2017
DOI: 10.1515/jomb-2016-0032
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Preanalytical Nonconformity Management Regarding Primary Tube Mixing in Brazil

Abstract: SummaryBackgroundThe multifaceted clinical laboratory process is divided in three essential phases: the preanalytical, analytical and postanalytical phase. Problems emerging from the preanalytical phase are responsible for more than 60% of laboratory errors. This report is aimed at highlighting and discussing nonconformity (e.g., nonstandardized procedures) in primary blood tube mixing immediately after blood collection by venipuncture with evacuated tube systems.MethodsFrom January 2015 to December 2015, fift… Show more

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Cited by 5 publications
(3 citation statements)
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“…Besides that, the sample rejection criteria differ from one laboratory to the next [ 9 ]. There is a lack of professional data on reporting, root cause analysis, and laboratory error prevention strategies [ 10 ]. The aim of this research is to observe the frequency of complete blood count (CBC) sample rejection factors to improve the quality of results and reduce pre-analytical errors.…”
Section: Introductionmentioning
confidence: 99%
“…Besides that, the sample rejection criteria differ from one laboratory to the next [ 9 ]. There is a lack of professional data on reporting, root cause analysis, and laboratory error prevention strategies [ 10 ]. The aim of this research is to observe the frequency of complete blood count (CBC) sample rejection factors to improve the quality of results and reduce pre-analytical errors.…”
Section: Introductionmentioning
confidence: 99%
“…Laboratory errors are divided into pre-analytical, analytical and post analytical errors (Lima-Oliveira, et al 2017). Most times the analytical and post analytical phases are what pathologists, scientists and accreditation bodies concentrate on.…”
Section: Introductionmentioning
confidence: 99%
“…This has led to laboratories overlooking the pre-analytical errors and processes when preparing for accreditation. The introduction of pre analytical quality indicators by the international organization for standardization (ISO) has helped laboratories to identify and assess the nonconformities to the processes in relation to specifications described in the standard operation procedures/ literatures (Lima-Oliveira, et al 2017). The ISO quality indicators which are generally accepted as the basis for the assessment of the pre analytical phase of the total testing process has the capacity for modification, based on individual laboratory practice (Da Rin.…”
Section: Introductionmentioning
confidence: 99%