Peter A Kavsak, Sameer Sharif, Craig Ainsworth, Jinhui Ma, Shawn E Mondoux, Dennis T Ko, Andrew Worster
{"title":"ALARRM: A laboratory approach for rapid risk-assessment for myocardial infarction.","authors":"Peter A Kavsak, Sameer Sharif, Craig Ainsworth, Jinhui Ma, Shawn E Mondoux, Dennis T Ko, Andrew Worster","doi":"10.1016/j.cca.2025.120630","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Current pathways using high-sensitivity cardiac troponin (hs-cTn) to rule in and rule out myocardial infarction (MI) are assay specific. This requires clinicians and laboratories to use the correct assay-specific cutoffs, deltas, and time between measurements for optimal decision making. To overcome these challenges, we developed a new common laboratory pathway (i.e., ALARRM: a laboratory approach for rapid risk-assessment for MI) to aid in early risk stratification for MI in the emergency department (ED) using the combined validated clinical chemistry score (CCS) and common change criteria (3C) algorithm. The objective of our study was to assess the diagnostic performance (sensitivity and specificity) and effectiveness (combination of rule out/low risk and rule in/high risk) of ALARRM.</p><p><strong>Methods: </strong>The study cohort (n = 855) consisted of patients presenting to the ED with acute coronary syndrome symptoms and had two blood samples collected three hours apart for measurement of Abbott hs-cTnI, Ortho hs-cTnI, Roche hs-cTnT, glucose, and creatinine (for the estimated glomerular filtration rate (eGFR) calculation). We also assessed the European society of cardiology (ESC) single sample assay-specific cutoffs with both ALARRM and ESC criteria being assessed for index MI in the cohort.</p><p><strong>Results: </strong>The sensitivity for MI using ALARRM was 100 % for all three assays, however this was not the case for the ESC single cutoffs where the Ortho hs-cTnI assay missed 4 MIs. The specificities in patients with serial measurements with ALARRM were > 90 %, with the overall effectiveness for ALARRM being 61 % (95 %CI: 58 to 64) for Roche, 80 % (95 %CI: 77 to 82) for Abbott, and 89 % (95 %CI: 86 to 91) for Ortho.</p><p><strong>Conclusion: </strong>The ALARRM pathway represents a highly efficacious and common approach using hs-cTn for early risk stratification for MI.</p>","PeriodicalId":10205,"journal":{"name":"Clinica Chimica Acta","volume":" ","pages":"120630"},"PeriodicalIF":2.9000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinica Chimica Acta","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.cca.2025.120630","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICAL LABORATORY TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Current pathways using high-sensitivity cardiac troponin (hs-cTn) to rule in and rule out myocardial infarction (MI) are assay specific. This requires clinicians and laboratories to use the correct assay-specific cutoffs, deltas, and time between measurements for optimal decision making. To overcome these challenges, we developed a new common laboratory pathway (i.e., ALARRM: a laboratory approach for rapid risk-assessment for MI) to aid in early risk stratification for MI in the emergency department (ED) using the combined validated clinical chemistry score (CCS) and common change criteria (3C) algorithm. The objective of our study was to assess the diagnostic performance (sensitivity and specificity) and effectiveness (combination of rule out/low risk and rule in/high risk) of ALARRM.
Methods: The study cohort (n = 855) consisted of patients presenting to the ED with acute coronary syndrome symptoms and had two blood samples collected three hours apart for measurement of Abbott hs-cTnI, Ortho hs-cTnI, Roche hs-cTnT, glucose, and creatinine (for the estimated glomerular filtration rate (eGFR) calculation). We also assessed the European society of cardiology (ESC) single sample assay-specific cutoffs with both ALARRM and ESC criteria being assessed for index MI in the cohort.
Results: The sensitivity for MI using ALARRM was 100 % for all three assays, however this was not the case for the ESC single cutoffs where the Ortho hs-cTnI assay missed 4 MIs. The specificities in patients with serial measurements with ALARRM were > 90 %, with the overall effectiveness for ALARRM being 61 % (95 %CI: 58 to 64) for Roche, 80 % (95 %CI: 77 to 82) for Abbott, and 89 % (95 %CI: 86 to 91) for Ortho.
Conclusion: The ALARRM pathway represents a highly efficacious and common approach using hs-cTn for early risk stratification for MI.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.