Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy
From May 1995 through October 2001, 19 infants less than 90 days old underwent surgical correction of total anomalous pulmonary venous connection. In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operativ...
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Veröffentlicht in: | Asian cardiovascular & thoracic annals 2003-03, Vol.11 (1), p.18-22 |
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creator | Anil Kumar, Dharmapuram Kumar, Raghavan Nair Suresh Narasinga Rao, Pantula Mahmoud, Hassan Mohamed Chandran, Sushil Dhir, Achal Kumar Saxena, Dileep Kumar Azhagappan, Sivan Pillay Pillai, Velayudhan Ramakrishna Venkitachalam, Chokkanathapura Gopalakrishnan Fikree, Mohamed Amin Nazer, Yoosuph Abdul Cartmill, Timothy Boyd Mrutyunjaya Rao, Ivatury |
description | From May 1995 through October 2001, 19 infants less than 90 days old underwent surgical correction of total anomalous pulmonary venous connection. In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operative deaths. The vertical vein was not ligated in 6 cases for various reasons. Two patients died during reoperation for early pulmonary venous obstruction. In the late follow-up, 2 babies required reoperation for late anastomotic stricture; one needed additional balloon dilatation. Of the 14 surviving patients, one had a small residual gradient and infrequent supraventricular tachycardia, the others were asymptomatic and without gradients. Surgical correction of total anomalous pulmonary venous connection can be carried out in early infancy with low mortality and morbidity. However, associated complex cardiac anomalies and small caliber pulmonary arteries and veins carry higher risks. Recurrent pulmonary venous obstruction and diffuse pulmonary vein stenosis are causes of early reoperation and poor surgical outcome. |
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In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operative deaths. The vertical vein was not ligated in 6 cases for various reasons. Two patients died during reoperation for early pulmonary venous obstruction. In the late follow-up, 2 babies required reoperation for late anastomotic stricture; one needed additional balloon dilatation. Of the 14 surviving patients, one had a small residual gradient and infrequent supraventricular tachycardia, the others were asymptomatic and without gradients. Surgical correction of total anomalous pulmonary venous connection can be carried out in early infancy with low mortality and morbidity. However, associated complex cardiac anomalies and small caliber pulmonary arteries and veins carry higher risks. Recurrent pulmonary venous obstruction and diffuse pulmonary vein stenosis are causes of early reoperation and poor surgical outcome.</description><identifier>ISSN: 0218-4923</identifier><identifier>EISSN: 1816-5370</identifier><identifier>DOI: 10.1177/021849230301100106</identifier><identifier>PMID: 12692017</identifier><language>eng</language><publisher>London, England: Asian Soc Cardio Surg</publisher><subject>Cardiac Surgical Procedures - methods ; Female ; Heart Defects, Congenital - surgery ; Humans ; Infant ; Infant, Newborn ; Ligation - methods ; Male ; Pulmonary Veins - physiopathology ; Pulmonary Veins - surgery ; Reoperation ; Retrospective Studies ; Treatment Outcome</subject><ispartof>Asian cardiovascular & thoracic annals, 2003-03, Vol.11 (1), p.18-22</ispartof><rights>2003 SAGE Publications</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c291t-34eb6a0366725bf6c92d337ee7f79732805e57d5b9c50c376ce74780cc6dd39c3</citedby><cites>FETCH-LOGICAL-c291t-34eb6a0366725bf6c92d337ee7f79732805e57d5b9c50c376ce74780cc6dd39c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/021849230301100106$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/021849230301100106$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21799,27903,27904,43600,43601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12692017$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anil