Key result
Cardiogoniometry demonstrated a diagnostic sensitivity of 69% for detecting non-ST-segment elevation acute coronary syndrome at hospital admission, which was significantly higher than first ECG (28%) and serial troponin (50%).
Why the study?
Does Cardiogoniometry (CGM) improve the early detection of NSTE-ACS and relevant coronary stenosis in patients presenting with acute chest pain without ST-segment elevation?
Observational (n=216)
Blinded review board
Yes
Does Cardiogoniometry (CGM) improve the early detection of NSTE-ACS and relevant coronary stenosis in patients presenting with acute chest pain without ST-segment elevation?
Absolute Event Rate: 69% vs 28%
p-value: p=<0.001
Cardiogoniometry (CGM) provides higher sensitivity than standard 12-lead ECG and conventional troponin at admission for detecting NSTE-ACS and relevant coronary stenosis, making it a potentially useful complementary triage tool.
BACKGROUND: Cardiogoniometry (CGM) is a novel electrocardiac method utilising computer-assisted three-dimensional information on cardiac potentials. OBJECTIVE: To investigate the potential of CGM in discriminating non-ST-segment elevation acute coronary syndrome (NSTE-ACS) and relevant coronary stenosis upon hospital admission by prospectively comparing its sensitivity, specificity and accuracy against those of a single troponin test and a 12-lead ECG performed on admission DESIGN: A multicenter prospective observational trial. SETTING: Eight interventional cardiac centres in Germany. PATIENTS: A cohort of 216 patients (mean age 67 years, 34.7 % female) who presented with acute chest pain or dyspnoea without ST-segment elevation and were scheduled for coronary angiography within 72 h of admission. INTERVENTION: Pre-angiography screening by CGM, troponin test, 12-lead ECG MAIN OUTCOME MEASURES: ECG, troponin and CGM on admission compared with final diagnosis of NSTE-ACS or relevant diameter stenosis ≥70 % verified by an independent review board and an angiographic core laboratory. RESULTS: NSTE-ACS was finally confirmed in 162 cases, whereas the remaining 54 cases without proof of NSTE-ACS served as controls. Diagnostic sensitivity for NSTE-ACS was 28, 50 and 69 % and specificity 78, 96 and 54 % for first ECG, serial troponin and first CGM, respectively. Accuracy was 40, 62 and 65 %. The sensitivity of the tests to detect relevant coronary stenosis (n = 126) was 32, 53 and 74 %, respectively. The sensitivity of CGM to detect NSTE-ACS (65 %) or relevant stenosis (71 %) was high even in patients with normal troponin and ECG. CONCLUSIONS: CGM can detect NSTE-ACS at first medical contact. CGM in conjunction with traditional markers, 12-lead ECG and troponin may effectively aid early decision making in patients presenting with acute chest pain.
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Tölg et al. (2012) conducted an observational in Non-ST-segment elevation acute coronary syndrome (NSTE-ACS) (n=216). Cardiogoniometry (CGM) vs. 12-lead ECG and troponin test was evaluated on Diagnostic sensitivity for NSTE-ACS (p=<0.001). Cardiogoniometry demonstrated a diagnostic sensitivity of 69% for detecting non-ST-segment elevation acute coronary syndrome at hospital admission, which was significantly higher than first ECG (28%) and serial troponin (50%).
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