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Histopathology of Cryoballoon Ablation-Induced Phrenic Nerve Injury
Cryoballoon‐Induced Phrenic Nerve Injury Introduction Hemi‐diaphragmatic paralysis is the most common complication associated with cryoballoon ablation for atrial fibrillation, yet the histopathology of phrenic nerve injury has not been well described. Methods and Results A preclinical randomized st...
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Published in: | Journal of cardiovascular electrophysiology 2014-02, Vol.25 (2), p.187-194 |
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creator | ANDRADE, JASON G. DUBUC, MARC FERREIRA, JOSE GUERRA, PETER G. LANDRY, EVELYN COULOMBE, NICOLAS RIVARD, LENA MACLE, LAURENT THIBAULT, BERNARD TALAJIC, MARIO ROY, DENIS KHAIRY, PAUL |
description | Cryoballoon‐Induced Phrenic Nerve Injury
Introduction
Hemi‐diaphragmatic paralysis is the most common complication associated with cryoballoon ablation for atrial fibrillation, yet the histopathology of phrenic nerve injury has not been well described.
Methods and Results
A preclinical randomized study was conducted to characterize the histopathology of phrenic nerve injury induced by cryoballoon ablation and assess the potential for electromyographic (EMG) monitoring to limit phrenic nerve damage. Thirty‐two dogs underwent cryoballoon ablation of the right superior pulmonary vein with the objective of inducing phrenic nerve injury. Animals were randomized 1:1 to standard monitoring (i.e., interruption of ablation upon reduction in diaphragmatic motion) versus EMG guidance (i.e., cessation of ablation upon a 30% reduction in the diaphragmatic compound motor action potential [CMAP] amplitude). The acute procedural endpoint was achieved in all dogs. Phrenic nerve injury was characterized by Wallerian degeneration, with subperineural injury to large myelinated axons and evidence of axonal regeneration. The degree of phrenic nerve injury paralleled the reduction in CMAP amplitude (P = 0.007). Animals randomized to EMG guidance had a lower incidence of acute hemi‐diaphragmatic paralysis (50% vs 100%; P = 0.001), persistent paralysis at 30 days (21% vs 75%; multivariate odds ratio 0.12, 95% confidence interval [0.02, 0.69], P = 0.017), and a lesser severity of histologic injury (P = 0.001). Mature pulmonary vein ablation lesion characteristics, including circumferentiality and transmurality, were similar in both groups.
Conclusion
Phrenic nerve injury induced by cryoballoon ablation is axonal in nature and characterized by Wallerian degeneration, with potential for recovery. An EMG‐guided approach is superior to standard monitoring in limiting phrenic nerve damage. |
doi_str_mv | 10.1111/jce.12296 |
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Introduction
Hemi‐diaphragmatic paralysis is the most common complication associated with cryoballoon ablation for atrial fibrillation, yet the histopathology of phrenic nerve injury has not been well described.
Methods and Results
A preclinical randomized study was conducted to characterize the histopathology of phrenic nerve injury induced by cryoballoon ablation and assess the potential for electromyographic (EMG) monitoring to limit phrenic nerve damage. Thirty‐two dogs underwent cryoballoon ablation of the right superior pulmonary vein with the objective of inducing phrenic nerve injury. Animals were randomized 1:1 to standard monitoring (i.e., interruption of ablation upon reduction in diaphragmatic motion) versus EMG guidance (i.e., cessation of ablation upon a 30% reduction in the diaphragmatic compound motor action potential [CMAP] amplitude). The acute procedural endpoint was achieved in all dogs. Phrenic nerve injury was characterized by Wallerian degeneration, with subperineural injury to large myelinated axons and evidence of axonal regeneration. The degree of phrenic nerve injury paralleled the reduction in CMAP amplitude (P = 0.007). Animals randomized to EMG guidance had a lower incidence of acute hemi‐diaphragmatic paralysis (50% vs 100%; P = 0.001), persistent paralysis at 30 days (21% vs 75%; multivariate odds ratio 0.12, 95% confidence interval [0.02, 0.69], P = 0.017), and a lesser severity of histologic injury (P = 0.001). Mature pulmonary vein ablation lesion characteristics, including circumferentiality and transmurality, were similar in both groups.
