Pregled bibliografske jedinice broj: 1143957
Reporting of activated thromboplastin time (aPTT): Could we achieve better comparability of the results?
Reporting of activated thromboplastin time (aPTT): Could we achieve better comparability of the results? // Biochemia medica, 31 (2021), 2; 020708, 7 doi:10.11613/BM.2021.020708 (međunarodna recenzija, članak, znanstveni)
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Naslov
Reporting of activated thromboplastin time
(aPTT): Could we achieve better comparability
of the results?
Autori
Bronić, Ana ; Margetić, Sandra ; Coen Herak, Desiree ; Milić, Marija ; Krešić, Branka ; Radišić Biljak, Vanja ; Leniček Krleža, Jasna
Izvornik
Biochemia medica (1330-0962) 31
(2021), 2;
020708, 7
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
activated partial thromboplastin time ; external quality assessment ; harmonization
Sažetak
Introduction: Activated partial thromboplastin time (aPTT) is determined and reported as clotting time in seconds aPTT(s), but it is presumed that reporting results as patient-to- normal clotting time ratio, aPTT(r), could minimize within- laboratory variability. The aim of study was to investigate differences in reporting aPTT results that can affect comparability of the results among Croatian laboratories and suggest further steps for its harmonization. Materials and methods: The questionnaire on aPTT reporting practice was distributed to 83 laboratories through Survey Monkey application in March 2019 as the part of the first regular round of Croatian Centre for Quality Assessment in Laboratory Medicine proficiency testing. Results: The survey response rate was 0.49. Majority of laboratories report aPTT results as both, seconds and ratio. Participants reported use of 23 different aPTT(s) reference intervals along with 17 different combinations of reagent/coagulometer and 25 aPTT(s) denominators of different origin for aPTT(r) calculation. Despite the same aPTT(s) results, the use of different denominators caused a dispersion of aPTT(r) results that can lead to exceeding external quality assessment performance criteria of 7%, particularly when results were compared for the same reagent group only. By applying aPTT(s) reference interval mean as denominator for calculation of aPTT(r) reference interval better concordance to harmonized one was obtained (17 vs. 27 ; χ2 = 3.972 ; P = 0.046). Conclusion: In order to improve comparability of the results, laboratories are advised to use mean of aPTT(s) reference interval as denominator for aPTT(r) calculation. Type of coagulometer need to be considered when evaluating aPTT proficiency test results and its currently acceptable limit of performance evaluated accordingly.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Ustanove:
Klinički bolnički centar Osijek,
Klinička bolnica "Sveti Duh",
KBC Split,
Klinika za traumatologiju,
Klinički bolnički centar Zagreb,
Medicinski fakultet, Split,
Klinika za dječje bolesti
Profili:
Jasna Leniček Krleža
(autor)
Desiree Coen Herak
(autor)
Marija Milić
(autor)
Ana Bronić
(autor)
Sandra Margetić
(autor)
Vanja Radišić Biljak
(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