Pregled bibliografske jedinice broj: 1188105
Analytical validation of 39 clinical chemistry tests and 17 immunoassays on the Alinity analytical system
Analytical validation of 39 clinical chemistry tests and 17 immunoassays on the Alinity analytical system // Scandinavian journal of clinical & laboratory investigation, 82 (2022), 3; 199-209 doi:10.1080/00365513.2022.2056856 (međunarodna recenzija, članak, stručni)
CROSBI ID: 1188105 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Analytical validation of 39 clinical chemistry tests
and 17 immunoassays on the Alinity analytical system
Autori
Lapić, Ivana ; Šegulja, Dragana ; Dukić, Kristina ; Bogić, Anamarija ; Lončar Vrančić, Ana ; Komljenović, Sven ; Šparakl, Tajana ; Grdiša Teodorović, Katarina ; Cigula Kurajica, Vlasta ; Baršić Lapić, Ivana ; Kralik Oguić, Saša ; Kozmar, Ana ; Vogrinc, Željka ; Rogić, Dunja
Izvornik
Scandinavian journal of clinical & laboratory investigation (0036-5513) 82
(2022), 3;
199-209
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
clinical chemistry tests ; immunoassays ; validation study ; precision ; method comparison ; Alinity
Sažetak
The aim of this study was to perform the analytical validation of Alinity c and i analyzers (Abbott Laboratories, Chicago, IL, USA) for 39 clinical chemistry tests and 17 immunoassays. Precision was evaluated at least at two concentration levels for 5 days in quintuplicate, following CLSI EP15-A3. Method comparison included parallel analysis of leftover routine samples on Alinity analyzers and the previously used Cobas c501 and e601 (Roche Diagnostics, Mannheim, Germany). Linearity was tested by preparing sequential sample dilutions with high analyte concentration, following the CLSI EP6 document. For clinical chemistry tests, within-run coefficients of variation (CV) were up to 6.0% (beta-2-microglobulin), while between-run CVs up to 5.4% (immunoglobulin M). Among immunoassays, the highest within-run CV was obtained for vitamin B12 (6.9%), while between-run for CA 19-9 (4.3%). Complete agreement with Roche analyzers was observed for 16 (41%) clinical chemistry assays and 6 (35%) immunoassays. Half of all evaluated assays did not meet the desirable biological variation criteria for bias, being especially exceeded for alpha1-antitrypsin, apolipoprotein A1, ceruloplasmin, complement C3 and C4, hemoglobin A1c, lipoprotein (a) and myoglobin, as well as some tumor markers (CA 125, CEA, fPSA, AFP, and ferritin), hormones (cortisol, DHEA-S, insulin) and vitamins (25-OHD). Linearity in the tested ranges was confirmed. Overall, this study revealed that precision criteria derived from manufacturer's claims were not satisfied for all assays while comparison study for some assays yielded differences that imply the need for additional assay evaluation prior to introduction into routine practice.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Klinički bolnički centar Zagreb,
Opća županijska bolnica Požega
Profili:
Željka Vogrinc
(autor)
Ana Kozmar
(autor)
SAŠA KRALIK OGUIĆ
(autor)
Dunja Rogić
(autor)
Dragana Šegulja
(autor)
ANA LONČAR VRANČIĆ
(autor)
Ivana Lapić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE