Literature DB >> 15976099

Postanalytical external quality assessment of blood glucose and hemoglobin A1c: an international survey.

Svein Skeie1, Carmen Perich, Carmen Ricos, Agnes Araczki, Andrea R Horvath, Wytze P Oosterhuis, Tanya Bubner, Gunnar Nordin, Rhena Delport, Geir Thue, Sverre Sandberg.   

Abstract

BACKGROUND: Diabetes mellitus (DM) is diagnosed and monitored worldwide by blood glucose (BG) and glycohemoglobin A(1c) (HbA(1c)) testing, respectively. Methods for quality assessment of clinician interpretations of changes in these laboratory results have been developed. This study uses survey responses from general practitioners (GPs) in different countries to investigate possible differences in interpretation of results, as well as the feasibility of performing international postanalytical external quality assessment surveys (P-EQAS).
METHODS: GPs recruited from 7 countries received questionnaires requesting interpretation of changes in a potentially diagnostic capillary BG result and an HbA(1c) value obtained during monitoring of a patient with type 2 DM. GPs were asked to estimate clinically significant differences between 2 consecutive laboratory results [critical difference (CD)/reference change value] for both BG and HbA(1c). The CDs reported by GPs were used to calculate the analytical variation (CV(a)), which was taken as the quality specification for analytical imprecision. Participants received national benchmarking feedback reports after the survey.
RESULTS: The study included responses from 2538 GPs. CDs in BG results showed the same pattern and were comparable among countries. Calculated median CV(a) values would be possible to attain at 80% confidence but not at the conventional 95% confidence. For HbA(1c), the same pattern was shown across countries, but with lower changes considered true when HbA(1c) increased than when it decreased. Despite the consistent pattern, variations among GPs were considerable in all countries.
CONCLUSIONS: Assessments of CDs for BG and HbA(1c) were similar internationally, and quality specifications for these analytes based on clinicians' opinions are therefore interchangeable among countries. International P-EQAS may contribute to a more rational use of laboratory services and clinical guidelines.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15976099     DOI: 10.1373/clinchem.2005.048488

Source DB:  PubMed          Journal:  Clin Chem        ISSN: 0009-9147            Impact factor:   8.327


  6 in total

1.  'Allowable Limits of Performance' for External Quality Assurance Programs - an Approach to Application of the Stockholm Criteria by the RCPA Quality Assurance Programs.

Authors:  Graham Rd Jones; Kenneth Sikaris; Janice Gill
Journal:  Clin Biochem Rev       Date:  2012-11

Review 2.  From evidence to best practice in laboratory medicine.

Authors:  A Rita Horvath
Journal:  Clin Biochem Rev       Date:  2013-08

3.  Warfarin monitoring in nursing homes assessed by case histories. Do recommendations and electronic alerts affect judgements?

Authors:  Reyes Serrano Teruel; Geir Thue; Svein Ivar Fylkesnes; Sverre Sandberg; Ann Helen Kristoffersen
Journal:  Scand J Prim Health Care       Date:  2017-08-04       Impact factor: 2.581

Review 4.  Quality Assurance in Clinical Chemistry: A Touch of Statistics and A Lot of Common Sense.

Authors:  Elvar Theodorsson
Journal:  J Med Biochem       Date:  2016-05-09       Impact factor: 3.402

Review 5.  External Quality Assessment beyond the analytical phase: an Australian perspective.

Authors:  Tony Badrick; Stephanie Gay; Euan J McCaughey; Andrew Georgiou
Journal:  Biochem Med (Zagreb)       Date:  2017-02-15       Impact factor: 2.313

6.  Feasibility of using self-reported patient data in a national diabetes register.

Authors:  Karianne Fjeld Løvaas; John G Cooper; Sverre Sandberg; Thomas Røraas; Geir Thue
Journal:  BMC Health Serv Res       Date:  2015-12-15       Impact factor: 2.655

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.