Guideline on the requirements of external quality assessment programs in molecular pathology
Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
van Krieken, J. Han [verfasserIn] Normanno, Nicola [verfasserIn] Blackhall, Fiona [verfasserIn] Boone, Elke [verfasserIn] Botti, Gerardo [verfasserIn] Carneiro, Fatima [verfasserIn] Celik, Ilhan [verfasserIn] Ciardiello, Fortunato [verfasserIn] Cree, Ian A. [verfasserIn] Deans, Zandra C. [verfasserIn] Edsjö, Anders [verfasserIn] Groenen, Patricia J. T. A. [verfasserIn] Kamarainen, Outi [verfasserIn] Kreipe, Hans H. [verfasserIn] Ligtenberg, Marjolijn J. L. [verfasserIn] Marchetti, Antonio [verfasserIn] Murray, Samuel [verfasserIn] Opdam, Frank J. M. [verfasserIn] Patterson, Scott D. [verfasserIn] Patton, Simon [verfasserIn] Pinto, Carmine [verfasserIn] Rouleau, Etienne [verfasserIn] Schuuring, Ed [verfasserIn] Sterck, Silke [verfasserIn] Taron, Miquel [verfasserIn] Tejpar, Sabine [verfasserIn] Timens, Wim [verfasserIn] Thunnissen, Erik [verfasserIn] van de Ven, Peter M. [verfasserIn] Siebers, Albert G. [verfasserIn] Dequeker, Elisabeth [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2012 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Virchows Archiv - Berlin : Springer, 1847, 462(2012), 1 vom: 19. Dez., Seite 27-37 |
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| Übergeordnetes Werk: |
volume:462 ; year:2012 ; number:1 ; day:19 ; month:12 ; pages:27-37 |
| Links: |
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| DOI / URN: |
10.1007/s00428-012-1354-4 |
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| Katalog-ID: |
SPR005761409 |
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| 520 | |a Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. | ||
| 650 | 4 | |a Molecular pathology |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a External quality assessment |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Oncology |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Guideline |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Normanno, Nicola |e verfasserin |4 aut | |
| 700 | 1 | |a Blackhall, Fiona |e verfasserin |4 aut | |
| 700 | 1 | |a Boone, Elke |e verfasserin |4 aut | |
| 700 | 1 | |a Botti, Gerardo |e verfasserin |4 aut | |
| 700 | 1 | |a Carneiro, Fatima |e verfasserin |4 aut | |
| 700 | 1 | |a Celik, Ilhan |e verfasserin |4 aut | |
| 700 | 1 | |a Ciardiello, Fortunato |e verfasserin |4 aut | |
| 700 | 1 | |a Cree, Ian A. |e verfasserin |4 aut | |
| 700 | 1 | |a Deans, Zandra C. |e verfasserin |4 aut | |
| 700 | 1 | |a Edsjö, Anders |e verfasserin |4 aut | |
| 700 | 1 | |a Groenen, Patricia J. T. A. |e verfasserin |4 aut | |
| 700 | 1 | |a Kamarainen, Outi |e verfasserin |4 aut | |
| 700 | 1 | |a Kreipe, Hans H. |e verfasserin |4 aut | |
| 700 | 1 | |a Ligtenberg, Marjolijn J. L. |e verfasserin |4 aut | |
| 700 | 1 | |a Marchetti, Antonio |e verfasserin |4 aut | |
| 700 | 1 | |a Murray, Samuel |e verfasserin |4 aut | |
| 700 | 1 | |a Opdam, Frank J. M. |e verfasserin |4 aut | |
| 700 | 1 | |a Patterson, Scott D. |e verfasserin |4 aut | |
| 700 | 1 | |a Patton, Simon |e verfasserin |4 aut | |
| 700 | 1 | |a Pinto, Carmine |e verfasserin |4 aut | |
| 700 | 1 | |a Rouleau, Etienne |e verfasserin |4 aut | |
| 700 | 1 | |a Schuuring, Ed |e verfasserin |4 aut | |
| 700 | 1 | |a Sterck, Silke |e verfasserin |4 aut | |
| 700 | 1 | |a Taron, Miquel |e verfasserin |4 aut | |
| 700 | 1 | |a Tejpar, Sabine |e verfasserin |4 aut | |
| 700 | 1 | |a Timens, Wim |e verfasserin |4 aut | |
| 700 | 1 | |a Thunnissen, Erik |e verfasserin |4 aut | |
| 700 | 1 | |a van de Ven, Peter M. |e verfasserin |4 aut | |
| 700 | 1 | |a Siebers, Albert G. |e verfasserin |4 aut | |
| 700 | 1 | |a Dequeker, Elisabeth |e verfasserin |4 aut | |
