Pre-analytical errors and patient safety
Laboratory medicine, as a specialty that had prioritized quality control, has always been at the forefront of error reduction. In the last decades, a dramatic decrease of analytical errors has been experienced, while a relatively high frequency of errors has been documented in the pre-analytical pha...
Ausführliche Beschreibung
Autor*in: |
Plebani Mario [verfasserIn] |
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Englisch |
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2012 |
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In: Journal of Medical Biochemistry - Society of Medical Biochemists of Serbia, Belgrade, 2008, 31(2012), 4, Seite 265-270 |
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Übergeordnetes Werk: |
volume:31 ; year:2012 ; number:4 ; pages:265-270 |
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DOAJ079398537 |
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(DE-627)DOAJ079398537 (DE-599)DOAJ50fe69287378497bb2ffa01963d3f1da DE-627 ger DE-627 rakwb eng QD415-436 Plebani Mario verfasserin aut Pre-analytical errors and patient safety 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Laboratory medicine, as a specialty that had prioritized quality control, has always been at the forefront of error reduction. In the last decades, a dramatic decrease of analytical errors has been experienced, while a relatively high frequency of errors has been documented in the pre-analytical phase. Most pre-analytical errors, which account for up to 70% of all mistakes made in laboratory diagnostics, arise during patient preparation, and sample collection, transportation, preparation for analysis and storage. However, while it has been reported that the pre-analytical phase is error-prone, only recently has it been demonstrated that most of these errors occur in the 'pre-pre-analytical phase', which comprises the initial procedures of the testing process performed outside the laboratory walls by healthcare personnel outside the direct control of the clinical laboratory. Developments in automation and information technologies have played a major role in decreasing some pre-analytical errors and, in particular, the automation of repetitive, error prone and bio-hazardous pre-analytical processes performed within the laboratory walls has effectively decreased errors in specimen preparation, centrifugation, aliquot preparation, pipetting and sorting. However, more efforts should be made to improve the appropriateness of test request, patient and sample identification procedures and other pre-analytical steps performed outside the laboratory walls. quality indicators errors in laboratory medicine pre-analytical phase pre-pre-analytical phase total testing process quality specifications Biochemistry In Journal of Medical Biochemistry Society of Medical Biochemists of Serbia, Belgrade, 2008 31(2012), 4, Seite 265-270 (DE-627)557575117 (DE-600)2405112-3 14528266 nnns volume:31 year:2012 number:4 pages:265-270 https://doaj.org/article/50fe69287378497bb2ffa01963d3f1da kostenfrei https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2012/1452-82581204265P.pdf kostenfrei https://doaj.org/toc/1452-8258 Journal toc kostenfrei https://doaj.org/toc/1452-8266 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2027 GBV_ILN_2055 GBV_ILN_2111 AR 31 2012 4 265-270 |
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Laboratory medicine, as a specialty that had prioritized quality control, has always been at the forefront of error reduction. In the last decades, a dramatic decrease of analytical errors has been experienced, while a relatively high frequency of errors has been documented in the pre-analytical phase. Most pre-analytical errors, which account for up to 70% of all mistakes made in laboratory diagnostics, arise during patient preparation, and sample collection, transportation, preparation for analysis and storage. However, while it has been reported that the pre-analytical phase is error-prone, only recently has it been demonstrated that most of these errors occur in the 'pre-pre-analytical phase', which comprises the initial procedures of the testing process performed outside the laboratory walls by healthcare personnel outside the direct control of the clinical laboratory. Developments in automation and information technologies have played a major role in decreasing some pre-analytical errors and, in particular, the automation of repetitive, error prone and bio-hazardous pre-analytical processes performed within the laboratory walls has effectively decreased errors in specimen preparation, centrifugation, aliquot preparation, pipetting and sorting. However, more efforts should be made to improve the appropriateness of test request, patient and sample identification procedures and other pre-analytical steps performed outside the laboratory walls. |
abstractGer |
Laboratory medicine, as a specialty that had prioritized quality control, has always been at the forefront of error reduction. In the last decades, a dramatic decrease of analytical errors has been experienced, while a relatively high frequency of errors has been documented in the pre-analytical phase. Most pre-analytical errors, which account for up to 70% of all mistakes made in laboratory diagnostics, arise during patient preparation, and sample collection, transportation, preparation for analysis and storage. However, while it has been reported that the pre-analytical phase is error-prone, only recently has it been demonstrated that most of these errors occur in the 'pre-pre-analytical phase', which comprises the initial procedures of the testing process performed outside the laboratory walls by healthcare personnel outside the direct control of the clinical laboratory. Developments in automation and information technologies have played a major role in decreasing some pre-analytical errors and, in particular, the automation of repetitive, error prone and bio-hazardous pre-analytical processes performed within the laboratory walls has effectively decreased errors in specimen preparation, centrifugation, aliquot preparation, pipetting and sorting. However, more efforts should be made to improve the appropriateness of test request, patient and sample identification procedures and other pre-analytical steps performed outside the laboratory walls. |
abstract_unstemmed |
Laboratory medicine, as a specialty that had prioritized quality control, has always been at the forefront of error reduction. In the last decades, a dramatic decrease of analytical errors has been experienced, while a relatively high frequency of errors has been documented in the pre-analytical phase. Most pre-analytical errors, which account for up to 70% of all mistakes made in laboratory diagnostics, arise during patient preparation, and sample collection, transportation, preparation for analysis and storage. However, while it has been reported that the pre-analytical phase is error-prone, only recently has it been demonstrated that most of these errors occur in the 'pre-pre-analytical phase', which comprises the initial procedures of the testing process performed outside the laboratory walls by healthcare personnel outside the direct control of the clinical laboratory. Developments in automation and information technologies have played a major role in decreasing some pre-analytical errors and, in particular, the automation of repetitive, error prone and bio-hazardous pre-analytical processes performed within the laboratory walls has effectively decreased errors in specimen preparation, centrifugation, aliquot preparation, pipetting and sorting. However, more efforts should be made to improve the appropriateness of test request, patient and sample identification procedures and other pre-analytical steps performed outside the laboratory walls. |
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title_short |
Pre-analytical errors and patient safety |
url |
https://doaj.org/article/50fe69287378497bb2ffa01963d3f1da https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2012/1452-82581204265P.pdf https://doaj.org/toc/1452-8258 https://doaj.org/toc/1452-8266 |
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