Key result
LoopLens ECG and VCG markers show modest repeatability with a median ICC of ~0.47.
Why the study?
Physiological names do not fully determine the measurement definition of an ECG or VCG marker, motivating an audit of how values in one implementation (LoopLens 10.1) vary across repeat recordings, reconstruction matrices, and boundary references.
Observational (n=10,187)
Question-specific non-independent analyst blinding for replication test partition
No
This exploratory audit of the LoopLens 10.1 ECG/VCG pipeline demonstrates substantial short-term repeat variation in routine clinical ECGs and widespread sensitivity of calculated markers to VCG reconstruction matrices and fiducial boundary definitions, highlighting that physiological marker names do not guarantee measurement stability or interchangeability.
Objective Physiological names do not fully determine the measurement definition of an electrocardiogram (ECG) or vectorcardiogram (VCG) marker. We examined how the values of one implementation (LoopLens 10.1) change between routine recordings 0–2 h apart, between two reconstruction matrices and between boundary references, in a catalog of 2,005 markers. Approach: Development-data audits in MIMIC-IV-ECG (15,693 pairs; 5,648 recordings for the matrix comparison), expert-boundary comparison in LUDB, repeat pairs from PTB-XL and public randomized QT controls. Replication was prespecified in a person-disjoint test partition, previously opened for other analyses. Main results: The median ICC(A,1) of 1,958 estimable non-circular markers was 0.468 (311 reached 0.75); an ICC cannot separate error, change and low between-person spread. The repeatability coefficient (RC, 1.96 SD of paired differences, including true change) was 27.27 ms for QRS duration, 61.78 ms for QT corrected by the Fridericia formula (QTcF) and 82.41° for the QRS-T area angle. Under author-fixed rules, replacing the Kors with the inverse Dower matrix gave 1,045 dependent, 684 conditional and no stable outputs among 1,729 non-identical estimable non-circular ones, yet ± 4-ms boundary shifts alone gave 496 dependent of 1,724; 29 circular markers were not classified. Against LUDB experts (amplitudes normalized per lead), the median P-onset error was + 14 ms with extreme-boundary and + 1 ms with lead-median references. PTB-XL repeat variation (pairs up to 24 h apart) had equal or lower point estimates than MIMIC (R 0.77–0.99), with no class decided. In public randomized recordings, the production (standard LoopLens) and source-annotation routes differed in 7 of 16 estimable treatment contrasts (exploratory, unadjusted). In the test partition, the historical matrix classification and P availability replicated; repeatability criteria were not met, with higher test ICCs.
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Leo Probst (2026) conducted an observational in Routine diagnostic ECG/VCG evaluation (n=10,187). LoopLens 10.1 ECG/VCG marker pipeline (repeat variation, Kors vs inverse Dower reconstruction matrix, and boundary reference comparisons) vs. Repeated recordings 0-2 h apart, Kors reconstruction matrix, and expert boundary annotations was evaluated on Short-interval repeat variation of 1,958 estimable non-circular ECG/VCG markers (median intraclass correlation coefficient [ICC(A,1)] and repeatability coefficients [RC]). LoopLens 10.1 ECG/VCG markers showed a median ICC of 0.468 across 15,693 pairs 0-2 h apart (RC 27.27 ms for QRS, 61.78 ms for QTcF), with 60.4% of non-circular outputs dependent on matrix choice.
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