2025 SIRM／SIC共识 文件：急性性胸痛患者的管理

SIRM/SIC consensus document on the management of patients with acute chest pain

Antonio Esposito ${ }^{1}$ . Riccardo Faletti ${ }^{2}$ . Anna Palmisano ${ }^{1}$ . Marco Gatti ${ }^{2}$ . Sara Settun ${ }^{3}$ . Cesare Mantini ${ }^{4}$ .Piergiuseppe Agostoni ${ }^{5}$ . Daniele Andreini ${ }^{6}$ . Francesco Barilla ${ }^{7}$ . Andrea Barison ${ }^{89}$ . Paolo Calabr ${ }^{10,11}$ .Matteo Cameli ${ }^{12}$ . Scipione Carerj ${ }^{13}$ . Carlo Catalano ${ }^{14}$ . Marcello Chiocchi ${ }^{15}$ . Marco Ticheo Ciccone ${ }^{16}$ .

Matteo Cameli12·Scipione Carerj13·Carlo Catalano14·Marcello Chiocchi15·Marco Matteo Ciccone16.

Antonio Curcio ${ }^{17}$ . Fabrizio D'Ascenzo ${ }^{18,19}$ . Serena Dell'Aversana ${ }^{20}$ . Fabio Falzea ${ }^{21}$ . Marco Francone ${ }^{22,47}$ .

Nicola Galea14. Andrea Giovagnoni23. Marco Guglielmo24. Andrea Laghi25. Carlo Liguia26. Luigi Lovato27.

Riccardo Marano28.Rocco Antonio Montone29,30. Doralisa Morrone31, Luigi Natale32.Savina Nodari33.

Michele Oppizzi ${ }^{34}$ . Stefania Paolillo ${ }^{35}$ .Alberto Polimeniro ${ }^{17,36}$ .Gianluca Pontone ${ }^{37}$ . Italo Porto 38.

Silvia Pradella $^{39}$ . Vincenzo Russo $^{40}$ . Vincenzo Russo $^{27}$ . Luca Saba $^{41}$ . Gianfranco Sinagra $^{42}$ . Massimo Slavich $^{43}$ .

Carmen Spacarotella35· Davide Tore44· Davide Vignale1· Carmine Dario Vizza45· Saverio Muscoli46·

Pasquale Perrone Filardi ${ }^{35}$ . Ciro Indolfi ${ }^{17}$

© The Author(s) 2025

Abstract

Acute chest pain is a common and challenging reason for emergency department visits and requires prompt and systematic evaluation to address potential life-threatening conditions, minimize risks and manage emergency department overcrowding.This updated consensus statement outlines the appropriate management of patients presenting to the emergency department with acute chest pain, emphasizing the timing and utility of non-invasive advanced imaging(particularly coronary computed tomography angiography) aiming to improve rapid and accurate diagnosis of both cardiac or non-cardiac causes improving patient safety, outcomes, and resource utilization efficiency. The writing committee was composed of members and experts from both the Italian Society of Cardiology(SIC) and the Italian Society of Medical and Interventional Radiology(SIRM)who worked jointly to create a cohesive approach in the field of acute chest pain. This structured approach may streamline diagnostic workflows in the emergency setting and support earlier, more appropriate patient management.

Keywords Acute chest pain· Acute coronary syndrome· Coronary Computed Tomography Angiography (CCTA)·Cardiac Magnetic Resonance (CMR)· Emergency department· Consensus statement

Abbreviations

AAS Acute aortic syndrome

ACP,Acute chest pain

ACS Acute coronary syndrome

AD Aortic dissection

AMI Acute myocardial infarction

CAD Coronary artery disease

CCTA Coronary computed tomography angiography

CMR Cardiac magnetic resonance

CXR Chest radiography

CTPA Computed tomography pulmonary

angiography

ECG Electrocardiogram

ECV Extracellular volume

ED Emergency department

hs-cTnI High-sensitivity cardiac troponin I

hs-cTnT High-sensitivity cardiac troponin T

ICA Invasive coronary angiography

LCE Late contrast enhancement

LIE Late iodine enhancement

MINOCAe Acute myocardial infarction with non-obstructive coronary arteries

NSTEMI Non-ST-Elevation myocardial infarction

PE Pulmonary embolism

PET Positron emission tomography

SPECT Single photon emission computed

tomography

STEMI ST-elevation myocardial infarction

TTE Transthoracic echocardiography

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|TRO|Triple rule out| |---|---| |UA|Unstable angina|

Introduction

Acute chest pain(ACP) is one of the most frequent causes of emergency department(ED) admissions and represents a clinically challenging condition. ACP can be the symptom of life-threatening pathophysiological processes requiring immediate intervention, as well as the expression of a minor clinical conditions, sometimes exacerbated by psychologi-cal factors such as stress or anxiety. Therefore, patients pre-senting with ACP should never be underestimated and must receive immediate attention. At the same time, a rational approach is essential to avoid unnecessary risks and prevent ED overcrowding, as widely documented, taking advan-tage of new technologies and modern clinical-diagnostic approaches to achieve maximum efficiency[1]. The need for a unified clinical-diagnostic pathway among specialists creation of this document. Developed collaboratively by the Italian Society of Cardiology(SIC) and the Italian Society of Medical and Interventional Radiology(SIRM), this docu-ment focuses on defining diagnostic pathways, with particu-lar emphasis on non-invasive imaging techniques.

