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Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care
BACKGROUND: Currently used biomarkers for cardiac ischemia are elevated in blood plasma after a delay of several hours and therefore unable to detect acute coronary syndrome (ACS) in a very early stage. General practitioners (GPs), however, are often confronted with patients suspected of ACS within...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358877/ https://www.ncbi.nlm.nih.gov/pubmed/18412949 http://dx.doi.org/10.1186/1471-2261-8-8 |
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author | Bruins Slot, Madeleine HE van der Heijden, Geert JMG Rutten, Frans H van der Spoel, Onno P Mast, E Gijs Bredero, Ad C Doevendans, Pieter A Glatz, Jan FC Hoes, Arno W |
author_facet | Bruins Slot, Madeleine HE van der Heijden, Geert JMG Rutten, Frans H van der Spoel, Onno P Mast, E Gijs Bredero, Ad C Doevendans, Pieter A Glatz, Jan FC Hoes, Arno W |
author_sort | Bruins Slot, Madeleine HE |
collection | PubMed |
description | BACKGROUND: Currently used biomarkers for cardiac ischemia are elevated in blood plasma after a delay of several hours and therefore unable to detect acute coronary syndrome (ACS) in a very early stage. General practitioners (GPs), however, are often confronted with patients suspected of ACS within hours after onset of complaints. This ongoing study aims to evaluate the added diagnostic value beyond clinical assessment for a rapid bedside test for heart-type fatty-acid binding protein (H-FABP), a biomarker that is detectable as soon as one hour after onset of ischemia. METHODS: Participating GPs perform a blinded H-FABP rapid bedside test (Cardiodetect(®)) in patients with symptoms suggestive of ACS such as chest pain or discomfort at rest. All patients, whether referred to hospital or not, undergo electrocardiography (ECG) and venapunction for a plasma troponin test within 12–36 hours after onset of complaints. A final diagnosis will be established by an expert panel consisting of two cardiologists and one general practitioner (blinded to the H-FABP test result), using all available patient information, also including signs and symptoms. The added diagnostic value of the H-FABP test beyond history taking and physical examination will be determined with receiver operating characteristic curves derived from multivariate regression analysis. CONCLUSION: Reasons for presenting the design of our study include the prevention of publication bias and unacknowledged alterations in the study aim, design or data-analysis. To our knowledge this study is the first to assess the diagnostic value of H-FABP outside a hospital-setting. Several previous hospital-based studies showed the potential value of H-FABP in diagnosing ACS. Up to now however it is unclear whether these results are equally promising when the test is used in primary care. The first results are expected in the end of 2008. |
format | Text |
id | pubmed-2358877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23588772008-04-29 Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care Bruins Slot, Madeleine HE van der Heijden, Geert JMG Rutten, Frans H van der Spoel, Onno P Mast, E Gijs Bredero, Ad C Doevendans, Pieter A Glatz, Jan FC Hoes, Arno W BMC Cardiovasc Disord Study Protocol BACKGROUND: Currently used biomarkers for cardiac ischemia are elevated in blood plasma after a delay of several hours and therefore unable to detect acute coronary syndrome (ACS) in a very early stage. General practitioners (GPs), however, are often confronted with patients suspected of ACS within hours after onset of complaints. This ongoing study aims to evaluate the added diagnostic value beyond clinical assessment for a rapid bedside test for heart-type fatty-acid binding protein (H-FABP), a biomarker that is detectable as soon as one hour after onset of ischemia. METHODS: Participating GPs perform a blinded H-FABP rapid bedside test (Cardiodetect(®)) in patients with symptoms suggestive of ACS such as chest pain or discomfort at rest. All patients, whether referred to hospital or not, undergo electrocardiography (ECG) and venapunction for a plasma troponin test within 12–36 hours after onset of complaints. A final diagnosis will be established by an expert panel consisting of two cardiologists and one general practitioner (blinded to the H-FABP test result), using all available patient information, also including signs and symptoms. The added diagnostic value of the H-FABP test beyond history taking and physical examination will be determined with receiver operating characteristic curves derived from multivariate regression analysis. CONCLUSION: Reasons for presenting the design of our study include the prevention of publication bias and unacknowledged alterations in the study aim, design or data-analysis. To our knowledge this study is the first to assess the diagnostic value of H-FABP outside a hospital-setting. Several previous hospital-based studies showed the potential value of H-FABP in diagnosing ACS. Up to now however it is unclear whether these results are equally promising when the test is used in primary care. The first results are expected in the end of 2008. BioMed Central 2008-04-15 /pmc/articles/PMC2358877/ /pubmed/18412949 http://dx.doi.org/10.1186/1471-2261-8-8 Text en Copyright © 2008 Bruins Slot 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 | Study Protocol Bruins Slot, Madeleine HE van der Heijden, Geert JMG Rutten, Frans H van der Spoel, Onno P Mast, E Gijs Bredero, Ad C Doevendans, Pieter A Glatz, Jan FC Hoes, Arno W Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title | Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title_full | Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title_fullStr | Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title_full_unstemmed | Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title_short | Heart-type Fatty acid-binding protein in Acute Myocardial infarction Evaluation (FAME): Background and design of a diagnostic study in primary care |
title_sort | heart-type fatty acid-binding protein in acute myocardial infarction evaluation (fame): background and design of a diagnostic study in primary care |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358877/ https://www.ncbi.nlm.nih.gov/pubmed/18412949 http://dx.doi.org/10.1186/1471-2261-8-8 |
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