Assessment of the Nova StatSensor whole blood point-of-care creatinine analyzer for the measurement of kidney function in screening for chronic kidney disease

Abstract Background: Point-of-care testing for creatinine using a fingerprick sample and resultant estimated glomerular filtration rate has potential for screening for chronic kidney disease in community settings. This study assessed the applicability of the Nova StatSensor creatinine analyzer for this purpose. Methods: Fingerprick samples from 100 patients (63 renal, 37 healthy volunteers; range 46–962 μmol/L) were assayed using two StatSensor analyzers. Lithium heparin venous plasma samples collected simultaneously were assayed in duplicate using the isotope dilution mass spectrometry-aligned Roche Creatinine Plus enzymatic assay on a Hitachi Modular P unit. Method comparison statistics and the ability of the StatSensor to correctly categorise estimated glomerular filtration rate above or below 60 mL/min were calculated pre- and post-alignment with the laboratory method. Results: StatSensor 1 creatinine results (y) were much lower than the laboratory (y=0.75x+10.2, average bias –47.3, 95% limits of agreement –208 to +113 μmol/L). For estimated glomerular filtration rates above or below 60 mL/min, 100% and 87% of results respectively agreed with the laboratory estimated glomerular filtration rate (79% and 96% post-alignment). StatSensor 2 statistics were similar. The 95% limits of agreement between StatSensor creatinine results were –35 to +34 μmol/L. Conclusions: Isotope dilution mass spectrometry alignment of the StatSensor will identify most patients with estimated glomerular filtration rate <60 mL/min, but there will be many falsely low estimated glomerular filtration rate results that require laboratory validation. Creatinine results need improvement. Clin Chem Lab Med 2010;48:1113–9.

[1]  K. Adeli,et al.  A patient with a leg rash, pedal edema, renal failure, and thrombocytopenia. , 2009, Clinical chemistry.

[2]  J. Nichols,et al.  Evaluation of the IRMA TRUpoint and i-STAT creatinine assays. , 2007, Clinica chimica acta; international journal of clinical chemistry.

[3]  S. Chadban,et al.  Screening for chronic kidney disease in Australia: a pilot study in the community and workplace. , 2010, Kidney international. Supplement.

[4]  Tom Greene,et al.  Using Standardized Serum Creatinine Values in the Modification of Diet in Renal Disease Study Equation for Estimating Glomerular Filtration Rate , 2006, Annals of Internal Medicine.

[5]  David W. Johnson,et al.  Chronic kidney disease (CKD) management in general practice , 2007 .

[6]  M. Peake,et al.  Measurement of serum creatinine--current status and future goals. , 2006, The Clinical biochemist. Reviews.

[7]  R. Bender,et al.  A General Regression Procedure for Method Transformation. Application of Linear Regression Procedures for Method Comparison Studies in Clinical Chemistry, Part III , 1988, Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie.

[8]  D. Preiss,et al.  The influence of a cooked-meat meal on estimated glomerular filtration rate , 2007, Annals of clinical biochemistry.

[9]  M. Panteghini Enzymatic assays for creatinine: time for action. , 2008, Clinical chemistry and laboratory medicine.

[10]  J M Bland,et al.  Statistical methods for assessing agreement between two methods of clinical measurement , 1986 .

[11]  Virtudes Alvarez,et al.  Within-subject biological variation in disease: collated data and clinical consequences , 2007, Annals of clinical biochemistry.

[12]  A. Killeen,et al.  Creatinine measurement: state of the art in accuracy and interlaboratory harmonization. , 2005, Archives of pathology & laboratory medicine.

[13]  Tom Greene,et al.  Expressing the Modification of Diet in Renal Disease Study equation for estimating glomerular filtration rate with standardized serum creatinine values. , 2007, Clinical chemistry.

[14]  David W. Johnson,et al.  Implementation of the routine reporting of eGFR in Australia and New Zealand , 2008, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[15]  David W Dunstan,et al.  Prevalence of kidney damage in Australian adults: The AusDiab kidney study. , 2003, Journal of the American Society of Nephrology : JASN.

[16]  D. Altman,et al.  STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.

[17]  Yang Qiu,et al.  CKD in the United States: Kidney Early Evaluation Program (KEEP) and National Health and Nutrition Examination Survey (NHANES) 1999-2004. , 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[18]  W Greg Miller,et al.  Recommendations for improving serum creatinine measurement: a report from the Laboratory Working Group of the National Kidney Disease Education Program. , 2006, Clinical chemistry.

[19]  H. Thomsen,et al.  In which patients should serum creatinine be measured before iodinated contrast medium administration? , 2005, European Radiology.

[20]  T. Mathew,et al.  Chronic kidney disease and automatic reporting of estimated glomerular filtration rate: revised recommendations , 2007, The Medical journal of Australia.

[21]  J. Coresh,et al.  Prevalence of chronic kidney disease in the United States. , 2007, JAMA.