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Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads

Electrocardiographic (ECG) T-wave endpoint (T(end)) identification suffers lack of reliability due to the presence of noise and variability among leads. T(end) identification can be improved by using global repolarization waveforms obtained by combining several leads. The dominant T-wave (DTW) is a...

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Autores principales: Giuliani, C., Agostinelli, A., Di Nardo, F., Fioretti, S., Burattini, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901195/
https://www.ncbi.nlm.nih.gov/pubmed/27347218
http://dx.doi.org/10.2174/1874120701610010043
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author Giuliani, C.
Agostinelli, A.
Di Nardo, F.
Fioretti, S.
Burattini, L.
author_facet Giuliani, C.
Agostinelli, A.
Di Nardo, F.
Fioretti, S.
Burattini, L.
author_sort Giuliani, C.
collection PubMed
description Electrocardiographic (ECG) T-wave endpoint (T(end)) identification suffers lack of reliability due to the presence of noise and variability among leads. T(end) identification can be improved by using global repolarization waveforms obtained by combining several leads. The dominant T-wave (DTW) is a global repolarization waveform that proved to improve T(end) identification when computed using the 15 (I to III, aVr, aVl, aVf, V1 to V6, X, Y, Z) leads usually available in clinics, of which only 8 (I, II, V1 to V6) are independent. The aim of the present study was to evaluate if the 8 independent leads are sufficient to obtain a DTW which allows a reliable T(end) identification. To this aim T(end) measures automatically identified from 15-dependent-lead DTWs of 46 control healthy subjects (CHS) and 103 acute myocardial infarction patients (AMIP) were compared with those obtained from 8-independent-lead DTWs. Results indicate that T(end) distributions have not statistically different median values (CHS: 340 ms vs. 340 ms, respectively; AMIP: 325 ms vs. 320 ms, respectively), besides being strongly correlated (CHS: ρ=0.97, AMIP: 0.88; P<10(-27)). Thus, measuring T(end) from the 15-dependent-lead DTWs is statistically equivalent to measuring T(end) from the 8-independent-lead DTWs. In conclusion, for the clinical purpose of automatic T(end) identification from DTW, the 8 independent leads can be used without a statistically significant loss of accuracy but with a significant decrement of computational effort. The lead dependence of 7 out of 15 leads does not introduce a significant bias in the T(end) determination from 15 dependent lead DTWs.
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spelling pubmed-49011952016-06-24 Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads Giuliani, C. Agostinelli, A. Di Nardo, F. Fioretti, S. Burattini, L. Open Biomed Eng J Article Electrocardiographic (ECG) T-wave endpoint (T(end)) identification suffers lack of reliability due to the presence of noise and variability among leads. T(end) identification can be improved by using global repolarization waveforms obtained by combining several leads. The dominant T-wave (DTW) is a global repolarization waveform that proved to improve T(end) identification when computed using the 15 (I to III, aVr, aVl, aVf, V1 to V6, X, Y, Z) leads usually available in clinics, of which only 8 (I, II, V1 to V6) are independent. The aim of the present study was to evaluate if the 8 independent leads are sufficient to obtain a DTW which allows a reliable T(end) identification. To this aim T(end) measures automatically identified from 15-dependent-lead DTWs of 46 control healthy subjects (CHS) and 103 acute myocardial infarction patients (AMIP) were compared with those obtained from 8-independent-lead DTWs. Results indicate that T(end) distributions have not statistically different median values (CHS: 340 ms vs. 340 ms, respectively; AMIP: 325 ms vs. 320 ms, respectively), besides being strongly correlated (CHS: ρ=0.97, AMIP: 0.88; P<10(-27)). Thus, measuring T(end) from the 15-dependent-lead DTWs is statistically equivalent to measuring T(end) from the 8-independent-lead DTWs. In conclusion, for the clinical purpose of automatic T(end) identification from DTW, the 8 independent leads can be used without a statistically significant loss of accuracy but with a significant decrement of computational effort. The lead dependence of 7 out of 15 leads does not introduce a significant bias in the T(end) determination from 15 dependent lead DTWs. Bentham Open 2016-04-30 /pmc/articles/PMC4901195/ /pubmed/27347218 http://dx.doi.org/10.2174/1874120701610010043 Text en © Giuliani et al.; Licensee Bentham Open. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Giuliani, C.
Agostinelli, A.
Di Nardo, F.
Fioretti, S.
Burattini, L.
Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title_full Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title_fullStr Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title_full_unstemmed Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title_short Automatic Identification of the Repolarization Endpoint by Computing the Dominant T-wave on a Reduced Number of Leads
title_sort automatic identification of the repolarization endpoint by computing the dominant t-wave on a reduced number of leads
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901195/
https://www.ncbi.nlm.nih.gov/pubmed/27347218
http://dx.doi.org/10.2174/1874120701610010043
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