Roadmap for harmonization of clinical laboratory measurement procedures.

Results between different clinical laboratory measurement procedures (CLMP) should be equivalent, within clinically meaningful limits, to enable optimal use of clinical guidelines for disease diagnosis and patient management. When laboratory test results are neither standardized nor harmonized, a different numeric result may be obtained for the same clinical sample. Unfortunately, some guidelines are based on test results from a specific laboratory measurement procedure without consideration of the possibility or likelihood of differences between various procedures. When this happens, aggregation of data from different clinical research investigations and development of appropriate clinical practice guidelines will be flawed. A lack of recognition that results are neither standardized nor harmonized may lead to erroneous clinical, financial, regulatory, or technical decisions. Standardization of CLMPs has been accomplished for several measurands for which primary (pure substance) reference materials exist and/or reference measurement procedures (RMPs) have been developed. However, the harmonization of clinical laboratory procedures for measurands that do not have RMPs has been problematic owing to inadequate definition of the measurand, inadequate analytical specificity for the measurand, inadequate attention to the commutability of reference materials, and lack of a systematic approach for harmonization. To address these problems, an infrastructure must be developed to enable a systematic approach for identification and prioritization of measurands to be harmonized on the basis of clinical importance and technical feasibility, and for management of the technical implementation of a harmonization process for a specific measurand.

[1]  Lothar Siekmann,et al.  State of the art in trueness and interlaboratory harmonization for 10 analytes in general clinical chemistry. , 2008, Archives of pathology & laboratory medicine.

[2]  C Heuck,et al.  The Stockholm Consensus Conference on quality specifications in laboratory medicine, 25-26 April 1999. , 1999, Scandinavian journal of clinical and laboratory investigation.

[3]  L M Thienpont,et al.  Trueness verification in European external quality assessment schemes: time to care about the quality of the samples , 2003, Scandinavian journal of clinical and laboratory investigation.

[4]  M. Panteghini,et al.  Biological variability of glycated hemoglobin. , 2010, Clinica chimica acta; international journal of clinical chemistry.

[5]  Callum G. Fraser,et al.  Strategies to set global analytical quality specifications in laboratory medicine: 10 years on from the Stockholm consensus conference , 2010 .

[6]  L. Thienpont,et al.  Traceability to a common standard for protein measurements by immunoassay for in-vitro diagnostic purposes. , 2010, Clinica chimica acta; international journal of clinical chemistry.

[7]  C. Sturgeon,et al.  Differences in recognition of the 1st WHO international reference reagents for hCG-related isoforms by diagnostic immunoassays for human chorionic gonadotropin. , 2009, Clinical chemistry.

[8]  David Armbruster,et al.  The Joint Committee for Traceability in Laboratory Medicine (JCTLM): a global approach to promote the standardisation of clinical laboratory test results. , 2007, The Clinical biochemist. Reviews.

[9]  Hubert W Vesper,et al.  Reference materials and commutability. , 2007, The Clinical biochemist. Reviews.

[10]  D. Bruns,et al.  [Current issues in measurement and reporting of urinary albumin excretion]. , 2010, Annales de biologie clinique.

[11]  J. Thijssen,et al.  Report of the IFCC Working Group for Standardization of Thyroid Function Tests; part 1: thyroid-stimulating hormone. , 2010, Clinical chemistry.

[12]  I. Zegers,et al.  Standardization of protein biomarker measurements: Is it feasible? , 2010, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[13]  M. Steffes,et al.  Toward standardization of insulin immunoassays. , 2009, Clinical chemistry.

[14]  R. Ekins Immunoassay standardization. , 1991, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[15]  Callum G. Fraser,et al.  Biological Variation: From Principles to Practice , 2001 .

[16]  Hubert W Vesper,et al.  Traceability in laboratory medicine. , 2009, Clinical chemistry.

[17]  NIH Consensus Statement on Management of Hepatitis C: 2002. , 2002, NIH consensus and state-of-the-science statements.

[18]  I. Zegers,et al.  Characterization of the new serum protein reference material ERM-DA470k/IFCC: value assignment by immunoassay. , 2010, Clinical chemistry.

[19]  Emons Hendrik,et al.  Characterization and Qualification of Commutable Reference Materials for Laboratory Medicine - Approved Guideline , 2010 .

[20]  S. Blirup-Jensen Protein Standardization III: Method Optimization. Basic Principles for Quantitative Determination of Human Serum Proteins on Automated Instruments Based on Turbidimetry or Nephelometry , 2001, Clinical Chemistry and Laboratory Medicine.

[21]  Mauro Panteghini,et al.  Traceability as a unique tool to improve standardization in laboratory medicine. , 2009, Clinical biochemistry.

[22]  A. Roddam,et al.  Assessing the clinical impact of prostate-specific antigen assay variability and nonequimolarity: a simulation study based on the population of the United Kingdom. , 2004, Clinical chemistry.

[23]  W Greg Miller,et al.  Why commutability matters. , 2006, Clinical chemistry.

[24]  C Franzini,et al.  Impact of reference materials on accuracy in clinical chemistry. , 1998, Clinical biochemistry.

[25]  M. Rose Follicle stimulating hormone: International standards and reference preparations for the calibration of immunoassays and bioassays , 1998 .

[26]  Angela M Caliendo,et al.  A commutable cytomegalovirus calibrator is required to improve the agreement of viral load values between laboratories. , 2009, Clinical chemistry.

[27]  I. Brandslund,et al.  ‘Likelihood-ratio’ and ‘odds’ applied to monitoring of patients as a supplement to ‘reference change value’ (RCV) , 2008, Clinical chemistry and laboratory medicine.

[28]  K. Polonsky,et al.  Standardization of C-peptide measurements. , 2008, Clinical chemistry.

[29]  W Greg Miller,et al.  Specimen materials, target values and commutability for external quality assessment (proficiency testing) schemes. , 2003, Clinica chimica acta; international journal of clinical chemistry.

[30]  M. Panteghini,et al.  Standardisation of cardiac troponin I measurement: past and present , 2010, Pathology.

[31]  G. Palomaki,et al.  Comparison of fresh frozen serum to proficiency testing material in College of American Pathologists surveys: alpha-fetoprotein, carcinoembryonic antigen, human chorionic gonadotropin, and prostate-specific antigen. , 2009, Archives of pathology & laboratory medicine.

[32]  Dietmar Schnorr,et al.  Interchangeability of measurements of total and free prostate-specific antigen in serum with 5 frequently used assay combinations: an update. , 2006, Clinical chemistry.

[33]  L. Thienpont Accuracy in clinical chemistry – who will kiss Sleeping Beauty awake? , 2008, Clinical chemistry and laboratory medicine.

[34]  C. Marano,et al.  To err is human. Building a safer health system , 2005 .

[35]  David Moher,et al.  Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. , 2004, Family practice.

[36]  G Lepschy,et al.  What is the Standard , 2002 .

[37]  L. Kohn,et al.  To Err Is Human : Building a Safer Health System , 2007 .

[38]  George G Klee,et al.  Glucose meter performance criteria for tight glycemic control estimated by simulation modeling. , 2010, Clinical chemistry.

[39]  J. García-Talavera,et al.  Serum TATI levels and clinical correlation in tumors of the head and neck. , 1991, Scandinavian journal of clinical and laboratory investigation. Supplementum.

[40]  George G Klee,et al.  Comparison of pooled fresh frozen serum to proficiency testing material in College of American Pathologists surveys: cortisol and immunoglobulin E. , 2005, Archives of pathology & laboratory medicine.