Key result
Use of potassium-sparing agents was associated with a lower amplitude spectrum area of ventricular fibrillation compared to other cardiovascular medications (OR 0.46; 95% CI 0.10-0.81; P < 0.012).
Why the study?
VF waveform analyses serve as a proxy for OHCA characteristics, but patient factors such as cardiovascular medication use might also influence VF waveform measures.
Does cardiovascular medication use affect the amplitude spectrum area of ventricular fibrillation in patients with out-of-hospital cardiac arrest?
Observational (n=990)
Does cardiovascular medication use affect the amplitude spectrum area of ventricular fibrillation in patients with out-of-hospital cardiac arrest?
Odds Ratio: 0.46 (95% CI 0.1–0.81)
p-value: p=< 0.012
Cardiovascular medication use has minimal independent effect on ventricular fibrillation waveform characteristics, indicating that AMSA can be used as a patient management tool in out-of-hospital cardiac arrest without adjusting for prior medication use.
Cardiovascular medications had minimal independent effect on AMSA; leaves open whether adjustment is needed for AMSA-guided OHCA management.
BACKGROUND: Ventricular fibrillation (VF) waveform analyses are considered a reliable proxy for OHCA characteristics in out-of-hospital cardiac arrest (OHCA), but patient characteristics such as cardiovascular medication use might also be associated with changes in VF waveform measures. OBJECTIVES: To assess associations between cardiovascular medication use and amplitude spectrum area (AMSA) of VF, while correcting for the presence of cardiovascular disease (CVD), CVD risk factors, and OHCA characteristics. METHODS: We included 990 VF patients from an OHCA registry in the Netherlands, with available information on medical history and cardiovascular medication use. Associations between cardiovascular medication use and AMSA were tested in a multivariate linear regression model, adjusting for CVD, CVD risk factors, and OHCA characteristics. Model performance was shown using R-square and R-change. We also calculated whether medication use was associated with faster dissolution of AMSA to lower values with increasing time delay. RESULTS: In the multivariate analysis, when corrected for CVD, CVD risk factors and OHCA characteristics, only potassium-sparing agents were associated with a lower AMSA when compared to patients using other cardiovascular medications (OR 0.46 [95% CI 0.10-0.81]; P < 0.012). The decrease in AMSA with increasing EMS-call-to-ECG delay was the same for patients with and without cardiovascular medication use (all P > 0.05). Only a small part of the variance in AMSA could be explained by medication use (R-square 0.003- 0.026). Adding OHCA characteristics to the model resulted in the largest R square change (0.09-0.15). CONCLUSIONS: It is unlikely that there is a strong and clinically relevant independent pharmacologic effect of cardiovascular medication use on AMSA. In OHCA, AMSA might be used as patient management tool without considering cardiovascular medication use.
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Hulleman et al. (2020) conducted an observational in Out-of-hospital cardiac arrest with ventricular fibrillation (n=990). Cardiovascular medication use (specifically potassium-sparing agents) vs. Other cardiovascular medications or no cardiovascular medication use was evaluated on Amplitude spectrum area (AMSA) of ventricular fibrillation (OR 0.46, 95% CI 0.10-0.81, p=< 0.012). Use of potassium-sparing agents was associated with a lower amplitude spectrum area of ventricular fibrillation compared to other cardiovascular medications (OR 0.46; 95% CI 0.10-0.81; P < 0.012).
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