Pregled bibliografske jedinice broj: 984952
Validation of a 6-part differential hematology analyzer Siemens Advia 2120i
Validation of a 6-part differential hematology analyzer Siemens Advia 2120i // 5th EFLM-UEMS European Joint Congress in Laboratory Medicine Laboratory Medicine at the Clinical Interface
Antalya, Turska, 2018. str. 293-293 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Validation of a 6-part differential hematology analyzer Siemens Advia 2120i
Autori
Čičak, Helena ; Petro, Dubravka ; Dojder, Ana ; Radišić Biljak, Vanja ; Šimundić, Ana-Maria
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
5th EFLM-UEMS European Joint Congress in Laboratory Medicine Laboratory Medicine at the Clinical Interface
Mjesto i datum
Antalya, Turska, 10.10.2018. - 13.10.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
hematology analyzer, validation, quality goals, biological variation
Sažetak
Purpose: The aim of this study was to perform the validation of a 6-part differential hematology analyzer Siemens Advia 2120i (Erlangen, Germany), prior to its routine implementation. Materials and methods: Our validation protocol combined the CLSI H26-A2: 2010 and the ICHS 2014 guidelines, and included: precision (within and between run), accuracy (comparison with reference analyzer – 300 samples), linearity, carryover, confirmation of a LoB, determination of a LoD and LoQ. TE% was calculated for all measured parameters. Acceptance criteria were based on: manufacturer technical specifications (Siemens), 2016 state- of-the-art criteria (Vis and Huisman) and biological variation. Analysis was done using MedCalc 16.2.0 statistical software (MedCalc Software bvba, Ostend, Belgium). Results: The lowest within and between run precision CVs were observed for MCV (0.3% and 0.6%, respectively). Bland& ; Altman plot did not reveal statistically significant bias for any of the measured parameters: WBC (difference (%): 1.0, 95%CI:-10, 2 to 8.1), RBC (difference (%):-1.4, 95%CI:-4.3 to 1.5), Hb (difference (%):-0.2, 95%CI:-2.5 to 2.1) and Plt (difference (%):-6.9, 95%CI:-2.4 to 16.1). mLinearity was confirmed for all tested parameters (r> ; 0.99). The carryover estimates ranged from 0.1% for Plt to 0.8% for WBC and were within the manufacturers specifications (≤1%). Manufacturers claims for LoB were confirmed. The estimated LoD and LoQ were 0.05x10* 9 /L and 0.1x10* 9 /L for WBC, while for Plt values were 2x10* 9 /L and 3x10* 9 /L, respectively. The calculated TE% ranged from 2.35% for Hb to 12.33 for Plt. Conclusions: Hematology analyzer Siemens Advia 2120i is completely in accordance with the predefined quality goals and is suitable for everyday routine practice.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinička bolnica "Sveti Duh"