Clinical profile of congestive cardiomyopathy in children
The clinical profile of 23 children with congestive cardiomyopathy was reviewed to detect any factors that might be predictive for their survival. Factors examined include age at onset (less than 2 versus greater than 2 years), gender, severity of the clinical picture including data from the chest r...
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| Veröffentlicht in: | Journal of the American College of Cardiology 1990, Vol.15 (1), p.189-193 |
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| container_title | Journal of the American College of Cardiology |
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| creator | SU-CHUNG CHEN NOURI, S BALFOUR, I JUREIDINI, S APPLETON, R. S |
| description | The clinical profile of 23 children with congestive cardiomyopathy was reviewed to detect any factors that might be predictive for their survival. Factors examined include age at onset (less than 2 versus greater than 2 years), gender, severity of the clinical picture including data from the chest radiograph, electrocardiogram (ECG), echocardiogram, hemodynamic study and endomyocardial biopsy. Follow-up study ranged from 1 month to 14 years (mean 43 months). There were 12 survivors and 11 nonsurvivors; the 1 year mortality rate was 30% (7 of 23), and the 5 year mortality rate was 44% (10 of 23). Age at onset, gender, cardiothoracic ratio on chest radiograph, pattern of infarction, ST-T changes or arrhythmia on ECG and left ventricular end-diastolic pressure were nonpredictive of outcome. However, low shortening fraction (mean 11.5% in nonsurvivors versus 20.9% in survivors, p less than 0.01), familial cardiomyopathy and endocardial fibroelastosis indicated a very poor prognosis. |
| doi_str_mv | 10.1016/0735-1097(90)90199-Y |
| format | Article |
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S</creator><creatorcontrib>SU-CHUNG CHEN ; NOURI, S ; BALFOUR, I ; JUREIDINI, S ; APPLETON, R. S</creatorcontrib><description>The clinical profile of 23 children with congestive cardiomyopathy was reviewed to detect any factors that might be predictive for their survival. Factors examined include age at onset (less than 2 versus greater than 2 years), gender, severity of the clinical picture including data from the chest radiograph, electrocardiogram (ECG), echocardiogram, hemodynamic study and endomyocardial biopsy. Follow-up study ranged from 1 month to 14 years (mean 43 months). There were 12 survivors and 11 nonsurvivors; the 1 year mortality rate was 30% (7 of 23), and the 5 year mortality rate was 44% (10 of 23). Age at onset, gender, cardiothoracic ratio on chest radiograph, pattern of infarction, ST-T changes or arrhythmia on ECG and left ventricular end-diastolic pressure were nonpredictive of outcome. However, low shortening fraction (mean 11.5% in nonsurvivors versus 20.9% in survivors, p less than 0.01), familial cardiomyopathy and endocardial fibroelastosis indicated a very poor prognosis.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/0735-1097(90)90199-Y</identifier><identifier>PMID: 2295732</identifier><identifier>CODEN: JACCDI</identifier><language>eng</language><publisher>New York, NY: Elsevier Science</publisher><subject>Biological and medical sciences ; Biopsy ; Cardiology. Vascular system ; Cardiomyopathy, Dilated - diagnosis ; Cardiomyopathy, Dilated - mortality ; Child ; Echocardiography ; Electrocardiography ; Female ; Heart ; Humans ; Male ; Medical sciences ; Myocarditis. 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S</creatorcontrib><title>Clinical profile of congestive cardiomyopathy in children</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>The clinical profile of 23 children with congestive cardiomyopathy was reviewed to detect any factors that might be predictive for their survival. Factors examined include age at onset (less than 2 versus greater than 2 years), gender, severity of the clinical picture including data from the chest radiograph, electrocardiogram (ECG), echocardiogram, hemodynamic study and endomyocardial biopsy. Follow-up study ranged from 1 month to 14 years (mean 43 months). There were 12 survivors and 11 nonsurvivors; the 1 year mortality rate was 30% (7 of 23), and the 5 year mortality rate was 44% (10 of 23). Age at onset, gender, cardiothoracic ratio on chest radiograph, pattern of infarction, ST-T changes or arrhythmia on ECG and left ventricular end-diastolic pressure were nonpredictive of outcome. However, low shortening fraction (mean 11.5% in nonsurvivors versus 20.9% in survivors, p less than 0.01), familial cardiomyopathy and endocardial fibroelastosis indicated a very poor prognosis.