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Description of an Automated Method for Urea Nitrogen Determination in Bronchoalveolar Lavage Fluid (BALF) of Neonates and Infants.
Pocino, Krizia; Minucci, Angelo; Manieri, Rocco; Conti, Giorgio; De Luca, Daniele; Capoluongo, Ettore Domenico.
Afiliação
  • Pocino K; Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy krizia.pocino@gmail.com.
  • Minucci A; Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy.
  • Manieri R; Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy.
  • Conti G; Pediatric Intensive Care Unit, Department of Critical Care University Hospital "A. Gemelli," Catholic University of the Sacred Heart, Rome, Italy.
  • De Luca D; Pediatric Intensive Care Unit, Department of Critical Care University Hospital "A. Gemelli," Catholic University of the Sacred Heart, Rome, Italy Division of Pediatrics and Neonatal Critical Care, South Paris University Hospitals Medical Center, "A. Beclere," APHP, Paris, France.
  • Capoluongo ED; Institute of Biochemistry and Clinical Biochemistry, Catholic University of the Sacred Heart, Rome, Italy.
J Lab Autom ; 20(6): 636-41, 2015 Dec.
Article em En | MEDLINE | ID: mdl-25586999
ABSTRACT
Bronchoalveolar lavage (BAL) partially recovers both the instilled saline and the alveolar fluid, so-called epithelial lining fluid (ELF), but a correction for the dilution due to the BAL technique itself is needed to know the amount of recovered ELF. In this regard, urea nitrogen may be useful and has been proposed to calculate ELF. The aim of the present study was to develop and validate a new method to measure urea nitrogen in BAL fluid (BALF). We used 19 BALF samples obtained from neonates and infants with different respiratory conditions. The urea nitrogen assay was carried out on Cobas c311 analyzer (Roche Diagnostics). A validation study shows that the method is perfectly linear (R(2) = 0.999), sensitive (limit of detection = 0.055 mg/dL; limit of quantification = 0.16 mg/dL), repeatable (low = 0.15 ± 0.02, 13.3%; high = 1.80 ± 0.02, 1.1%), reproducible (low = 0.14 ± 0.02, 14.2 %; high = 1.76 ± 0.04, 2.2 %) with accuracy ranging between 93-96%. Our results support the robustness of validated procedure since the described method appears simple, precise, rapid, and suitable for routine analysis. Thus, it may be used to correct concentration of various noncellular BAL components and calculate their ELF amounts in neonates and infants.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ureia / Líquido da Lavagem Broncoalveolar / Automação Laboratorial Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ureia / Líquido da Lavagem Broncoalveolar / Automação Laboratorial Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2015 Tipo de documento: Article