key: cord-0030324-23t439m2
authors: Schnaubelt, Sebastian; Eibensteiner, Felix; Oppenauer, Julia; Kornfehl, Andrea; Brock, Roman; Poschenreithner, Laura; Du, Na; Baldi, Enrico; Schlager, Oliver; Niessner, Alexander; Domanovits, Hans; Roth, Dominik; Sulzgruber, Patrick
title: The Feasibility of Ultra-Sensitive Phonocardiography in Acute Chest Pain Patients of a Tertiary Care Emergency Department (ScorED Feasibility Study)
date: 2022-04-14
journal: J Pers Med
DOI: 10.3390/jpm12040631
sha: a48976d117a2a92ad505fca568f7283c889bc7e1
doc_id: 30324
cord_uid: 23t439m2

Background: Thoracic pain is one of the most frequent chief complaints at emergency departments (EDs). However, a respective workup in cases without clear electrocardiographic signs is complex. In addition, after having ruled out acute coronary syndrome (ACS), patients are often left with an unclear etiology of their symptoms. Ultra-sensitive phonocardiography is already used to rule out stable coronary artery disease (CAD); however, its feasibility in an ED-setting remains unknown. Methods: We prospectively used ultra-sensitive phonocardiography via the CADScor(®)System to measure hemodynamically stable patients with the chief complaint of chest pain during routine waiting times at a high-volume tertiary ED. Results: A total of 101 patients (49% male; 94% Caucasian; 61 (51–71) years; BMI 28.3 (24.2–31.6)) were enrolled. Patient workflow was not hindered, and no adverse events were recorded. In 80% of cases, a score was successfully calculated, with 74% at the first, 5% at the second, and 1% at the third attempt. Feasibility was judged as 9.0 (±1.8) by the patients, and 8.9 (±2.6) by the investigators on a 10-point Likert scale. Conclusions: Ultra-sensitive phonocardiography was found to be feasible in acute chest pain patients presenting to a tertiary ED. Thus, the CAD score measured during routine waiting times could potentially serve as an additional tool in a diagnostic pathway for thoracic pain.

Thoracic pain is one of the most frequent chief complaints in emergency medicine [1, 2] . While the majority of patients are eventually discharged with a non-cardiac/low-risk symptom etiology, acute coronary syndrome (ACS) must first be ruled out [2] . Currently, a combination of patients' clinical presentation, electrocardiogram (ECG), and laboratory markers is recommended, potentially supplemented by scores [1] . Cases with normal or unspecific ECGs are complex, and often result in clinicians' uncertainty on how to proceed [3] . Thus, novel tools for cardiovascular risk prediction in emergency departments 2 of 9 (ED) and the following workup are needed. In this regard, surrogate markers for coronary artery disease (CAD) can be utilized: significant coronary artery stenosis generates turbulations in coronary blood flow, evident as intracoronary murmurs. Specific acoustic signal patterns combined with analysis techniques can identify these murmurs, and therefore hint towards existing CAD [4, 5] . This approach using highly sensitive microphones, named phonocardiography, appears as non-invasive, inexpensive, and simple to perform [6, 7] . We therefore aimed at assessing its feasibility in the setting of our tertiary-care, high-volume ED which provides comprehensive emergency and intensive care medicine [8, 9] . Since phonocardiography has so far only been used and validated in stable CAD and in orderly and well-structured settings, such as outpatient clinics [10] [11] [12] , providing data on its feasibility in busy and mostly overcrowded EDs [13] seems vital for further respective research endeavors: an ED not only differs from normal wards, outpatient departments, or even general physician offices in terms of time and resource management possibilities, there is also an increased physical and psychological strain on the personnel, further impacting on ED-reproducibility of measures that have previously been only assessed outside this unique environment [13] [14] [15] [16] [17] .

Patients >40 years in stable cardiorespiratory condition presenting to the ED with the chief complaint of chest pain were screened.

Ultra-sensitive phonocardiography was prospectively performed using the CADScor ® System (algorithm version 3.1, Acarix A/S, Denmark), a palm-sized portable device with an adhesive sensor applied to the patient's chest (fourth left intercostal space) [7] . The measurement is performed via 3 min of recording with four breath holds for a reduction of acoustic interference. A numeric value regarding a continuum of risk is calculated (0-99 risk scale: low ≤20 points, intermediate 21-29, high ≥30) [7] . The score is calculated immediately after the recording using an integrated algorithm performing an analysis of the heart sounds together with age, gender, and blood pressure information. Combined with clinical risk evaluation, the CAD score shows good diagnostic accuracy for stable CAD detection [7, 10] , with a low-risk score (≤20) having a negative predictive value of up to 97%, thereby reliably ruling out stable CAD [7, [10] [11] [12] . Further, it can perform a reclassification of intermediate risk patients to low risk [12] .