The sections regarding the clinical evaluation of a patient with ACP and the first- and second-line diagnostic exams are available as supplementary data.

Definition, epidemiology, and etiologies of ACP

ACP is defined as non-traumatic chest pain of new onset or acutely changed in its pattern of onset, intensity, or dura-tion. The term“ACP” refers to a broad range of thoracic symptoms, including true precordial pain or sensations such as pressure, tightness, heaviness, crushing, or burn-ing. These sensations may also occur outside the chest and radiate to other areas of the body, such as the shoulder, arm,neck, upper abdomen, or jaw. ACP represents approximately 8-10% of annual ED admissions among patients aged over 18 years old, with roughly 5% of these caused by acute coro-nary syndrome(ACS)[2]. Therefore, in most cases, ACP originates from non-cardiac causes, while about 15% of cases remain undiagnosed [3]. It has been estimated that more than one-fifth of medico-legal expenses are related to the inappropriate discharge of patients with ACS from EDs.Thus, an accurate assessment of ACP is essential to stratify the risk of ACS, a condition that can be life-threatening for the patient. While clinical presentation, electrocardiographic findings, and cardiac necrosis markers can sometimes

<EndOfPara>provide diagnostic confirmation of acute myocardial infarc-tion(AMI), they are sometimes insufficient to distinguish ACS from the many potential cardiac or non-cardiac etiolo-gies of ACP.

Preliminary assessment of patients with ACP

History,pain characteristics,and clinical examination

The initial clinical evaluation of a patient with ACP should focus on the rapid identification and treatment of poten-tially life-threatening conditions such as ACS, aortic dis-section(AD), pulmonary embolism(PE) and infarct-like myocarditis.

Symptoms described as chest pressure, tightness, heavi-ness, or burning should be considered indicative of ACS(Fig. 1). In cases of ACS, the pain may also manifest in other areas of the body, such as the shoulder, arm, neck,back, upper abdomen, or jaw. Other potentially associated symptoms include dyspnea, nausea, vomiting, sweating,fatigue, or altered mental status, which can sometimes be the main presenting symptom. Conversely, symptoms described as hyperacute, fleeting, related to inspiration(pleuritic) or position, or localized to a single point are unlikely related to myocardial ischemia. Chest pain is traditionally classified as "typical" or "atypical." However, according to the 2021 international guidelines from the AHA/ACC/ASE/CHEST/SAEM/SCCT/SCM [2], it is now preferable to use the terms“cardiac,” “possibly cardiac,” and “non-cardiac” to describe the likely cause of chest pain. Chest pain should be consid-ered stable when symptoms are chronic and associated with identifiable triggers such as physical exertion or emotional stress. The clinical assessment should include a detailed description of chest pain and related symptoms, including their onset, duration, location, radiation, and alleviating or exacerbating factors. Additionally, a complete evaluation of cardiovascular risk factors and the patient's medical history should supplement the symptom analysis. Any results from previous diagnostic tests for coronary artery disease (CAD)should also be reviewed.

The clinical assessment should aim to identify signs asso-ciated with a high-risk of morbidity and mortality, such as:

● signs of reduced cardiac output,(e.g., tachycardia, hypo-tension, cold extremities, low urine output, altered men-tal status)

● signs of heart failure(e.g., pulmonary edema, elevated jugular venous pressure, peripheral edema)

● new onset of a new systolic murmur suggestive of acute mitral regurgitation or a ventricular septal defect

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Acute Chest Pain Characteristics

 Fig.1 Acute Chest Pain Characteristics

Signs suggesting alternative etiologies to ACS include:

● fever(endocarditis or pneumonia)

● differential blood pressure between pulses(aortic dissec-tion)

● pulmonary abnormalities detected on auscultation or chest X-ray(pneumonia or pneumothorax)

● pericardial friction rub(pericarditis)

or other cardiac murmurs(e.g., aortic stenosis, endocar-ditis).

Electrocardiogram(ECG)

Electrocardiogram(ECG) is a cornerstone of the initial assessment and management of patients presenting with ACP. For patients with suspected ACS, an ECG should be performed and interpreted as soon as possible[2].

The ECG must be promptly analyzed to identify signs of acute infarction or ischemia. If such signs are present,further management should proceed according to current guidelines for ST-elevation myocardial infarction(STEMI)or non-ST- elevation ACS(NSTE-ACS), which includes non-ST-elevation myocardial infarction(NSTEMI) and unstable angina(UA). Patients with non-ischemic ECG pat-terns should undergo a clinical decision pathway based on additional evaluations.

ECGs can be classified into three categories(Fig. 2):

(1) STEMI or STEMI-equivalent

(2) Ischemic ST-segment or T-wave abnormalities

(3) Non-ischemic patterns, which include normal ECGs,non-specific findings, left ventricular hypertrophy(with or without ST-T segment changes), left or right bundle branch block, or ventricular paced rhythm that do not meet the Sgarbossa criteria[4] or modified Sgarbossa criteria[5] for AMI.

In the setting of UA/NSTEMI:(1) UA diagnosis is based on the presence of new, worsening, resting chest pain or occurring with minimal exertion without any elevation in biomarkers indicating myocardial injury or necrosis.(2) The presence of ECG abnormalities increases the diagnostic probability; however, ECG changes may be completely absent in more than one-third of patients with NSTEMI.(3) The prognostic value of T-wave inversions is lower compared to ST-segment depression. ST-segment depression also serves as a quantitative prognostic marker of risk(number of leads used and severity of ST-segment depression).

