The effect of the localisation of an underlying ST-elevation myocardial infarction on the VF-waveform: A multi-centre
J Nas1, L H van Dongen2, J Thannhauser1
1Department of Cardiology, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, the Netherlands.
Insights
Amplitude spectrum area (AMSA) during ventricular fibrillation (VF) is lower in out-of-hospital cardiac arrest (OHCA) patients with ST-elevation myocardial infarction (STEMI). This VF waveform characteristic is most pronounced with inferior STEMI, suggesting potential for earlier STEMI diagnosis.
Area of Science:
- Cardiology
- Medical Technology
- Emergency Medicine
Background:
- Ventricular fibrillation (VF) waveform characteristics, like amplitude spectrum area (AMSA), are investigated for identifying underlying myocardial infarction (MI) during cardiac arrest.
- Previous studies indicate lower AMSA values in patients with MI, with waveform characteristics varying based on MI location relative to ECG recording direction.
Purpose of the Study:
- To investigate the association between AMSA values derived from defibrillator recordings and the presence and localization of ST-elevation myocardial infarction (STEMI) in out-of-hospital cardiac arrest (OHCA) patients.
Main Methods:
- A multi-center cohort study involving 754 OHCA patients.
- AMSA was calculated from defibrillator pad-ECG recordings.
- STEMI localization was determined through ECG, angiography, or autopsy.
Main Results:
- Statistically significant differences in AMSA values were observed across no STEMI, anterior STEMI, and inferior STEMI groups in both study cohorts.
- Univariate analysis revealed significantly lower AMSA in inferior STEMI compared to no STEMI.
- Adjusted analyses showed numerically lowest AMSA for inferior STEMI, with a greater relative difference compared to anterior STEMI.
Conclusions:
- This OHCA study demonstrates significantly lower AMSA in the presence of underlying STEMI, particularly for inferior STEMI.
- Further research is warranted to confirm the impact of STEMI localization on VF waveforms for potential earlier diagnosis during VF.
Introduction:
In cardiac arrest, ventricular fibrillation (VF) waveform characteristics such as amplitude spectrum area (AMSA) are studied to identify an underlying myocardial infarction (MI). Observational studies report lower AMSA-values in patients with than without underlying MI. Moreover, experimental studies with 12-lead ECG-recordings show lowest VF-characteristics when the MI-localisation matches the ECG-recording direction. However, out-of-hospital cardiac arrest (OHCA)-studies with defibrillator-derived VF-recordings are lacking.
Methods:
Multi-centre (Amsterdam/Nijmegen, the Netherlands) cohort-study on the association between AMSA, ST-elevation MI (STEMI) and its localisation. AMSA was calculated from defibrillator pad-ECG recordings (proxy for lead II, inferior vantage point); STEMI-localisation was determined using ECG/angiography/autopsy findings.
Results:
We studied AMSA-values in 754 OHCA-patients. There were statistically significant differences between no STEMI, anterior STEMI and inferior STEMI (Nijmegen: no STEMI 13.0mVHz [7.9-18.6], anterior STEMI 7.5mVHz [5.6-13.8], inferior STEMI 7.5mVHz [5.4-11.8], p = 0.006. Amsterdam: 11.7mVHz [5.0-21.9], 9.6mVHz [4.6-17.2], and 6.9mVHz [3.2-16.0], respectively, p = 0.001). Univariate analyses showed significantly lower AMSA-values in inferior STEMI vs. no STEMI; there was no significant difference between anterior and no STEMI. After correction for confounders, adjusted absolute AMSA-values were numerically lowest for inferior STEMI in both cohorts, and the relative differences in AMSA between inferior and no STEMI was 1.4-1.7 times larger than between anterior and no STEMI.
Conclusion:
This multi-centre VF-waveform OHCA-study showed significantly lower AMSA in case of underlying STEMI, with a more pronounced difference for inferior than for anterior STEMI. Confirmative studies on the impact of STEMI-localisation on the VF-waveform are warranted, and might contribute to earlier diagnosis of STEMI during VF.
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