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Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'

BACKGROUND: In 1999 a four-level hierarchy of evidence was promoted by the National Health and Medical Research Council in Australia. The primary purpose of this hierarchy was to assist with clinical practice guideline development, although it was co-opted for use in systematic literature reviews an...

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Autores principales: Merlin, Tracy, Weston, Adele, Tooher, Rebecca
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700132/
https://www.ncbi.nlm.nih.gov/pubmed/19519887
http://dx.doi.org/10.1186/1471-2288-9-34
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author Merlin, Tracy
Weston, Adele
Tooher, Rebecca
author_facet Merlin, Tracy
Weston, Adele
Tooher, Rebecca
author_sort Merlin, Tracy
collection PubMed
description BACKGROUND: In 1999 a four-level hierarchy of evidence was promoted by the National Health and Medical Research Council in Australia. The primary purpose of this hierarchy was to assist with clinical practice guideline development, although it was co-opted for use in systematic literature reviews and health technology assessments. In this hierarchy interventional study designs were ranked according to the likelihood that bias had been eliminated and thus it was not ideal to assess studies that addressed other types of clinical questions. This paper reports on the revision and extension of this evidence hierarchy to enable broader use within existing evidence assessment systems. METHODS: A working party identified and assessed empirical evidence, and used a commissioned review of existing evidence assessment schema, to support decision-making regarding revision of the hierarchy. The aim was to retain the existing evidence levels I-IV but increase their relevance for assessing the quality of individual diagnostic accuracy, prognostic, aetiologic and screening studies. Comprehensive public consultation was undertaken and the revised hierarchy was piloted by individual health technology assessment agencies and clinical practice guideline developers. After two and a half years, the hierarchy was again revised and commenced a further 18 month pilot period. RESULTS: A suitable framework was identified upon which to model the revision. Consistency was maintained in the hierarchy of "levels of evidence" across all types of clinical questions; empirical evidence was used to support the relationship between study design and ranking in the hierarchy wherever possible; and systematic reviews of lower level studies were themselves ascribed a ranking. The impact of ethics on the hierarchy of study designs was acknowledged in the framework, along with a consideration of how harms should be assessed. CONCLUSION: The revised evidence hierarchy is now widely used and provides a common standard against which to initially judge the likelihood of bias in individual studies evaluating interventional, diagnostic accuracy, prognostic, aetiologic or screening topics. Detailed quality appraisal of these individual studies, as well as grading of the body of evidence to answer each clinical, research or policy question, can then be undertaken as required.
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spelling pubmed-27001322009-06-23 Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence' Merlin, Tracy Weston, Adele Tooher, Rebecca BMC Med Res Methodol Research Article BACKGROUND: In 1999 a four-level hierarchy of evidence was promoted by the National Health and Medical Research Council in Australia. The primary purpose of this hierarchy was to assist with clinical practice guideline development, although it was co-opted for use in systematic literature reviews and health technology assessments. In this hierarchy interventional study designs were ranked according to the likelihood that bias had been eliminated and thus it was not ideal to assess studies that addressed other types of clinical questions. This paper reports on the revision and extension of this evidence hierarchy to enable broader use within existing evidence assessment systems. METHODS: A working party identified and assessed empirical evidence, and used a commissioned review of existing evidence assessment schema, to support decision-making regarding revision of the hierarchy. The aim was to retain the existing evidence levels I-IV but increase their relevance for assessing the quality of individual diagnostic accuracy, prognostic, aetiologic and screening studies. Comprehensive public consultation was undertaken and the revised hierarchy was piloted by individual health technology assessment agencies and clinical practice guideline developers. After two and a half years, the hierarchy was again revised and commenced a further 18 month pilot period. RESULTS: A suitable framework was identified upon which to model the revision. Consistency was maintained in the hierarchy of "levels of evidence" across all types of clinical questions; empirical evidence was used to support the relationship between study design and ranking in the hierarchy wherever possible; and systematic reviews of lower level studies were themselves ascribed a ranking. The impact of ethics on the hierarchy of study designs was acknowledged in the framework, along with a consideration of how harms should be assessed. CONCLUSION: The revised evidence hierarchy is now widely used and provides a common standard against which to initially judge the likelihood of bias in individual studies evaluating interventional, diagnostic accuracy, prognostic, aetiologic or screening topics. Detailed quality appraisal of these individual studies, as well as grading of the body of evidence to answer each clinical, research or policy question, can then be undertaken as required. BioMed Central 2009-06-11 /pmc/articles/PMC2700132/ /pubmed/19519887 http://dx.doi.org/10.1186/1471-2288-9-34 Text en Copyright ©2009 Merlin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Merlin, Tracy
Weston, Adele
Tooher, Rebecca
Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title_full Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title_fullStr Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title_full_unstemmed Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title_short Extending an evidence hierarchy to include topics other than treatment: revising the Australian 'levels of evidence'
title_sort extending an evidence hierarchy to include topics other than treatment: revising the australian 'levels of evidence'
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700132/
https://www.ncbi.nlm.nih.gov/pubmed/19519887
http://dx.doi.org/10.1186/1471-2288-9-34
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