Pregled bibliografske jedinice broj: 949895
PERFORMANCE EVALUATION OF ROCHE ELECSYS SEROLOGICAL SCREENING ASSAYS ON THE NEW COBAS e 801 AMONG BLOOD DONORS IN COMPARISON TO ABBOTT PRISM/ARCHITECT ASSAYS
PERFORMANCE EVALUATION OF ROCHE ELECSYS SEROLOGICAL SCREENING ASSAYS ON THE NEW COBAS e 801 AMONG BLOOD DONORS IN COMPARISON TO ABBOTT PRISM/ARCHITECT ASSAYS // Vox Sanguinis
Toronto, Kanada, 2018. str. 191-191 (poster, međunarodna recenzija, sažetak, stručni)
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Naslov
PERFORMANCE EVALUATION OF ROCHE ELECSYS SEROLOGICAL SCREENING ASSAYS ON THE NEW COBAS e 801 AMONG BLOOD DONORS IN COMPARISON TO ABBOTT PRISM/ARCHITECT ASSAYS
Autori
Miletić, Manuela ; Stojić Vidović, Miljana ; Strauss-Patko, Maja ; Jukić, Irena
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Vox Sanguinis
/ - , 2018, 191-191
Skup
35th International Congress of the ISBT
Mjesto i datum
Toronto, Kanada, 02.06.2018. - 06.06.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Elecsys e 801 ; Prism tests: Blood Donor Screening Assays
Sažetak
Background: The Croatian Institute of Transfusion Medicine routinely screens all regular and first-time-donors with serology assays for HIV (HIV antigen/antibody), HCV (anti-HCV), HBV (HBsAg) and Syphilis (anti-TP) in addition to the respective ID-NAT assay. A method comparison between Roche Cobas e 801 and Abbott Prism/Architect on these parameters were carried out between October 2017 and January 2018. Aim: The aim of the study was to evaluate the specificity as one of the key performance criteria for the platforms, Roche Cobas e 801 and Abbott Prism/Architect on the main four screening serology parameters. Methods: The following assays were used: Elecsys® HIV Duo, Elecsys® Anti-HCV II, Elecsys® HBsAg II, Elecsys® Syphilis and Prism HIV Ag/Ab Combo, Prism HCV, Prism HBsAg as well as Architect Syphilis TP. The following verification methods were used to decide on false or correct positive results: immunoblot, HIV-1 Ag, 3rd HIV combination assay (HIV) ; immunoblot, HCV Ag, 3rd anti-HCV assays (HCV) ; HBsAg Confirmatory tests, hepatitis B serological profile (HBsAg) ; immunoblot, TPHA, RPR, 3rd syphilis ELISA (syphilis) ; in addition to triplex ID-NAT (HBV DNA, HCV RNA and HIV 1/2 RNA). Results: The specificity results on Cobas e 801 Elecsys® HIV Duo were 99.85% (n=4073), 99.90% for Elecsys® Anti-HCV II (n=4006), 100% for Elecsys® HBsAg II (n=4073) and 99.93% (n=4052) for Elecsys® Syphilis. For Abbott Prism, the specificity for HIV Ag/Ab Combo was 100%, 99.93% for HCV and 99.98% for HBsAg ; Abbott Architect Syphilis TP revealed a specificity of 100%. Summary/Conclusions: The observed specificity performance data of the Roche Cobas e 801 Elecsys screening assays were similar to the respective Abbott Prism/Architect assays which showed a slightly higher specificity, but not statistically different. Taking into consideration, that the tested blood donor population was unselected and comprised of approx. 85%-repeat, regular donors and approx. 15% first-time donors, a certain, however very difficult to quantify bias due to a cleaning-out process over many years of routine use can be a putative cause of slightly different specificity results of new and established screening assays. Both platforms can be considered suitable for blood donor screening.
Izvorni jezik
Engleski
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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