In patients with STEMI, the sum of ST-segment eleva-tions across all leads(ESTE) is a clinical marker of ischemic myocardium and myocardium-at-risk.

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 Fig.2 Classification and ECG Criteria in Patients with Acute Coro-nary Syndrome. Panel A. This panel illustrates the classification of acute coronary syndromes(ACS) based on ECG changes, cardiac biomarkers, and the extent of myocardial injury. Patients with unsta-ble angina or NSTEMI may present with ST-segment depression or T-wave inversion on ECG, though the ECG may appear normal or with nonspecific ST-T changes. In NSTEMI, elevated high-sativit-ity cardiac troponins(hs-cTnT or hs-cTnI) indicate subendocardial infarction, typically caused by partial coronary occlusion. STEMI is characterized by ST-segment elevation and transmural infarction due to complete coronary occlusion. Elevated hs-cTn refers to val-ues above the 99th percentile of the upper reference limit. Panel B.ECG examples illustrating the original and Smith-modified Sgarbossa

criteria for AMI in left bundle branch block(LBBB) or ventricu-lar-paced rhythms. The left illustration shows concordant ST eleva-tion≥1 mm in leads with a positive QRS complex; the middle illus-tration shows excessively discordant ST elevation≥5 mm (original criterion) or ≥25% of the depth of the preceding S-wave (Smith-mod-ified criterion) in leads with a predominantly negative QRS complex;and the right illustration shows concordant ST depression≥1 mm in leads V1-V3. Abbreviations AMI, acute myocardial infarction; ACS,acute coronary syndrome; ECG, electrocardiogram; hs-cTn, high-sen-sitivity cardiac troponin; LBBB, left bundle branch block; NSTEMI,non-ST-segment elevation myocardial infarction; STEMI, ST- seg-ment elevation myocardial infarction

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Troponins

High-sensitivity cardiac troponin T(hs-cTnT) and high-sensi-tivity cardiac troponin I(hs-cTnI) are the preferred serum bio-markers for evaluating patients with suspected ACS. Troponin concentrations should be reported as whole numbers in nano-grams per liter (ng/L). Sex-specific 99th percentile cut-offs are recommended to increase diagnostic sensitivity in women and specificity in men. Serial measurement using 0h/1h or 0h/2h algorithms are recommended for timely rule-in and rule-out [6].

1st level imaging: chest X-ray and echocardiography

Both chest X-ray and echocardiography are low cost and widely available first level imaging modalities that provides very useful information in patients with ACP able to help the differential diagnosis, to detect signs with prognostic value and to guide the patient's management. A description about the role of chest X-ray and echocardiography in the setting of ACP is reported in the supplementary materials(supplementary 3.4.1 and 3.4.2, respectively).

Risk stratification using clinical and laboratory data-based algorithms

The pre-test probability assessment, combined with the calculation of risk scores, are critical elements in evaluat-ing ACP patients. For instance, in the setting of suspected angina, the ESC guidelines recommend an assessment of pre-test probability of CAD, based on age, sex, and pain characteristics [7]. The kind of pain and any associated ges-turing (Levine sign) can guide clinicians in formulating a diagnostic hypothesis. However, these are just probability estimates based on very simple criteria; therefore, even a high pre-test probability of CAD does not necessarily mean that CAD is the cause of the patient's symptoms and ED access, and vice-versa in the case of low pre-test probabil-ity. The chest pain score aims to facilitate the differentia-tion between ischemic and non-ischemic chest pain [8]. A description of most used scores is reported in the supple-mentary materials (supplementary 4.1) and supplementary Table 1 (Table S1).

2nd level imaging: coronary CT angiography, cardiac magnetic resonance,stress imaging

Technological and methodological advances have made coronary CT angiography(CCTA) the clinical reference standard for ruling-out obstructive CAD. Hence, CCTA

<EndOfPara>is considered a safe and effective diagnostic tool highly recommended in patients with low-to-intermediate risk ACP and normal troponins/ECG, allowing to reduce hospital stay and costs. Moreover, CCTA, eventually integrated with emerging advanced scanning techniques like late contrast enhancement CT and stress-CT perfu-sion, plays a growing role in managing"troponinos,"preventing unnecessary catheterizations and improving differential diagnosis. This CCTA complementary role is particularly important in the current high-sensitivity troponins(hs-cTn) era, because the wide adoption of hs-cTn has improved sensitivity in the diagnosis of ACS, but also increases false positives, making CCTA a valuable complementary tool to reduce unnecessary catheteriza-tion. Emerging CCTA techniques like FFR-CT and CT-perfusion show promise but require further clinical vali-dation. Cardiac magnetic resonance(CMR) represents the reference imaging technique for myocardial tissue characterization, useful for distinguishing ischemic from non-ischemic damage. Its limited availability makes it an imaging modality poorly used in the emergency setting,but it plays a fundamental role for a temporally deferred evaluation aimed to reveal the nature and the extension of myocardial injury in selected patients. Advanced CMR techniques(mapping) help in providing more precise diag-nosis. Stress Imaging could be indicated for intermediate-risk patients without ECG changes and normal troponin levels. It includes stress-echocardiography, SPECT,PET,and stress CMR. While CCTA has largely replaced these tests, functional imaging remains valuable in specific cases with technical limitations or contrast agent allergies. A more extensive discussion of second-level techniques in the context of ACP can be found in the supplementary materials(supplementary 5.1, 5.2 and 5.3).

