Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure
Patients with thalassemia major present chronic hemolysis and require regular blood transfusions which may cause iron overload cardiomyopathy and chronic heart failure. Hemochromatosis is characterized by excessive iron accumulation in tissues, and heart involvement is the main cause of death in pat...
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Veröffentlicht in: | Arquivos brasileiros de cardiologia 2013-01, Vol.100 (1), p.75-81 |
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creator | Rodrigues, Alexandre Guimarães-Filho, Fábio Villaça Braga, João Carlos Ferreira Rodrigues, Cássia Spínola Custódio Waib, Paulo Fabron-Junior, Antonio Tan, Doralice Marvulle França, Ana Cristina C V Okoshi, Marina Politi Okoshi, Katashi |
description | Patients with thalassemia major present chronic hemolysis and require regular blood transfusions which may cause iron overload cardiomyopathy and chronic heart failure. Hemochromatosis is characterized by excessive iron accumulation in tissues, and heart involvement is the main cause of death in patients with thalassemia.
The aim of this study was to evaluate cardiac structure and function by conventional Doppler echocardiography and tissue Doppler imaging in patients with TM and no clinical evidence of heart failure.
This is a prospective observational study including 18 patients with thalassemia major (TM) receiving regular blood transfusion. To separately evaluate anemia and blood transfusion effects, two gender, age, weight, and height-matched control groups were included: one with healthy individuals (Healthy, n=18) and one with iron deficient anemia patients (Anemia, n=18). Statistical analysis was performed using ANOVA followed by Tukey's test or Kruskal-Wallis's and Dunn's test.
The following echocardiographic variables presented significantly higher values in TM than the Anemia and Healthy groups: left atrium volume index (Healthy: 16.4±6.08; Anemia: 17.9±7.02; TM: 24.1±8.30 cm³/m²); mitral septal E/Em ratio (Healthy: 6.55±1.60; Anemia: 6.74±0.74; TM: 8.10±1.31); and duration of reverse pulmonary vein flow [Healthy: 74.0 (59.0-74.0); Anemia: 70.5 (67.0-74.0); TM: 111 (87.0-120) ms]. The mitral E/A ratio was higher in TM than Anemia (Healthy: 1.80±0.40; Anemia: 1.80±0.24; TM: 2.03±0.34). No differences were found in left ventricular structures and systolic function indexes.
Conventional Doppler echocardiography and tissue Doppler allow changes in left ventricular diastolic function to be identified in asymptomatic patients with thalassemia major. |
doi_str_mv | 10.1590/S0066-782X2013005000001 |
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The aim of this study was to evaluate cardiac structure and function by conventional Doppler echocardiography and tissue Doppler imaging in patients with TM and no clinical evidence of heart failure.
This is a prospective observational study including 18 patients with thalassemia major (TM) receiving regular blood transfusion. To separately evaluate anemia and blood transfusion effects, two gender, age, weight, and height-matched control groups were included: one with healthy individuals (Healthy, n=18) and one with iron deficient anemia patients (Anemia, n=18). Statistical analysis was performed using ANOVA followed by Tukey's test or Kruskal-Wallis's and Dunn's test.
The following echocardiographic variables presented significantly higher values in TM than the Anemia and Healthy groups: left atrium volume index (Healthy: 16.4±6.08; Anemia: 17.9±7.02; TM: 24.1±8.30 cm³/m²); mitral septal E/Em ratio (Healthy: 6.55±1.60; Anemia: 6.74±0.74; TM: 8.10±1.31); and duration of reverse pulmonary vein flow [Healthy: 74.0 (59.0-74.0); Anemia: 70.5 (67.0-74.0); TM: 111 (87.0-120) ms]. The mitral E/A ratio was higher in TM than Anemia (Healthy: 1.80±0.40; Anemia: 1.80±0.24; TM: 2.03±0.34). No differences were found in left ventricular structures and systolic function indexes.
Conventional Doppler echocardiography and tissue Doppler allow changes in left ventricular diastolic function to be identified in asymptomatic patients with thalassemia major.</description><identifier>EISSN: 1678-4170</identifier><identifier>DOI: 10.1590/S0066-782X2013005000001</identifier><identifier>PMID: 23295250</identifier><language>eng</language><publisher>Brazil</publisher><subject>Adolescent ; Adult ; Age Factors ; Anemia - etiology ; Anemia - physiopathology ; beta-Thalassemia - complications ; beta-Thalassemia - physiopathology ; beta-Thalassemia - therapy ; Chelation Therapy ; Child ; Echocardiography, Doppler - methods ; Epidemiologic Methods ; Female ; Hemochromatosis - etiology ; Hemochromatosis - physiopathology ; Hemodynamics ; Hemolysis - physiology ; Humans ; Iron Chelating Agents - therapeutic use ; Male ; Sex Factors ; Transfusion Reaction ; Ventricular Function ; Young Adult</subject><ispartof>Arquivos brasileiros de cardiologia, 2013-01, Vol.100 (1), p.75-81</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,865,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23295250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodrigues, Alexandre</creatorcontrib><creatorcontrib>Guimarães-Filho, Fábio Villaça</creatorcontrib><creatorcontrib>Braga, João Carlos Ferreira</creatorcontrib><creatorcontrib>Rodrigues, Cássia Spínola Custódio</creatorcontrib><creatorcontrib>Waib, Paulo</creatorcontrib><creatorcontrib>Fabron-Junior, Antonio</creatorcontrib><creatorcontrib>Tan, Doralice Marvulle</creatorcontrib><creatorcontrib>França, Ana Cristina C V</creatorcontrib><creatorcontrib>Okoshi, Marina Politi</creatorcontrib><creatorcontrib>Okoshi, Katashi</creatorcontrib><title>Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure</title><title>Arquivos brasileiros de cardiologia</title><addtitle>Arq Bras Cardiol</addtitle><description>Patients with thalassemia major present chronic hemolysis and require regular blood transfusions which may cause iron overload cardiomyopathy and chronic heart failure. Hemochromatosis is characterized by excessive iron accumulation in tissues, and heart involvement is the main cause of death in patients with thalassemia.
