Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Autovalidation and automation of the postanalytical phase of routine hematology and coagulation analyses in a university hospital laboratory (CROSBI ID 250066)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Mlinarić, Ana ; Miloš, Marija ; Coen Herak, Desiree ; Fuček, Mirjana ; Rimac, Vladimira ; Zadro, Renata ; Rogić, Dunja Autovalidation and automation of the postanalytical phase of routine hematology and coagulation analyses in a university hospital laboratory // Clinical chemistry and laboratory medicine, 56 (2018), 3; 454-462. doi: 10.1515/cclm-2017-0402

Podaci o odgovornosti

Mlinarić, Ana ; Miloš, Marija ; Coen Herak, Desiree ; Fuček, Mirjana ; Rimac, Vladimira ; Zadro, Renata ; Rogić, Dunja

engleski

Autovalidation and automation of the postanalytical phase of routine hematology and coagulation analyses in a university hospital laboratory

Background: The need to satisfy high-throughput demands for laboratory tests continues to be a challenge. Therefore, we aimed to automate postanalytical phase in hematology and coagulation laboratory by autovalidation of complete blood count (CBC) and routine coagulation test results (prothrombin time [PT], international normalized ratio [PT-INR], activated partial thromboplastin time [APTT], fibrinogen, antithrombin activity [AT] and thrombin time [TT]). Work efficacy and turnaround time (TAT) before and after implementation of automated solutions will be compared. Methods: Ordering panels tailored to specific patient populations were implemented. Rerun and reflex testing rules were set in the respective analyzers’ software (Coulter DxH Connectivity 1601, Beckman Coulter, FL, USA ; AutoAssistant, Siemens Healthcare Diagnostics, Germany), and sample status information was transferred into the laboratory information system. To evaluate if the automation improved TAT and efficacy, data from manually verified results in September and October of 2015 were compared with the corresponding period in 2016 when autovalidation was implemented. Results: Autovalidation rates of 63% for CBC and 65% for routine coagulation test results were achieved. At the TAT of 120 min, the percentage of reported results increased substantially for all analyzed tests, being above 90% for CBC, PT, PT-INR and fibrinogen and 89% for APTT. This output was achieved with three laboratory technicians less compared with the period when the postanalytical phase was not automated. Conclusions: Automation allowed optimized laboratory workflow for specific patient populations, thereby ensuring standardized results reporting. Autovalidation of test results proved to be an efficient tool for improvement of laboratory work efficacy and TAT.

autovalidation ; complete blood count ; postanalytical phase ; routine coagulation tests ; turnaround time

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

56 (3)

2018.

454-462

objavljeno

1434-6621

1437-4331

10.1515/cclm-2017-0402

Povezanost rada

Kliničke medicinske znanosti

Poveznice
Indeksiranost