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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Veröffentlicht in:Resuscitation 2011-08, Vol.82 (8), p.1041-1046
Hauptverfasser: Body, Richard, McDowell, Garry, Carley, Simon, Wibberley, Christopher, Ferguson, Jamie, Mackway-Jones, Kevin
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container_end_page 1046
container_issue 8
container_start_page 1041
container_title Resuscitation
container_volume 82
creator Body, Richard
McDowell, Garry
Carley, Simon
Wibberley, Christopher
Ferguson, Jamie
Mackway-Jones, Kevin
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. 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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. 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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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