We have located links that may give you full text access.
JOURNAL ARTICLE
RESEARCH SUPPORT, NON-U.S. GOV'T
Automatic Identification of Reentry Mechanisms and Critical Sites During Atrial Tachycardia by Analyzing Areas of Activity.
IEEE Transactions on Bio-medical Engineering 2018 October
OBJECTIVE: Atrial tachycardia (AT) still poses a major challenge in catheter ablation. Although state-of-the-art electroanatomical mapping systems allow to acquire several thousand intracardiac electrograms (EGMs), algorithms for diagnostic analysis are mainly limited to the amplitude of the signal (voltage map) and the local activation time (LAT map). We applied spatio-temporal analysis of EGM activity to generate maps indicating reentries and diastolic potentials, thus identifying and localizing the driving mechanism of AT.
METHODS: First, the time course of active surface area ASA is determined during one basic cycle length (BCL). The chamber cycle length coverage cCLC reflects the relative duration within one BCL for which activity was present in each individual atrium. A local cycle length coverage lCLC is computed for circular subareas with 20 mm diameter. The simultaneous active surface area sASA is determined to indicate the spatial extent of depolarizing tissue.
RESULTS: Combined analysis of these spatial scales allowed to correctly identify and localize the driving mechanism: cCLC values of 100% were indicative for atria harbouring a reentrant driver. lCLC could detect micro reentries within an area of 1.65 $\pm$ 1.28 cm $^2$ in simulated data and differentiate them against focal sources. Middiastolic potentials, being potential targets for catheter ablation, were identified as areas showing confined activity based on sASA values.
CONCLUSION: The concept of spatio-temporal activity analysis proved successful and correctly indicated the tachycardia mechanism in 20 simulated AT scenarios and three clinical data sets.
SIGNIFICANCE: Automatic interpretation of intracardiac mapping data could help to improve the treatment strategy in complex cases of AT.
METHODS: First, the time course of active surface area ASA is determined during one basic cycle length (BCL). The chamber cycle length coverage cCLC reflects the relative duration within one BCL for which activity was present in each individual atrium. A local cycle length coverage lCLC is computed for circular subareas with 20 mm diameter. The simultaneous active surface area sASA is determined to indicate the spatial extent of depolarizing tissue.
RESULTS: Combined analysis of these spatial scales allowed to correctly identify and localize the driving mechanism: cCLC values of 100% were indicative for atria harbouring a reentrant driver. lCLC could detect micro reentries within an area of 1.65 $\pm$ 1.28 cm $^2$ in simulated data and differentiate them against focal sources. Middiastolic potentials, being potential targets for catheter ablation, were identified as areas showing confined activity based on sASA values.
CONCLUSION: The concept of spatio-temporal activity analysis proved successful and correctly indicated the tachycardia mechanism in 20 simulated AT scenarios and three clinical data sets.
SIGNIFICANCE: Automatic interpretation of intracardiac mapping data could help to improve the treatment strategy in complex cases of AT.
Full text links
Trending Papers
A Personalized Approach to the Management of Congestion in Acute Heart Failure.Heart International 2023
Potential Mechanisms of the Protective Effects of the Cardiometabolic Drugs Type-2 Sodium-Glucose Transporter Inhibitors and Glucagon-like Peptide-1 Receptor Agonists in Heart Failure.International Journal of Molecular Sciences 2024 Februrary 21
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app