Two-Hour Algorithm for Triage toward Rule-Out and Rule-In of Acute Myocardial Infarction by Use of High-Sensitivity Cardiac Troponin I
The early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm that uses high-sensitivity cardiac troponin I (hs-cTnI). We prospectively enrolled 1435 (derivation cohort) and 1194 (external validation cohor...
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Published in | Clinical chemistry (Baltimore, Md.) Vol. 62; no. 3; pp. 494 - 504 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.03.2016
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Subjects | |
Online Access | Get full text |
ISSN | 0009-9147 1530-8561 |
DOI | 10.1373/clinchem.2015.249508 |
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Abstract | The early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm that uses high-sensitivity cardiac troponin I (hs-cTnI).
We prospectively enrolled 1435 (derivation cohort) and 1194 (external validation cohort) patients presenting with suspected AMI to the emergency department. The final diagnosis was adjudicated by 2 independent cardiologists. hs-cTnI was measured at presentation and after 2 h in a blinded fashion. We derived and validated a diagnostic algorithm incorporating hs-cTnI values at presentation and absolute changes within the first 2 h.
AMI was the final diagnosis in 17% of patients in the derivation and 13% in the validation cohort. The 2-h algorithm developed in the derivation cohort classified 56% of patients as rule-out, 17% as rule-in, and 27% as observation. Resulting diagnostic sensitivity and negative predictive value (NPV) were 99.2% and 99.8% for rule-out; specificity and positive predictive value (PPV) were 95.2% and 75.8% for rule-in. Applying the 2-h algorithm in the external validation cohort, 60% of patients were classified as rule-out, 13% as rule-in, and 27% as observation. Diagnostic sensitivity and NPV were 98.7% and 99.7% for rule-out; specificity and PPV were 97.4% and 82.2% for rule-in. Thirty-day survival was 100% for rule-out patients in both cohorts.
A simple algorithm incorporating hs-cTnI baseline values and absolute 2-h changes allowed a triage toward safe rule-out or accurate rule-in of AMI in the majority of patients. |
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AbstractList | The early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm that uses high-sensitivity cardiac troponin I (hs-cTnI). We prospectively enrolled 1435 (derivation cohort) and 1194 (external validation cohort) patients presenting with suspected AMI to the emergency department. The final diagnosis was adjudicated by 2 independent cardiologists. hs-cTnI was measured at presentation and after2hinablinded fashion. We derived and validated a diagnostic algorithm incorporating hscTnI values at presentation and absolute changes within the first 2 h. AMI was the final diagnosis in 17% of patients in the derivation and 13% in the validation cohort. The 2-h algorithm developed in the derivation cohort classified 56% of patients as rule-out, 17% as rule-in, and 27% as observation. Resulting diagnostic sensitivity and negative predictive value (NPV) were 99.2% and 99.8% for rule-out; specificity and positive predictive value (PPV) were 95.2% and 75.8% for rule-in. Applying the 2-h algorithm in the external validation cohort, 60% of patients were classified as rule-out, 13% as rule-in, and 27% as observation. Diagnostic sensitivity and NPV were 98.7% and 99.7% for rule-out; specificity and PPV were 97.4% and 82.2% for rule-in. Thirty-day survival was 100% for rule-out patients in both cohorts. A simple algorithm incorporating hs-cTnI baseline values and absolute 2-h changes allowed a triage toward safe rule-out or accurate rule-in of AMI in the majority of patients. BACKGROUNDThe early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm that uses high-sensitivity cardiac troponin I (hs-cTnI).METHODSWe prospectively enrolled 1435 (derivation cohort) and 1194 (external validation cohort) patients presenting with suspected AMI to the emergency department. The final diagnosis was adjudicated by 2 independent cardiologists. hs-cTnI was measured at presentation and after 2 h in a blinded fashion. We derived and validated a diagnostic algorithm incorporating hs-cTnI values at presentation and absolute changes within the first 2 h.RESULTSAMI was the final diagnosis in 17% of patients in the derivation and 13% in the validation cohort. The 2-h algorithm developed in the derivation cohort classified 56% of patients as rule-out, 17% as rule-in, and 27% as observation. Resulting diagnostic sensitivity and negative predictive value (NPV) were 99.2% and 99.8% for rule-out; specificity and positive predictive value (PPV) were 95.2% and 75.8% for rule-in. Applying the 2-h algorithm in the external validation cohort, 60% of patients were classified as rule-out, 13% as rule-in, and 27% as observation. Diagnostic sensitivity and NPV were 98.7% and 99.7% for rule-out; specificity and PPV were 97.4% and 82.2% for rule-in. Thirty-day survival was 100% for rule-out patients in both cohorts.CONCLUSIONSA simple algorithm incorporating hs-cTnI baseline values and absolute 2-h changes allowed a triage toward safe rule-out or accurate rule-in of AMI in the majority of patients. The early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm that uses high-sensitivity cardiac troponin I (hs-cTnI). We prospectively enrolled 1435 (derivation cohort) and 1194 (external validation cohort) patients presenting with suspected AMI to the emergency department. The final diagnosis was adjudicated by 2 independent cardiologists. hs-cTnI was measured at presentation and after 2 h in a blinded fashion. We derived and validated a diagnostic algorithm incorporating hs-cTnI values at presentation and absolute changes within the first 2 h. AMI was the final diagnosis in 17% of patients in the derivation and 13% in the validation cohort. The 2-h algorithm developed in the derivation cohort classified 56% of patients as rule-out, 17% as rule-in, and 27% as observation. Resulting diagnostic sensitivity and negative predictive value (NPV) were 99.2% and 99.8% for rule-out; specificity and positive predictive value (PPV) were 95.2% and 75.8% for rule-in. Applying the 2-h algorithm in the external validation cohort, 60% of patients were classified as rule-out, 13% as rule-in, and 27% as observation. Diagnostic sensitivity and NPV were 98.7% and 99.7% for rule-out; specificity and PPV were 97.4% and 82.2% for rule-in. Thirty-day survival was 100% for rule-out patients in both cohorts. A simple algorithm incorporating hs-cTnI baseline values and absolute 2-h changes allowed a triage toward safe rule-out or accurate rule-in of AMI in the majority of patients. |
