Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD > 17) undergoing scar-related ventricular tachycardia ablation

Abstract Aims Ventricular tachycardia (VT) non-inducibility in response to programmed ventricular stimulation (PVS) is a widely used procedural endpoint for VT ablation despite inconclusive evidence with respect to clinical outcomes in high-risk patients. The aim is to determine the utility of acute...

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Veröffentlicht in:Europace (London, England) England), 2024-07, Vol.26 (7)
Hauptverfasser: Sipko, Joseph, Baranowski, Bryan, Bhargava, Mandeep, Callahan, Thomas D, Dresing, Thomas J, Higuchi, Koji, Hussein, Ayman A, Kanj, Mohamed, Lee, Justin, Martin, David O, Nakhla, Shady, Rickard, John J, Saliba, Walid I, Taigen, Tyler, Wazni, Oussama M, Santangeli, Pasquale, Sroubek, Jakub
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container_issue 7
container_start_page
container_title Europace (London, England)
container_volume 26
creator Sipko, Joseph
Baranowski, Bryan
Bhargava, Mandeep
Callahan, Thomas D
Dresing, Thomas J
Higuchi, Koji
Hussein, Ayman A
Kanj, Mohamed
Lee, Justin
Martin, David O
Nakhla, Shady
Rickard, John J
Saliba, Walid I
Taigen, Tyler
Wazni, Oussama M
Santangeli, Pasquale
Sroubek, Jakub
description Abstract Aims Ventricular tachycardia (VT) non-inducibility in response to programmed ventricular stimulation (PVS) is a widely used procedural endpoint for VT ablation despite inconclusive evidence with respect to clinical outcomes in high-risk patients. The aim is to determine the utility of acute post-ablation VT inducibility as a predictor of VT recurrence, mortality, or mortality equivalent in high-risk patients. Methods and results We conducted a retrospective analysis of high-risk patients (defined as PAINESD > 17) who underwent scar-related VT ablation at our institution between July 2010 and July 2022. Patients’ response to PVS (post-procedure) was categorized into three groups: Group A, no clinical VT or VT with cycle length > 240 ms inducible; Group B, only non-clinical VT with cycle length > 240 ms induced; and Group C, all other outcomes (including cases where no PVS was performed). The combined primary endpoint included death, durable left ventricular assist device placement, and cardiac transplant (Cox analysis). Ventricular tachycardia recurrence was considered a secondary endpoint (competing risk analysis). Of the 1677 VT ablation cases, 123 cases met the inclusion criteria for analysis. During a 19-month median follow-up time (interquartile range 4–43 months), 82 (66.7%) patients experienced the composite primary endpoint. There was no difference between Groups A and C with respect to the primary [hazard ratio (HR) = 1.21 (0.94–1.57), P = 0.145] or secondary [HR = 1.18 (0.91–1.54), P = 0.210] outcomes. These findings persisted after multivariate adjustments. The size of Group B (n = 13) did not permit meaningful statistical analysis. Conclusion The results of post-ablation PVS do not significantly correlate with long-term outcomes in high-risk (PAINESD > 17) VT ablation patients. Graphical Abstract Graphical Abstract
doi_str_mv 10.1093/europace/euae185
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The aim is to determine the utility of acute post-ablation VT inducibility as a predictor of VT recurrence, mortality, or mortality equivalent in high-risk patients. Methods and results We conducted a retrospective analysis of high-risk patients (defined as PAINESD &gt; 17) who underwent scar-related VT ablation at our institution between July 2010 and July 2022. Patients’ response to PVS (post-procedure) was categorized into three groups: Group A, no clinical VT or VT with cycle length &gt; 240 ms inducible; Group B, only non-clinical VT with cycle length &gt; 240 ms induced; and Group C, all other outcomes (including cases where no