Conclusion
Phrenic nerve injury induced by cryoballoon ablation is axonal in nature and characterized by Wallerian degeneration, with potential for recovery. An EMG‐guided approach is superior to standard monitoring in limiting phrenic nerve damage.</description><identifier>ISSN: 1045-3873</identifier><identifier>EISSN: 1540-8167</identifier><identifier>DOI: 10.1111/jce.12296</identifier><identifier>PMID: 24102792</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; arrhythmia ; atrial fibrillation ; catheter ablation ; complications ; cryoballoon ; cryoballoon; pulmonary vein isolation ; Cryosurgery - adverse effects ; Dogs ; Neuromuscular Monitoring - methods ; Peripheral Nerve Injuries - etiology ; Peripheral Nerve Injuries - pathology ; Peripheral Nerve Injuries - prevention & control ; phrenic nerve ; Phrenic Nerve - injuries ; Phrenic Nerve - pathology ; pulmonary vein isolation ; Treatment Outcome</subject><ispartof>Journal of cardiovascular electrophysiology, 2014-02, Vol.25 (2), p.187-194</ispartof><rights>2013 Wiley Periodicals, Inc.</rights><rights>Journal compilation © 2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3916-50d517123c74f89996878457c04452a599d81e5f6ff4b174e0abecb7c29be52a3</citedby><cites>FETCH-LOGICAL-c3916-50d517123c74f89996878457c04452a599d81e5f6ff4b174e0abecb7c29be52a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24102792$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ANDRADE, JASON G.</creatorcontrib><creatorcontrib>DUBUC, MARC</creatorcontrib><creatorcontrib>FERREIRA, JOSE</creatorcontrib><creatorcontrib>GUERRA, PETER G.</creatorcontrib><creatorcontrib>LANDRY, EVELYN</creatorcontrib><creatorcontrib>COULOMBE, NICOLAS</creatorcontrib><creatorcontrib>RIVARD, LENA</creatorcontrib><creatorcontrib>MACLE, LAURENT</creatorcontrib><creatorcontrib>THIBAULT, BERNARD</creatorcontrib><creatorcontrib>TALAJIC, MARIO</creatorcontrib><creatorcontrib>ROY, DENIS</creatorcontrib><creatorcontrib>KHAIRY, PAUL</creatorcontrib><title>Histopathology of Cryoballoon Ablation-Induced Phrenic Nerve Injury</title><title>Journal of cardiovascular electrophysiology</title><addtitle>J Cardiovasc Electrophysiol</addtitle><description>Cryoballoon‐Induced Phrenic Nerve Injury
Introduction
Hemi‐diaphragmatic paralysis is the most common complication associated with cryoballoon ablation for atrial fibrillation, yet the histopathology of phrenic nerve injury has not been well described.
Methods and Results
A preclinical randomized study was conducted to characterize the histopathology of phrenic nerve injury induced by cryoballoon ablation and assess the potential for electromyographic (EMG) monitoring to limit phrenic nerve damage. Thirty‐two dogs underwent cryoballoon ablation of the right superior pulmonary vein with the objective of inducing phrenic nerve injury. Animals were randomized 1:1 to standard monitoring (i.e., interruption of ablation upon reduction in diaphragmatic motion) versus EMG guidance (i.e., cessation of ablation upon a 30% reduction in the diaphragmatic compound motor action potential [CMAP] amplitude). The acute procedural endpoint was achieved in all dogs. Phrenic nerve injury was characterized by Wallerian degeneration, with subperineural injury to large myelinated axons and evidence of axonal regeneration. The degree of phrenic nerve injury paralleled the reduction in CMAP amplitude (P = 0.007). Animals randomized to EMG guidance had a lower incidence of acute hemi‐diaphragmatic paralysis (50% vs 100%; P = 0.001), persistent paralysis at 30 days (21% vs 75%; multivariate odds ratio 0.12, 95% confidence interval [0.02, 0.69], P = 0.017), and a lesser severity of histologic injury (P = 0.001). Mature pulmonary vein ablation lesion characteristics, including circumferentiality and transmurality, were similar in both groups.
