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    <subfield code="a">10.1016/j.bspc.2023.105056</subfield>
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    <subfield code="a">ART-2023-134124</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Pérez, Cristina</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-8334-4786</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">QT interval time lag in response to heart rate changes during stress test for Coronary Artery Disease diagnosis</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2023</subfield>
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    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Background: Slow adaptation of the QT interval to abrupt changes in heart rate (HR) can enhance ventricular heterogeneity and has been suggested as a marker of arrhythmic risk. Most investigations on QT rate adaptation lag have been performed in response to step-like HR changes. However, abrupt HR changes are difficult to induce or observe in ECG recordings under ambulatory conditions.

Objective: We aim to evaluate the power of indices related to the QT lag in response to ramp-like HR changes in stress test to assess CAD risk.

Methods: We quantified the lag between the actual QT series and the memoryless expected QT series, which was obtained by fitting a hyperbolic regression model to the instantaneous QT and HR measurements in stages where their behavior could be assumed stationary. The proposed methodology was applied to analyze ECG stress tests of a subset of 448 patients presenting different risk levels for Coronary Artery Disease (CAD). The QT lag was estimated separately in the exercise and recovery phases.

Results: An increase in the estimated QT lag during exercise (from 25 to 36 s) and a decrease during recovery (from 57 to 39 s) were associated with higher CAD risk. The difference between these lags showed significant capacity for CAD risk stratification.

Conclusion: The QT lag in response to HR changes can be quantified from a stress test. QT lag values in response to ramp-like HR changes are in ranges comparable to those quantified from abrupt HR changes and show clinical significance to stratify CAD risk.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/T39-23R</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/EUR/ERC-2014-StG-638284</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Pueyo, Esther</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1960-407X</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Martínez, Juan Pablo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7503-3339</subfield>
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    <subfield code="a">Viik, Jari</subfield>
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    <subfield code="a">Laguna, Pablo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3434-9254</subfield>
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    <subfield code="b">Dpto. Ingeniería Electrón.Com.</subfield>
    <subfield code="c">Área Teoría Señal y Comunicac.</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">86 (2023), 105056 [13 pp.]</subfield>
    <subfield code="p">Biomed. signal proces. control</subfield>
    <subfield code="t">Biomedical Signal Processing and Control</subfield>
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