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10.1007/s00428-012-1354-4 doi (DE-627)SPR005761409 (SPR)s00428-012-1354-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.47 bkl van Krieken, J. Han verfasserin aut Guideline on the requirements of external quality assessment programs in molecular pathology 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. Molecular pathology (dpeaa)DE-He213 External quality assessment (dpeaa)DE-He213 Oncology (dpeaa)DE-He213 Guideline (dpeaa)DE-He213 Normanno, Nicola verfasserin aut Blackhall, Fiona verfasserin aut Boone, Elke verfasserin aut Botti, Gerardo verfasserin aut Carneiro, Fatima verfasserin aut Celik, Ilhan verfasserin aut Ciardiello, Fortunato verfasserin aut Cree, Ian A. verfasserin aut Deans, Zandra C. verfasserin aut Edsjö, Anders verfasserin aut Groenen, Patricia J. T. A. verfasserin aut Kamarainen, Outi verfasserin aut Kreipe, Hans H. verfasserin aut Ligtenberg, Marjolijn J. L. verfasserin aut Marchetti, Antonio verfasserin aut Murray, Samuel verfasserin aut Opdam, Frank J. M. verfasserin aut Patterson, Scott D. verfasserin aut Patton, Simon verfasserin aut Pinto, Carmine verfasserin aut Rouleau, Etienne verfasserin aut Schuuring, Ed verfasserin aut Sterck, Silke verfasserin aut Taron, Miquel verfasserin aut Tejpar, Sabine verfasserin aut Timens, Wim verfasserin aut Thunnissen, Erik verfasserin aut van de Ven, Peter M. verfasserin aut Siebers, Albert G. verfasserin aut Dequeker, Elisabeth verfasserin aut Enthalten in Virchows Archiv Berlin : Springer, 1847 462(2012), 1 vom: 19. Dez., Seite 27-37 (DE-627)254910645 (DE-600)1463276-7 1432-2307 nnns volume:462 year:2012 number:1 day:19 month:12 pages:27-37 https://dx.doi.org/10.1007/s00428-012-1354-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.47 ASE AR 462 2012 1 19 12 27-37 |
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10.1007/s00428-012-1354-4 doi (DE-627)SPR005761409 (SPR)s00428-012-1354-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.47 bkl van Krieken, J. Han verfasserin aut Guideline on the requirements of external quality assessment programs in molecular pathology 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. Molecular pathology (dpeaa)DE-He213 External quality assessment (dpeaa)DE-He213 Oncology (dpeaa)DE-He213 Guideline (dpeaa)DE-He213 Normanno, Nicola verfasserin aut Blackhall, Fiona verfasserin aut Boone, Elke verfasserin aut Botti, Gerardo verfasserin aut Carneiro, Fatima verfasserin aut Celik, Ilhan verfasserin aut Ciardiello, Fortunato verfasserin aut Cree, Ian A. verfasserin aut Deans, Zandra C. verfasserin aut Edsjö, Anders verfasserin aut Groenen, Patricia J. T. A. verfasserin aut Kamarainen, Outi verfasserin aut Kreipe, Hans H. verfasserin aut Ligtenberg, Marjolijn J. L. verfasserin aut Marchetti, Antonio verfasserin aut Murray, Samuel verfasserin aut Opdam, Frank J. M. verfasserin aut Patterson, Scott D. verfasserin aut Patton, Simon verfasserin aut Pinto, Carmine verfasserin aut Rouleau, Etienne verfasserin aut Schuuring, Ed verfasserin aut Sterck, Silke verfasserin aut Taron, Miquel verfasserin aut Tejpar, Sabine verfasserin aut Timens, Wim verfasserin aut Thunnissen, Erik verfasserin aut van de Ven, Peter M. verfasserin aut Siebers, Albert G. verfasserin aut Dequeker, Elisabeth verfasserin aut Enthalten in Virchows Archiv Berlin : Springer, 1847 462(2012), 1 vom: 19. Dez., Seite 27-37 (DE-627)254910645 (DE-600)1463276-7 1432-2307 nnns volume:462 year:2012 number:1 day:19 month:12 pages:27-37 https://dx.doi.org/10.1007/s00428-012-1354-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.47 ASE AR 462 2012 1 19 12 27-37 |
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10.1007/s00428-012-1354-4 doi (DE-627)SPR005761409 (SPR)s00428-012-1354-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.47 bkl van Krieken, J. Han verfasserin aut Guideline on the requirements of external quality assessment programs in molecular pathology 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. Molecular pathology (dpeaa)DE-He213 External quality assessment (dpeaa)DE-He213 Oncology (dpeaa)DE-He213 Guideline (dpeaa)DE-He213 Normanno, Nicola verfasserin aut Blackhall, Fiona verfasserin aut Boone, Elke verfasserin aut Botti, Gerardo verfasserin aut Carneiro, Fatima verfasserin aut Celik, Ilhan verfasserin aut Ciardiello, Fortunato verfasserin aut Cree, Ian A. verfasserin aut Deans, Zandra C. verfasserin aut Edsjö, Anders verfasserin aut Groenen, Patricia