Measurements were conducted during routine waiting times in a separate quiet room, a supine position, and after 5 min of rest. Results were blinded to patients and treating physicians or nurses. An overview of the measuring procedure can be found in Supplementary Table S1 [18] .

The primary study outcome was the utilization feasibility of the CADScor ® System. The overall study population was stratified into subgroups concerning gender, CAD history, and CAD score details, which were then compared. Continuous variables are presented as means and standard deviations or medians and interquartile-ranges, and compared via a Kruskal-Wallis test. Categorical data are presented as counts and percentages, and compared using χ 2 -square test. Due to the pilot study character and the main outcome merely being feasibility, no sample size calculation was performed, and a team of experts decided upon 100 patients. Statistical significance was defined by two-tailed p-values of <0.05. Data analysis was performed using SPSS 22.0 (IBM, Armonk, NY, USA). Figure 1 gives an overview of the main study results. A total of 101 patients (49% male; 94% Caucasian; 61 (51-71) years; BMI 28.3 (24.2-31.6)) were included in this study from August to October 2021. No study inclusion hindered or slowed down the patient workflow. No adverse events were recorded. Further data, including details of the current complaints of the whole cohort and stratified into subgroups, are shown in Table 1 . In brief, conventionally known associations of gender, previously-known CAD, and wellestablished risk factors [19] were observed. Table 2 depicts CAD score details and feasibility data. A total of 44% of patients fell into the subgroup of ≤20 points. As age, gender, and hypertension/blood pressure data were integrated in the internal calculation process, they naturally differed in the subgroups. Figure 1 gives an overview of the main study results. A total of 101 patients (4 94% Caucasian; 61 (51-71) years; BMI 28.3 (24.2-31.6)) were included in this stu August to October 2021. No study inclusion hindered or slowed down the patient w No adverse events were recorded. Further data, including details of the current comp the whole cohort and stratified into subgroups, are shown in Table 1 . In brief, conve known associations of gender, previously-known CAD, and well-established risk fa were observed. Table 2 depicts CAD score details and feasibility data. A total o patients fell into the subgroup of ≤20 points. As age, gender, and hypertension/blood data were integrated in the internal calculation process, they naturally differe subgroups. Table 1 . Patient's demographics, including chronic conditions and details of their current episode of chest pain. Values are given for the total study cohort and subgroups concerning gender, known coronary artery disease (CAD), calculated CAD score, and final diagnosis regarding acute coronary syndrome (ACS). Categorical data are presented as counts and percentages, continuous data as medians and interquartile ranges (IQRs). Categorical data are analyzed using a test for linear association (Maentel-Haenszel chi-square test), continuous data using Kruskal-Wallis test for testing within the subgroups. BMI = body mass index; SpO2 = oxygen saturation; FiO2 = fraction of inspiratory oxygen; AHTN = arterial hypertension; HLP = hyperlipidaemia; DM = diabetes mellitus; MCI = myocardial infarction; CKI = chronic kidney injury; PAD = peripheral artery disease; baPWV = brachial-ankle pulse-wave velocity; cfPWV = carotid-femoral pulse-wave velocity; AP = angina pectoris; HEART = History, ECG, Age, Risk factors, and Troponin; GRACE = Global Registry of Acute Coronary Events; NYHA = New York Heart Association; ECG = electrocardiogram; IMCU = intermediate care unit. In 80% of cases, a score was successfully calculated, with 74% at the first, 5% at the second, and 1% at the third attempt. The measurement was stopped by the patient in 9% of cases (e.g., due to incapability to follow necessary breathing commands), and by the investigator in 10% (e.g., due to occurring arrhythmia or tachycardia). In 2% of cases, a measurement was not possible due to technical reasons including inconsistent data analysis by the device (e.g., due to extra systoles or high heart rates) or too weak sound signals.

Feasibility was judged as 9.0 (±1.8) by the patients and 8.9 (±2.6) by the investigators on a 10-point Likert scale (10 being the maximum favorable estimation of feasibility in the current setting of the respective evaluator).

Descriptive laboratory data are found in the Supplementary Table S2 .

We demonstrated sufficient feasibility of ultra-sensitive phonocardiography via CAD score in acute chest pain patients at a high-volume ED. Routine workflow was not hindered, no adverse events were noted, and a CAD score was calculated in 3 4 of cases at the first attempt. Feasibility was rated high by patients and investigators, and the system suggested a high functionality even under the time-and place-restricting conditions of a busy ED. In times of overcrowded EDs with increasing additional duties, such as comprehensive intensive care, as well as the physical and emotional strain on the staff [13] [14] [15] [16] [17] , this knowledge seems vital: for instance, the measurements could not have been accepted by the personnel or the patients, time or spatial resources could have not been available, or the busy environment could have prevented sufficient phonocardiographic results. Of note, feasibility was the primary outcome of this study, and not clinical diagnoses or outcomes. To provide data on feasibility was important to build a base for following larger trials.