PVS was performed). The combined primary endpoint included death, durable left ventricular assist device placement, and cardiac transplant (Cox analysis). Ventricular tachycardia recurrence was considered a secondary endpoint (competing risk analysis). Of the 1677 VT ablation cases, 123 cases met the inclusion criteria for analysis. During a 19-month median follow-up time (interquartile range 4–43 months), 82 (66.7%) patients experienced the composite primary endpoint. There was no difference between Groups A and C with respect to the primary [hazard ratio (HR) = 1.21 (0.94–1.57), P = 0.145] or secondary [HR = 1.18 (0.91–1.54), P = 0.210] outcomes. These findings persisted after multivariate adjustments. The size of Group B (n = 13) did not permit meaningful statistical analysis. Conclusion The results of post-ablation PVS do not significantly correlate with long-term outcomes in high-risk (PAINESD &gt; 17) VT ablation patients. Graphical Abstract Graphical Abstract</description><identifier>ISSN: 1099-5129</identifier><identifier>ISSN: 1532-2092</identifier><identifier>EISSN: 1532-2092</identifier><identifier>DOI: 10.1093/europace/euae185</identifier><identifier>PMID: 39031021</identifier><language>eng</language><publisher>UK: Oxford University Press</publisher><subject>Ablation ; Aged ; Cardiac arrhythmia ; Catheter Ablation ; Cicatrix - etiology ; Cicatrix - physiopathology ; Clinical outcomes ; Female ; Heart transplantation ; Humans ; Male ; Middle Aged ; Mortality ; Recurrence ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Risk groups ; Statistical analysis ; Tachycardia ; Tachycardia, Ventricular - diagnosis ; Tachycardia, Ventricular - etiology ; Tachycardia, Ventricular - physiopathology ; Tachycardia, Ventricular - surgery ; Treatment Outcome ; Ventricle</subject><ispartof>Europace (London, England), 2024-07, Vol.26 (7)</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c321t-a1200c890028edcff5dff3eb9d73ad0086713615a6912631b4649b14f178c3643</cites><orcidid>0009-0008-3990-7407 ; 0000-0003-2490-5106 ; 0000-0002-4495-3845 ; 0000-0002-9218-1966 ; 0000-0001-5281-7598 ; 0009-0002-1419-1808 ; 0000-0003-2823-9243 ; 0000-0002-6711-7284 ; 0000-0002-8359-1525 ; 0000-0002-1258-8118 ; 0000-0002-0023-9666</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1605,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39031021$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sipko, Joseph</creatorcontrib><creatorcontrib>Baranowski, Bryan</creatorcontrib><creatorcontrib>Bhargava, Mandeep</creatorcontrib><creatorcontrib>Callahan, Thomas D</creatorcontrib><creatorcontrib>Dresing, Thomas J</creatorcontrib><creatorcontrib>Higuchi, Koji</creatorcontrib><creatorcontrib>Hussein, Ayman A</creatorcontrib><creatorcontrib>Kanj, Mohamed</creatorcontrib><creatorcontrib>Lee, Justin</creatorcontrib><creatorcontrib>Martin, David O</creatorcontrib><creatorcontrib>Nakhla, Shady</creatorcontrib><creatorcontrib>Rickard, John J</creatorcontrib><creatorcontrib>Saliba, Walid I</creatorcontrib><creatorcontrib>Taigen, Tyler</creatorcontrib><creatorcontrib>Wazni, Oussama M</creatorcontrib><creatorcontrib>Santangeli, Pasquale</creatorcontrib><creatorcontrib>Sroubek, Jakub</creatorcontrib><title>Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD &gt; 17) undergoing scar-related ventricular tachycardia ablation</title><title>Europace (London, England)</title><addtitle>Europace</addtitle><description>Abstract Aims Ventricular tachycardia (VT) non-inducibility in response to programmed ventricular stimulation (PVS) is a widely used procedural endpoint for VT ablation despite inconclusive evidence with respect to clinical outcomes in high-risk patients. The aim is to determine the utility of acute post-ablation VT inducibility as a predictor of VT recurrence, mortality, or mortality equivalent in high-risk patients. Methods and results We conducted a