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Clinical decision making in patients presenting to the Emergency Department with chest pain remains a challenge; while only 10% to 20% are ultimately diagnosed with acute myocardial infarction (AMI), it is important to not miss any patient with an AMI. The European Society of Cardiology (ESC) 0/1 algorithm allows rapid triage of chest pain patients based on the change in high-sensitivity cardiac troponin (hs-cTn) over the first hour after presentation, dividing patients into rule-out, observation and rule-in categories. However, there appears to be some variation in the accuracy of this approach across different population cohorts and there is little data on outcomes in the rule-out and observation categories. To better understand the accuracy and prognostic value of the ESC 0/1 algorithm globally, Chiang and colleagues1 performed a systematic review and meta-analysis that identified that 10 cohorts with over 11 000 patients -- about 18% were assigned to rule-in, 27% to observation and 55% to rule-out categories, depending on the specific c-Tn assay. The pooled sensitivity of the ESC 0/1 algorithm for AMI diagnosis was over 98% with a mortality rate in the rule-out category of only 0.1% (95% CI=0.0% to 0.4%) at 30 days and 0.8% (95% CI=0.5% to 1.2%) at 1 year. However, the mortality rate for patients in the observation group was 0.7% (95% CI=0.3% to 1.2%) at 30 days and increased to 8.1% (95% CI=6.1% to 10.4%) at 1 year, similar to the mortality rate in the rule-in group.
In an editorial, Chapman and Mills2 summarise these data (figure 1) and conclude: “While many emergency departments will already have implemented rapid rule-out pathways for acute myocardial infarction, some have not, particularly those in the USA. There is a plethora of data evaluating high-sensitivity troponin testing in patients with suspected acute coronary syndrome, including two prospective, randomised controlled trials, demonstrating very low rates of future myocardial infarction or death as far as 1 year after index presentation. It is time to take advantage of these strategies to reduce overcrowding, mitigate the associated risks of hospitalisation and prevent harm.”
Stopyra and colleagues3 compared two other rapid rule-out pathways for AMI in 5788 patients presenting to the emergency department at three sites in the USA. The History ECG Age Risk factor Troponin (HEART) Pathway classified 38% of patients as low-risk and only 0.4% of these low risk patient had a major adverse cardiac event (MACE) at 30 days; a negative predictive value of 99.6%. In comparison, the Emergency Department Assessment of Chest pain Score (EDACS) classified 58% of patient as low risk but the 30 day MACE in these patients was 1.0% yielding a slightly lower negative predictive value of 99.0%. (figure 2) The authors conclude: “EDACS identifies a larger proportion of patients as low-risk than the HEART Pathway, but has a higher missed major adverse cardiac events rate at 30 days.”
Professor Brody comments4 that “Crowding of our hospitals and emergency departments (EDs) is not a new issue, but the COVID-19 pandemic has now taken it to another level. The recent pressures highlight the importance of sparing vital inpatient resources for those who really need them.” Clearly we should use rapid triage approaches to the patient with chest pain but “Should you use the 1 hour algorithm, the High-Sensitivity Troponin in the Evaluation of patients with suspected Acute Coronary Syndrome (High-STEACS) algorithm or should you incorporate clinical features by adopting the HEART pathway or Emergency Department Assessment of Chest Pain (EDACS) decision aid?” While there is no simple answer to balancing accuracy vs efficiency, “It is also important to consider the patient’s perspective. There is evidence that patients who are allowed to engage in shared decision-making with their clinician are more likely to choose to leave the hospital without further investigations than those who receive standard, clinician-guided care.”
An additional challenge in patients presenting with chest pain is management of those who have a myocardial infarction but no obstructive coronary disease (MINOCA). In a series of 255 patients with MINOCA, Vago and colleagues5 report that cardiac magnetic resonance imaging (CMR) soon (at a mean of 2.7 days) after presentation was diagnostic in 86% -- myocarditis in 54%, myocardial infarction in 22%, and takotsubo cardiomyopathy in 10% . (figure 3) Furthermore, the patients with a normal CMR had a 4 year mortality of 0%.
A state-of-the art review article in this issue of Heart6 discusses the clinical role of advanced left ventricular imaging in adults with aortic stenosis and how parameters such as global longitudinal strain on echocardiography, late-gadolinium enhancement on CMR, exercise hemodynamics and serum biomarkers are being utilised in ongoing clinical trials of earlier intervention for aortic stenosis. Another review article by Shan and Pellikka7 discusses the distinctive characteristics of aortic stenosis in women and how these sex differences might impact diagnosis, management and clinical outcomes. (figure 4)
The Education in Heart article in this issue,8 outlines the causes and epidemiology of non-bacterial thrombotic endocarditis (NBTE), discusses the pathophysiology, and emphasises key principles in diagnosis and management. As the authors summarise: “NBTE is a rare condition associated with autoimmune disease, malignancy and hypercoagulable states, and characterised by sterile friable vegetations composed of fibrin and platelets with high risk of systemic embolism. Most patients are asymptomatic and the condition is commonly diagnosed at post-mortem. A high index of clinical suspicion is therefore required for diagnosis. Management requires differentiation of NBTE from infective endocarditis, definition of the underlying cause, assessment of valve lesions with echocardiography and prevention of systemic embolism by means of anticoagulant treatment. Surgery is rarely indicated, except in patients with haemodynamic compromise, valve failure or high risk of embolism.”
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication Not required.
Provenance and peer review Commissioned; internally peer reviewed.
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