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) |
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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 |
format | Article |
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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</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 > 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 > 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</description><subject>Ablation</subject><subject>Aged</subject><subject>Cardiac arrhythmia</subject><subject>Catheter Ablation</subject><subject>Cicatrix - etiology</subject><subject>Cicatrix - physiopathology</subject><subject>Clinical outcomes</subject><subject>Female</subject><subject>Heart transplantation</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Risk groups</subject><subject>Statistical analysis</subject><subject>Tachycardia</subject><subject>Tachycardia, Ventricular - diagnosis</subject><subject>Tachycardia, Ventricular - etiology</subject><subject>Tachycardia, Ventricular - physiopathology</subject><subject>Tachycardia, Ventricular - surgery</subject><subject>Treatment Outcome</subject><subject>Ventricle</subject><issn>1099-5129</issn><issn>1532-2092</issn><issn>1532-2092</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0EoqVw54QscSlCKR47TuIL0qoUqFQBEnCOHHuy65KNU_-ptB-Jb4nRbnvgQk_zpPm9J808Ql4COwOmxDvMwS_aYBEaoZOPyDFIwSvOFH9cNFOqksDVEXkW4zVjrOVKPiVHQjEBjMMx-b0yOSFdfEzVErxBm4OeqJttNm5wk0s76iLVhfCBLgGtM6koP1IzudmZAvucjN9iLC66cetNFVz8RRedHM4p0tNvq8svF98_0PcU2jc0zxbD2rt5TaPRoQo46YSW3hY4OJMnHWjSZrMrS-s01UPZOz8_J09GPUV8cZgn5OfHix_nn6urr58uz1dXlREcUqWBM2Y6xRjv0JpxlHYcBQ7KtkJbxrqmBdGA1I0C3ggY6qZWA9QjtJ0RTS1OyOk-t7zjJmNM_dZFg9OkZ_Q59qJEiA6k7B6Cln8rLlVBX_-DXvsc5nJIL4DXdV0ioVBsT5ngYww49ktwWx12PbD-b-P9XeP9ofFieXUIzsMW7b3hruICvN0DPi__j_sD4KW6DA</recordid><startdate>20240702</startdate><enddate>20240702</enddate><creator>Sipko, Joseph</creator><creator>Baranowski, Bryan</creator><creator>Bhargava, Mandeep</creator><creator>Callahan, Thomas D</creator><creator>Dresing, Thomas J</creator><creator>Higuchi, Koji</creator><creator>Hussein, Ayman A</creator><creator>Kanj, Mohamed</creator><creator>Lee, Justin</creator><creator>Martin, David O</creator><creator>Nakhla, Shady</creator><creator>Rickard, John J</creator><creator>Saliba, Walid I</creator><creator>Taigen, Tyler</creator><creator>Wazni, Oussama M</creator><creator>Santangeli, Pasquale</creator><creator>Sroubek, Jakub</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><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></search><sort><creationdate>20240702</creationdate><title>Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD > 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 & 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 > 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 > 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</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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