• Carmen Ricós, Maria Vicenta Doménech, and Carmen Perich.
• Laboratoris Clinics Hospital Universitari Vall d'Hebron, Barcelona, Spain. cricos@hg.vhebron.es
• Clin Chem Lab Med. 2004 Jan 1; 42 (7): 858-62.

AbstractInterpretation of laboratory test results requires comparison to some type of reference value or reference interval. These comparisons can be cross-sectional (population-based reference interval and cut-off values) or longitudinal (reference change value). Quality specifications for cross-sectional comparison have been established by determining the influence of analytical bias and imprecision on the percentage of the healthy population falling outside the reference limits, when sharing population-based reference intervals in a Gaussian distribution of results. Quality specifications for longitudinal comparisons are equally important and are often overlooked, since less work has been done in this area. Some criteria suggest that a difference between consecutive results designates a true change in a patient health status when the difference is higher than the within-subject biological variation plus the within-laboratory analytical variation. In this chapter we discuss the clinical considerations and laboratory-related factors that must be considered when quality specifications are applied to sharing reference comparisons. Real life experience shows that different analytical methods can produce comparable results when common quality goals are established, and quality can be achieved through a willingness to work together. Within the existing organization, the current specifications for analytical quality and a dedication to quality health care makes it possible to achieve transferability between laboratories within a geographic area.

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