J. T. A. verfasserin aut Kamarainen, Outi verfasserin aut Kreipe, Hans H. verfasserin aut Ligtenberg, Marjolijn J. L. verfasserin aut Marchetti, Antonio verfasserin aut Murray, Samuel verfasserin aut Opdam, Frank J. M. verfasserin aut Patterson, Scott D. verfasserin aut Patton, Simon verfasserin aut Pinto, Carmine verfasserin aut Rouleau, Etienne verfasserin aut Schuuring, Ed verfasserin aut Sterck, Silke verfasserin aut Taron, Miquel verfasserin aut Tejpar, Sabine verfasserin aut Timens, Wim verfasserin aut Thunnissen, Erik verfasserin aut van de Ven, Peter M. verfasserin aut Siebers, Albert G. verfasserin aut Dequeker, Elisabeth verfasserin aut Enthalten in Virchows Archiv Berlin : Springer, 1847 462(2012), 1 vom: 19. Dez., Seite 27-37 (DE-627)254910645 (DE-600)1463276-7 1432-2307 nnns volume:462 year:2012 number:1 day:19 month:12 pages:27-37 https://dx.doi.org/10.1007/s00428-012-1354-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.47 ASE AR 462 2012 1 19 12 27-37 |
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10.1007/s00428-012-1354-4 doi (DE-627)SPR005761409 (SPR)s00428-012-1354-4-e DE-627 ger DE-627 rakwb eng 610 ASE 44.47 bkl van Krieken, J. Han verfasserin aut Guideline on the requirements of external quality assessment programs in molecular pathology 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. Molecular pathology (dpeaa)DE-He213 External quality assessment (dpeaa)DE-He213 Oncology (dpeaa)DE-He213 Guideline (dpeaa)DE-He213 Normanno, Nicola verfasserin aut Blackhall, Fiona verfasserin aut Boone, Elke verfasserin aut Botti, Gerardo verfasserin aut Carneiro, Fatima verfasserin aut Celik, Ilhan verfasserin aut Ciardiello, Fortunato verfasserin aut Cree, Ian A. verfasserin aut Deans, Zandra C. verfasserin aut Edsjö, Anders verfasserin aut Groenen, Patricia J. T. A. verfasserin aut Kamarainen, Outi verfasserin aut Kreipe, Hans H. verfasserin aut Ligtenberg, Marjolijn J. L. verfasserin aut Marchetti, Antonio verfasserin aut Murray, Samuel verfasserin aut Opdam, Frank J. M. verfasserin aut Patterson, Scott D. verfasserin aut Patton, Simon verfasserin aut Pinto, Carmine verfasserin aut Rouleau, Etienne verfasserin aut Schuuring, Ed verfasserin aut Sterck, Silke verfasserin aut Taron, Miquel verfasserin aut Tejpar, Sabine verfasserin aut Timens, Wim verfasserin aut Thunnissen, Erik verfasserin aut van de Ven, Peter M. verfasserin aut Siebers, Albert G. verfasserin aut Dequeker, Elisabeth verfasserin aut Enthalten in Virchows Archiv Berlin : Springer, 1847 462(2012), 1 vom: 19. Dez., Seite 27-37 (DE-627)254910645 (DE-600)1463276-7 1432-2307 nnns volume:462 year:2012 number:1 day:19 month:12 pages:27-37 https://dx.doi.org/10.1007/s00428-012-1354-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.47 ASE AR 462 2012 1 19 12 27-37 |
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van Krieken, J. Han @@aut@@ Normanno, Nicola @@aut@@ Blackhall, Fiona @@aut@@ Boone, Elke @@aut@@ Botti, Gerardo @@aut@@ Carneiro, Fatima @@aut@@ Celik, Ilhan @@aut@@ Ciardiello, Fortunato @@aut@@ Cree, Ian A. @@aut@@ Deans, Zandra C. @@aut@@ Edsjö, Anders @@aut@@ Groenen, Patricia J. T. A. @@aut@@ Kamarainen, Outi @@aut@@ Kreipe, Hans H. @@aut@@ Ligtenberg, Marjolijn J. L. @@aut@@ Marchetti, Antonio @@aut@@ Murray, Samuel @@aut@@ Opdam, Frank J. M. @@aut@@ Patterson, Scott D. @@aut@@ Patton, Simon @@aut@@ Pinto, Carmine @@aut@@ Rouleau, Etienne @@aut@@ Schuuring, Ed @@aut@@ Sterck, Silke @@aut@@ Taron, Miquel @@aut@@ Tejpar, Sabine @@aut@@ Timens, Wim @@aut@@ Thunnissen, Erik @@aut@@ van de Ven, Peter M. @@aut@@ Siebers, Albert G. @@aut@@ Dequeker, Elisabeth @@aut@@ |
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van Krieken, J. Han |
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van Krieken, J. Han ddc 610 bkl 44.47 misc Molecular pathology misc External quality assessment misc Oncology misc Guideline Guideline on the requirements of external quality assessment programs in molecular pathology |
