ArticleComputing in cardiology2020
Experimental Validation of a Novel Extracellular-Based Source Representation of Acute Myocardial Ischemia.
Article in Computing in cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 3 citations in OpenAlex.
- Tipping the scales of understanding: An engineering approach to design and implement whole-body cardiac electrophysiology experimental models.Frontiers in physiology · 2023Article
- Uncertainty Quantification in Simulations of Myocardial Ischemia.Computing in cardiology · 2021Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
Electrocardiographic imaging (ECGI) based detection of myocardial ischemia requires an accurate formulation of the source model, which includes a relationship between extracellular and transmembrane potentials (TMPs). In this study, we used high-resolution intramural experimental recordings and forward modeling to examine the relationship between extracellular potentials and TMPs during myocardial ischemia. We measured extracellular electro-grams from intramural plunge needle arrays during seven controlled ischemia episodes in an animal model. We used three TMP source representations: (1) parameterized and distance-based (defined previously), (2) extracellular-based linear transform, and (3) extracellular-based sigmoidal transform. TMPs for each source formulation were then used to compute extracellular potentials by calculating the passive bidomain forward solution throughout the myocardium. We compared measured and computed potentials. Linear and sigmoidal approaches produced improved results compared to the parameterized method. The RMSE, SC, and TC of linear, sigmoidal, and parameterized methods were 0.85 mV, 1.21 mV, and 3.37 mV; 0.91, 0.88, and 0.47; 0.90, 0.77, and 0.33 respectively. We found extracellular-based calculations of TMPs produced superior forward computations compared to parameterized zones.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.