Pulmonary vascular disease in complete transposition of the great arteries: A study of 200 patients
Lung specimens of 200 patients with transposition of the great arteries were examined microscopically for evidence of pulmonary vascular disease. In patients with an intact ventricular septum or a small ventricular septal defect, advanced pulmonary vascular disease was uncommon; only 9 of 107 such p...
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Veröffentlicht in: | The American journal of cardiology 1974-07, Vol.34 (1), p.75-82 |
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description | Lung specimens of 200 patients with transposition of the great arteries were examined microscopically for evidence of pulmonary vascular disease. In patients with an intact ventricular septum or a small ventricular septal defect, advanced pulmonary vascular disease was uncommon; only 9 of 107 such patients (8.4 percent) demonstrated greater than grade 2 (Heath-Edwards) pulmonary vascular disease. A persistent large patent ductus arteriosus appeared to promote progressive pulmonary vascular disease in this group since each of the five infants less than 1 year of age with grade 3 or 4 disease had this lesion. In contrast, pulmonary vascular disease was common in patients with a large ventricular septal defect; 37 of 93 patients (40 percent) with this defect had greater than grade 2 pulmonary vascular disease. Among patients more than 1 year of age, 26 of 35 (75 percent) had grade 4 disease. The catheterization data suggest that the calculated pulmonary vascular resistance may underestimate the degree of disease, probably by overestimating the pulmonary blood flow (Fick method). Pulmonic stenosis appeared to protect the lungs from progressive pulmonary vascular disease, and pulmonary arterial banding was protective when performed before age 6 months. Our studies indicate that a persistent large patent ductus arteriosus should be closed as early as possible in view of its association with advanced pulmonary vascular disease in these patients. In infants with a large ventricular septal defect, pulmonary arterial banding or corrective surgery with closure of the defect should be performed between the ages of 4 and 6 months to prevent progressive pulmonary vascular damage. |
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In patients with an intact ventricular septum or a small ventricular septal defect, advanced pulmonary vascular disease was uncommon; only 9 of 107 such patients (8.4 percent) demonstrated greater than grade 2 (Heath-Edwards) pulmonary vascular disease. A persistent large patent ductus arteriosus appeared to promote progressive pulmonary vascular disease in this group since each of the five infants less than 1 year of age with grade 3 or 4 disease had this lesion. In contrast, pulmonary vascular disease was common in patients with a large ventricular septal defect; 37 of 93 patients (40 percent) with this defect had greater than grade 2 pulmonary vascular disease. Among patients more than 1 year of age, 26 of 35 (75 percent) had grade 4 disease. The catheterization data suggest that the calculated pulmonary vascular resistance may underestimate the degree of disease, probably by overestimating the pulmonary blood flow (Fick method). Pulmonic stenosis appeared to protect the lungs from progressive pulmonary vascular disease, and pulmonary arterial banding was protective when performed before age 6 months. Our studies indicate that a persistent large patent ductus arteriosus should be closed as early as possible in view of its association with advanced pulmonary vascular disease in these patients. In infants with a large ventricular septal defect, pulmonary arterial banding or corrective surgery with closure of the defect should be performed between the ages of 4 and 6 months to prevent progressive pulmonary vascular damage.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/0002-9149(74)90096-4</identifier><identifier>PMID: 4835757</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Atrophy - pathology ; Atrophy - physiopathology ; Autopsy ; Cardiac Catheterization ; Ductus Arteriosus, Patent - complications ; Ductus Arteriosus, Patent - surgery ; Heart Septal Defects, Ventricular - complications ; Heart Septal Defects, Ventricular - pathology ; Heart Septum ; Humans ; Hypertension, Pulmonary - pathology ; Hypertension, Pulmonary - physiopathology ; Hypertrophy - pathology ; Hypertrophy - physiopathology ; Pulmonary Artery - pathology ; Pulmonary Artery - physiopathology ; Pulmonary Circulation ; Pulmonary Valve Stenosis - complications ; Pulmonary Veins - pathology ; Pulmonary Veins - physiopathology ; Transposition of Great Vessels - complications ; Vascular Diseases - classification ; Vascular Diseases - etiology ; Vascular Diseases - pathology ; Vascular Diseases - physiopathology ; Vascular Diseases - prevention & control ; Vascular Resistance</subject><ispartof>The American journal of cardiology, 1974-07, Vol.34 (1), p.75-82</ispartof><rights>1974</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-5812c2752bfa00a78cc951ab6618c8ebf348dfa252def63b536ee13adeb12b873</citedby><cites>FETCH-LOGICAL-c423t-5812c2752bfa00a78cc951ab6618c8ebf348dfa252def63b536ee13adeb12b873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0002-9149(74)90096-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4835757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Newfeld, Edgar A.