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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1016/j.jacep.2019.11.004</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">146809</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">ART-2020-146809</subfield>
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  <datafield tag="041" ind1=" " ind2=" ">
    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Soto-Iglesias D</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Cardiac Magnetic Resonance-Guided Ventricular Tachycardia Substrate Ablation.</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2020</subfield>
  </datafield>
  <datafield tag="520" ind1="3" ind2=" ">
    <subfield code="a">Objectives
This study assessed the feasibility and potential benefit of performing ventricular tachycardia (VT) substrate ablation procedures guided by cardiac magnetic resonance (CMR)-derived pixel signal intensity (PSI) maps.
Background
CMR-aided VT ablation using PSI maps from late gadolinium enhancement-CMR (LGE-CMR), together with electroanatomical map (EAM) information, has been shown to improve outcomes of VT substrate ablation.
Methods
Eighty-four patients with scar-dependent monomorphic VT who underwent substrate ablation were included in the study. In the last 28 (33%) consecutive patients, the procedure was guided by CMR. Procedural data, as well as acute and follow-up outcomes, were compared between patients who underwent guided CMR and 2 control groups: 1) patients who had PSI maps were available but the EAM was acquired and used to select the ablation targets (CMR aided); and 2) patients with no CMR-derived PSI maps available (no CMR).
Results
Mean procedure duration was lower in CMR-guided substrate ablation compared with CMR-aided and no CMR (107 ± 59 min vs. 203 ± 68 min and 227 ± 52 min; p &lt; 0.001 for both comparisons). CMR-guided ablation required less fluoroscopy time than CMR-aided ablation and no CMR (10 ± 4 min vs. 23 ± 11 min and 20 ± 9 min, respectively; p &lt; 0.001 for both comparisons) and less radiofrequency time (15 ± 8 min vs. 20 ± 15 min and 26 ± 10 min; p = 0.16 and p &lt; 0.001, respectively). After substrate ablation, VT inducibility was lower in CMR-guided ablation compared with CMR-aided ablation and no CMR (18% vs. 32% and 46%; p = 0.35 and p = 0.04, respectively), without significant differences in complications. After 12 months, VT recurrence was lower in those who underwent CMR-guided ablation compared with no CMR (log-rank: 0.019), with no differences with CMR-aided ablation.
Conclusions
CMR-guided VT ablation is feasible and safe, significantly reduces the procedural, fluoroscopy, and radiofrequency times, and is associated with a higher noninducibility rate and lower VT recurrence after substrate ablation.</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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  <datafield tag="536" ind1=" " ind2=" ">
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RTC-2015-3515-1</subfield>
    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RTC-2016-5445-1</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
    <subfield code="a">by-nc-nd</subfield>
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    <subfield code="a">CARDIAC &amp; CARDIOVASCULAR SYSTEMS</subfield>
    <subfield code="b">26 / 141 = 0.184</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
    <subfield code="e">T1</subfield>
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    <subfield code="a">2.278</subfield>
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    <subfield code="a">Physiology (medical)</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">Cardiology and Cardiovascular Medicine</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">info:eu-repo/semantics/article</subfield>
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    <subfield code="a">Penela D</subfield>
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    <subfield code="a">Jáuregui B</subfield>
    <subfield code="0">(orcid)0000-0001-9187-1773</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Acosta J</subfield>
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    <subfield code="a">Fernández-Armenta J</subfield>
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    <subfield code="a">Linhart M</subfield>
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    <subfield code="a">Zucchelli G</subfield>
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    <subfield code="a">Syrovnev V</subfield>
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    <subfield code="a">Terés C</subfield>
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    <subfield code="a">Perea RJ</subfield>
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    <subfield code="a">Prat-González S</subfield>
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    <subfield code="g">6, 4 (2020), 436 - 447</subfield>
    <subfield code="t">JACC: Clinical Electrophysiology</subfield>
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