Gradient variability in hypertrophic cardiomyopathy: New insights from computer‐assisted, high fidelity, rest and exercise hemodynamic analysis
Objectives This study examines the intrapatient variability in peak instantaneous left ventricular outflow tract (LVOT) gradients and aortic pulse pressures during rest, exercise, and after ventricular ectopy. Background Although the variability in LVOT gradients in patients with hypertrophic cardio...
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Veröffentlicht in: | Catheterization and cardiovascular interventions 2019-07, Vol.94 (1), p.E37-E43 |
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description | Objectives
This study examines the intrapatient variability in peak instantaneous left ventricular outflow tract (LVOT) gradients and aortic pulse pressures during rest, exercise, and after ventricular ectopy.
Background
Although the variability in LVOT gradients in patients with hypertrophic cardiomyopathy (HCM) is well known, the predictors of such variation are not. We hypothesized that quantitative invasive analysis of gradient variation could identify useful predictors of maximal gradients.
Methods
Variability in continuously recorded, high‐fidelity left ventricular and aortic pressure waveforms were evaluated by computer‐assisted analysis in the resting state (N = 659 beats) and during supine exercise (N = 379 beats) in a symptomatic patient with a resting LVOT gradient >30 mmHg and frequent ventricular ectopy.
Results
At rest, the peak left ventricular and aortic pressures at the time of the peak instantaneous LVOT gradient for all sinus and postectopic beats followed consistent regression slopes characterizing the potential energy loss between the LV cavity and aorta. During exercise, similar regression slopes were identified, and these converged with the resting slopes at the point of the maximal measured LVOT gradient. Component analysis of the LVOT gradient suggests that resting beat‐to‐beat variability provides information similar to post‐ectopic pressures for predicting maximal gradients in obstructive‐variant HCM.
Conclusions
Our study suggests that computer‐assisted analysis of hemodynamic variability in HCM may prove useful in characterizing the severity of obstruction. Further study is warranted to confirm the reproducibility and utility of this finding in a population with clinically significant exercise‐induced gradients. |
doi_str_mv | 10.1002/ccd.27998 |
format | Article |
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This study examines the intrapatient variability in peak instantaneous left ventricular outflow tract (LVOT) gradients and aortic pulse pressures during rest, exercise, and after ventricular ectopy.
Background
Although the variability in LVOT gradients in patients with hypertrophic cardiomyopathy (HCM) is well known, the predictors of such variation are not. We hypothesized that quantitative invasive analysis of gradient variation could identify useful predictors of maximal gradients.
Methods
Variability in continuously recorded, high‐fidelity left ventricular and aortic pressure waveforms were evaluated by computer‐assisted analysis in the resting state (N = 659 beats) and during supine exercise (N = 379 beats) in a symptomatic patient with a resting LVOT gradient >30 mmHg and frequent ventricular ectopy.
Results
At rest, the peak left ventricular and aortic pressures at the time of the peak instantaneous LVOT gradient for all sinus and postectopic beats followed consistent regression slopes characterizing the potential energy loss between the LV cavity and aorta. During exercise, similar regression slopes were identified, and these converged with the resting slopes at the point of the maximal measured LVOT gradient. Component analysis of the LVOT gradient suggests that resting beat‐to‐beat variability provides information similar to post‐ectopic pressures for predicting maximal gradients in obstructive‐variant HCM.
