This study evaluated the types and frequencies of pre-examination errors recorded in the chemical pathology laboratory at the University Hospital of the West Indies, Jamaica. This was a retrospective analysis of errors recorded over a three year period. Data analysis was done on an average of 519,084 samples collected and tested per year. Samples included blood, urine, stool and other fluids. Pre-examination errors were identified and recorded following visual inspection of the samples and corresponding request forms by laboratory staff, then subsequently by the Senior Medical Technologist. Errors were generally classified as inappropriate sample (58 %), inappropriate form (23.4 %), inappropriate sample volume (9.3 %) and inappropriate sample tube (9.3 %). Over 90 % of recorded pre-examination errors were related to blood samples while urine samples accounted for 6.8 % error. Pre-examination errors were lower at this study location than elsewhere. Measures aimed at reducing instances of these errors are recommended for improved laboratory quality output.
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http://dx.doi.org/10.1007/s12291-013-0348-6 | DOI Listing |
Clin Chem Lab Med
December 2018
National Health Commission of the People's Republic of China, No. 1, Xizhimenwai South Road, Xicheng District, Beijing 100044, P.R.China, Phone: +86-010-68792197.
Background As effective quality management tools, quality indicators (QIs) are widely used in laboratory medicine. This study aimed to analyze the results of QIs, identify errors and provide quality specifications (QSs) based on the state-of-the-art. Methods Clinical laboratories all over China participated in the QIs survey organized by the National Health Commission of People' Republic of China from 2015 to 2017.
View Article and Find Full Text PDFDiagnosis (Berl)
March 2018
British Columbia Patient Safety and Learning System, Vancouver, BC, Canada.
Background: Incident reporting systems are useful tools to raise awareness of patient safety issues associated with healthcare error, including errors associated with the medical laboratory.
Methods: Previously, we presented the analysis of data compiled by the British Columbia Patient Safety & Learning System over a 3-year period. A second comparable set was collected and analyzed to determine if reported error rates would tend to remain stable or change.
J Clin Diagn Res
August 2017
Senior Lecturer and Head, Sub-Department of Chemical Pathology, Department of Pathology, Faculty of Medical Sciences, The University of the West Indies, Mona, Kingston 7, Jamaica.
Introduction: The Chemical Pathology Laboratory at the University Hospital of the West Indies (UHWI) processes specimens received from inpatients, the outpatient department and other medical facilities in Jamaica. Specific rejection criteria are used to determine samples unsuitable for analysis. It has been noted that despite efforts to reduce the number of unacceptable samples received in the laboratory, the problem persists.
View Article and Find Full Text PDFClin Biochem
December 2016
Section of Clinical Biochemistry, University of Verona, Verona, Italy.
The total testing process comprises a number of phases of laboratory testing, which can be broadly considered as comprising pre-examination, examination and post-examination activities. Although each phase is crucial to providing accurate and meaningful laboratory results, the pre-examination phase of testing is where most laboratory errors currently occur, and thus requires special attention. The activities in this phase include sample collection, handling, transportation, processing and storage, which are frequently outside the control of the laboratory performing the tests.
View Article and Find Full Text PDFHell J Nucl Med
June 2015
317-1 Daemyeong 5-dong, Nam-gu, Daegu 705-717, Korea.
Objective: The Dixon sequence is acquired for attenuation correction (AC) of positron emission tomography (PET) data in integrated PET/magnetic resonance (MR). However it sometimes misclassifies soft tissue and fat in μ-map. In the present study, we investigated factors related to this misclassification and their clinical impacts.
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