Conclusion
Phrenic nerve injury induced by cryoballoon ablation is axonal in nature and characterized by Wallerian degeneration, with potential for recovery. An EMG‐guided approach is superior to standard monitoring in limiting phrenic nerve damage.</description><subject>Animals</subject><subject>arrhythmia</subject><subject>atrial fibrillation</subject><subject>catheter ablation</subject><subject>complications</subject><subject>cryoballoon</subject><subject>cryoballoon; pulmonary vein isolation</subject><subject>Cryosurgery - adverse effects</subject><subject>Dogs</subject><subject>Neuromuscular Monitoring - methods</subject><subject>Peripheral Nerve Injuries - etiology</subject><subject>Peripheral Nerve Injuries - pathology</subject><subject>Peripheral Nerve Injuries - prevention & control</subject><subject>phrenic nerve</subject><subject>Phrenic Nerve - injuries</subject><subject>Phrenic Nerve - pathology</subject><subject>pulmonary vein isolation</subject><subject>Treatment Outcome</subject><issn>1045-3873</issn><issn>1540-8167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp10c1u1DAUBWALUdFSWPACKBIbWKT19W-8rKK2M1U1gFSExMZynBuaIRMP9qSQt8d02i6Q8MZefPfIOpeQN0BPIJ_TtccTYMyoZ-QIpKBlBUo_z28qZMkrzQ_Jy5TWlAJXVL4gh0wAZdqwI1Iv-rQLW7e7DUP4PhehK-o4h8YNQwhjcdYMbteHsVyO7eSxLT7dRhx7X6ww3mGxHNdTnF-Rg84NCV8_3Mfky8X5Tb0orz9eLuuz69JzA6qUtJWggXGvRVcZY1SlKyG1p0JI5qQxbQUoO9V1ogEtkLoGfaM9Mw1mwI_J-33uNoafE6ad3fTJ4zC4EcOULCjJBNdCVZm--4euwxTH_DsLwmimFYDJ6sNe-RhSitjZbew3Ls4WqP3brM3N2vtms337kDg1G2yf5GOVGZzuwa9-wPn_SfaqPn-MLPcTeQX4-2nCxR9Waa6l_bq6tFqzxc23q5X9zP8AjayPVA</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>ANDRADE, JASON G.</creator><creator>DUBUC, MARC</creator><creator>FERREIRA, JOSE</creator><creator>GUERRA, PETER G.</creator><creator>LANDRY, EVELYN</creator><creator>COULOMBE, NICOLAS</creator><creator>RIVARD, LENA</creator><creator>MACLE, LAURENT</creator><creator>THIBAULT, BERNARD</creator><creator>TALAJIC, MARIO</creator><creator>ROY, DENIS</creator><creator>KHAIRY, PAUL</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QP</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201402</creationdate><title>Histopathology of Cryoballoon Ablation-Induced Phrenic Nerve Injury</title><author>ANDRADE, JASON G. ; DUBUC, MARC ; FERREIRA, JOSE ; GUERRA, PETER G. ; LANDRY, EVELYN ; COULOMBE, NICOLAS ; RIVARD, LENA ; MACLE, LAURENT ; THIBAULT, BERNARD ; TALAJIC, MARIO ; ROY, DENIS ; KHAIRY, PAUL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3916-50d517123c74f89996878457c04452a599d81e5f6ff4b174e0abecb7c29be52a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>arrhythmia</topic><topic>atrial fibrillation</topic><topic>catheter ablation</topic><topic>complications</topic><topic>cryoballoon</topic><topic>cryoballoon; pulmonary vein isolation</topic><topic>Cryosurgery - adverse effects</topic><topic>Dogs</topic><topic>Neuromuscular Monitoring - methods</topic><topic>Peripheral Nerve Injuries - etiology</topic><topic>Peripheral Nerve Injuries - pathology</topic><topic>Peripheral Nerve Injuries - prevention & control</topic><topic>phrenic nerve</topic><topic>Phrenic Nerve - injuries</topic><topic>Phrenic Nerve - pathology</topic><topic>pulmonary vein isolation</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ANDRADE, JASON G.</creatorcontrib><creatorcontrib>DUBUC, MARC</creatorcontrib><creatorcontrib>FERREIRA, JOSE</creatorcontrib><creatorcontrib>GUERRA, PETER G.