Kumar, Dharmapuram</creatorcontrib><creatorcontrib>Kumar, Raghavan Nair Suresh</creatorcontrib><creatorcontrib>Narasinga Rao, Pantula</creatorcontrib><creatorcontrib>Mahmoud, Hassan Mohamed</creatorcontrib><creatorcontrib>Chandran, Sushil</creatorcontrib><creatorcontrib>Dhir, Achal Kumar</creatorcontrib><creatorcontrib>Saxena, Dileep Kumar</creatorcontrib><creatorcontrib>Azhagappan, Sivan Pillay</creatorcontrib><creatorcontrib>Pillai, Velayudhan Ramakrishna</creatorcontrib><creatorcontrib>Venkitachalam, Chokkanathapura Gopalakrishnan</creatorcontrib><creatorcontrib>Fikree, Mohamed Amin</creatorcontrib><creatorcontrib>Nazer, Yoosuph Abdul</creatorcontrib><creatorcontrib>Cartmill, Timothy Boyd</creatorcontrib><creatorcontrib>Mrutyunjaya Rao, Ivatury</creatorcontrib><title>Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy</title><title>Asian cardiovascular & thoracic annals</title><addtitle>Asian Cardiovasc Thorac Ann</addtitle><description>From May 1995 through October 2001, 19 infants less than 90 days old underwent surgical correction of total anomalous pulmonary venous connection. In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operative deaths. The vertical vein was not ligated in 6 cases for various reasons. Two patients died during reoperation for early pulmonary venous obstruction. In the late follow-up, 2 babies required reoperation for late anastomotic stricture; one needed additional balloon dilatation. Of the 14 surviving patients, one had a small residual gradient and infrequent supraventricular tachycardia, the others were asymptomatic and without gradients. Surgical correction of total anomalous pulmonary venous connection can be carried out in early infancy with low mortality and morbidity. However, associated complex cardiac anomalies and small caliber pulmonary arteries and veins carry higher risks. Recurrent pulmonary venous obstruction and diffuse pulmonary vein stenosis are causes of early reoperation and poor surgical outcome.</description><subject>Cardiac Surgical Procedures - methods</subject><subject>Female</subject><subject>Heart Defects, Congenital - surgery</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Ligation - methods</subject><subject>Male</subject><subject>Pulmonary Veins - physiopathology</subject><subject>Pulmonary Veins - surgery</subject><subject>Reoperation</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><issn>0218-4923</issn><issn>1816-5370</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78AQ_SkyfrziTbpD3Ksn6AoMjqNaRpultpkzXZIvvvTemCB0HmMDA87zszLyGXCLeIQkyBYj4rKAMGiAAI_IBMMEeeZkzAIZkMQDoQJ-Q0hE8AYMjyY3KClBcUUEzI_ZvZqMYnrk6Wbqva5M66TrWuD8lr33bOKr9LPowdBnNnrdHbxtmksclC-XaXPNlaWb07J0e1aoO52Pcz8n6_WM4f0-eXh6f53XOqaYHblM1MyRUwzgXNyprrglaMCWNELQrBaA6ZyUSVlYXOQDPBtREzkYPWvKpYodkZuR59N9599SZsZdcEbdpWWRNPlIKhyIpcRJCOoPYuBG9qufFNF5-RCHJIT_5NL4qu9u592ZnqV7KPKwLTEQhqZeSn672N3_5veTMq1s1q_d14I0OMt40LUKrQKKvsYIEoY-XsByYLhg8</recordid><startdate>200303</startdate><enddate>200303</enddate><creator>Anil Kumar, Dharmapuram</creator><creator>Kumar, Raghavan Nair Suresh</creator><creator>Narasinga Rao, Pantula</creator><creator>Mahmoud, Hassan Mohamed</creator><creator>Chandran, Sushil</creator><creator>Dhir, Achal Kumar</creator><creator>Saxena, Dileep Kumar</creator><creator>Azhagappan, Sivan Pillay</creator><creator>Pillai, Velayudhan Ramakrishna</creator><creator>Venkitachalam, Chokkanathapura Gopalakrishnan</creator><creator>Fikree, Mohamed Amin</creator><creator>Nazer, Yoosuph Abdul</creator><creator>Cartmill, Timothy Boyd</creator><creator>Mrutyunjaya Rao, Ivatury</creator><general>Asian Soc Cardio Surg</general><general>SAGE Publications</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>200303</creationdate><title>Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy</title><author>Anil Kumar, Dharmapuram ; Kumar, Raghavan Nair Suresh ; Narasinga Rao, Pantula ; Mahmoud, Hassan Mohamed ; Chandran, Sushil ; Dhir, Achal Kumar ; Saxena, Dileep Kumar ; Azhagappan, Sivan Pillay ; Pillai, Velayudhan Ramakrishna ; Venkitachalam, Chokkanathapura Gopalakrishnan ; Fikree, Mohamed Amin ; Nazer, Yoosuph Abdul ; Cartmill, Timothy Boyd ; Mrutyunjaya Rao, Ivatury</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c291t-34eb6a0366725bf6c92d337ee7f79732805e57d5b9c50c376ce74780cc6dd39c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Cardiac Surgical Procedures - methods</topic><topic>Female</topic><topic>Heart Defects, Congenital - surgery</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Ligation - methods</topic><topic>Male</topic><topic>Pulmonary Veins - physiopathology</topic><topic>Pulmonary Veins - surgery</topic><topic>Reoperation</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><toplevel>online_resources</toplevel><creatorcontrib>Anil Kumar, Dharmapuram</creatorcontrib><creatorcontrib>Kumar, Raghavan Nair Suresh</creatorcontrib><creatorcontrib>Narasinga Rao, Pantula</creatorcontrib><creatorcontrib>Mahmoud, Hassan Mohamed</creatorcontrib><creatorcontrib>Chandran, Sushil</creatorcontrib><creatorcontrib>Dhir, Achal Kumar</creatorcontrib><creatorcontrib>Saxena, Dileep Kumar</creatorcontrib><creatorcontrib>Azhagappan, Sivan Pillay</creatorcontrib><creatorcontrib>Pillai, Velayudhan Ramakrishna</creatorcontrib><creatorcontrib>Venkitachalam, Chokkanathapura Gopalakrishnan</creatorcontrib><creatorcontrib>Fikree, Mohamed Amin</creatorcontrib><creatorcontrib>Nazer, Yoosuph Abdul</creatorcontrib><creatorcontrib>Cartmill, Timothy Boyd</creatorcontrib><creatorcontrib>Mrutyunjaya Rao, Ivatury</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>Asian cardiovascular & thoracic annals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anil Kumar, Dharmapuram</au><au>Kumar, Raghavan Nair Suresh</au><au>Narasinga Rao, Pantula</au><au>Mahmoud, Hassan Mohamed</au><au>Chandran, Sushil</au><au>Dhir, Achal Kumar</au><au>Saxena, Dileep Kumar</au><au>Azhagappan, Sivan Pillay</au><au>Pillai, Velayudhan Ramakrishna</au><au>Venkitachalam, Chokkanathapura Gopalakrishnan</au><au>Fikree, Mohamed Amin</au><au>Nazer, Yoosuph Abdul</au><au>Cartmill, Timothy Boyd</au><au>Mrutyunjaya Rao, Ivatury</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy</atitle><jtitle>Asian cardiovascular & thoracic annals</jtitle><addtitle>Asian Cardiovasc Thorac Ann</addtitle><date>2003-03</date><risdate>2003</risdate><volume>11</volume><issue>1</issue><spage>18</spage><epage>22</epage><pages>18-22</pages><issn>0218-4923</issn><eissn>1816-5370</eissn><abstract>From May 1995 through October 2001, 19 infants less than 90 days old underwent surgical correction of total anomalous pulmonary venous connection. In 15 babies with isolated total anomalous pulmonary venous connection, there was one operative death. In 4 with complex anomalies, there were 2 operative deaths. The vertical vein was not ligated in 6 cases for various reasons. Two patients died during reoperation for early pulmonary venous obstruction. In the late follow-up, 2 babies required reoperation for late anastomotic stricture; one needed additional balloon dilatation. Of the 14 surviving patients, one had a small residual gradient and infrequent supraventricular tachycardia, the others were asymptomatic and without gradients. Surgical correction of total anomalous pulmonary venous connection can be carried out in early infancy with low mortality and morbidity. However, associated complex cardiac anomalies and small caliber pulmonary arteries and veins carry higher risks. Recurrent pulmonary venous obstruction and diffuse pulmonary vein stenosis are causes of early reoperation and poor surgical outcome.</abstract><cop>London, England</cop><pub>Asian Soc Cardio Surg</pub><pmid>12692017</pmid><doi>10.1177/021849230301100106</doi><tpages>5</tpages></addata></record> |
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subjects | Cardiac Surgical Procedures - methods Female Heart Defects, Congenital - surgery Humans Infant Infant, Newborn Ligation - methods Male Pulmonary Veins - physiopathology Pulmonary Veins - surgery Reoperation Retrospective Studies Treatment Outcome |
title | Repair of Total Anomalous Pulmonary Venous Connection in Early Infancy |
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