</creatorcontrib><creatorcontrib>Paul, Milton H.</creatorcontrib><creatorcontrib>Muster, Alexander J.</creatorcontrib><creatorcontrib>Idriss, Farouk S.</creatorcontrib><title>Pulmonary vascular disease in complete transposition of the great arteries: A study of 200 patients</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>Lung specimens of 200 patients with transposition of the great arteries were examined microscopically for evidence of pulmonary vascular disease. In patients with an intact ventricular septum or a small ventricular septal defect, advanced pulmonary vascular disease was uncommon; only 9 of 107 such patients (8.4 percent) demonstrated greater than grade 2 (Heath-Edwards) pulmonary vascular disease. A persistent large patent ductus arteriosus appeared to promote progressive pulmonary vascular disease in this group since each of the five infants less than 1 year of age with grade 3 or 4 disease had this lesion. In contrast, pulmonary vascular disease was common in patients with a large ventricular septal defect; 37 of 93 patients (40 percent) with this defect had greater than grade 2 pulmonary vascular disease. Among patients more than 1 year of age, 26 of 35 (75 percent) had grade 4 disease. The catheterization data suggest that the calculated pulmonary vascular resistance may underestimate the degree of disease, probably by overestimating the pulmonary blood flow (Fick method). Pulmonic stenosis appeared to protect the lungs from progressive pulmonary vascular disease, and pulmonary arterial banding was protective when performed before age 6 months. Our studies indicate that a persistent large patent ductus arteriosus should be closed as early as possible in view of its association with advanced pulmonary vascular disease in these patients. In infants with a large ventricular septal defect, pulmonary arterial banding or corrective surgery with closure of the defect should be performed between the ages of 4 and 6 months to prevent progressive pulmonary vascular damage.</description><subject>Atrophy - pathology</subject><subject>Atrophy - physiopathology</subject><subject>Autopsy</subject><subject>Cardiac Catheterization</subject><subject>Ductus Arteriosus, Patent - complications</subject><subject>Ductus Arteriosus, Patent - surgery</subject><subject>Heart Septal Defects, Ventricular - complications</subject><subject>Heart Septal Defects, Ventricular - pathology</subject><subject>Heart Septum</subject><subject>Humans</subject><subject>Hypertension, Pulmonary - pathology</subject><subject>Hypertension, Pulmonary - physiopathology</subject><subject>Hypertrophy - pathology</subject><subject>Hypertrophy - physiopathology</subject><subject>Pulmonary Artery - pathology</subject><subject>Pulmonary Artery - physiopathology</subject><subject>Pulmonary Circulation</subject><subject>Pulmonary Valve Stenosis - complications</subject><subject>Pulmonary Veins - pathology</subject><subject>Pulmonary Veins - physiopathology</subject><subject>Transposition of Great Vessels - complications</subject><subject>Vascular Diseases - classification</subject><subject>Vascular Diseases - etiology</subject><subject>Vascular Diseases - pathology</subject><subject>Vascular Diseases - physiopathology</subject><subject>Vascular Diseases - prevention & control</subject><subject>Vascular Resistance</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxTAQhoMoery8gUJWootqbm1TF4KINxB0oeuQplONtE3NpIJvb4_n4NLVMPyXYT5CDjk744wX54wxkVVcVSelOq0Yq4pMbZAF12WV8YrLTbL4s-yQXcSPeeU8L7bJttIyL_NyQdzz1PVhsPGbfll0U2cjbTyCRaB-oC70YwcJaIp2wDGgTz4MNLQ0vQN9i2ATtTFB9IAX9IpimprvpSwYo6NNHoaE-2SrtR3CwXrukdfbm5fr--zx6e7h-uoxc0rIlOWaCyfKXNStZcyW2rkq57YuCq6dhrqVSjetFblooC1kncsCgEvbQM1FrUu5R45XvWMMnxNgMr1HB11nBwgTGi2UkoVks1GtjC4GxAitGaPvZwaGM7Nka5bgzBKcKZX5ZWvUHDta9091D81faA1z1i9XOsxPfnmIBt0MwEHjI7hkmuD_P_ADBFWJTg</recordid><startdate>197407</startdate><enddate>197407</enddate><creator>Newfeld, Edgar A.</creator><creator>Paul, Milton H.</creator><creator>Muster, Alexander J.</creator><creator>Idriss, Farouk S.