Further research seems warranted in two major domains:

First, a CAD score should be evaluated as a potential additional triage tool in chest pain patients-not (only) towards discrimination of ACS vs. non-ACS, but rather concerning its potential power to provide additional information on patients' CAD status right from the start of their evaluation. This especially applies to those patients not being able to provide an estimation on their coronary artery status, or those in whom anamnesis is not sufficiently possible (e.g., language barriers, dementia, etc.). Hints towards a CAD score potentially identifying sicker patients (e.g., lower SpO2, higher cfPWV, or higher NT-proBNP values) should be investigated in future research as well.

Second, and of higher priority, the CAD score performs very well in ruling out stable CAD. Applying this information, alternative diagnoses for the chief complaint of chest pain can become more probable after having already ruled out ACS via the known standard algorithm. Currently, many patients are discharged with provisional diagnoses of their complaints, for instance musculoskeletal thoracic pain or radiating gastric pain [20] . However, with CAD forming a major international health burden with growing incidences [21] , ruling out ACS may in the future not be enough. In fact, after having ruled out ACS, rather than discharging patients with an unknown etiology of their symptoms, a further sub-classification into two groups seems thinkable: (1) stable CAD ruled out by CAD score, making a non-cardiac symptom etiology more probable; (2) stable CAD not ruled out by CAD score, making further workup at a cardiologist's office or a cardiologic outpatient department a logical next step to be advised. With an increasing emphasis on shared decision making, and expensive resources often being consumed with little effect on clinical outcome [22] , this cost-and time-effective approach could aid in prioritizing care for individuals who are at particular risk for major adverse cardiac events (MACE). A recently shown prognostic potential of the CAD score towards all-cause mortality and future myocardial infarction emphasizes these thoughts [23] .

A study setting with a larger sample size and specially designed to investigate the above-raised points should be aimed for in future research endeavors.

Ultra-sensitive phonocardiography in chest pain patients presenting to an emergency department is feasible.

The CAD score is already utilized to rule out stable coronary artery disease. • After having ruled out acute coronary syndrome via a guideline-directed algorithm, the CADScor ® System could help to classify chest pain patients into those with and without coronary artery disease, making a specific further cardiovascular workup possible.

Ultra-sensitive phonocardiography is feasible in acute chest pain patients presenting to a tertiary emergency department. Thus, a CAD score measured during routine waiting times could potentially serve as an additional tessera in a diagnostic pathway for thoracic pain after having ruled out acute coronary syndrome. Informed Consent Statement: Informed consent was obtained from all subjects involved in the study.

The data underlying this article will be shared on reasonable request to the corresponding author.

ESC Guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation

Update on the emergency department diagnosis and risk stratification of acute chest pain

Non-cardiac chest pain patients in the emergency department: Do physicians have a plan how to diagnose and treat them? A retrospective study

Audible Coronary Artery Stenosis

Coronary artery disease and low frequency heart sound signatures

Acoustic Detection of Coronary Artery Disease

A novel approach to diagnosing coronary artery disease: Acoustic detection of coronary turbulence

The Impact of the COVID-19 Pandemic on Incidences of Atrial Fibrillation and Electrical Cardioversion at a Tertiary Care Emergency Department: An Inter-and Intra-year Analysis

Aspects of intensive care medicine in emergency medicine

Diagnosing coronary artery disease by sound analysis from coronary stenosis induced turbulent blood flow: Diagnostic performance in patients with stable angina pectoris

Diagnostic performance of an acoustic-based system for coronary artery disease risk stratification

Coronary artery disease risk reclassification by a new acoustic-based score

Emergency department overcrowding: Analysis and strategies to manage an international phenomenon

Emergency department crowding affects triage processes

A longitudinal assessment of occupational stress in Emergency Department Nursing Staff

Office or Emergency Department: What's the difference?

Emergency Medicine Residents Experience Acute Stress While Working in the Emergency Department

CADScor®System User Manual; Acarix: Malmo

A review on coronary artery disease, its risk factors, and therapeutics

Description of chest pain patients in a Norwegian emergency department

Atherosclerotic Coronary Heart Disease Epidemiology, Classification and Management

Acute Chest Pain in the Emergency Department

Advanced heart sound analysis as a new prognostic marker in stable coronary artery disease

We thank all personnel involved in acquiring the study data. We especially acknowledge Michael Unterrieder and the rest of the "ABI-Team" of the Department of Emergency Medicine, Medical University of Vienna, Austria.

The authors declare no conflict of interest.