Clinical-diagnostic pathways for patients with ACP

Risk classification in ACS

Based on the initial ECG and markers of myocardial necrosis, patients with suspected ACS are categorized as follows:

● Patients with ACP(or equivalent symptoms) and per-sistent ST-segment elevation(or equivalent ST-segment elevation patterns) on ECG: STEMI.

● Patients with ACP(or equivalent symptoms) but without persistent ST-segment elevation(or equivalent ST- seg-ment elevation patterns) on ECG, with elevated and/or

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decreased cTn levels, with at least one value above the 99th percentile of the upper reference limit: NSTEMI.

● Patients with ACP in the absence of signs of acute car-diomyocyte damage/necrosis, accompanied by specific clinical symptoms: prolonged angina(>20 min) at rest;new-onset severe angina; increasing frequency or dura-tion of angina, or angina occurring with minimal exer-tion; or angina occurring after a recent AMI: unstable angina.

STEMI and high/very high-risk NSTEMI

Within the setting of ACP, prompt and accurate identifica-tion of high-risk patients is crucial, as missed diagnoses and inappropriate discharges have been linked to a high mor-tality rate(2-4%). It is essential to promptly identify ACS patients and establish different pathways for NSTEMI and STEMI. An initial evaluation should consider the patient's risk factors, as suggested by the latest ESC guidelines[7].The likelihood that ACP has cardiac origin increases in the presence of multiple risk factors, such as a family history of premature cardiovascular atherosclerotic disease, famil-ial hypercholesterolemia, smoking, hypertension, diabetes mellitus, dyslipidemia, obesity, and kidney failure. Based on these cardiovascular risk factors, patients can already be classified into high and low-risk categories. The risk assess-ment and initial ECG findings will guide the rapid referral of STEMI patients or high/very high-risk NSTEMI patients for revascularization(Table 1). As suggested by international guidelines[7], it is essential to minimize delays and ensure the ideal time intervals for diagnosis and revascularization.The AHA/ACC consensus document outlines all recom-mendations for managing patients with ACP and suspected ACS[2]. For STEMI patients, revascularization should be

Table 1 Criteria for High-Risk and Very High-Risk NSTEMI

Very-High-Risk NSTEMI

Hemodynamic instability or cardiogenic shock

Recurrent/ongoing chest pain refractory to medical therapy

Cardiac arrest after presentation or life-threatening arrhythmias

Mechanical complications

Acute heart failure due to ongoing ischemia

Recurrent dynamic ECG changes suggestive of ischemia, especially intermittent ST-segment elevation

High-Risk NSTEMI

NSTEMI confirmed by recommended hs-cTn algorithms

Dynamic ST-segment and T-wave changes

Transient ST-segment elevation

GRACE risk score> 140

performed as soon as possible[7]. Specifically, immediate primary percutaneous coronary intervention is highly rec-ommended for patients with symptom onset within 12 hours and should be performed within 60 minutes in centers with 24/7 interventional cardiology service and within 90 min-utes for patients admitted to spoke centers or transported by ambulance. For NSTEMI patients with any high-risk fea-tures, an early invasive strategy(within 24 hours) should be considered, including invasive coronary angiography(ICA)with possible angioplasty within 24 hours of diagnosis[7].

For NSTEMI patients requiring the exclusion of obstruc-tive CAD,CT may play a role only if the local organizational model allows CCTA to be available before ICA, without causing delays in the angiography itself. In an organizational model with prompt availability of CCTA, CCTA can be per-formed before ICA to reduce the number of unnecessary catheterizations.

The setting of presumptive diagnosis of Acute Aortic Syndrome(AAS) and Pulmonary Embolism(PE) is reported in the supplementary materials(supplementary 6.2.1).

Non-high risk and uncertain diagnosis

The term“non-high risk” refers to patients who do not show clear signs of AMI or hemodynamic instability and who have a low-to-intermediate probability of ACS[7,9]. This category includes patients with ACP of possible cardiac origin but without a definitive clinical, electrocar-diographic, or laboratory diagnosis of ACS[10, 11]. These patients are often diagnosed with conditions like acute myo-carditis, Takotsub syndrome, or, less commonly, an acute presentation of an unrecognized non-ischemic cardiomyo-pathy. However, a variable percentage of these patients may have ACS without the characteristics of high-risk STEMI or NSTEMI. In such cases, a preliminary evaluation using CCTA can be a valid alternative to immediate ICA[9].Comprehensive clinical assessment, including evaluation of diabetes status and duration, is essential, as long-standing diabetes(over 10 years) is associated with a high likelihood of significant coronary calcifications, which could reduce the accuracy of CCTA[12].

