A FABP-ulous ‘rule out’ strategy? Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction
Abstract Objective Many Emergency Departments (EDs) utilise ‘triple marker’ testing with CK-MB, myoglobin and troponin I (cTnI) to exclude acute myocardial infarction (AMI) within hours of presentation. We evaluated the ability of 8 biomarkers to rapidly exclude AMI at the point of presentation and...
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description | Abstract Objective Many Emergency Departments (EDs) utilise ‘triple marker’ testing with CK-MB, myoglobin and troponin I (cTnI) to exclude acute myocardial infarction (AMI) within hours of presentation. We evaluated the ability of 8 biomarkers to rapidly exclude AMI at the point of presentation and investigated whether ‘triple marker’ testing represents the optimal multimarker strategy. Methods We recruited patients who presented to the ED with suspected cardiac chest pain occurring within 24 h. Blood was drawn at the time of presentation. Diagnostic value was assessed by calculating the area under the ROC curve (AUC) and a multivariate model was constructed by logistic regression. The primary outcome was a diagnosis of AMI, established by ≥12-h troponin testing in all patients. Results 705 included patients underwent venepuncture a median of 3.5 h after symptom onset. Heart fatty acid binding protein (H-FABP) had an AUC of 0.86 (95% CI 0.82–0.90), which was significantly higher than any other biomarker including cTnI. While no single biomarker could enable exclusion of AMI, multivariate analysis identified cTnI and H-FABP as the optimal biomarker combination. Combined with clinical risk stratification, this strategy had a sensitivity of 96.9%, specificity of 54.7%, PPV 32.4% and NPV 98.8%. Conclusions We have derived an algorithm that would enable AMI to be immediately excluded in 315 (44.7%) patients at the cost of missing 6 AMIs per 1000 patients treated. While the risk is likely to be unacceptable for clinical implementation, we have highlighted an area for future development using serial testing and increasingly sensitive assays. |
doi_str_mv | 10.1016/j.resuscitation.2011.03.015 |
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Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Body, Richard ; McDowell, Garry ; Carley, Simon ; Wibberley, Christopher ; Ferguson, Jamie ; Mackway-Jones, Kevin</creator><creatorcontrib>Body, Richard ; McDowell, Garry ; Carley, Simon ; Wibberley, Christopher ; Ferguson, Jamie ; Mackway-Jones, Kevin</creatorcontrib><description>Abstract Objective Many Emergency Departments (EDs) utilise ‘triple marker’ testing with CK-MB, myoglobin and troponin I (cTnI) to exclude acute myocardial infarction (AMI) within hours of presentation. We evaluated the ability of 8 biomarkers to rapidly exclude AMI at the point of presentation and investigated whether ‘triple marker’ testing represents the optimal multimarker strategy. Methods We recruited patients who presented to the ED with suspected cardiac chest pain occurring within 24 h. Blood was drawn at the time of presentation. Diagnostic value was assessed by calculating the area under the ROC curve (AUC) and a multivariate model was constructed by logistic regression. The primary outcome was a diagnosis of AMI, established by ≥12-h troponin testing in all patients. Results 705 included patients underwent venepuncture a median of 3.5 h after symptom onset. Heart fatty acid binding protein (H-FABP) had an AUC of 0.86 (95% CI 0.82–0.90), which was significantly higher than any other biomarker including cTnI. While no single biomarker could enable exclusion of AMI, multivariate analysis identified cTnI and H-FABP as the optimal biomarker combination. Combined with clinical risk stratification, this strategy had a sensitivity of 96.9%, specificity of 54.7%, PPV 32.4% and NPV 98.8%. Conclusions We have derived an algorithm that would enable AMI to be immediately excluded in 315 (44.7%) patients at the cost of missing 6 AMIs per 1000 patients treated. While the risk is likely to be unacceptable for clinical implementation, we have highlighted an area for future development using serial testing and increasingly sensitive assays.