3. Values of extended white blood cell indicators in the diagnosis of sepsis in children

Nguyen Thi Duyen, Nguyen Thi Thanh Tam, Luong Thi Nghiem, Hoang Thi Bich Ngoc, Tran Thi Ngan, Nguyen Van Hai, Tran Thi Thuy Lanh, Nguyen Thi Thu Nga, Nguyen Thanh Binh

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Abstract

Sepsis is one of the primary causes of children mortality. Early diagnosis of sepsis decreases mortality, and hospital stay duration, and improves prognosis. This study aimed to determine the diagnostic value of extended granulocyte indicators in children with sepsis. From February 2022 to February 2023, a cross-sectional, retrospective descriptive study was conducted on three patient groups, including 120 patients with sepsis, 60 patients with local infection, and 120 healthy children. White blood cells (WBC), immature granulocytes (IG#, IG%), and novel neutrophil indices (NE-SFL, NE-SSC, NE-WY) were measured and compared in 3 groups. The results showed that IG# and IG% indicators were statistically significant differences between the sepsis and other groups. Using the area under the ROC curve, IG#, IG% was better than WBC, neutrophil percentage (NEU%) in the differential diagnosis of sepsis and local infection of 0.77 and 0.76 respectively. The IG# indicator has sensitivity (Se) = 71.2% and Specificity (Sp) = 73.3% at the optimal cutoff threshold of 0.045 G/L. The IG% indicator has Se = 72.6% and Sp = 71.0% at the optimal cut-off threshold of 0.45%. Other neutrophil indicators, such as NE-SFL, NE-SSC, and NE-WY, did not reveal statistically significant differences between patient groups. Conclusion: IG# = 0.045 G/L and IG% = 0.45% are the optimal cut-off values for IG# and IG%, respectively, in diagnosing sepsis with an AUC of 0.77 and 0.76.

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References

1. Rudd KE, Johnson SC, Agesa KM, et al. Global, regional, and national sepsis incidence and mortality, 1990-2017: analysis for the Global Burden of Disease Study. Lancet (London, England). 2020; 395(10219): 200-11.
2. Biban P, Teggi M, Gaffuri M, et al. Cell Population Data (CPD) for Early Recognition of Sepsis and Septic Shock in Children: A Pilot Study. Frontier Pediatric. 2021; 9: 642377.
3. Pavare J, Grope I, Gardovska D. Assessment of Immature Granulocytes Percentage to Predict Severe Bacterial Infection in Latvian Children: An Analysis of Secondary Data. Medicina (Mex). 2018; 54(4): 56.
4. Van der Geest PJ, Mohseni M, Brouwer R, van der Hoven B, Steyerberg EW, Groeneveld ABJ. Immature granulocytes predict microbial infection and its adverse sequelae in the intensive care unit. J Crit Care. 2014; 29(4): 523-527.
5. Nguyễn Thị Trúc Lệ, Dương Phước Lực. Khảo sát số lượng tế bào bạch cầu hạt chưa trưởng thành trong máu bằng máy đếm tế bào tự động ở người bệnh tại bệnh viện đa khoa Long An, Tạp chí Y học thành phố Hồ Chí Minh. 7, 2023.
6. Garner J, Jarvis W, Emori TG, Horan T, Hughes J. CDC Definitions for Nosocomial Infections. Am J Infect Control. 1988;16:128-140.
7. MacQueen BC, Christensen RD, Yoder BA, et al. Comparing automated vs manual leukocyte differential counts for quantifying the “left shift” in the blood of neonates. J Perinatol Off J Calif Perinat Assoc. 2016; 36(10): 843-848.
8. Roehrl MHA, Lantz D, Sylvester C, Wang JY. Age-Dependent Reference Ranges for Automated Assessment of Immature Granulocytes and Clinical Significance in an Outpatient Setting. Arch Pathol Lab Med. 2011; 135(4): 471-477.