Development of diastolic heart failure in a 6-year follow-up study in patients after acute myocarditis

BackgroundThe aim of this study was to analyse the long-term prognosis of patients with acute myocarditis (AMC) who had been discharged from hospital while having normal left ventricular (LV) function.Methods and results50 patients with acute myocarditis who underwent endomyocardial biopsies (EMBs)...

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Veröffentlicht in:Heart (British Cardiac Society) 2011-05, Vol.97 (9), p.709-714
Hauptverfasser: Escher, Felicitas, Westermann, Dirk, Gaub, Regina, Pronk, Johannes, Bock, Thomas, Al-Saadi, Nidal, Kühl, Uwe, Schultheiss, Heinz-Peter, Tschöpe, Carsten
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container_end_page 714
container_issue 9
container_start_page 709
container_title Heart (British Cardiac Society)
container_volume 97
creator Escher, Felicitas
Westermann, Dirk
Gaub, Regina
Pronk, Johannes
Bock, Thomas
Al-Saadi, Nidal
Kühl, Uwe
Schultheiss, Heinz-Peter
Tschöpe, Carsten
description BackgroundThe aim of this study was to analyse the long-term prognosis of patients with acute myocarditis (AMC) who had been discharged from hospital while having normal left ventricular (LV) function.Methods and results50 patients with acute myocarditis who underwent endomyocardial biopsies (EMBs) were prospectively studied. Their clinical condition was examined during a mean follow-up period of 72 (54–78) months, including tissue Doppler imaging (TDI). 4% (2/50) died, and 6% (3/50) developed dilated cardiomyopathy. 45/50 (90%) showed a normal or improvement in LV function over time. In the course of the follow-up, 49% (22/45) suffered from heart failure symptoms despite a normal ejection fraction (HFNEF). This was associated with an abnormal E/A ratio, an impaired deceleration time of early mitral flow velocity and isovolumic relaxation time, and a pathological increase in the LV filling index E/E′, in contrast to patients without heart failure symptoms (E/E′septal 10.9 (9.3–13.8) vs 6.8 (6.4–9.1); p=0.001). Plasma N-terminal proB-type natriuretic peptide levels were increased threefold in patients with HFNEF (19.9 (10.6–24.1) vs 7.3 (4.2–11.9) pmol/l; p=0.006).ConclusionsIt is assumed that the evidence for AMC is associated not only with the risk of developing LV dilatation but also with an increased risk of symptomatic diastolic dysfunction after several years.
doi_str_mv 10.1136/hrt.2010.199489
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Their clinical condition was examined during a mean follow-up period of 72 (54–78) months, including tissue Doppler imaging (TDI). 4% (2/50) died, and 6% (3/50) developed dilated cardiomyopathy. 45/50 (90%) showed a normal or improvement in LV function over time. In the course of the follow-up, 49% (22/45) suffered from heart failure symptoms despite a normal ejection fraction (HFNEF). This was associated with an abnormal E/A ratio, an impaired deceleration time of early mitral flow velocity and isovolumic relaxation time, and a pathological increase in the LV filling index E/E′, in contrast to patients without heart failure symptoms (E/E′septal 10.9 (9.3–13.8) vs 6.8 (6.4–9.1); p=0.001). Plasma N-terminal proB-type natriuretic peptide levels were increased threefold in patients with HFNEF (19.9 (10.6–24.1) vs 7.3 (4.2–11.9) pmol/l; p=0.006).ConclusionsIt is assumed that the evidence for AMC is associated not only with the risk of developing LV dilatation but also with an increased risk of symptomatic diastolic dysfunction after several years.</description><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/hrt.2010.199489</identifier><identifier>PMID: 21134904</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><subject>Acute Disease ; Adult ; Biological and medical sciences ; Cardiology ; Cardiology. Vascular system ; Cardiomyopathy ; cardiomyopathy dilated ; Cardiovascular disease ; Diastolic dysfunction ; Female ; Flow velocity ; Gangrene ; Genome, Viral ; Heart ; Heart attacks ; Heart failure ; Heart failure, cardiogenic pulmonary edema, cardiac enlargement ; Heart Failure, Diastolic - etiology ; Heart Failure, Diastolic - physiopathology ; Hospitalization - statistics &amp; numerical data ; Hospitals ; Humans ; Immunohistochemistry ; Inflammation ; Magnetic Resonance Angiography ; Male ; Medical sciences ; Middle Aged ; Morbidity ; Mortality ; myocarditis ; Myocarditis - complications ; Myocarditis. Cardiomyopathies ; Prospective Studies ; Rodents ; Ventricular Dysfunction, Left - etiology</subject><ispartof>Heart (British Cardiac Society), 2011-05, Vol.97 (9), p.709-714</ispartof><rights>2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright: 2011 (c) 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b534t-5eb23ed9436260a31752e42dd3b1dc1b78a631a630a079d83ac71331039cfab23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://heart.bmj.com/content/97/9/709.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://heart.bmj.com/content/97/9/709.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,315,782,786,3200,23580,27933,27934,77610,77641</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24077273$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21134904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Escher, Felicitas</creatorcontrib><creatorcontrib>Westermann, Dirk</creatorcontrib><creatorcontrib>Gaub, Regina</creatorcontrib><creatorcontrib>Pronk, Johannes</creatorcontrib><creatorcontrib>Bock, Thomas</creatorcontrib><creatorcontrib>Al-Saadi, Nidal</creatorcontrib><creatorcontrib>Kühl, Uwe</creatorcontrib><creatorcontrib>Schultheiss, Heinz-Peter</creatorcontrib><creatorcontrib>Tschöpe, Carsten</creatorcontrib><title>Development of diastolic heart failure in a 6-year follow-up study in patients after acute myocarditis</title><title>Heart (British Cardiac Society)</title><addtitle>Heart</addtitle><description>BackgroundThe aim of this study was to analyse the long-term prognosis of patients with acute myocarditis (AMC) who had been discharged from hospital while having normal left ventricular (LV) function.Methods and results50 patients with acute myocarditis who underwent endomyocardial biopsies (EMBs) were prospectively studied. Their clinical condition was examined during a mean follow-up period of 72 (54–78) months, including tissue Doppler imaging (TDI). 4% (2/50) died, and 6% (3/50) developed dilated cardiomyopathy. 45/50 (90%) showed a normal or improvement in LV function over time. In the course of the follow-up, 49% (22/45) suffered from heart failure symptoms despite a normal ejection fraction (HFNEF). This was associated with an abnormal E/A ratio, an impaired deceleration time of early mitral flow velocity and isovolumic relaxation time, and a pathological increase in the LV filling index E/E′, in contrast to patients without heart failure symptoms (E/E′septal 10.9 (9.3–13.8) vs 6.8 (6.4–9.1); p=0.001). Plasma N-terminal proB-type natriuretic peptide levels were increased threefold in patients with HFNEF (19.9 (10.6–24.1) vs 7.3 (4.2–11.9) pmol/l; p=0.006).ConclusionsIt is assumed that the evidence for AMC is associated not only with the risk of developing LV dilatation but also with an increased risk of symptomatic diastolic dysfunction after several years.</description><subject>Acute Disease</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cardiology</subject><subject>Cardiology. Vascular system</subject><subject>Cardiomyopathy</subject><subject>cardiomyopathy dilated</subject><subject>Cardiovascular disease</subject><subject>Diastolic dysfunction</subject><subject>Female</subject><subject>Flow velocity</subject><subject>Gangrene</subject><subject>Genome, Viral</subject><subject>Heart</subject><subject>Heart attacks</subject><subject>Heart failure</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Heart Failure, Diastolic - etiology</subject><subject>Heart Failure, Diastolic - physiopathology</subject><subject>Hospitalization - statistics &amp; numerical data</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Magnetic Resonance Angiography</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>myocarditis</subject><subject>Myocarditis - complications</subject><subject>Myocarditis. 