</description><identifier>ISSN: 0300-9572</identifier><identifier>EISSN: 1873-1570</identifier><identifier>DOI: 10.1016/j.resuscitation.2011.03.015</identifier><identifier>PMID: 21561701</identifier><identifier>CODEN: RSUSBS</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Acute coronary syndromes ; Acute myocardial infarction ; Acute-Phase Proteins ; Algorithms ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Bayes Theorem ; Biological and medical sciences ; Biomarkers - blood ; Brain natriuretic peptide ; Cardiology. Vascular system ; CK-MB ; Coronary heart disease ; Creatine Kinase, MB Form - blood ; d-Dimer ; Diagnosis ; Diagnosis, Differential ; Emergency ; Fatty Acid-Binding Proteins - blood ; Female ; Fibrin Fibrinogen Degradation Products - metabolism ; Heart ; Heart fatty acid binding protein ; Humans ; Intensive care medicine ; Lipocalin-2 ; Lipocalins - blood ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; Myeloperoxidase ; Myocardial Infarction - blood ; Myoglobin ; Myoglobin - blood ; Natriuretic Peptide, Brain - blood ; Peroxidase - blood ; Prospective Studies ; Proto-Oncogene Proteins - blood ; Risk Assessment ; ROC Curve ; Sensitivity and Specificity ; Troponin I - blood ; Troponins</subject><ispartof>Resuscitation, 2011-08, Vol.82 (8), p.1041-1046</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-3ba00c4de4d91d8054b74a96d26e79452ce8e796c53c2d5006b691bd426786cb3</citedby><cites>FETCH-LOGICAL-c467t-3ba00c4de4d91d8054b74a96d26e79452ce8e796c53c2d5006b691bd426786cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.resuscitation.2011.03.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24387075$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21561701$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Body, Richard</creatorcontrib><creatorcontrib>McDowell, Garry</creatorcontrib><creatorcontrib>Carley, Simon</creatorcontrib><creatorcontrib>Wibberley, Christopher</creatorcontrib><creatorcontrib>Ferguson, Jamie</creatorcontrib><creatorcontrib>Mackway-Jones, Kevin</creatorcontrib><title>A FABP-ulous ‘rule out’ strategy? Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction</title><title>Resuscitation</title><addtitle>Resuscitation</addtitle><description>Abstract Objective Many Emergency Departments (EDs) utilise ‘triple marker’ testing with CK-MB, myoglobin and troponin I (cTnI) to exclude acute myocardial infarction (AMI) within hours of presentation. We evaluated the ability of 8 biomarkers to rapidly exclude AMI at the point of presentation and investigated whether ‘triple marker’ testing represents the optimal multimarker strategy. Methods We recruited patients who presented to the ED with suspected cardiac chest pain occurring within 24 h. Blood was drawn at the time of presentation. Diagnostic value was assessed by calculating the area under the ROC curve (AUC) and a multivariate model was constructed by logistic regression. The primary outcome was a diagnosis of AMI, established by ≥12-h troponin testing in all patients. Results 705 included patients underwent venepuncture a median of 3.5 h after symptom onset. Heart fatty acid binding protein (H-FABP) had an AUC of 0.86 (95% CI 0.82–0.90), which was significantly higher than any other biomarker including cTnI. While no single biomarker could enable exclusion of AMI, multivariate analysis identified cTnI and H-FABP as the optimal biomarker combination. Combined with clinical risk stratification, this strategy had a sensitivity of 96.9%, specificity of 54.7%, PPV 32.4% and NPV 98.8%. Conclusions We have derived an algorithm that would enable AMI to be immediately excluded in 315 (44.7%) patients at the cost of missing 6 AMIs per 1000 patients treated. While the risk is likely to be unacceptable for clinical implementation, we have highlighted an area for future development using serial testing and increasingly sensitive assays.