</creatorcontrib><creatorcontrib>LANDRY, EVELYN</creatorcontrib><creatorcontrib>COULOMBE, NICOLAS</creatorcontrib><creatorcontrib>RIVARD, LENA</creatorcontrib><creatorcontrib>MACLE, LAURENT</creatorcontrib><creatorcontrib>THIBAULT, BERNARD</creatorcontrib><creatorcontrib>TALAJIC, MARIO</creatorcontrib><creatorcontrib>ROY, DENIS</creatorcontrib><creatorcontrib>KHAIRY, PAUL</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiovascular electrophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ANDRADE, JASON G.</au><au>DUBUC, MARC</au><au>FERREIRA, JOSE</au><au>GUERRA, PETER G.</au><au>LANDRY, EVELYN</au><au>COULOMBE, NICOLAS</au><au>RIVARD, LENA</au><au>MACLE, LAURENT</au><au>THIBAULT, BERNARD</au><au>TALAJIC, MARIO</au><au>ROY, DENIS</au><au>KHAIRY, PAUL</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histopathology of Cryoballoon Ablation-Induced Phrenic Nerve Injury</atitle><jtitle>Journal of cardiovascular electrophysiology</jtitle><addtitle>J Cardiovasc Electrophysiol</addtitle><date>2014-02</date><risdate>2014</risdate><volume>25</volume><issue>2</issue><spage>187</spage><epage>194</epage><pages>187-194</pages><issn>1045-3873</issn><eissn>1540-8167</eissn><abstract>Cryoballoon‐Induced Phrenic Nerve Injury
Introduction
Hemi‐diaphragmatic paralysis is the most common complication associated with cryoballoon ablation for atrial fibrillation, yet the histopathology of phrenic nerve injury has not been well described.
Methods and Results
A preclinical randomized study was conducted to characterize the histopathology of phrenic nerve injury induced by cryoballoon ablation and assess the potential for electromyographic (EMG) monitoring to limit phrenic nerve damage. Thirty‐two dogs underwent cryoballoon ablation of the right superior pulmonary vein with the objective of inducing phrenic nerve injury. Animals were randomized 1:1 to standard monitoring (i.e., interruption of ablation upon reduction in diaphragmatic motion) versus EMG guidance (i.e., cessation of ablation upon a 30% reduction in the diaphragmatic compound motor action potential [CMAP] amplitude). The acute procedural endpoint was achieved in all dogs. Phrenic nerve injury was characterized by Wallerian degeneration, with subperineural injury to large myelinated axons and evidence of axonal regeneration. The degree of phrenic nerve injury paralleled the reduction in CMAP amplitude (P = 0.007). Animals randomized to EMG guidance had a lower incidence of acute hemi‐diaphragmatic paralysis (50% vs 100%; P = 0.001), persistent paralysis at 30 days (21% vs 75%; multivariate odds ratio 0.12, 95% confidence interval [0.02, 0.69], P = 0.017), and a lesser severity of histologic injury (P = 0.001). Mature pulmonary vein ablation lesion characteristics, including circumferentiality and transmurality, were similar in both groups.
Conclusion
Phrenic nerve injury induced by cryoballoon ablation is axonal in nature and characterized by Wallerian degeneration, with potential for recovery. An EMG‐guided approach is superior to standard monitoring in limiting phrenic nerve damage.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24102792</pmid><doi>10.1111/jce.12296</doi><tpages>8</tpages></addata></record> |
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subjects | Animals arrhythmia atrial fibrillation catheter ablation complications cryoballoon cryoballoon pulmonary vein isolation Cryosurgery - adverse effects Dogs Neuromuscular Monitoring - methods Peripheral Nerve Injuries - etiology Peripheral Nerve Injuries - pathology Peripheral Nerve Injuries - prevention & control phrenic nerve Phrenic Nerve - injuries Phrenic Nerve - pathology pulmonary vein isolation Treatment Outcome |
title | Histopathology of Cryoballoon Ablation-Induced Phrenic Nerve Injury |
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