This information, combined with local factors such as the type of CT scanner available and the expertise of car-diovascular radiologists in interpreting CCTAs, can influ-ence the decision to use CT in the diagnostic workup of a patient with more than 10 years of history of diabetes and ACP. In patients with ACP and low-to-intermediate risk but with unknown CAD, CCTA plays a critical role in ruling out obstructive CAD(stenosis>50%) and in characterizing the atherosclerotic coronary substrate[9]. A diagnostic strategy involving CCTA within 24 hours(preferably within 8 hours to optimize ED workflow and patient experience) provides non-invasive access to coronary anatomical assessment,

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 Fig.3 Clinical Cases of Acute Chest Pain. Panel A: Imaging findings of acute infarct-like myocarditis in a 20-year-old male. The first three images(top row) are curved multiplanar reconstructions(cMPRs)of the left anterior descending, circumflex, and right coronary arter-ies from coronary computed tomography angiography(CCTA), all showing no obstructive coronary disease. The fourth image on the top row is a short-axis late iodine enhancement(LIE) reconstruc-tion highlighting subepicardial enhancement in the inferolateral wall,suggestive of myocardial injury. The bottom row depicts the corre-sponding cardiovascular magnetic resonance(CMR) findings: short-axis T2 short-tau inversion-recovery(T2-STIR) image demonstrating regional myocardial edema; color-coded quantitative T2 map show-ing increased T2 values; color-coded native T1 map showing elevated native T1; and late gadolinium enhancement(LGE) image confirm-ing subepicardial necrosis in the same distribution. Panel B: Imag-ing findings of myocardial infarction with non-obstructive coronary arteries(MINOCA) in a 36-year-old male. The top row presents two cardiac phases(diastolic and systolic) of short-axis cine steady-state free precession(cine-SSFP) illustrating akinesia of the basal-infero-lateral wall, followed by a quantitative T2 map. The T2 map shows a central hypo-intense core consistent with intramyocardial hemor-rhage, surrounded by a rim of increased T2 values indicating myo-cardial edema. The bottom row depicts short-axis T2 short-tau inversion-recovery(T2-STIR) image confirming myocardial edema with a central dark zone(hemorrhage); late gadolinium enhancement(LGE) image demonstrating a transmural enhancement pattern with a central hypo-enhanced region of microvascular obstruction; and a native T1 map showing elevated T1 values within the infarcted myo-cardium. Panel C: Imaging findings of reverse Takotsubo cardiomyo-

including the detection of coronary anomalies. CCTA is highly sensitive for both diagnosing obstructive CAD and detecting non- obstructive CAD, which can guide optimized clinical management after the acute phase(Fig. 3). The

pathy in a 40-year-old female. The top row shows curved multipla-nar reconstructions(cMPRs) of the left anterior descending(LAD),left circumflex(LCx), and right coronary arteries(RCA) from coro-nary computed tomography angiography(CCTA), all demonstrat-ing patent, non-obstructive coronaries, followed by a left-ventricular long-axis T2 short-tau inversion-recovery(T2-STIR) image depicting diffuse myocardial edema that predominates in the basal segments.The bottom row includes diastolic and systolic three-dimensional blood-pool volume-rendered models illustrating basal akinesia with compensatory apical hyperkinesia; a long-axis late iodine enhance-ment(LIE)/late gadolinium enhancement(LGE) image showing no evidence of myocardial necrosis. Panel D: Imaging findings of non-ST-elevation myocardial infarction(NSTEMI) in a 44-year-old male(peak high-sensitivity troponin T: 287 ng/L). The top row depicts curved multiplanar reconstructions(cMPRs) of the left ante-rior descending(LAD), left circumflex(LCx), and right coronary arteries(RCA) from coronary computed tomography angiography(CCTA). A mixed-attenuation plaque with ulceration causing severe stenosis is evident in the proximal LAD, whereas the LCx and RCA are free of significant disease. The bottom row shows two short-axis(basal and mid-ventricular) and one long-axis late iodine enhance-ment(LIE) images. All demonstrate absence of LIE, indicating no established myocardial necrosis despite the culprit LAD lesion.Abbreviations cMPRs, Curved multiplanar reconstructions; CCTA,Coronary Computed Tomography Angiography; LIE, Late Iodine Enhancement; STIR, Short-TI Inversion Recovery; LGE, Late gado-linium enhancement; MINOCA, Myocardial Infarction with Non-Obstructive Coronary Arteries; SSFP, Steady-state free precession;NSTEMI: Non-ST- elevation myocardial infarction

CCTA use in the ED also allows the exclusion of alterna-tive diagnoses(such as AD or PE), which can sometimes be unexpected. Additionally, when integrated with a multipara-metric approach, including a LCE/LIE scan, CCTA allows

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not only a rapid rule-out of significant CAD or identification of patients who need revascularization but also a prompt dif-ferential diagnosis such as myocarditis, MINOCA, or acute cardiomyopathies, all within a“one-stop-shop” approach[13] (Fig. 3). However, the interpretation of LCE/LIE still requires considerable expertise[14], awaiting the broader availability of CT scanners with spectral cardiac imaging capabilities, which could significantly improve LCE/LIE quality and contrast-to-noise ratios. In patients with non-obstructive CAD or normal coronary arteries, the use of CCTA is likely to facilitate early discharge and prevent unnecessary ICA. A more extensive discussion can be found in the supplementary materials(supplementary 5.1).