The aim of this study was to evaluate cardiac structure and function by conventional Doppler echocardiography and tissue Doppler imaging in patients with TM and no clinical evidence of heart failure.
This is a prospective observational study including 18 patients with thalassemia major (TM) receiving regular blood transfusion. To separately evaluate anemia and blood transfusion effects, two gender, age, weight, and height-matched control groups were included: one with healthy individuals (Healthy, n=18) and one with iron deficient anemia patients (Anemia, n=18). Statistical analysis was performed using ANOVA followed by Tukey's test or Kruskal-Wallis's and Dunn's test.
The following echocardiographic variables presented significantly higher values in TM than the Anemia and Healthy groups: left atrium volume index (Healthy: 16.4±6.08; Anemia: 17.9±7.02; TM: 24.1±8.30 cm³/m²); mitral septal E/Em ratio (Healthy: 6.55±1.60; Anemia: 6.74±0.74; TM: 8.10±1.31); and duration of reverse pulmonary vein flow [Healthy: 74.0 (59.0-74.0); Anemia: 70.5 (67.0-74.0); TM: 111 (87.0-120) ms]. The mitral E/A ratio was higher in TM than Anemia (Healthy: 1.80±0.40; Anemia: 1.80±0.24; TM: 2.03±0.34). No differences were found in left ventricular structures and systolic function indexes.
Conventional Doppler echocardiography and tissue Doppler allow changes in left ventricular diastolic function to be identified in asymptomatic patients with thalassemia major.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Anemia - etiology</subject><subject>Anemia - physiopathology</subject><subject>beta-Thalassemia - complications</subject><subject>beta-Thalassemia - physiopathology</subject><subject>beta-Thalassemia - therapy</subject><subject>Chelation Therapy</subject><subject>Child</subject><subject>Echocardiography, Doppler - methods</subject><subject>Epidemiologic Methods</subject><subject>Female</subject><subject>Hemochromatosis - etiology</subject><subject>Hemochromatosis - physiopathology</subject><subject>Hemodynamics</subject><subject>Hemolysis - physiology</subject><subject>Humans</subject><subject>Iron Chelating Agents - therapeutic use</subject><subject>Male</subject><subject>Sex Factors</subject><subject>Transfusion Reaction</subject><subject>Ventricular Function</subject><subject>Young Adult</subject><issn>1678-4170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo10EtLxDAUBeAgiDM-_oJm6aZ6kzRNu5RhfMCACxXclZs0tZG2qUmKzL-34ng2Z_NxFoeQKwY3TFZw-wJQFJkq-TsHJgAk_IYdkTUrVJnlTMGKnMb4CcC5EvKErLjgleQS1kRvTecNhsb5j4BTt6dupKnDHmO0gzN0wuTsmCL1I9W99w1NAcfYztH5MVIcG2o62y9qAd8udX5OtLMYEm3R9XOw5-S4xT7ai0Ofkbf77evmMds9Pzxt7nbZxBlLWcEFMA6QK42tqKAAW-XS8KpRVV7JokTUucqtNkwILQ0I23BoDTJgwLUUZ-T6b3cK_mu2MdWDi8b2PY7Wz7FmghVClcsDC7080FkPtqmn4AYM-_r_F_ED-F9lPA</recordid><startdate>201301</startdate><enddate>201301</enddate><creator>Rodrigues, Alexandre</creator><creator>Guimarães-Filho, Fábio Villaça</creator><creator>Braga, João Carlos Ferreira</creator><creator>Rodrigues, Cássia Spínola Custódio</creator><creator>Waib, Paulo</creator><creator>Fabron-Junior, Antonio</creator><creator>Tan, Doralice Marvulle</creator><creator>França, Ana Cristina C V</creator><creator>Okoshi, Marina Politi</creator><creator>Okoshi, Katashi</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201301</creationdate><title>Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure</title><author>Rodrigues, Alexandre ; Guimarães-Filho, Fábio Villaça ; Braga, João Carlos Ferreira ; Rodrigues, Cássia Spínola Custódio ; Waib, Paulo ; Fabron-Junior, Antonio ; Tan, Doralice Marvulle ; França, Ana Cristina C V ; Okoshi, Marina Politi ; Okoshi, Katashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-6230120047baf39060e945c29d7949568aab474ebc133b5c03ed20fca10102b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Anemia - etiology</topic><topic>Anemia - physiopathology</topic><topic>beta-Thalassemia - complications</topic><topic>beta-Thalassemia - physiopathology</topic><topic>beta-Thalassemia - therapy</topic><topic>Chelation Therapy</topic><topic>Child</topic><topic>Echocardiography, Doppler - methods</topic><topic>Epidemiologic Methods</topic><topic>Female</topic><topic>Hemochromatosis - etiology</topic><topic>Hemochromatosis - physiopathology</topic><topic>Hemodynamics</topic><topic>Hemolysis - physiology</topic><topic>Humans</topic><topic>Iron Chelating Agents - therapeutic use</topic><topic>Male</topic><topic>Sex Factors</topic><topic>Transfusion Reaction</topic><topic>Ventricular Function</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodrigues, Alexandre</creatorcontrib><creatorcontrib>Guimarães-Filho, Fábio Villaça</creatorcontrib><creatorcontrib>Braga, João Carlos Ferreira</creatorcontrib><creatorcontrib>Rodrigues, Cássia Spínola Custódio</creatorcontrib><creatorcontrib>Waib, Paulo</creatorcontrib><creatorcontrib>Fabron-Junior, Antonio</creatorcontrib><creatorcontrib>Tan, Doralice Marvulle</creatorcontrib><creatorcontrib>França, Ana Cristina C V</creatorcontrib><creatorcontrib>Okoshi, Marina Politi</creatorcontrib><creatorcontrib>Okoshi, Katashi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Arquivos brasileiros de cardiologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodrigues, Alexandre</au><au>Guimarães-Filho, Fábio Villaça</au><au>Braga, João Carlos Ferreira</au><au>Rodrigues, Cássia Spínola Custódio</au><au>Waib, Paulo</au><au>Fabron-Junior, Antonio</au><au>Tan, Doralice Marvulle</au><au>França, Ana Cristina C V</au><au>Okoshi, Marina Politi</au><au>Okoshi, Katashi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure</atitle><jtitle>Arquivos brasileiros de cardiologia</jtitle><addtitle>Arq Bras Cardiol</addtitle><date>2013-01</date><risdate>2013</risdate><volume>100</volume><issue>1</issue><spage>75</spage><epage>81</epage><pages>75-81</pages><eissn>1678-4170</eissn><abstract>Patients with thalassemia major present chronic hemolysis and require regular blood transfusions which may cause iron overload cardiomyopathy and chronic heart failure. Hemochromatosis is characterized by excessive iron accumulation in tissues, and heart involvement is the main cause of death in patients with thalassemia.
The aim of this study was to evaluate cardiac structure and function by conventional Doppler echocardiography and tissue Doppler imaging in patients with TM and no clinical evidence of heart failure.
This is a prospective observational study including 18 patients with thalassemia major (TM) receiving regular blood transfusion. To separately evaluate anemia and blood transfusion effects, two gender, age, weight, and height-matched control groups were included: one with healthy individuals (Healthy, n=18) and one with iron deficient anemia patients (Anemia, n=18). Statistical analysis was performed using ANOVA followed by Tukey's test or Kruskal-Wallis's and Dunn's test.
The following echocardiographic variables presented significantly higher values in TM than the Anemia and Healthy groups: left atrium volume index (Healthy: 16.4±6.08; Anemia: 17.9±7.02; TM: 24.1±8.30 cm³/m²); mitral septal E/Em ratio (Healthy: 6.55±1.60; Anemia: 6.74±0.74; TM: 8.10±1.31); and duration of reverse pulmonary vein flow [Healthy: 74.0 (59.0-74.0); Anemia: 70.5 (67.0-74.0); TM: 111 (87.0-120) ms]. The mitral E/A ratio was higher in TM than Anemia (Healthy: 1.80±0.40; Anemia: 1.80±0.24; TM: 2.03±0.34). No differences were found in left ventricular structures and systolic function indexes.
Conventional Doppler echocardiography and tissue Doppler allow changes in left ventricular diastolic function to be identified in asymptomatic patients with thalassemia major.</abstract><cop>Brazil</cop><pmid>23295250</pmid><doi>10.1590/S0066-782X2013005000001</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Factors Anemia - etiology Anemia - physiopathology beta-Thalassemia - complications beta-Thalassemia - physiopathology beta-Thalassemia - therapy Chelation Therapy Child Echocardiography, Doppler - methods Epidemiologic Methods Female Hemochromatosis - etiology Hemochromatosis - physiopathology Hemodynamics Hemolysis - physiology Humans Iron Chelating Agents - therapeutic use Male Sex Factors Transfusion Reaction Ventricular Function Young Adult |
title | Echocardiography in thalassemic patients on blood transfusions and chelation without heart failure |
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