Errors in laboratory medicine and patient safety: the road ahead
The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and...
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| Autor*in: |
Plebani, Mario [verfasserIn] |
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E-Artikel |
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| Erschienen: |
Walter de Gruyter ; 2007 |
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©2007 by Walter de Gruyter Berlin New York |
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| Umfang: |
8 |
| Reproduktion: |
Walter de Gruyter Online Zeitschriften |
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| Übergeordnetes Werk: |
Enthalten in: Clinical chemistry and laboratory medicine - Berlin [u.a.] : De Gruyter, 1998, 45(2007), 6 vom: 19. Juni, Seite 700-707 |
| Übergeordnetes Werk: |
volume:45 ; year:2007 ; number:6 ; day:19 ; month:06 ; pages:700-707 ; extent:8 |
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10.1515/CCLM.2007.170 |
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| 520 | |a The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. | ||
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10.1515/CCLM.2007.170 doi artikel_Grundlieferung.pp (DE-627)NLEJ246720417 DE-627 ger DE-627 rakwb Plebani, Mario verfasserin aut Errors in laboratory medicine and patient safety: the road ahead Walter de Gruyter 2007 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ©2007 by Walter de Gruyter Berlin New York The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. Walter de Gruyter Online Zeitschriften analytical quality clinical laboratories errors in laboratory medicine patient safety pre- and post-analytical phases total testing process Enthalten in Clinical chemistry and laboratory medicine Berlin [u.a.] : De Gruyter, 1998 45(2007), 6 vom: 19. Juni, Seite 700-707 (DE-627)NLEJ248235222 (DE-600)1492732-9 1437-4331 nnns volume:45 year:2007 number:6 day:19 month:06 pages:700-707 extent:8 https://doi.org/10.1515/CCLM.2007.170 Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-DGR GBV_NL_ARTICLE AR 45 2007 6 19 06 700-707 8 |
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10.1515/CCLM.2007.170 doi artikel_Grundlieferung.pp (DE-627)NLEJ246720417 DE-627 ger DE-627 rakwb Plebani, Mario verfasserin aut Errors in laboratory medicine and patient safety: the road ahead Walter de Gruyter 2007 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ©2007 by Walter de Gruyter Berlin New York The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. Walter de Gruyter Online Zeitschriften analytical quality clinical laboratories errors in laboratory medicine patient safety pre- and post-analytical phases total testing process Enthalten in Clinical chemistry and laboratory medicine Berlin [u.a.] : De Gruyter, 1998 45(2007), 6 vom: 19. Juni, Seite 700-707 (DE-627)NLEJ248235222 (DE-600)1492732-9 1437-4331 nnns volume:45 year:2007 number:6 day:19 month:06 pages:700-707 extent:8 https://doi.org/10.1515/CCLM.2007.170 Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-DGR GBV_NL_ARTICLE AR 45 2007 6 19 06 700-707 8 |
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10.1515/CCLM.2007.170 doi artikel_Grundlieferung.pp (DE-627)NLEJ246720417 DE-627 ger DE-627 rakwb Plebani, Mario verfasserin aut Errors in laboratory medicine and patient safety: the road ahead Walter de Gruyter 2007 8 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier ©2007 by Walter de Gruyter Berlin New York The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. Walter de Gruyter Online Zeitschriften analytical quality clinical laboratories errors in laboratory medicine patient safety pre- and post-analytical phases total testing process Enthalten in Clinical chemistry and laboratory medicine Berlin [u.a.] : De Gruyter, 1998 45(2007), 6 vom: 19. Juni, Seite 700-707 (DE-627)NLEJ248235222 (DE-600)1492732-9 1437-4331 nnns volume:45 year:2007 number:6 day:19 month:06 pages:700-707 extent:8 https://doi.org/10.1515/CCLM.2007.170 Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-DGR GBV_NL_ARTICLE AR 45 2007 6 19 06 700-707 8 |
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The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. ©2007 by Walter de Gruyter Berlin New York |
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The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. ©2007 by Walter de Gruyter Berlin New York |
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The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. Moreover, a fundamental shift in improving patient safety in laboratory medicine is to move from error reporting to risk management. Clin Chem Lab Med 2007;45:700–7. ©2007 by Walter de Gruyter Berlin New York |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ246720417</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506100849.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">220814s2007 xx |||||o 00| ||und c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1515/CCLM.2007.170</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">artikel_Grundlieferung.pp</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ246720417</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Plebani, Mario</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Errors in laboratory medicine and patient safety: the road ahead</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="b">Walter de Gruyter</subfield><subfield code="c">2007</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">8</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">©2007 by Walter de Gruyter Berlin New York</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The Institute of Medicine (IOM) report, To err is human, galvanized a dramatically increased level of concern about adverse events and patient safety in healthcare, including errors in laboratory medicine. While a significant decrease in the error rates of clinical laboratories has been achieved and documented in recent decades, available evidence demonstrates that the pre- and post-analytical phases of the total testing process are more vulnerable to errors than the analytical phase. However, analytical quality is still a major issue, particularly in some areas of laboratory medicine such as immunoassaying. In the present paper, current trends and factors that could effect future changes in the frequency and types of errors in laboratory services are analyzed and discussed. A more effective integration of automation and information technology could allow clinical laboratories to identify, control and decrease error rates in the total testing process, but interdepartmental cooperation and communication with clinicians and other stakeholders are essential to improving patient safety. 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