Low risk of CAD and presumptive diagnosis of peri-myocarditis or myo-pericarditis

Patients presenting with low-risk ACP(negative ECG for ischemic changes, negative cTn levels, and resolved chest pain) but with known or suspected CAD based on clinical evaluation or pre-test probability scores may be discharged with a recommendation for short-term functional or ana-tomical imaging tests[5, 9]. Both strategies demonstrate high negative predictive value for the diagnosis of ischemia(functional imaging tests: stress echocardiography[15],SPECT[16], stress CMR[17] and obstructive CCTA[18]).However, in patients without previous anatomical coronary studies(invasive or non-invasive), CCTA is preferable to functional imaging strategies because it can also identify non-obstructive CAD. This enables better prognostic strati-fication and optimization of therapeutic approaches, posi-tively impacting on long term outcomes[19].

Patients with ACP and no ECG signs suggestive of ischemic changes represent a significant subset of patients with troponin dispersion[20]. In these cases, troponin eleva-tion may be due to various cardiac or non-cardiac causes.Based on the enzyme curve, these patients can be classi-fied as having acute or chronic myocardial injury[21]. For patients with acute myocardial injury, even in the absence of ECG ischemic criteria, it is recommended to rule out obstructive CAD, preferably using CCTA[22, 23]. If the test is negative, CMR is recommended either during hospi-talization or with short- term priority to identify myocardial causes of acute troponin dispersion, such as stress cardio-myopathy[24], MINOCA[25], or acute myocarditis[26](Fig. 3). CMR should be performed as soon as possible, as its diagnostic sensitivity decreases over time, in the days or weeks after the acute event[27].

As previously mentioned, recent studies have proposed CCTA with LCE/LIE as a valid alternative to CMR, capa-ble of providing all necessary information in a single exam

[28], thereby improving organizational efficiency and patient safety.

For patients with chronic myocardial injury,CAD evalu-ation can follow the timing used for low-risk patients. In cases with suspected dilated, inflammatory, infiltrative, or hypertrophic cardiomyopathy(based on clinical, echocar-diographic, or laboratory findings), CMR may be indicated to confirm the diagnosis[9]. A more extensive discussion can be found in the supplementary materials(supplementary 5.1 and 5.2).

Very low risk of CAD and presumptive diagnosis of non-cardiac chest pain

In patients where clinical evaluation indicates a very low risk of cardiovascular chest pain, non-cardiac causes must be considered. These may range from benign self-limiting conditions to severe syndromes requiring prompt recognition and timely treatment. Clinical evaluation, integrated with laboratory tests, plays a key role in guiding differential diag-noses. Imaging orders should be tailored to the individual patient, guided by clinical presentation(especially symp-toms), vital signs, and laboratory tests. PE can present with few or mild symptoms. When suspected, elevated D- dimer levels warrant CTPA. AAS may manifest as persistent, non-specific chest pain unrelied for hours, requiring echocardi-ographic and/or CT evaluation. A more extensive discussion can be found in the supplementary materials(supplementary 5.1).“Non-cardiovascular chest pain” often originates from other thoracic structures, such as the pleura, lungs, esopha-gus, or chest wall(skin, muscles, or skeleton). Additionally,pain may be“referred” from abdominal organs like the stom-ach, gallbladder, or pancreas. Proper symptom interpretation based on pain characteristics(acute, constrictive, burning,or dull), location(anterior, posterior, shoulder, radiating to arms or neck), or evolution(relieved by rest, associated with nausea, sweating, fever, etc.) and a thorough physical exami-nation to identify associated signs of a pathological process are essential for guiding diagnostic workup and necessary tests. Low-impact imaging tools such as chest X-ray, TTE, or abdominal ultrasound may be valuable depending on the pri-mary clinical suspicion. Specific considerations for potential non-cardiac causes of chest pain(Fig. 4) include:

● Lungs: Conditions such as PE(potentially life-threatening-ing), pneumonia, pleuritis, or pneumothorax.

● Esophagus: Commonly inflammatory causes. Gas-troesophageal reflux disease can mimic angina, while esophagitis may result from drug therapy and should always be investigated. Esophageal motility disorders may also cause pain.

- Chest Wall: Non-traumatic causes include muscle and cartilage inflammation(costochondritis), rheu-

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Fig.4 Diagnostic Algorithm for Non-Cardiac Chest Pain.Abbreviations CAD, coronary artery disease; CT, computed tomography; EGD, esophago-gastrodeuodenoscopy; GERD,gastroesophageal reflux disease;IMH, intramural hematoma;PAU, penetrating atheroscle-rotic ulcer; X-Ray, radiography;Echo, Ultrasound as appropri-ate(e.g.,cardiac,abdominal,vascular, musculoskeletal).*:includes the measurement of cardiac biomarkers and D-dimer, complete blood count,and inflammatory markers

 matic diseases, systemic inflammatory conditions, or rarer causes like fibromyalgia or infectious conditions like herpes zoster. Pain may also indicate primary or secondary osseous or muscular neoplasms, typically localized. Radiographic or ultrasound imaging helps pinpoint the lesion and guide further diagnostic steps.

● Psychosomatic Pain: Panic attacks can mimic cardiac chest pain.

● Referred Pain from Abdominal Causes: Gastrointes-tinal conditions such as peptic ulcers, biliary colic, or pancreatitis may present as chest pain.

Organizational and logistical aspects

Collaboration among different specialists, primarily car-diologists and radiologists, is essential to optimise the diagnostic and therapeutic pathway of patients with ACP in the ED. Key challenges include:

● Shared diagnostic pathways(Fig.5) to be implemented in the clinical practice.