Conclusions
Our study suggests that computer‐assisted analysis of hemodynamic variability in HCM may prove useful in characterizing the severity of obstruction. Further study is warranted to confirm the reproducibility and utility of this finding in a population with clinically significant exercise‐induced gradients.</description><identifier>ISSN: 1522-1946</identifier><identifier>EISSN: 1522-726X</identifier><identifier>DOI: 10.1002/ccd.27998</identifier><identifier>PMID: 30474252</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Adult ; Aorta ; Arterial Pressure ; Brockenbrough‐Braunwald‐Morrow sign ; Cardiac Catheterization ; Cardiomyopathy ; Cardiomyopathy, Hypertrophic - diagnosis ; Cardiomyopathy, Hypertrophic - physiopathology ; Diagnosis, Computer-Assisted ; dynamic obstruction ; ectopy ; Energy loss ; Exercise ; Exercise Test ; Heart ; Hemodynamics ; high fidelity pressure measurements ; Humans ; hypertrophic cardiomyopathy ; LVOT gradient ; Male ; multisensor catheter ; Potential energy ; Predictive Value of Tests ; Rest ; Severity of Illness Index ; Signal Processing, Computer-Assisted ; Slopes ; supine submaximal exercise ; Time Factors ; VALVULAR AND STRUCTURAL HEART DISEASES (E‐only ) ; Variability ; Ventricle ; Ventricular Function, Left ; Ventricular Outflow Obstruction - diagnosis ; Ventricular Outflow Obstruction - physiopathology ; Ventricular Premature Complexes - diagnosis ; Ventricular Premature Complexes - physiopathology ; Ventricular Pressure</subject><ispartof>Catheterization and cardiovascular interventions, 2019-07, Vol.94 (1), p.E37-E43</ispartof><rights>2018 The Authors. published by Wiley Periodicals, Inc.</rights><rights>2018 The Authors. Catheterization and Cardiovascular Interventions published by Wiley Periodicals, Inc.</rights><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4108-d24fb89f62b1cf84e117e674dd9185404fc8d1f57971b6270bf005ded3dc439c3</citedby><cites>FETCH-LOGICAL-c4108-d24fb89f62b1cf84e117e674dd9185404fc8d1f57971b6270bf005ded3dc439c3</cites><orcidid>0000-0003-1062-3677</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fccd.27998$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fccd.27998$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30474252$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bauch, Terry D.</creatorcontrib><creatorcontrib>Smith, Alexandra J.</creatorcontrib><creatorcontrib>Murgo, Joseph P.</creatorcontrib><creatorcontrib>Watts, James A.</creatorcontrib><creatorcontrib>Rubal, Bernard J.</creatorcontrib><title>Gradient variability in hypertrophic cardiomyopathy: New insights from computer‐assisted, high fidelity, rest and exercise hemodynamic analysis</title><title>Catheterization and cardiovascular interventions</title><addtitle>Catheter Cardiovasc Interv</addtitle><description>Objectives
This study examines the intrapatient variability in peak instantaneous left ventricular outflow tract (LVOT) gradients and aortic pulse pressures during rest, exercise, and after ventricular ectopy.
Background
Although the variability in LVOT gradients in patients with hypertrophic cardiomyopathy (HCM) is well known, the predictors of such variation are not. We hypothesized that quantitative invasive analysis of gradient variation could identify useful predictors of maximal gradients.
Methods
Variability in continuously recorded, high‐fidelity left ventricular and aortic pressure waveforms were evaluated by computer‐assisted analysis in the resting state (N = 659 beats) and during supine exercise (N = 379 beats) in a symptomatic patient with a resting LVOT gradient >30 mmHg and frequent ventricular ectopy.
Results
At rest, the peak left ventricular and aortic pressures at the time of the peak instantaneous LVOT gradient for all sinus and postectopic beats followed consistent regression slopes characterizing the potential energy loss between the LV cavity and aorta. During exercise, similar regression slopes were identified, and these converged with the resting slopes at the point of the maximal measured LVOT gradient. Component analysis of the LVOT gradient suggests that resting beat‐to‐beat variability provides information similar to post‐ectopic pressures for predicting maximal gradients in obstructive‐variant HCM.