</description><subject>Acute coronary syndromes</subject><subject>Acute myocardial infarction</subject><subject>Acute-Phase Proteins</subject><subject>Algorithms</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Bayes Theorem</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Brain natriuretic peptide</subject><subject>Cardiology. Vascular system</subject><subject>CK-MB</subject><subject>Coronary heart disease</subject><subject>Creatine Kinase, MB Form - blood</subject><subject>d-Dimer</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Emergency</subject><subject>Fatty Acid-Binding Proteins - blood</subject><subject>Female</subject><subject>Fibrin Fibrinogen Degradation Products - metabolism</subject><subject>Heart</subject><subject>Heart fatty acid binding protein</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Lipocalin-2</subject><subject>Lipocalins - blood</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Myeloperoxidase</subject><subject>Myocardial Infarction - blood</subject><subject>Myoglobin</subject><subject>Myoglobin - blood</subject><subject>Natriuretic Peptide, Brain - blood</subject><subject>Peroxidase - blood</subject><subject>Prospective Studies</subject><subject>Proto-Oncogene Proteins - blood</subject><subject>Risk Assessment</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><subject>Troponin I - blood</subject><subject>Troponins</subject><issn>0300-9572</issn><issn>1873-1570</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNktGK1DAUhoso7uzqK0hAxKvWk6ZtWgSXcdl1hQUF9TqkyemSsZOMSSr2bq_2GfT19klMmVHRK6-SwHfO-fP_J8ueUigo0ObFpvAYpqBMlNE4W5RAaQGsAFrfy1a05SynNYf72QoYQN7VvDzKjkPYAACrO_4wOypp3VAOdJXdrsnF-vX7fBrdFMjdzXc_jUjcFO9ufpAQvYx4PZ-SS5Q-kkHGOBOpjCa9sdrYa7LzLqKxRFpNonc7Z9NjcJ54uUsYflPjFJJK4oZUOEUk29kp6bWRIzF2kF4tn3iUPRjkGPDx4TzJPl2cfzy7zK_evXl7tr7KVdXwmLNeAqhKY6U7qluoq55Xsmt02SDvqrpU2KZLo2qmSl0DNH3T0V5XZcPbRvXsJHu-75t0f5kwRLE1QeE4SovJANHyNpnGoE3kyz2pvAvB4yB23mylnwUFseQgNuKvHMSSgwAmUg6p-slhztRvUf-u_WV8Ap4dABmUHAcvrTLhD1exlgNfGp3vOUyufDXoRRqIVqE2HlUU2pn_FPTqnz5qNNak0Z9xxrBxk7fJeEFFKAWID8vqLJtDKUAJnLGf9gzGpw</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Body, Richard</creator><creator>McDowell, Garry</creator><creator>Carley, Simon</creator><creator>Wibberley, Christopher</creator><creator>Ferguson, Jamie</creator><creator>Mackway-Jones, Kevin</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110801</creationdate><title>A FABP-ulous ‘rule out’ strategy? Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction</title><author>Body, Richard ; McDowell, Garry ; Carley, Simon ; Wibberley, Christopher ; Ferguson, Jamie ; Mackway-Jones, Kevin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-3ba00c4de4d91d8054b74a96d26e79452ce8e796c53c2d5006b691bd426786cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acute coronary syndromes</topic><topic>Acute myocardial infarction</topic><topic>Acute-Phase Proteins</topic><topic>Algorithms</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Bayes Theorem</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Brain natriuretic peptide</topic><topic>Cardiology. Vascular system</topic><topic>CK-MB</topic><topic>Coronary heart disease</topic><topic>Creatine Kinase, MB Form - blood</topic><topic>d-Dimer</topic><topic>Diagnosis</topic><topic>Diagnosis, Differential</topic><topic>Emergency</topic><topic>Fatty Acid-Binding Proteins - blood</topic><topic>Female</topic><topic>Fibrin Fibrinogen Degradation Products - metabolism</topic><topic>Heart</topic><topic>Heart fatty acid binding protein</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Lipocalin-2</topic><topic>Lipocalins - blood</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Myeloperoxidase</topic><topic>Myocardial Infarction - blood</topic><topic>Myoglobin</topic><topic>Myoglobin - blood</topic><topic>Natriuretic Peptide, Brain - blood</topic><topic>Peroxidase - blood</topic><topic>Prospective Studies</topic><topic>Proto-Oncogene Proteins - blood</topic><topic>Risk Assessment</topic><topic>ROC