● Availability of advanced imaging. Advanced radiologi-cal imaging, in particular CCTA, plays a key role in the management of a sub-population of subjects present-

ing to ED with ACP. However, the clinical context of subjects with ACP requiring management including CT evaluation, determines the need for CT technology and expertise to address immediately, 24 h day, the possible suspicion of acute aortic syndrome, which in any case requires the acquisition of CT with cardiosynchronisa-tion for the correction evaluation of the aortic root, and the need for cardioradiological expertise capable of handling all phases of preparation, acquisition and reporting of a cardiac CT examination within 24 h of the arrival of the subject with ACP in the ED.Hence, a state of the art CT scanner with cardiac synchronization capabilities should be always available for patients from ED, as well as a general radiologist able to diagnostically assess patients with suspected AAS. The cardiac CT for ACP can be deferred up to 24-h, hence different delivery strategies can be implemented according to local organisational context:(a) all radiologists providing emergency-service trained to perform advanced cardiac imaging, which is certainly the more complex and difficult to implement in many contexts;(b) deferred execution, within 24 h,of cardiac CT by the cardiovascular CT imaging service in contexts where there is a group of radiologists dedi-cated to cardiac imaging, associated to the activation of a weekend on-call service;(c) activation of teleradiol-ogy support services for emergency rooms in smaller and

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 Fig.5 Acute Chest Pain Diagnostic Flow Chart, Blood tests include but are not limited to complete blood count, renal, profile high-sensi-tivity cardiac troponins(hs-cTn),C-reactive protein(CRP),D-dimer,and NT-pro BNP. Risk stratification for patients with NSTE-ACS is based on the elements described in the 2023 ESC Guidelines[7].Abbreviations AAS, acute aortic syndrome; ACP, acute chest pain;CAD, coronary artery disease; CCTA, coronary computed tomogra-phy angiography; CMR, cardiac magnetic resonance; ECG, electro-

peripheral settings, through the creation of cardiac imag-ing networks on a territorial, regional or national basis.

● All the strategies cited above are supported by the adequate training in cardiovascular imaging that radi-ologists receive during residency and by the continu-ous training initiatives available, like those by SIRM's Cardioradiology section[29].

• Outpatient Pathways for advanced cardiac imaging. In some cases deferred follow-up with advanced cardiac imaging could be indicated after ED dismission, hence specific pathways allowing these patients to access the necessary diagnostic method in the days or weeks fol-lowing their access to the ED, should be impemented.

Organizational and logistical aspects are further addressed in the supplementary materials.

A more extensive discussion of organizational and logis-tical aspects can be found in the supplementary materials(supplementary 7.1). The central illustration(Fig. 5) pre-sents a suggested approach based on currently available evidence and the insights of experts involved in drafting the document.

<EndOfPara>cardiogram; ED, emergency department; GRACE, Global Registry of Acute Coronary Events; hs-cTn, high-sensitivity cardiac troponin; LIE, late iodine enhancement; NSTE-ACS, non-ST-elevation acute coronary syndrome; PCL, percutaneous coronary intervention; PE,pulmonary embolism; X-Ray, radiography; STEI, ST-elevation myocardial infarction; TTE, transthoracic echocardiography; UA,unstable angina; US, Ultrasound

Conclusions

This SIRM-SIC document outlines the appropriate manage-ment of patients presenting to the ED with ACP, emphasiz-ing the timing and utility of non-invasive imaging for rapid and accurate diagnosis of cardiac or non-cardiac causes.The document aims to improve diagnostic pathways across Italian hospitals and foster cardiologist-radiologist collabo-ration, improving patient safety, outcomes, and resource utilization efficiency.

Supplementary Information The online version contains supplemen-tary material available at https://doi.org/10.1007/s11547-025-02076-x.

Open Access This article is licensed under a Creative Commons Attri-bution 4.0 International License, which permits use, sharing, adapta-tion, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source,provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will

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Authors and Affiliations

Antonio Esposito1·Riccardo Faletti2·Anna Palmisano1·Marco Gatti2·Sara Seitun3·Cesare Mantini4·Piergiuseppe Agostoni5·Daniele Andreini6·Francesco Barilla7·Andrea Barison8·Paolo Calabr0,11·Matteo Cameli12·Scipione Carerj13·Carlo Catalano14·Marcello Chiocchi15·Marco Matteo Ciccone16.Antonio Curcio17·Fabrizio D'Ascenzo18,19·Serena Dell'Aversana20·Fabio Falzea21·Marco Francone22,47.Nicola Galea14·Andrea Giovagnoni23·Marco Guglielmo24·Andrea Laghi25·Carlo Liguoli Lovato27·Riccardo Marano28·Rocco Antonio Montone29,30·Doralisa Morrone31·Luigi Natale32·Savina Nodari33.Michele Oppizzi34·Stefania Paollilo35·Alberto Polimeni17,36·Gianluca Pontone37·Italo Porto38.Silvia Pradella39·Vincenzo Russo40·Vincenzo Russo27·Luca Saba41·Gianfranco Sinagra42·Massimo Slavich43.Carmen Spacarotella35· Davide Tore44· Davide Vignale1· Carmine Dario Vizza45· Saverio Muscoli46.Pasquale Perrone Filardi35·Ciro Indolfi17

