2008, Number 3
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Rev Mex Pediatr 2008; 75 (3)
Sensibility and specificity of smears of buffy coat stained with Gram in the diagnosis of neonatal sepsis
Ballesteros DOJC, Tena RD, García EG, Vega GA, Ramírez OMR, Sosa MJ, Tapia RC, Mendoza ZRM
Language: Spanish
References: 13
Page: 97-102
PDF size: 97.61 Kb.
ABSTRACT
Objective. To calculate the sensibility and specificity of the smears of buffy coat (BC) stained with Gram and an from another laboratory exams for the diagnosis of neonatal sepsis, taking as «gold standard» the haemocultive.
Material and methods. The validation of the results of the BC smears the tint of the BC and of those of the exams of laboratory was done in 38 neonates where the diagnosis of sepsis was you confirmed and those of 10 neonates with negative laboratory exams for the diagnosis of sepsis.
Results. Among the 38 with sepsis, the protein C reactive was high in 31 (81.5%) and the smears of the BC were positives in 29 (76.3%); neutrophilia was found in 28 (73.6%) and the vacuolization of the neutrophiles in 22 (52.6%). The biggest sensibility was for protein C reactive protein (82%) followed by the smear of BC (76%) and the haemocultive (73%): although all of them had a low specificity.
Conclusions. The smear of the BC stained with Gram is an advisable technical procedure in the diagnosis of sepsis neonatal: it is accessible, economic, simple and easy in expert hands.
REFERENCES
Murguía M, Mancilla J. Programa de actualización continua en neonatología. Libro 7. Intersistemas editores. México 2004; 433-439, 467-480.
López H, Reynés J, Álvarez E, et al. Primer Consenso de sepsis neonatal (2003). Acta Pediátrica Mexicana 2003; 24(Supl. 1) S1-S11.
Goldstein B, Giroir B, Randolph A, et al. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatric Critical Care Medicine 2005; 6(1): 1-8.
Ballesteros JC, Rodríguez C, Morales M, et al. Indicadores de infección temprana en septicemia neonatal. Revista Mexicana de Pediatría 1996; 63(1): 17-24.
Jawetz E, Melnick J, Adelberg E. Microbiología médica. 14° ed. México: Manual Moderno. México. 1992: 636-637.
Fernández P, Pertegas S. Pruebas diagnósticas, sensibilidad y especificidad. Cad Aten Primaria 2003; 10: 120-124. www.fisterra.com/mbe/investiga/pruebas_diagnosticas/pruebas_diagnosticas.asp
Buttery JP. Blood cultures in newborns and children: optimizing an everyday test. Arch Dis Child Fetal and Neonatal edition 2002; 87(1): 25-28.
Scheloyka RL, Chai MK, Yoder BA, Hensley D, Brockett RM, Ascher DP. Volume of blood required to detect common neonatal pathogens. J Pediatr 1996; 129(2): 275-278.
Stoll BJ, Gordon T, Korones SB, Shankaran S, Tyson JE, Bauer CR et al. Late-onset sepsis in very low birth weight neonates: a report from the National Institute of Child Health and Human Development Neonatal Research Network. J Pediatr 1996; 129(7): 63-71.
Sanghvi KP, Tudehope DI. Neonatal bacterial sepsis in a neonatal intensive care unit: a 5 year analysis. Journal of Paediatrics and Child Health 1996; 32(4): 333-338.
Mathur NB, Saxena LM, Sarkar P, Puri RK. Superiority of acridine orange-stained buffy coat smears for diagnosis of partially treated neonatal septicemia. Acta Paediatr 1993; 82(6-7): 533-535.
Hechavarría SJC, Armaignac FG, Suárez DR. Infección nosocomial en la Unidad de Cuidados Intensivos. Medisan 2001; 5(3): 12-17. http://www.bvs.sld.cu/revistas/san/vol5_4_01/san 02401.pdf
Ristuccia PA, Hoefner RA, Digamon-Beltrán M, Cunha BA. Detection of bacteremia by buffy coat smears. Scand J Infect Dis 1987; 19(2): 215-217.