Curve</topic><topic>Sensitivity and Specificity</topic><topic>Troponin I - blood</topic><topic>Troponins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Body, Richard</creatorcontrib><creatorcontrib>McDowell, Garry</creatorcontrib><creatorcontrib>Carley, Simon</creatorcontrib><creatorcontrib>Wibberley, Christopher</creatorcontrib><creatorcontrib>Ferguson, Jamie</creatorcontrib><creatorcontrib>Mackway-Jones, Kevin</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Resuscitation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Body, Richard</au><au>McDowell, Garry</au><au>Carley, Simon</au><au>Wibberley, Christopher</au><au>Ferguson, Jamie</au><au>Mackway-Jones, Kevin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A FABP-ulous ‘rule out’ strategy? Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction</atitle><jtitle>Resuscitation</jtitle><addtitle>Resuscitation</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>82</volume><issue>8</issue><spage>1041</spage><epage>1046</epage><pages>1041-1046</pages><issn>0300-9572</issn><eissn>1873-1570</eissn><coden>RSUSBS</coden><abstract>Abstract Objective Many Emergency Departments (EDs) utilise ‘triple marker’ testing with CK-MB, myoglobin and troponin I (cTnI) to exclude acute myocardial infarction (AMI) within hours of presentation. We evaluated the ability of 8 biomarkers to rapidly exclude AMI at the point of presentation and investigated whether ‘triple marker’ testing represents the optimal multimarker strategy. Methods We recruited patients who presented to the ED with suspected cardiac chest pain occurring within 24 h. Blood was drawn at the time of presentation. Diagnostic value was assessed by calculating the area under the ROC curve (AUC) and a multivariate model was constructed by logistic regression. The primary outcome was a diagnosis of AMI, established by ≥12-h troponin testing in all patients. Results 705 included patients underwent venepuncture a median of 3.5 h after symptom onset. Heart fatty acid binding protein (H-FABP) had an AUC of 0.86 (95% CI 0.82–0.90), which was significantly higher than any other biomarker including cTnI. While no single biomarker could enable exclusion of AMI, multivariate analysis identified cTnI and H-FABP as the optimal biomarker combination. Combined with clinical risk stratification, this strategy had a sensitivity of 96.9%, specificity of 54.7%, PPV 32.4% and NPV 98.8%. Conclusions We have derived an algorithm that would enable AMI to be immediately excluded in 315 (44.7%) patients at the cost of missing 6 AMIs per 1000 patients treated. While the risk is likely to be unacceptable for clinical implementation, we have highlighted an area for future development using serial testing and increasingly sensitive assays.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>21561701</pmid><doi>10.1016/j.resuscitation.2011.03.015</doi><tpages>6</tpages></addata></record> |
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subjects | Acute coronary syndromes Acute myocardial infarction Acute-Phase Proteins Algorithms Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Bayes Theorem Biological and medical sciences Biomarkers - blood Brain natriuretic peptide Cardiology. Vascular system CK-MB Coronary heart disease Creatine Kinase, MB Form - blood d-Dimer Diagnosis Diagnosis, Differential Emergency Fatty Acid-Binding Proteins - blood Female Fibrin Fibrinogen Degradation Products - metabolism Heart Heart fatty acid binding protein Humans Intensive care medicine Lipocalin-2 Lipocalins - blood Logistic Models Male Medical sciences Middle Aged Myeloperoxidase Myocardial Infarction - blood Myoglobin Myoglobin - blood Natriuretic Peptide, Brain - blood Peroxidase - blood Prospective Studies Proto-Oncogene Proteins - blood Risk Assessment ROC Curve Sensitivity and Specificity Troponin I - blood Troponins |
title | A FABP-ulous ‘rule out’ strategy? Heart fatty acid binding protein and troponin for rapid exclusion of acute myocardial infarction |
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