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Evaluation of the 25-hydroxy vitamin D assay on a fully automated liquid chromatography mass spectrometry system, the Thermo Scientific Cascadion SM Clinical Analyzer with the Cascadion 25-hydroxy vitamin D assay in a routine clinical laboratory.
Benton, Sally C; Tetteh, Godwin K; Needham, Sarah-Jayne; Mücke, Jakob; Sheppard, Leanne; Alderson, Steven; Ruppen, Corinne; Curti, Maurus; Redondo, Maurice; Milan, Anna M.
  • Benton SC; Berkshire and Surrey Pathology Services, Frimley Park Hospital NHS Trust, Camberley, UK.
  • Tetteh GK; NHS Bowel Cancer Screening Programme Southern Hub, Royal Surrey County Hospital, Surrey GU2 7YS, UK.
  • Needham SJ; Berkshire and Surrey Pathology Services, Frimley Park Hospital NHS Trust, Camberley, UK.
  • Mücke J; Berkshire and Surrey Pathology Services, Frimley Park Hospital NHS Trust, Camberley, UK.
  • Sheppard L; Viollier AG, Allschwil, Switzerland.
  • Alderson S; Department of Clinical Biochemistry, Liverpool Clinical Laboratories, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
  • Ruppen C; Berkshire and Surrey Pathology Services, Frimley Park Hospital NHS Trust, Camberley, UK.
  • Curti M; Viollier AG, Allschwil, Switzerland.
  • Redondo M; Viollier AG, Allschwil, Switzerland.
  • Milan AM; Viollier AG, Allschwil, Switzerland.
Clin Chem Lab Med ; 58(6): 1010-1017, 2020 Jun 25.
Article en En | MEDLINE | ID: mdl-31851610
ABSTRACT
Background Liquid chromatography-tandem mass spectrometry (LC-MS/MS) offers advantages over immunoassay due to its increased specificity and ability to multiplex metabolites within a single run. Wide scale adoption of LC-MS/MS in routine clinical laboratories is restricted in part due to the high level of technical expertise required. The Thermo Scientific™ Cascadion™ SM Clinical Analyzer is the first fully automated, random access clinical analyser that utilises LC-MS/MS technology. We report an analytical validation of the 25-hydroxy vitamin D2 and D3 assays on the Cascadion Analyzer and an assessment of its performance within a routine clinical laboratory. Methods Analyser usability was assessed by staff with no previous experience of LC-MS/MS. An analytical validation included analysis of 154 patient samples on two different Cascadion Analyzers and a four-way method comparison of 146 patient samples on Roche and Siemens immunoassays and an in-house LC-MS/MS method. Accuracy was assessed using external quality assurance and reference materials. Seven third party IQC materials were tested on Cascadion. Results Cascadion proved easy to use by scientific and non-scientific staff. The assay passed all validation criteria. Excellent agreement was demonstrated between two different Cascadions (y = 0.97x + 3.9 nmol/L, r2 > 0.99). A method comparison demonstrated no significant difference (p > 0.05) between the Cascadion and the Roche immunoassay. A significant difference (p < 0.0001) was observed between the Cascadion and an LC-MS/MS and Siemens methods. Results obtained from EQA and reference material showed a mean bias of +3.09% and all samples were within ±10% of assigned concentrations. All third party IQC samples tested were compatible for use with Cascadion. Conclusions The Cascadion Analyzer is a fully automated LC-MS/MS system that requires no prior LC-MS/MS expertise. The vitamin D assays demonstrated excellent performance with high levels of accuracy.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina D / Análisis Químico de la Sangre / Cromatografía Liquida / Espectrometría de Masas en Tándem / Laboratorios Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vitamina D / Análisis Químico de la Sangre / Cromatografía Liquida / Espectrometría de Masas en Tándem / Laboratorios Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article