Riccardo Faletti riccardo.faletti@unito.it

1 Experimental Imaging Centre, Radiology Unit, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University,Milan, Italy

2 Department of Surgical Sciences, Radiology Unit, University of Turin, Via Genova 3, 10126 Turin, Italy

3 Department of Radiology, IRCCS Opede Policlinico San Martino, Genoa, Italy

4 Department of Neuroscience, Imaging and Clinical Sciences,‘G.d'Annunzio' University,Chieti,Italy

5 Monzino Cardiology Center, IRCCS, Milan, Italy

6 Division of University Cardiology, IRCCS Ospedale Galeazzi Sant/Ambrogio,Milan, Italy

7 Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy

8 Cardiology and Cardiovascular Medicine Department,Fondazione Tosana Gabriele Monasterio, Pisa, Italy

9 Interdisciplinary Center for Health Science, Scuola Superiore Sant'Anna, Pisa, Italy

10 Sant'Anna E San Sebastiano Hospital, Caserta, Italy

11 Division of Cardiology, University of Campania“Luigi Vanvitelli”, Caserta, Italy

12 Department of Medical Biotechnologies, Division of Cardiology, University of Siena, Siena, Italy

13 Department of Clinical and Experimental Medicine,University of Messina, Messina, Italy

14 Department of Radiological, Oncological and Pathological Sciences,“La Sapienza” University of Rome, Rome, Italy

15 Department of Biomedicine and Prevention, Division of Diagnostic Imaging, University of Rome“Tor Vergata”,Rome, Italy

16 Cardiology Unit, Department of Precision and Regenerative Medicine and Ionian Area(DiMePRe-J), University of Bari Medical School, Bari, Italy

17 Division of Cardiology, Department of Pharmacy,Health and Nutritional Sciences, University of Calabria,87036 Rende, Italy

18 Division of Cardiology, Cardiovascular and Thoracic Department,"Citta Della Salute E Della Scienza" Hospital,Turin, Italy

19 Department of Medical Sciences, University of Turin, Turin,Italy

20 Department of Radiology, Santa Maria Delle Grazie Hospital, ASL Napoli 2 Nord, Pozuzi, Italy

21 Centro ECORAD Di Villa San Giovanni, Reggio Calabria,Italy

22 Department of Biomedical Sciences, Humanitas University,Pieve Emanuele, Italy

23 Department of Radiology, University Hospital“Ospedali Riunitn”, Ancona, Italy

4 Division of Heart and Lungs, Department of Cardiology,Utrecht University Medical Center, Utrecht, The Netherlands

25 Department of Medical Surgical Sciences and Translational Medicine, Sapienza-University of Rome, Radiology Unit-Sant'Andrea University Hospital, Rome, Italy

26 UOC Diagnostica Per Immagini,P.O. San Giovanni Bosco-ASL Na1 Centro, Napoli, Via F.M. Briganti 255,80144 Naples, Italy

27 Department of Pediatric and Adult Cardio-Thoracovascular,Acondematologic and Emergencies Radiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna,Italy

28 Department of Radiological and Hematological Sciences,Section of Radiology, Universita Cattolica del Sacro Cuore,Rome, Italy

29 Department of Cardiovascular and Pulmonary Sciences,Catholic University of the Sacred Heart, Rome, Italy

30 Department of Cardiovascular Sciences, Fondazione Policlinico Universitaire A. Gemelli IRCCS, Rome, Italy

31 Department of Surgical, Medical and Molecular Pathology and of Critical Sciences, University of Pisa, Pisa, Italy

32 Department of Radiological Sciences, Institute of Radiology,Catholic University of Rome, A. Gemelli University Hospital, Rome, Italy

33 Department of Cardiology, University of Brescia and ASST Spedali Civil Di Brescia, Italy

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34 Unit of Clinical Cardiology, IRCCS San Raffaele, Milan,Italy

35 Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy

36 Division of Interventional Cardiology, Anunzniata Hospital,Cosenza, Italy

${}^{37}$ Department of Perioperative Cardiology and Cardiovascular Imaging,Centro Cardiologico Monzino IRCSS,Milan,Italy

${}^{38}$ Cardiovascular Disease Unit, IRCCS Ospedale Policlinico San Martino, IRCCS Italian Cardiology Network, Genoa,Italy

39 Department of Radiology, Careggi University Hospital,Florence, Italy

40 Cardiology Unit, Department of Medical Translational Sciences, University of Campania“Luigi Vanvitelli”-Monaldi Hospital, Naples, Italy

${}^{41}$ Department of Radiology, Azienda Ospedaliero Universitaria, University of Cagliari, Cagliari, Italy

$\boxed{42}$ Cardiovascular Department, Azienda Sanitaria Universitaria Giuliano-Isontina, University of Trieste,Trieste, Italy

43 Department of Cardiology, IRCCS San Raffaele Scientific Institute,Milan, Italy

$\overline{44}$ Radiology Unit, Department of Diagnostic Imaging and Interventional Radiology,"Citta della Salute e della Scienza"- Molinette Hospital, Turin, Italy

${}^{45}$ Department of Cardiovascular and Respiratory Sciences,Sapienza University of Rome, Rome, Italy

46 Department of Cardiology, Policlinico Tor Vergata, Rome,Italy

$\boxed{47}$ IRCCS Humanitas Research Hospital,Rozzano,Italy