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Due to increased convenience and faster test results, interest in point-of-care testing (PoCT) has grown significantly. Though PoCT may improve the speed and convenience of testing, the devices need to be fit for their intended purpose. Our aim was to verify the performance of Roche cobas b 101 and Abbott Afinion 2 for C-reactive protein (CRP), lipid studies and glycated haemoglobin (HbA1c), and Siemens Atellica DCA for HbA1c. For all PoCT analysers and measurands, accuracy was assessed by method comparison with central laboratory analysers. Passing-Bablok linear regression was performed, and Bland-Altman plots were generated. The proportion of samples within the Royal College of Pathologists of Australasia Quality Assurance Programs Analytical Performance Specifications (RCPAQAP APS) was assessed. Within-run and between-day imprecision was assessed and compared with manufacturer claims and biological variation or clinical guidelines for desirable imprecision. For CRP, both evaluated PoCT analysers had all samples within the RCPAQAP APS and had optimal imprecision according to biological variation. For lipid studies, the Roche cobas b 101 had most samples within the RCPAQAP APS, with two of 22 cholesterol, one of 22 high-density-lipoprotein-cholesterol (HDL-C) and zero of 22 triglyceride comparisons outside the RCPAQAP APS. The Abbott Afinion 2 had a positive bias with all three measured parameters, although the effect was more limited in the calculated parameters cholesterol:HDL-C ratio, non-HDL-C and low-density-lipoprotein-cholesterol (LDL-C). For HbA1c, all analysers had acceptable imprecision for monitoring with coefficient of variation (CV) <3% and minimal bias at the treatment target (HbA1c 53 mmol/mol or 7.0%). However, significant biases were apparent at higher or lower HbA1c for all analysers. All evaluated analysers were fit for purpose for CRP and for serial monitoring of HbA1c, although bias in some analysers was present at extremes of HbA1c. For lipid studies, the Roche cobas b 101 had fewer results outside the RCPAQAP allowable limits, and better precision. The Abbott Afinion 2 had a positive bias on both the cholesterol and HDL-C, but there is limited clinical impact when calculating cholesterol:HDL-C, LDL-C and non-HDL-C.
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http://dx.doi.org/10.1016/j.pathol.2023.07.004 | DOI Listing |
Pathology
December 2023
Biochemistry, Canterbury Health Laboratories, Christchurch, New Zealand; Te Whatu Ora - Health New Zealand Waitaha Canterbury, Christchurch, New Zealand.
Due to increased convenience and faster test results, interest in point-of-care testing (PoCT) has grown significantly. Though PoCT may improve the speed and convenience of testing, the devices need to be fit for their intended purpose. Our aim was to verify the performance of Roche cobas b 101 and Abbott Afinion 2 for C-reactive protein (CRP), lipid studies and glycated haemoglobin (HbA1c), and Siemens Atellica DCA for HbA1c.
View Article and Find Full Text PDFClin Chem Lab Med
January 2024
AACB/RCPAQAP Vitamins Advisory Committee, St Leonards, NSW, Australia.
Objectives: Monitoring serum vitamin A (retinol) and vitamin E (α-tocopherol) concentrations is common practice for assessing nutritional status. Measurement of these vitamins can be challenging due to several factors. Whilst the RCPAQAP Vitamins: Serum Program assists participating laboratories in harmonisation, the materials provided do not contain the analogues of retinol and α-tocopherol that may be present in real patient samples.
View Article and Find Full Text PDFBackground: Laboratory identification of lupus anticoagulants (LA), an important component of the clinical diagnosis of the autoimmune disorder antiphospholipid syndrome (APS), is challenged by the heterogeneity of tests available, the diagnostic and laboratory approach undertaken, and the heterogeneity of the autoantibodies present.
Aim: : To assess the laboratory approach for investigation of LA, as well as the utility of various tests and test approaches, given a difficult clinical scenario in which LA might or might not be present.
Methods: Ninety-three participants in the Royal College of Pathologists of Australasia (RCPA) Haematology Quality Assurance Program (QAP) were sent 4 mL of a complex but strongly positive LA sample blinded to the nature of the abnormality.