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610 ASE 44.47 bkl Guideline on the requirements of external quality assessment programs in molecular pathology Molecular pathology (dpeaa)DE-He213 External quality assessment (dpeaa)DE-He213 Oncology (dpeaa)DE-He213 Guideline (dpeaa)DE-He213 |
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van Krieken, J. Han Normanno, Nicola Blackhall, Fiona Boone, Elke Botti, Gerardo Carneiro, Fatima Celik, Ilhan Ciardiello, Fortunato Cree, Ian A. Deans, Zandra C. Edsjö, Anders Groenen, Patricia J. T. A. Kamarainen, Outi Kreipe, Hans H. Ligtenberg, Marjolijn J. L. Marchetti, Antonio Murray, Samuel Opdam, Frank J. M. Patterson, Scott D. Patton, Simon Pinto, Carmine Rouleau, Etienne Schuuring, Ed Sterck, Silke Taron, Miquel Tejpar, Sabine Timens, Wim Thunnissen, Erik van de Ven, Peter M. Siebers, Albert G. Dequeker, Elisabeth |
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guideline on the requirements of external quality assessment programs in molecular pathology |
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Guideline on the requirements of external quality assessment programs in molecular pathology |
| abstract |
Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. |
| abstractGer |
Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. |
| abstract_unstemmed |
Abstract Molecular pathology is an integral part of daily diagnostic pathology and used for classification of tumors, for prediction of prognosis and response to therapy, and to support treatment decisions. For these reasons, analyses in molecular pathology must be highly reliable and hence external quality assessment (EQA) programs are called for. Several EQA programs exist to which laboratories can subscribe, but they vary in scope, number of subscribers, and execution. The guideline presented in this paper has been developed with the purpose to harmonize EQA in molecular pathology. It presents recommendations on how an EQA program should be organized, provides criteria for a reference laboratory, proposes requirements for EQA test samples, and defines the number of samples needed for an EQA program. Furthermore, a system for scoring of the results is proposed as well as measures to be taken for poorly performing laboratories. Proposals are made regarding the content requirements of an EQA report and how its results should be communicated. Finally, the need for an EQA database and a participant manual are elaborated. It is the intention of this guideline to improve EQA for molecular pathology in order to provide more reliable molecular analyses as well as optimal information regarding patient selection for treatment. |
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| container_issue |
1 |
| title_short |
Guideline on the requirements of external quality assessment programs in molecular pathology |
| url |
https://dx.doi.org/10.1007/s00428-012-1354-4 |
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| author2 |
Normanno, Nicola Blackhall, Fiona Boone, Elke Botti, Gerardo Carneiro, Fatima Celik, Ilhan Ciardiello, Fortunato Cree, Ian A. Deans, Zandra C. Edsjö, Anders Groenen, Patricia J. T. A. Kamarainen, Outi Kreipe, Hans H. Ligtenberg, Marjolijn J. L. Marchetti, Antonio Murray, Samuel Opdam, Frank J. M. Patterson, Scott D. Patton, Simon Pinto, Carmine Rouleau, Etienne Schuuring, Ed Sterck, Silke Taron, Miquel Tejpar, Sabine Timens, Wim Thunnissen, Erik van de Ven, Peter M. Siebers, Albert G. Dequeker, Elisabeth |
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Normanno, Nicola Blackhall, Fiona Boone, Elke Botti, Gerardo Carneiro, Fatima Celik, Ilhan Ciardiello, Fortunato Cree, Ian A. Deans, Zandra C. Edsjö, Anders Groenen, Patricia J. T. A. Kamarainen, Outi Kreipe, Hans H. Ligtenberg, Marjolijn J. L. Marchetti, Antonio Murray, Samuel Opdam, Frank J. M. Patterson, Scott D. Patton, Simon Pinto, Carmine Rouleau, Etienne Schuuring, Ed Sterck, Silke Taron, Miquel Tejpar, Sabine Timens, Wim Thunnissen, Erik van de Ven, Peter M. Siebers, Albert G. Dequeker, Elisabeth |
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| doi_str |
10.1007/s00428-012-1354-4 |
| up_date |
2024-07-03T18:30:55.232Z |
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| score |
7.3985844 |