infect Dis. 2010; 51: e38.

Weiss SL, Parker B, Bullock ME, et all. Defining pediatric sepsis by different criteria: discrepancies in populations and implications for clinical practice. Pediatr Crit Care Med. 2012; 13: e219.

Lucignano B, Ranno S, Liesenfeld O, et al. Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis. J Clin Microbiol. 2011; 49: 2252.

Dhanani S, Cox PN. Infectious syndromes in the pediatric intensive care unit. In: Fuhrman & Zimmerman's Pediatric Critical Care, 4th ed, Fuhrman BP, Zimmerman JJ (Eds), Elsevier Saunders, Philadelphia 2011. p.1336.

Van Waardenburg DA, Jansen TC, Vos GD, Buuman WA. Hypergycemia in children with meningococcal sepsis and septic shock: the relation between plasma levels of insulin and inflammatory mediators. J Clin Endocrinol Metab. 2006; 91: 3916.

Cotter JM, Hardee I, Moss A, et al. Procalcito10nin Use: Variation Across Hospitals and Trends Over Time. Hosp Pediatr 2021; 12: 20-24

Juutilainen A, Hamalainen S, Pulkki K, et al. Biomarkers for bacteremia and severe sepsis in hematological patients with neutropenic fever: multivariate logistic regression analysis and factor analysis. Leuk Lymphoma. 2011; 52: 2349.

Downes KJ, Weiss SL, Gerber Js, et al. A Pragmatic Biomarker-Driven Algorithm to Guide Antibiotic Use in the Pediatric Intensive Care Unit: The Optimizing Antibiotic Strategies in Sepsis (OASIS) Study. J Pediatric Infect Dis Soc. 2017; 6: 134.

Downes KJ, Fitzgerald JC, Weiss SL. Utility of Procalcitonin as a Biomarker for Sepsis in Children. J Clin Microbiol. 2020; 58: e01851-19.

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29 Nisan 2025

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