Conclusions
Our study suggests that computer‐assisted analysis of hemodynamic variability in HCM may prove useful in characterizing the severity of obstruction. Further study is warranted to confirm the reproducibility and utility of this finding in a population with clinically significant exercise‐induced gradients.</description><subject>Adult</subject><subject>Aorta</subject><subject>Arterial Pressure</subject><subject>Brockenbrough‐Braunwald‐Morrow sign</subject><subject>Cardiac Catheterization</subject><subject>Cardiomyopathy</subject><subject>Cardiomyopathy, Hypertrophic - diagnosis</subject><subject>Cardiomyopathy, Hypertrophic - physiopathology</subject><subject>Diagnosis, Computer-Assisted</subject><subject>dynamic obstruction</subject><subject>ectopy</subject><subject>Energy loss</subject><subject>Exercise</subject><subject>Exercise Test</subject><subject>Heart</subject><subject>Hemodynamics</subject><subject>high fidelity pressure measurements</subject><subject>Humans</subject><subject>hypertrophic cardiomyopathy</subject><subject>LVOT gradient</subject><subject>Male</subject><subject>multisensor catheter</subject><subject>Potential energy</subject><subject>Predictive Value of Tests</subject><subject>Rest</subject><subject>Severity of Illness Index</subject><subject>Signal Processing, Computer-Assisted</subject><subject>Slopes</subject><subject>supine submaximal exercise</subject><subject>Time Factors</subject><subject>VALVULAR AND STRUCTURAL HEART DISEASES (E‐only )</subject><subject>Variability</subject><subject>Ventricle</subject><subject>Ventricular Function, Left</subject><subject>Ventricular Outflow Obstruction - diagnosis</subject><subject>Ventricular Outflow Obstruction - physiopathology</subject><subject>Ventricular Premature Complexes - diagnosis</subject><subject>Ventricular Premature Complexes - physiopathology</subject><subject>Ventricular Pressure</subject><issn>1522-1946</issn><issn>1522-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc9OFTEUhxsjEUQXvABp4oqEC22n05m6MDFX-ZMQ3Gjirum0p0zJzHRs5wKz8xH0FXkSi_dCdMGqJ-l3vtPTH0J7lBxRQtixMfaIVVLWL9AOLRlbVEx8f7mpqeRiG71O6ZoQIgWTr9B2QXjFWcl20O_TqK2HYcI3Onrd-M5PM_YDbucR4hTD2HqDjY7Wh34Oo57a-T2-hNvMJH_VTgm7GHpsQj-uJoj3P3_plHyawB7iNgPYeQsP0kMcIU1YDxbDHUTjE-AW-mDnQfd5hh50N-fON2jL6S7B2825i76dfP66PFtcfDk9X368WBhOSb2wjLumlk6whhpXc6C0AlFxayWtS064M7WlrqxkRRvBKtI4QkoLtrCGF9IUu-jD2juumh6syX8QdafG6HsdZxW0V__fDL5VV-FGCUFrWrAseLcRxPBjlXdT12EV8xZJMVaSknEpZKYO1pSJIaUI7mkCJeohPZXTU3_Ty-z-v096Ih_jysDxGrj1HczPm9Ry-Wmt_AMsJqnZ</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Bauch, Terry D.</creator><creator>Smith, Alexandra J.</creator><creator>Murgo, Joseph P.</creator><creator>Watts, James A.</creator><creator>Rubal, Bernard J.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</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>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1062-3677</orcidid></search><sort><creationdate>20190701</creationdate><title>Gradient variability in hypertrophic cardiomyopathy: New insights from computer‐assisted, high fidelity, rest and exercise hemodynamic analysis</title><author>Bauch, Terry D. ; Smith, Alexandra J. ; Murgo, Joseph P. ; Watts, James A. ; Rubal, Bernard J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4108-d24fb89f62b1cf84e117e674dd9185404fc8d1f57971b6270bf005ded3dc439c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Aorta</topic><topic>Arterial Pressure</topic><topic>Brockenbrough‐Braunwald‐Morrow sign</topic><topic>Cardiac Catheterization</topic><topic>Cardiomyopathy</topic><topic>Cardiomyopathy, Hypertrophic - diagnosis</topic><topic>Cardiomyopathy, Hypertrophic - physiopathology</topic><topic>Diagnosis, Computer-Assisted</topic><topic>dynamic obstruction</topic><topic>ectopy</topic><topic>Energy loss</topic><topic>Exercise</topic><topic>Exercise Test</topic><topic>Heart</topic><topic>Hemodynamics</topic><topic>high fidelity pressure measurements</topic><topic>Humans</topic><topic>hypertrophic cardiomyopathy</topic><topic>LVOT gradient</topic><topic>Male</topic><topic>multisensor catheter</topic><topic>Potential energy</topic><topic>Predictive Value of Tests</topic><topic>Rest</topic><topic>Severity of Illness Index</topic><topic>Signal Processing, Computer-Assisted</topic><topic>Slopes</topic><topic>supine submaximal exercise</topic><topic>Time Factors</topic><topic>VALVULAR AND STRUCTURAL HEART DISEASES (E‐only )</topic><topic>Variability</topic><topic>Ventricle</topic><topic>Ventricular Function, Left</topic><topic>Ventricular Outflow Obstruction - diagnosis</topic><topic>Ventricular Outflow Obstruction - physiopathology</topic><topic>Ventricular Premature Complexes - diagnosis</topic><topic>Ventricular Premature Complexes - physiopathology</topic><topic>Ventricular Pressure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bauch, Terry D.