Key result
Unipolar voltage amplitudes are ~31% lower in myocardial scar but significant overlap limits accurate assessment.
Why the study?
Does unipolar voltage amplitude mapping accurately detect myocardial scar compared to DE-CMR in heart failure patients?
Observational (n=60)
Yes
Does unipolar voltage amplitude mapping accurately detect myocardial scar compared to DE-CMR in heart failure patients?
Absolute Event Rate: 7.1% vs 10.3%
p-value: p=<0.001
Unipolar voltage mapping has limited reliability for accurate myocardial scar assessment, particularly for epicardial measurements and areas with less than 75% scar extent, due to large intra- and inter-patient variability.
Unipolar voltage mapping lacks reliability for scar assessment in HF; leaves open whether refined criteria or multimodal imaging can improve accuracy.
BACKGROUND: Validation of voltage-based scar delineation has been limited to small populations using mainly endocardial measurements. The aim of this study is to compare unipolar voltage amplitudes (UnipV) with scar on delayed enhancement cardiac magnetic resonance imaging (DE-CMR). METHODS: Heart failure patients who underwent DE-CMR and electro-anatomic mapping were included. Thirty-three endocardial mapped patients and 27 epicardial mapped patients were investigated. UnipV were computed peak-to-peak. Electrograms were matched with scar extent of the corresponding DE-CMR segment using a 16-segment/slice model. Non-scar was defined as 0% scar, while scar was defined as 1-100% scar extent. RESULTS: UnipVs were moderately lower in scar than in non-scar (endocardial 7.1 [4.6-10.6] vs. 10.3 [7.4-14.2] mV; epicardial 6.7 [3.6-10.5] vs. 7.8 [4.2-12.3] mV; both p<0.001). The correlation between UnipV and scar extent was moderate for endocardial (R = -0.33, p<0.001), and poor for epicardial measurements (R = -0.07, p<0.001). Endocardial UnipV predicted segments with >25%, >50% and >75% scar extent with AUCs of 0.72, 0.73 and 0.76, respectively, while epicardial UnipV were poor scar predictors, independent of scar burden (AUC = 0.47-0.56). UnipV in non-scar varied widely between patients (p<0.001) and were lower in scar compared to non-scar in only 9/22 (41%) endocardial mapped patients and 4/19 (21%) epicardial mapped patients with scar. CONCLUSION: UnipV are slightly lower in scar compared to non-scar. However, significant UnipV differences between and within patients and large overlap between non-scar and scar limits the reliability of accurate scar assessment, especially in epicardial measurements and in segments with less than 75% scar extent.
No takes yet. Share an insight, caveat, or question.
Nguyên et al. (2017) conducted an observational in Heart failure (n=60). Unipolar voltage amplitude mapping vs. Non-scar tissue (0% scar extent on DE-CMR) was evaluated on Endocardial unipolar voltage amplitude in any-scar (1-100% scar extent) vs. non-scar (p=<0.001). Unipolar voltage amplitudes were only moderately lower in myocardial scar compared to non-scar tissue (endocardial 7.1 vs 10.3 mV), with significant overlap and inter-patient variability limiting accurate scar assessment.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: