임상검사실 측정방법의 일치화를 위한 추진방향
Roadmap for Harmonization of Clinical Laboratory Measurement Procedures
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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.
Abstract
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.
참고문헌 (38)
- Kohn LT, "To err is human: building a safer health system", pp.287~ (2000), National Academy Press
- Vesper HW, "Traceability in laboratory medicine", Clin Chem, 55, pp.1067~1075 (2009)
- ISO, "In vitro diagnostic medical devices-measurement of quantities in biological samples-metrological traceability of values assigned to calibrators and control materials. 1st ed", ISO 17511:2003(E), ~ (2003)
- Armbruster D, "The Joint Committee for Traceability in Laboratory Medicine (JCTLM): a global approach to promote the standardisation of clinical laboratory test results", Clin Biochem Rev, 28, pp.105~113 (2007)
- Panteghini M, "Traceability as a unique tool to improve standardization in laboratory medicine", Clin Biochem, 42, pp.236~240 (2009)
- Ekins R, "Immunoassay standardization", Scand J Clin Lab Invest, 51(205), pp.33~46 (1991)
- Thienpont LM, "Accuracy in clinical chemistry: who will kiss Sleeping Beauty awake?", Clin Chem Lab Med, 46, pp.1220~1222 (2008)
- Zegers I, "Characterization of the new serum protein reference material ERM-DA470k", IFCC: value assignment by immunoassay, 2010, pp.56, 1880~1888
- Little RR, "Standardization of C-peptide measurements", Clin Chem, 54, pp.1023~1026 (2008)
- Stephan C, "Interchangeability of measurements of total and free prostate-specific antigen in serum with 5 frequently used assay combinations: an update", Clin Chem, 52, pp.59~64 (2006)
- Miller WG, "Toward standardization of insulin immunoassays", Clin Chem, 55, pp.1011~1018 (2009)
- Thienpont LM, "Report of the IFCC Working Group for Standardization of Thyroid Function Tests; part 1: thyroid-stimulating hormone", Clin Chem, 56, pp.902~911 (2010)
- Rose MP, "Follicle stimulating hormone international standards and reference preparations for the calibration of immunoassays and bioassays", Clin Chim Acta, 273, pp.103~117 (1998)
- Tate JR, "Standardisation of cardiac troponin I measurement: past and present", Pathology, 42, pp.402~408 (2010)
- Sturgeon CM, "Differences in recognition of the 1st WHO international reference reagents for hCG-related isoforms by diagnostic immunoassays for human chorionic gonadotropin", Clin Chem, 55, pp.1484~1491 (2009)
- Thienpont LM, "Traceability to a common standard for protein measurements by immunoassay for in-vitro diagnostic purposes", Clin Chim Acta, 411, pp.2058~2061 (2010)
- Schimmel H, "Standardization of protein biomarker measurements: is it feasible?", Scand J Clin Lab Invest, 70(242), pp.27~33 (2010)
- Radin N, "What is a standard", Clin Chem, 13, pp.55~76 (1967)
- Miller WG, "Why commutability matters", Clin Chem, 52, pp.553~554 (2006)
- Vesper HW, "Reference materials and commutability", Clin Biochem Rev, 28, pp.139~147 (2007)
- Caliendo AM, "A commutable cytomegalovirus calibrator is required to improve the agreement of viral load values between laboratories", Clin Chem, 55, pp.1701~1710 (2009)
- CLSI, "Characterization and qualification of commutable reference materials for laboratory medicine: approved guideline", CLSI document C53-A, ~ (2010)
- Franzini C, "Impact of reference materials on accuracy in clinical chemistry", Clin Biochem, 31, pp.449~457 (1998)
- Thienpont LM, "Trueness verification in European external quality assessment schemes: time to care about the quality of the samples", Scand J Clin Lab Invest, 63, pp.195~202 (2003)
- Miller WG, "Specimen materials, target values and commutability for external quality assessment (proficiency testing) schemes", Clin Chim Acta, 327, pp.25~37 (2003)
- Bossuyt PM, "Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative", BMJ, 326, pp.41~44 (2003)
- Roddam AW, "Assessing the clinical impact of prostate-specific antigen assay variability and nonequimolarity: a simulation study based on the population of the United Kingdom", Clin Chem, 50, pp.1012~1016 (2004)
- "NIH consensus statement on management of hepatitis C: 2002", NIH Consens State Sci Statements, 19, pp.1~46 (2002)
- Petersen PH, "‘Likelihood-ratio’ and ‘odds’ applied to monitoring of patients as a supplement to ‘reference change value’ (RCV)", Clin Chem Lab Med, 46, pp.157~164 (2007)
- Karon BS, "Glucose meter performance criteria for tight glycemic control estimated by simulation modeling", Clin Chem, 56, pp.1091~1097 (2010)
- Kenny D, "Strategies to set global analytical quality specifications in laboratory medicine. Consensus agreement", Scand J Clin Lab Invest, 59, pp.475~585 (1999)
- Fraser CG, "Biological variation: from principles to practice" (2001), AACC Press
- Braga F, "Panteghini M. Biological variability of glycated hemoglobin", Clin Chim Acta, 411, pp.1606~1610 (2010)
- Miller WG, "Current issues in measurement and reporting of urinary albumin excretion", Clin Chem, 55, pp.24~38 (2009)
- Miller WG, "State of the art in trueness and inter-laboratory harmonization for 10 analytes in general clinical chemistry", Arch Pathol Lab Med, 132, pp.838~846 (2008)
- Palmer-Toy DE, "Comparison of pooled fresh frozen serum to proficiency testing material in College of American Pathologists surveys: cortisol and immunoglobulin E", Arch Pathol Lab Med, 129, pp.305~309 (2005)
- Schreiber WE, "Comparison of fresh frozen serum to proficiency testing material in College of American Pathologists Surveys: α-fetoprotein, carcinoembryonic antigen, human chorionic gonadotropin, and prostatespecific antigen", Arch Pathol Lab Med, 129, pp.331~337 (2005)
- Blirup-Jensen, "S. Protein standardization III: method optimization. Basic principles for quantitative determination of human serum proteins on automated instruments based on turbidimetry or nephelometry", Clin Chem Lab Med, 39, pp.1098~1109 (2001)
