Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction
Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, an...
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Veröffentlicht in: | The American journal of cardiology 1969-06, Vol.23 (6), p.818-821 |
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creator | Moss, Arthur J. Marcano, Bertrand Ruttenberg, Herbert D. Desilets, Donald T. Shapiro, Bertrand |
description | Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, and intrapulmonary right to left shunts were demonstrated in 4 of the 6 cases. These shunts appear to reflect venous admixture rather than true anatomic connections between the bronchial and pulmonary circulations. |
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Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, and intrapulmonary right to left shunts were demonstrated in 4 of the 6 cases. These shunts appear to reflect venous admixture rather than true anatomic connections between the bronchial and pulmonary circulations.</description><identifier>ISSN: 0002-9149</identifier><identifier>EISSN: 1879-1913</identifier><identifier>DOI: 10.1016/0002-9149(69)90376-2</identifier><identifier>PMID: 5785161</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Angiocardiography ; Arteriovenous Anastomosis ; Bronchial Arteries - pathology ; Child ; Cyanosis - complications ; Dilatation ; Female ; Heart Defects, Congenital - complications ; Heart Defects, Congenital - surgery ; Heart Septal Defects, Atrial - surgery ; Humans ; Male ; Postoperative Complications ; Pulmonary Circulation ; Pulmonary Valve Stenosis - surgery ; Tetralogy of Fallot - surgery</subject><ispartof>The American journal of cardiology, 1969-06, Vol.23 (6), p.818-821</ispartof><rights>1969</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-d5da7f65a8fae27c5766fe35bf090e5dca71c55c28d7a229a29e004a4adf4b33</citedby><cites>FETCH-LOGICAL-c357t-d5da7f65a8fae27c5766fe35bf090e5dca71c55c28d7a229a29e004a4adf4b33</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(69)90376-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5785161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moss, Arthur J.</creatorcontrib><creatorcontrib>Marcano, Bertrand</creatorcontrib><creatorcontrib>Ruttenberg, Herbert D.</creatorcontrib><creatorcontrib>Desilets, Donald T.</creatorcontrib><creatorcontrib>Shapiro, Bertrand</creatorcontrib><title>Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction</title><title>The American journal of cardiology</title><addtitle>Am J Cardiol</addtitle><description>Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, and intrapulmonary right to left shunts were demonstrated in 4 of the 6 cases. These shunts appear to reflect venous admixture rather than true anatomic connections between the bronchial and pulmonary circulations.</description><subject>Angiocardiography</subject><subject>Arteriovenous Anastomosis</subject><subject>Bronchial Arteries - pathology</subject><subject>Child</subject><subject>Cyanosis - complications</subject><subject>Dilatation</subject><subject>Female</subject><subject>Heart Defects, Congenital - complications</subject><subject>Heart Defects, Congenital - surgery</subject><subject>Heart Septal Defects, Atrial - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Postoperative Complications</subject><subject>Pulmonary Circulation</subject><subject>Pulmonary Valve Stenosis - surgery</subject><subject>Tetralogy of Fallot - surgery</subject><issn>0002-9149</issn><issn>1879-1913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1969</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9LAzEQxYMotVa_gcKeRA-rye4m2VwEKf4DwUvvYZrMamSb1CQr9Nu7tcWjp2F4783wfoScM3rDKBO3lNKqVKxRV0JdK1pLUVYHZMpaqUqmWH1Ipn-WY3KS0ue4MsbFhEy4bDkTbEoWLz5HWA_9KniImyJ9DD6nwvnCbMCH7Exhgn9H7zL0xQdCzIV1CSFhAV3GWKQhvjsziibEiCa74E_JUQd9wrP9nJHF48Ni_ly-vj29zO9fS1NzmUvLLchOcGg7wEoaLoXosObLjiqK3BqQzHBuqtZKqCoFlUJKG2jAds2yrmfkcnd2HcPXgCnrlUsG-x48hiHptmG8EbUcjc3OaGJIKWKn19GtxrqaUb1lqbeg9BaUFkr_stTVGLvY3x-WK7R_oT28Ub_b6Th2_HYYdTIOvUHrtiC0De7_Bz9hiYVE</recordid><startdate>196906</startdate><enddate>196906</enddate><creator>Moss, Arthur J.</creator><creator>Marcano, Bertrand</creator><creator>Ruttenberg, Herbert D.</creator><creator>Desilets, Donald T.</creator><creator>Shapiro, Bertrand</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>196906</creationdate><title>Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction</title><author>Moss, Arthur J. ; Marcano, Bertrand ; Ruttenberg, Herbert D. ; Desilets, Donald T. ; Shapiro, Bertrand</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-d5da7f65a8fae27c5766fe35bf090e5dca71c55c28d7a229a29e004a4adf4b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1969</creationdate><topic>Angiocardiography</topic><topic>Arteriovenous Anastomosis</topic><topic>Bronchial Arteries - pathology</topic><topic>Child</topic><topic>Cyanosis - complications</topic><topic>Dilatation</topic><topic>Female</topic><topic>Heart Defects, Congenital - complications</topic><topic>Heart Defects, Congenital - surgery</topic><topic>Heart Septal Defects, Atrial - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Postoperative Complications</topic><topic>Pulmonary Circulation</topic><topic>Pulmonary Valve Stenosis - surgery</topic><topic>Tetralogy of Fallot - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moss, Arthur J.</creatorcontrib><creatorcontrib>Marcano, Bertrand</creatorcontrib><creatorcontrib>Ruttenberg, Herbert D.</creatorcontrib><creatorcontrib>Desilets, Donald T.</creatorcontrib><creatorcontrib>Shapiro, Bertrand</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>Moss, Arthur J.</au><au>Marcano, Bertrand</au><au>Ruttenberg, Herbert D.</au><au>Desilets, Donald T.</au><au>Shapiro, Bertrand</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction</atitle><jtitle>The American journal of cardiology</jtitle><addtitle>Am J Cardiol</addtitle><date>1969-06</date><risdate>1969</risdate><volume>23</volume><issue>6</issue><spage>818</spage><epage>821</epage><pages>818-821</pages><issn>0002-9149</issn><eissn>1879-1913</eissn><abstract>Six children with surgically corrected cyanotic congenital heart disease were studied six months to four years after definitive repair. Five had tetralogy of Fallot, and 1 had severe valvular pulmonic stenosis with an atrial septal defect. The bronchial arteries were enlarged and tortuous in all, and intrapulmonary right to left shunts were demonstrated in 4 of the 6 cases. These shunts appear to reflect venous admixture rather than true anatomic connections between the bronchial and pulmonary circulations.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>5785161</pmid><doi>10.1016/0002-9149(69)90376-2</doi><tpages>4</tpages></addata></record> |
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subjects | Angiocardiography Arteriovenous Anastomosis Bronchial Arteries - pathology Child Cyanosis - complications Dilatation Female Heart Defects, Congenital - complications Heart Defects, Congenital - surgery Heart Septal Defects, Atrial - surgery Humans Male Postoperative Complications Pulmonary Circulation Pulmonary Valve Stenosis - surgery Tetralogy of Fallot - surgery |
title | Intrapulmonary shunts in cyanotic congenital heart disease after surgical correction |
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