</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>197407</creationdate><title>Pulmonary vascular disease in complete transposition of the great arteries: A study of 200 patients</title><author>Newfeld, Edgar A. ; Paul, Milton H. ; Muster, Alexander J. ; Idriss, Farouk S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-5812c2752bfa00a78cc951ab6618c8ebf348dfa252def63b536ee13adeb12b873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1974</creationdate><topic>Atrophy - pathology</topic><topic>Atrophy - physiopathology</topic><topic>Autopsy</topic><topic>Cardiac Catheterization</topic><topic>Ductus Arteriosus, Patent - complications</topic><topic>Ductus Arteriosus, Patent - surgery</topic><topic>Heart Septal Defects, Ventricular - complications</topic><topic>Heart Septal Defects, Ventricular - pathology</topic><topic>Heart Septum</topic><topic>Humans</topic><topic>Hypertension, Pulmonary - pathology</topic><topic>Hypertension, Pulmonary - physiopathology</topic><topic>Hypertrophy - pathology</topic><topic>Hypertrophy - physiopathology</topic><topic>Pulmonary Artery - pathology</topic><topic>Pulmonary Artery - physiopathology</topic><topic>Pulmonary Circulation</topic><topic>Pulmonary Valve Stenosis - complications</topic><topic>Pulmonary Veins - pathology</topic><topic>Pulmonary Veins - physiopathology</topic><topic>Transposition of Great Vessels - complications</topic><topic>Vascular Diseases - classification</topic><topic>Vascular Diseases - etiology</topic><topic>Vascular Diseases - pathology</topic><topic>Vascular Diseases - physiopathology</topic><topic>Vascular Diseases - prevention & control</topic><topic>Vascular Resistance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Newfeld, Edgar A.</creatorcontrib><creatorcontrib>Paul, Milton H.</creatorcontrib><creatorcontrib>Muster, Alexander J.</creatorcontrib><creatorcontrib>Idriss, Farouk S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Newfeld, Edgar A.</au><au>Paul, Milton H.</au><au>Muster, Alexander J.</au><au>Idriss, Farouk S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pulmonary vascular disease in complete transposition of the great arteries: A study of 200 patients</atitle><jtitle>The American journal of cardiology</jtitle><addtitle>Am J Cardiol</addtitle><date>1974-07</date><risdate>1974</risdate><volume>34</volume><issue>1</issue><spage>75</spage><epage>82</epage><pages>75-82</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><abstract>Lung specimens of 200 patients with transposition of the great arteries were examined microscopically for evidence of pulmonary vascular disease. In patients with an intact ventricular septum or a small ventricular septal defect, advanced pulmonary vascular disease was uncommon; only 9 of 107 such patients (8.4 percent) demonstrated greater than grade 2 (Heath-Edwards) pulmonary vascular disease. A persistent large patent ductus arteriosus appeared to promote progressive pulmonary vascular disease in this group since each of the five infants less than 1 year of age with grade 3 or 4 disease had this lesion. In contrast, pulmonary vascular disease was common in patients with a large ventricular septal defect; 37 of 93 patients (40 percent) with this defect had greater than grade 2 pulmonary vascular disease. Among patients more than 1 year of age, 26 of 35 (75 percent) had grade 4 disease. The catheterization data suggest that the calculated pulmonary vascular resistance may underestimate the degree of disease, probably by overestimating the pulmonary blood flow (Fick method). Pulmonic stenosis appeared to protect the lungs from progressive pulmonary vascular disease, and pulmonary arterial banding was protective when performed before age 6 months. Our studies indicate that a persistent large patent ductus arteriosus should be closed as early as possible in view of its association with advanced pulmonary vascular disease in these patients. In infants with a large ventricular septal defect, pulmonary arterial banding or corrective surgery with closure of the defect should be performed between the ages of 4 and 6 months to prevent progressive pulmonary vascular damage.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>4835757</pmid><doi>10.1016/0002-9149(74)90096-4</doi><tpages>8</tpages></addata></record> |
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subjects | Atrophy - pathology Atrophy - physiopathology Autopsy Cardiac Catheterization Ductus Arteriosus, Patent - complications Ductus Arteriosus, Patent - surgery Heart Septal Defects, Ventricular - complications Heart Septal Defects, Ventricular - pathology Heart Septum Humans Hypertension, Pulmonary - pathology Hypertension, Pulmonary - physiopathology Hypertrophy - pathology Hypertrophy - physiopathology Pulmonary Artery - pathology Pulmonary Artery - physiopathology Pulmonary Circulation Pulmonary Valve Stenosis - complications Pulmonary Veins - pathology Pulmonary Veins - physiopathology Transposition of Great Vessels - complications Vascular Diseases - classification Vascular Diseases - etiology Vascular Diseases - pathology Vascular Diseases - physiopathology Vascular Diseases - prevention & control Vascular Resistance |
title | Pulmonary vascular disease in complete transposition of the great arteries: A study of 200 patients |
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