retrospective analysis of high-risk patients (defined as PAINESD &gt; 17) who underwent scar-related VT ablation at our institution between July 2010 and July 2022. Patients’ response to PVS (post-procedure) was categorized into three groups: Group A, no clinical VT or VT with cycle length &gt; 240 ms inducible; Group B, only non-clinical VT with cycle length &gt; 240 ms induced; and Group C, all other outcomes (including cases where no PVS was performed). The combined primary endpoint included death, durable left ventricular assist device placement, and cardiac transplant (Cox analysis). Ventricular tachycardia recurrence was considered a secondary endpoint (competing risk analysis). Of the 1677 VT ablation cases, 123 cases met the inclusion criteria for analysis. During a 19-month median follow-up time (interquartile range 4–43 months), 82 (66.7%) patients experienced the composite primary endpoint. There was no difference between Groups A and C with respect to the primary [hazard ratio (HR) = 1.21 (0.94–1.57), P = 0.145] or secondary [HR = 1.18 (0.91–1.54), P = 0.210] outcomes. These findings persisted after multivariate adjustments. The size of Group B (n = 13) did not permit meaningful statistical analysis. Conclusion The results of post-ablation PVS do not significantly correlate with long-term outcomes in high-risk (PAINESD &gt; 17) VT ablation patients. 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17) undergoing scar-related ventricular tachycardia ablation</title><author>Sipko, Joseph ; Baranowski, Bryan ; Bhargava, Mandeep ; Callahan, Thomas D ; Dresing, Thomas J ; Higuchi, Koji ; Hussein, Ayman A ; Kanj, Mohamed ; Lee, Justin ; Martin, David O ; Nakhla, Shady ; Rickard, John J ; Saliba, Walid I ; Taigen, Tyler ; Wazni, Oussama M ; Santangeli, Pasquale ; Sroubek, Jakub</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-a1200c890028edcff5dff3eb9d73ad0086713615a6912631b4649b14f178c3643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Ablation</topic><topic>Aged</topic><topic>Cardiac arrhythmia</topic><topic>Catheter Ablation</topic><topic>Cicatrix - etiology</topic><topic>Cicatrix - physiopathology</topic><topic>Clinical outcomes</topic><topic>Female</topic><topic>Heart transplantation</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Recurrence</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Risk groups</topic><topic>Statistical analysis</topic><topic>Tachycardia</topic><topic>Tachycardia, Ventricular - diagnosis</topic><topic>Tachycardia, Ventricular - etiology</topic><topic>Tachycardia, Ventricular - physiopathology</topic><topic>Tachycardia, Ventricular - surgery</topic><topic>Treatment Outcome</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sipko, Joseph</creatorcontrib><creatorcontrib>Baranowski, Bryan</creatorcontrib><creatorcontrib>Bhargava, Mandeep</creatorcontrib><creatorcontrib>Callahan, Thomas D</creatorcontrib><creatorcontrib>Dresing, Thomas J</creatorcontrib><creatorcontrib>Higuchi, Koji</creatorcontrib><creatorcontrib>Hussein, Ayman A</creatorcontrib><creatorcontrib>Kanj, Mohamed</creatorcontrib><creatorcontrib>Lee, Justin</creatorcontrib><creatorcontrib>Martin, David O</creatorcontrib><creatorcontrib>Nakhla, Shady</creatorcontrib><creatorcontrib>Rickard, John J</creatorcontrib><creatorcontrib>Saliba, Walid I</creatorcontrib><creatorcontrib>Taigen, Tyler</creatorcontrib><creatorcontrib>Wazni, Oussama M</creatorcontrib><creatorcontrib>Santangeli, Pasquale</creatorcontrib><creatorcontrib>Sroubek, Jakub</creatorcontrib><collection>Access via Oxford University Press (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Europace (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sipko, Joseph</au><au>Baranowski, Bryan</au><au>Bhargava, Mandeep</au><au>Callahan, Thomas D</au><au>Dresing, Thomas J</au><au>Higuchi, Koji</au><au>Hussein, Ayman A</au><au>Kanj, Mohamed</au><au>Lee, Justin</au><au>Martin, David