Author | Cullen, Louise Parsonage, William A Rubini Gimenez, Maria Boeddinghaus, Jasper Mueller, Christian Reichlin, Tobias Than, Martin Nestelberger, Thomas Rentsch, Katharina Hawkins, Tracey Puelacher, Christian Kern, Vera Greenslade, Jaimi H Wildi, Karin Grimm, Karin Hammett, Christopher Pickering, John W Aldous, Sally Twerenbold, Raphael |
Author_xml | – sequence: 1 givenname: Jasper surname: Boeddinghaus fullname: Boeddinghaus, Jasper organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and, Department of Internal Medicine, University Hospital Basel, Basel, Switzerland – sequence: 2 givenname: Tobias surname: Reichlin fullname: Reichlin, Tobias organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and – sequence: 3 givenname: Louise surname: Cullen fullname: Cullen, Louise organization: Department of Emergency Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia, School of Public Health, The Queensland University of Technology, Brisbane, Australia – sequence: 4 givenname: Jaimi H surname: Greenslade fullname: Greenslade, Jaimi H organization: Department of Emergency Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia, School of Public Health, The Queensland University of Technology, Brisbane, Australia – sequence: 5 givenname: William A surname: Parsonage fullname: Parsonage, William A organization: School of Public Health, The Queensland University of Technology, Brisbane, Australia, School of Medicine, The University of Queensland, Brisbane, Australia – sequence: 6 givenname: Christopher surname: Hammett fullname: Hammett, Christopher organization: School of Medicine, The University of Queensland, Brisbane, Australia – sequence: 7 givenname: John W surname: Pickering fullname: Pickering, John W organization: Department of Medicine, University of Otago, Christchurch, New Zealand, Emergency Department, Christchurch Hospital, Christchurch, New Zealand – sequence: 8 givenname: Tracey surname: Hawkins fullname: Hawkins, Tracey organization: Department of Emergency Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia, School of Public Health, The Queensland University of Technology, Brisbane, Australia – sequence: 9 givenname: Sally surname: Aldous fullname: Aldous, Sally organization: Emergency Department, Christchurch Hospital, Christchurch, New Zealand – sequence: 10 givenname: Raphael surname: Twerenbold fullname: Twerenbold, Raphael organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and – sequence: 11 givenname: Karin surname: Wildi fullname: Wildi, Karin organization: Cardiovascular Research Institute Basel (CRIB) – sequence: 12 givenname: Thomas surname: Nestelberger fullname: Nestelberger, Thomas organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and, Department of Internal Medicine, University Hospital Basel, Basel, Switzerland – sequence: 13 givenname: Karin surname: Grimm fullname: Grimm, Karin organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and, Department of Internal Medicine, University Hospital Basel, Basel, Switzerland – sequence: 14 givenname: Maria surname: Rubini Gimenez fullname: Rubini Gimenez, Maria organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and – sequence: 15 givenname: Christian surname: Puelacher fullname: Puelacher, Christian organization: Cardiovascular Research Institute Basel (CRIB) – sequence: 16 givenname: Vera surname: Kern fullname: Kern, Vera organization: Cardiovascular Research Institute Basel (CRIB) – sequence: 17 givenname: Katharina surname: Rentsch fullname: Rentsch, Katharina organization: Laboratory Medicine, University Hospital Basel, Basel, Switzerland – sequence: 18 givenname: Martin surname: Than fullname: Than, Martin organization: Emergency Department, Christchurch Hospital, Christchurch, New Zealand – sequence: 19 givenname: Christian surname: Mueller fullname: Mueller, Christian organization: Cardiovascular Research Institute Basel (CRIB), Department of Cardiology, and |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26797687$$D View this record in MEDLINE/PubMed |
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Snippet | The early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h algorithm... BACKGROUNDThe early triage of patients toward rule-out and rule-in of acute myocardial infarction (AMI) is challenging. Therefore, we aimed to develop a 2-h... |
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SubjectTerms | Accuracy Acute coronary syndromes Algorithms Cardiovascular disease Clinical medicine Female Funding Heart attacks Hospitals Humans Hypothesis testing Laboratories Limit of Detection Male Middle Aged Myocardial infarction Myocardial Infarction - blood Myocardial Infarction - mortality Pain Predictive Value of Tests Prospective Studies Studies Time Factors Troponin I - blood |
Title | Two-Hour Algorithm for Triage toward Rule-Out and Rule-In of Acute Myocardial Infarction by Use of High-Sensitivity Cardiac Troponin I |
URI | https://www.ncbi.nlm.nih.gov/pubmed/26797687 https://www.proquest.com/docview/1770388662 https://www.proquest.com/docview/1768564479 |
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