</description><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Cardiology. Vascular system</subject><subject>Cardiomyopathy, Dilated - diagnosis</subject><subject>Cardiomyopathy, Dilated - mortality</subject><subject>Child</subject><subject>Echocardiography</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Heart</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocarditis. Cardiomyopathies</subject><subject>Myocardium - pathology</subject><subject>Prognosis</subject><subject>Survival Rate</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9j0tLxDAUhYMo4zj6DxS6ENFF9SZpkt7lMPiCATe6cFUyeTiRtB2bqdB_b8Eyq7M4H-dByCWFewpUPoDiIqeA6hbhDoEi5p9HZE6FKHMuUB2T-QE5JWcpfQOALCnOyIwxFIqzOcFVDE0wOma7rvUhuqz1mWmbL5f24ddlRnc2tPXQ7vR-O2Shycw2RNu55pyceB2Tu5h0QT6eHt9XL_n67fl1tVznWwZ0nxecoVTMCQuCjv3MI_dgrdYFWroBhp7LUkurC4dUgyk3oERBuXCltV7yBbn5zx0H_vTjrKoOybgYdePaPlUKBVeCFiN4NYH9pna22nWh1t1QTV9H_3rydRoP-043JqQDJiUik4r_AVJAYrc</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>SU-CHUNG CHEN</creator><creator>NOURI, S</creator><creator>BALFOUR, I</creator><creator>JUREIDINI, S</creator><creator>APPLETON, R. 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Vascular system</topic><topic>Cardiomyopathy, Dilated - diagnosis</topic><topic>Cardiomyopathy, Dilated - mortality</topic><topic>Child</topic><topic>Echocardiography</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Heart</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocarditis. Cardiomyopathies</topic><topic>Myocardium - pathology</topic><topic>Prognosis</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SU-CHUNG CHEN</creatorcontrib><creatorcontrib>NOURI, S</creatorcontrib><creatorcontrib>BALFOUR, I</creatorcontrib><creatorcontrib>JUREIDINI, S</creatorcontrib><creatorcontrib>APPLETON, R. S</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SU-CHUNG CHEN</au><au>NOURI, S</au><au>BALFOUR, I</au><au>JUREIDINI, S</au><au>APPLETON, R. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical profile of congestive cardiomyopathy in children</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>1990</date><risdate>1990</risdate><volume>15</volume><issue>1</issue><spage>189</spage><epage>193</epage><pages>189-193</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><coden>JACCDI</coden><abstract>The clinical profile of 23 children with congestive cardiomyopathy was reviewed to detect any factors that might be predictive for their survival. Factors examined include age at onset (less than 2 versus greater than 2 years), gender, severity of the clinical picture including data from the chest radiograph, electrocardiogram (ECG), echocardiogram, hemodynamic study and endomyocardial biopsy. Follow-up study ranged from 1 month to 14 years (mean 43 months). There were 12 survivors and 11 nonsurvivors; the 1 year mortality rate was 30% (7 of 23), and the 5 year mortality rate was 44% (10 of 23). Age at onset, gender, cardiothoracic ratio on chest radiograph, pattern of infarction, ST-T changes or arrhythmia on ECG and left ventricular end-diastolic pressure were nonpredictive of outcome. However, low shortening fraction (mean 11.5% in nonsurvivors versus 20.9% in survivors, p less than 0.01), familial cardiomyopathy and endocardial fibroelastosis indicated a very poor prognosis.</abstract><cop>New York, NY</cop><pub>Elsevier Science</pub><pmid>2295732</pmid><doi>10.1016/0735-1097(90)90199-Y</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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| ispartof | Journal of the American College of Cardiology, 1990, Vol.15 (1), p.189-193 |
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| language | eng |
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| source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; ScienceDirect Journals (5 years ago - present) |
| subjects | Biological and medical sciences Biopsy Cardiology. Vascular system Cardiomyopathy, Dilated - diagnosis Cardiomyopathy, Dilated - mortality Child Echocardiography Electrocardiography Female Heart Humans Male Medical sciences Myocarditis. Cardiomyopathies Myocardium - pathology Prognosis Survival Rate |
| title | Clinical profile of congestive cardiomyopathy in children |
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