Preanalytical quality improvement. In pursuit of harmony, on behalf of European Federation for Clinical Chemistry and Laboratory Medicine (EFLM) Working group for Preanalytical Phase (WG-PRE)

被引:99
作者
Lippi, Giuseppe [1 ,2 ]
Banfi, Giuseppe [3 ]
Church, Stephen [4 ]
Cornes, Michael [5 ]
De Carli, Gabriella [6 ]
Grankvist, Kjell [7 ]
Kristensen, Gunn B. [8 ]
Ibarz, Mercedes [9 ]
Panteghini, Mauro [10 ,11 ]
Plebani, Mario [12 ]
Nybo, Mads [13 ]
Smellie, Stuart [14 ]
Zaninotto, Martina [12 ]
Simundic, Ana-Maria [15 ]
机构
[1] Univ Parma, Azienda Osped, UO Diagnost Ematochim, I-43126 Parma, Italy
[2] Acad Hosp Parma, Diagnost Dept, Lab Clin Chem & Hematol, Parma, Italy
[3] Univ Milan, Dept Biomed Sci, Milan, Italy
[4] Becton Dickinson Diagnost, Oxford, England
[5] New Cross Hosp, Dept Clin Chem, Wolverhampton, W Midlands, England
[6] Natl Inst Infect Dis L Spallanzani, Dept Epidemiol & Pre Clin Res, Rome, Italy
[7] Umea Univ, Dept Med Biosci, Umea, Sweden
[8] Norwegian EQA Program NKK, Bergen, Norway
[9] Hosp Arnau Vilanova, Lab Clin, Lleida, Spain
[10] Univ Milan, Dept Lab Med & Clin, Pathol Unit, Luigi Sacco Univ Hosp, Milan, Italy
[11] European Federat Clin Chem & Lab Med EFLM, London, England
[12] Univ Hosp, Dept Lab Med, Padua, Italy
[13] Odense Univ Hosp, Dept Clin Biochem & Pharmacol, DK-5000 Odense, Denmark
[14] Cty Durham & Darlington Acute Hosp NHS Trust, Clin Lab, Bishop Auckland, New Zealand
[15] Univ Hosp Sestre Milosrdnice, Sch Med, Univ Dept Chem, Zagreb, Croatia
关键词
harmonization; laboratory errors; preanalytical variability; standardization; RESIDUAL PLATELET COUNT; ROUTINE COAGULATION; UTILIZATION MANAGEMENT; CENTRIFUGATION TIME; MANAGING DEMAND; PATIENT SAFETY; HEALTH-CARE; LIGHT MEAL; BLOOD; SAMPLE;
D O I
10.1515/cclm-2014-1051
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Laboratory diagnostics develop through different phases that span from test ordering (pre-preanalytical phase), collection of diagnostic specimens (preanalytical phase), sample analysis (analytical phase), results reporting (postanalytical phase) and interpretation (post-postanalytical phase). Although laboratory medicine seems less vulnerable than other clinical and diagnostic areas, the chance of errors is not negligible and may adversely impact on quality of testing and patient safety. This article, which continues a biennial tradition of collective papers on preanalytical quality improvement, is aimed to provide further contributions for pursuing quality and harmony in the preanalytical phase, and is a synopsis of lectures of the third European Federation of Clinical Chemistry and Laboratory Medicine (EFLM)-Becton Dickinson (BD) European Conference on Preanalytical Phase meeting entitled 'Preanalytical quality improvement. In pursuit of harmony' (Porto, 20-21 March 2015). The leading topics that will be discussed include unnecessary laboratory testing, management of test request, implementation of the European Union (EU) Directive on needlestick injury prevention, harmonization of fasting requirements for blood sampling, influence of physical activity and medical contrast media on in vitro diagnostic testing, recent evidence about the possible lack of necessity of the order of draw, the best practice for monitoring conditions of time and temperature during sample transportation, along with description of problems emerging from inappropriate sample centrifugation. In the final part, the article includes recent updates about preanalytical quality indicators, the feasibility of an External Quality Assessment Scheme (EQAS) for the preanalytical phase, the results of the 2nd EFLM WG-PRE survey, as well as specific notions about the evidence-based quality management of the preanalytical phase.
引用
收藏
页码:357 / 370
页数:14
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