</creatorcontrib><creatorcontrib>Smith, Alexandra J.</creatorcontrib><creatorcontrib>Murgo, Joseph P.</creatorcontrib><creatorcontrib>Watts, James A.</creatorcontrib><creatorcontrib>Rubal, Bernard J.</creatorcontrib><collection>Wiley Online Library Open Access</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Catheterization and cardiovascular interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bauch, Terry D.</au><au>Smith, Alexandra J.</au><au>Murgo, Joseph P.</au><au>Watts, James A.</au><au>Rubal, Bernard J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gradient variability in hypertrophic cardiomyopathy: New insights from computer‐assisted, high fidelity, rest and exercise hemodynamic analysis</atitle><jtitle>Catheterization and cardiovascular interventions</jtitle><addtitle>Catheter Cardiovasc Interv</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>94</volume><issue>1</issue><spage>E37</spage><epage>E43</epage><pages>E37-E43</pages><issn>1522-1946</issn><eissn>1522-726X</eissn><abstract>Objectives
This study examines the intrapatient variability in peak instantaneous left ventricular outflow tract (LVOT) gradients and aortic pulse pressures during rest, exercise, and after ventricular ectopy.
Background
Although the variability in LVOT gradients in patients with hypertrophic cardiomyopathy (HCM) is well known, the predictors of such variation are not. We hypothesized that quantitative invasive analysis of gradient variation could identify useful predictors of maximal gradients.
Methods
Variability in continuously recorded, high‐fidelity left ventricular and aortic pressure waveforms were evaluated by computer‐assisted analysis in the resting state (N = 659 beats) and during supine exercise (N = 379 beats) in a symptomatic patient with a resting LVOT gradient >30 mmHg and frequent ventricular ectopy.
Results
At rest, the peak left ventricular and aortic pressures at the time of the peak instantaneous LVOT gradient for all sinus and postectopic beats followed consistent regression slopes characterizing the potential energy loss between the LV cavity and aorta. During exercise, similar regression slopes were identified, and these converged with the resting slopes at the point of the maximal measured LVOT gradient. Component analysis of the LVOT gradient suggests that resting beat‐to‐beat variability provides information similar to post‐ectopic pressures for predicting maximal gradients in obstructive‐variant HCM.
Conclusions
Our study suggests that computer‐assisted analysis of hemodynamic variability in HCM may prove useful in characterizing the severity of obstruction. Further study is warranted to confirm the reproducibility and utility of this finding in a population with clinically significant exercise‐induced gradients.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>30474252</pmid><doi>10.1002/ccd.27998</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1062-3677</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aorta Arterial Pressure Brockenbrough‐Braunwald‐Morrow sign Cardiac Catheterization Cardiomyopathy Cardiomyopathy, Hypertrophic - diagnosis Cardiomyopathy, Hypertrophic - physiopathology Diagnosis, Computer-Assisted dynamic obstruction ectopy Energy loss Exercise Exercise Test Heart Hemodynamics high fidelity pressure measurements Humans hypertrophic cardiomyopathy LVOT gradient Male multisensor catheter Potential energy Predictive Value of Tests Rest Severity of Illness Index Signal Processing, Computer-Assisted Slopes supine submaximal exercise Time Factors VALVULAR AND STRUCTURAL HEART DISEASES (E‐only ) Variability Ventricle Ventricular Function, Left Ventricular Outflow Obstruction - diagnosis Ventricular Outflow Obstruction - physiopathology Ventricular Premature Complexes - diagnosis Ventricular Premature Complexes - physiopathology Ventricular Pressure |
title | Gradient variability in hypertrophic cardiomyopathy: New insights from computer‐assisted, high fidelity, rest and exercise hemodynamic analysis |
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