Am J Perinatol 2014; 31(10): 851-854
DOI: 10.1055/s-0033-1361938
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Adjusting for Bias in C-Reactive Protein Levels When Using a Vitros Slide Method in Infants

Mohamad T. Elabiad
1   Division of Neonatology, Department of Pediatrics, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
2   Department of Obstetrics & Gynecology, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
,
Kristopher L. Arheart
3   Division of Biostatistics and Pediatrics, Department of Epidemiology and Public Health, Miller School of Medicine, University of Miami, Miami, Florida
,
Sheldon B. Korones
1   Division of Neonatology, Department of Pediatrics, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
2   Department of Obstetrics & Gynecology, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
,
Massroor Pourcyrous
1   Division of Neonatology, Department of Pediatrics, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
2   Department of Obstetrics & Gynecology, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
4   Department of Physiology, University of Tennessee Health Science Center (UTHSC), Memphis, Tennessee
› Author Affiliations
Further Information

Publication History

26 September 2013

24 October 2013

Publication Date:
25 February 2014 (online)

Abstract

Objective Low total serum protein levels may cause a positive bias on C-reactive protein (CRP) detected by the Vitros 250 Chemistry System (Ortho-Clinical Diagnostics, Inc., Johnson & Johnson Co., Raritan, NJ). Low total serum protein levels are observed in some infants. Our objective was to define a cutoff value for normal levels of CRP measured on the Vitros System that is comparable to the cutoff value of 1.0 mg/dL measured by rate nephelometry on a Beckman Array System (Beckman Instruments Inc., Fullerton, CA).

Study Design CRP was prospectively measured on the same serum sample on Vitros and Beckman systems. Using a result of ≥1.0 as the “gold standard” definition of an abnormal CRP, measures of association were calculated.

Results CRP was measured in 981 blood samples that were collected from 361 infants. A cutoff CRP level using the Vitros system at 1.5 mg/dL had the highest sensitivity and negative predictive value comparable to 1.0 mg/dL measured by nephelometry. By regression analysis, each increase by 1 mg/dL by nephelometry caused an increase by 1.5 mg/dL on the Vitros system (R2 = 0.94; p < 0.001; slope = 0.66; 95% confidence intervals, 0.65, 0.67).

Conclusion In infants, when measuring CRP levels by Vitros CRP slide system, a normal reference level of 1.5 mg/dL instead of 1 mg/dL should be used.

 
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