O</au><au>Nakhla, Shady</au><au>Rickard, John J</au><au>Saliba, Walid I</au><au>Taigen, Tyler</au><au>Wazni, Oussama M</au><au>Santangeli, Pasquale</au><au>Sroubek, Jakub</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD &gt; 17) undergoing scar-related ventricular tachycardia ablation</atitle><jtitle>Europace (London, England)</jtitle><addtitle>Europace</addtitle><date>2024-07-02</date><risdate>2024</risdate><volume>26</volume><issue>7</issue><issn>1099-5129</issn><issn>1532-2092</issn><eissn>1532-2092</eissn><abstract>Abstract Aims Ventricular tachycardia (VT) non-inducibility in response to programmed ventricular stimulation (PVS) is a widely used procedural endpoint for VT ablation despite inconclusive evidence with respect to clinical outcomes in high-risk patients. The aim is to determine the utility of acute post-ablation VT inducibility as a predictor of VT recurrence, mortality, or mortality equivalent in high-risk patients. Methods and results We conducted a retrospective analysis of high-risk patients (defined as PAINESD &gt; 17) who underwent scar-related VT ablation at our institution between July 2010 and July 2022. Patients’ response to PVS (post-procedure) was categorized into three groups: Group A, no clinical VT or VT with cycle length &gt; 240 ms inducible; Group B, only non-clinical VT with cycle length &gt; 240 ms induced; and Group C, all other outcomes (including cases where no PVS was performed). The combined primary endpoint included death, durable left ventricular assist device placement, and cardiac transplant (Cox analysis). Ventricular tachycardia recurrence was considered a secondary endpoint (competing risk analysis). Of the 1677 VT ablation cases, 123 cases met the inclusion criteria for analysis. During a 19-month median follow-up time (interquartile range 4–43 months), 82 (66.7%) patients experienced the composite primary endpoint. There was no difference between Groups A and C with respect to the primary [hazard ratio (HR) = 1.21 (0.94–1.57), P = 0.145] or secondary [HR = 1.18 (0.91–1.54), P = 0.210] outcomes. These findings persisted after multivariate adjustments. The size of Group B (n = 13) did not permit meaningful statistical analysis. Conclusion The results of post-ablation PVS do not significantly correlate with long-term outcomes in high-risk (PAINESD &gt; 17) VT ablation patients. Graphical Abstract Graphical Abstract</abstract><cop>UK</cop><pub>Oxford University Press</pub><pmid>39031021</pmid><doi>10.1093/europace/euae185</doi><orcidid>https://orcid.org/0009-0008-3990-7407</orcidid><orcidid>https://orcid.org/0000-0003-2490-5106</orcidid><orcidid>https://orcid.org/0000-0002-4495-3845</orcidid><orcidid>https://orcid.org/0000-0002-9218-1966</orcidid><orcidid>https://orcid.org/0000-0001-5281-7598</orcidid><orcidid>https://orcid.org/0009-0002-1419-1808</orcidid><orcidid>https://orcid.org/0000-0003-2823-9243</orcidid><orcidid>https://orcid.org/0000-0002-6711-7284</orcidid><orcidid>https://orcid.org/0000-0002-8359-1525</orcidid><orcidid>https://orcid.org/0000-0002-1258-8118</orcidid><orcidid>https://orcid.org/0000-0002-0023-9666</orcidid><oa>free_for_read</oa></addata></record>
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subjects Ablation
Aged
Cardiac arrhythmia
Catheter Ablation
Cicatrix - etiology
Cicatrix - physiopathology
Clinical outcomes
Female
Heart transplantation
Humans
Male
Middle Aged
Mortality
Recurrence
Retrospective Studies
Risk Assessment
Risk Factors
Risk groups
Statistical analysis
Tachycardia
Tachycardia, Ventricular - diagnosis
Tachycardia, Ventricular - etiology
Tachycardia, Ventricular - physiopathology
Tachycardia, Ventricular - surgery
Treatment Outcome
Ventricle
title Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD > 17) undergoing scar-related ventricular tachycardia ablation
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