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Vascular system</topic><topic>Cardiomyopathy</topic><topic>cardiomyopathy dilated</topic><topic>Cardiovascular disease</topic><topic>Diastolic dysfunction</topic><topic>Female</topic><topic>Flow velocity</topic><topic>Gangrene</topic><topic>Genome, Viral</topic><topic>Heart</topic><topic>Heart attacks</topic><topic>Heart failure</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Heart Failure, Diastolic - etiology</topic><topic>Heart Failure, Diastolic - physiopathology</topic><topic>Hospitalization - statistics &amp; numerical data</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Magnetic Resonance Angiography</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>myocarditis</topic><topic>Myocarditis - complications</topic><topic>Myocarditis. Cardiomyopathies</topic><topic>Prospective Studies</topic><topic>Rodents</topic><topic>Ventricular Dysfunction, Left - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Escher, Felicitas</creatorcontrib><creatorcontrib>Westermann, Dirk</creatorcontrib><creatorcontrib>Gaub, Regina</creatorcontrib><creatorcontrib>Pronk, Johannes</creatorcontrib><creatorcontrib>Bock, Thomas</creatorcontrib><creatorcontrib>Al-Saadi, Nidal</creatorcontrib><creatorcontrib>Kühl, Uwe</creatorcontrib><creatorcontrib>Schultheiss, Heinz-Peter</creatorcontrib><creatorcontrib>Tschöpe, Carsten</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Heart (British Cardiac Society)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Escher, Felicitas</au><au>Westermann, Dirk</au><au>Gaub, Regina</au><au>Pronk, Johannes</au><au>Bock, Thomas</au><au>Al-Saadi, Nidal</au><au>Kühl, Uwe</au><au>Schultheiss, Heinz-Peter</au><au>Tschöpe, Carsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of diastolic heart failure in a 6-year follow-up study in patients after acute myocarditis</atitle><jtitle>Heart (British Cardiac Society)</jtitle><addtitle>Heart</addtitle><date>2011-05-01</date><risdate>2011</risdate><volume>97</volume><issue>9</issue><spage>709</spage><epage>714</epage><pages>709-714</pages><issn>1355-6037</issn><eissn>1468-201X</eissn><abstract>BackgroundThe aim of this study was to analyse the long-term prognosis of patients with acute myocarditis (AMC) who had been discharged from hospital while having normal left ventricular (LV) function.Methods and results50 patients with acute myocarditis who underwent endomyocardial biopsies (EMBs) were prospectively studied. Their clinical condition was examined during a mean follow-up period of 72 (54–78) months, including tissue Doppler imaging (TDI). 4% (2/50) died, and 6% (3/50) developed dilated cardiomyopathy. 45/50 (90%) showed a normal or improvement in LV function over time. In the course of the follow-up, 49% (22/45) suffered from heart failure symptoms despite a normal ejection fraction (HFNEF). This was associated with an abnormal E/A ratio, an impaired deceleration time of early mitral flow velocity and isovolumic relaxation time, and a pathological increase in the LV filling index E/E′, in contrast to patients without heart failure symptoms (E/E′septal 10.9 (9.3–13.8) vs 6.8 (6.4–9.1); p=0.001). Plasma N-terminal proB-type natriuretic peptide levels were increased threefold in patients with HFNEF (19.9 (10.6–24.1) vs 7.3 (4.2–11.9) pmol/l; p=0.006).ConclusionsIt is assumed that the evidence for AMC is associated not only with the risk of developing LV dilatation but also with an increased risk of symptomatic diastolic dysfunction after several years.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><pmid>21134904</pmid><doi>10.1136/hrt.2010.199489</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute Disease
Adult
Biological and medical sciences
Cardiology
Cardiology. Vascular system
Cardiomyopathy
cardiomyopathy dilated
Cardiovascular disease
Diastolic dysfunction
Female
Flow velocity
Gangrene
Genome, Viral
Heart
Heart attacks
Heart failure
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
Heart Failure, Diastolic - etiology
Heart Failure, Diastolic - physiopathology
Hospitalization - statistics & numerical data
Hospitals
Humans
Immunohistochemistry
Inflammation
Magnetic Resonance Angiography
Male
Medical sciences
Middle Aged
Morbidity
Mortality
myocarditis
Myocarditis - complications
Myocarditis. Cardiomyopathies
Prospective Studies
Rodents
Ventricular Dysfunction, Left - etiology
title Development of diastolic heart failure in a 6-year follow-up study in patients after acute myocarditis
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