Key result
Unipolar and bipolar voltage mapping show ~90% spatial concordance for site classification during sinus rhythm.
Why the study?
It is unclear to what extent factors like inter-electrode spacing and wavefront angle impact left atrial low voltage areas in clinical bipolar voltage mapping compared with unipolar mapping.
Does unipolar voltage mapping provide comparable localization of left atrial low voltage areas compared to bipolar voltage mapping in patients with atrial fibrillation?
Observational (n=28)
Does unipolar voltage mapping provide comparable localization of left atrial low voltage areas compared to bipolar voltage mapping in patients with atrial fibrillation?
Bipolar and unipolar voltage maps are highly correlated for localizing left atrial low voltage areas in both sinus rhythm and atrial fibrillation, suggesting theoretical confounders of bipolar mapping have limited clinical impact.
Supports comparable low-voltage localization by unipolar mapping in atrial fibrillation; hypothesis-generating without outcome data.
Background: Presence of left atrial low voltage substrate in bipolar voltage mapping is associated with increased arrhythmia recurrences following pulmonary vein isolation for atrial fibrillation (AF). Besides local myocardial fibrosis, bipolar voltage amplitudes may be influenced by inter-electrode spacing and bipole-to-wavefront-angle. It is unclear to what extent these impact low voltage areas (LVA) in the clinical setting. Alternatively, unipolar electrogram voltage is not affected by these factors but requires advanced filtering. Objectives: To assess the relationship between bipolar and unipolar voltage mapping in sinus rhythm (SR) and AF and identify if the electrogram recording mode affects the quantification and localization of LVA. Methods: Patients ( n = 28, 66±7 years, 46% male, 82% persistent AF, 32% redo-procedures) underwent high-density (>1,200 sites, 20 ± 10 sites/cm 2 , using a 20-pole 2-6-2 mm-spaced Lasso) voltage mapping in SR and AF. Bipolar LVA were defined using four different thresholds described in literature: <0.5 and <1 mV in SR, <0.35 and <0.5 mV in AF. The optimal unipolar voltage threshold resulting in the highest agreement in both unipolar and bipolar mapping modes was determined. The impact of the inter-electrode distance (2 vs. 6 mm) on the correlation was assessed. Regional analysis was performed using an 11-segment left atrial model. Results: Patients had relevant bipolar LVA (23 ± 23 cm 2 at <0.5 mV in SR and 42 ± 26 cm 2 at <0.5 mV in AF). 90 ± 5% (in SR) and 85 ± 5% (AF) of mapped sites were concordantly classified as high or low voltage in both mapping modes. Discordant mapping sites located to the border zone of LVA. Bipolar voltage mapping using 2 vs. 6 mm inter-electrode distances increased the portion of matched mapping points by 4%. The unipolar thresholds (y) which resulted in a high spatial concordance can be calculated from the bipolar threshold (x) using following linear equations: y = 1.06 x + 0.26 mV ( r = 0.994) for SR and y = 1.22 x + 0.12 mV ( r = 0.998) for AF. Conclusion: Bipolar and unipolar voltage maps are highly correlated, in SR and AF. While bipole orientation and inter-electrode spacing are theoretical confounders, their impact is unlikely to be of clinical importance for localization of LVA, when mapping is performed at high density with a 20-polar Lasso catheter.
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Nairn et al. (2020) conducted an observational in Atrial Fibrillation (n=28). Unipolar voltage mapping vs. Bipolar voltage mapping was evaluated on Concordant classification of mapped sites as high or low voltage in sinus rhythm. Unipolar and bipolar voltage mapping demonstrated high spatial concordance, with 90% of sites in sinus rhythm and 85% in atrial fibrillation concordantly classified as high or low voltage.
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