4.5 Article

The effect of the localisation of an underlying ST-elevation myocardial infarction on the VF-waveform: A multi-centre cardiac arrest study

期刊

RESUSCITATION
卷 168, 期 -, 页码 11-18

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.resuscitation.2021.08.049

关键词

Out-of-hospital cardiac arrest; Ventricular fibrillation; Waveform analysis; ST-elevation myocardial infarction

资金

  1. European Union's Horizon 2020 research and innovation program under acronym ESCAPE-NET [733381]
  2. COST (European Cooperation in Science and Technology) [CA19137]
  3. Netherlands CardioVascular Research Initiative
  4. Dutch Heart Foundation
  5. Dutch Federation of University Medical Centers
  6. Netherlands Organization for Health Research and Development
  7. Royal Netherlands Academy of Sciences [CVON2017-15, CVON2018-30]
  8. Stryker, Emergency Care, Redmond, WA USA

向作者/读者索取更多资源

This multi-center VF-waveform OHCA study demonstrated significantly lower AMSA in cases of underlying STEMI, with a more pronounced difference for inferior than for anterior STEMI. Further confirmatory studies are needed to investigate the impact of STEMI localization on the VF waveform, which may contribute to earlier diagnosis of STEMI 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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