The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease

From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome ( n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation ( n = 7), complex single right ventr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of thoracic and cardiovascular surgery 1995-04, Vol.109 (4), p.654-662
Hauptverfasser: Weldner, Paul W., Myers, John L., Gleason, Marie M., Cyran, Stephen E., Weber, Howard S., White, Michael G., Baylen, Barry G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 662
container_issue 4
container_start_page 654
container_title The Journal of thoracic and cardiovascular surgery
container_volume 109
creator Weldner, Paul W.
Myers, John L.
Gleason, Marie M.
Cyran, Stephen E.
Weber, Howard S.
White, Michael G.
Baylen, Barry G.
description From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome ( n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation ( n = 7), complex single right ventricle with subaortic stenosis ( n = 8), critical aortic stenosis with endocardial fibroelastosis ( n = 2), and malaligned primum atrial septal defect with coarctation ( n = 2). Age at operation ranged from 1 day to 3.9 months (mean 9 days, median 3.5 days). The operative mortality (< 30 days) was 33% (20 patients). Late mortality was 17% (10 patients). Nine of the 20 (45%) operative deaths occurred during the first 2 days after the operation as a result of sudden hemodynamic instability. All four infants with premature closure of the foramen ovale had pulmonary lymphangiectasia and died of pulmonary failure. Seven operative deaths have occurred in 36 patients since 1990 (19%); in the past 2 years, no operative deaths have occurred in 22 patients. Overall, there are 30 long-term survivors (50%). Twenty-one of these 30 infants have undergone a two-stage repair with a modified Fontan operation at 7.3 to 27.6 months of age (mean 18.1 months) with no mortality. Six patients have entered a three-stage repair strategy by undergoing a hemi-Fontan procedure at 6.8 to 23.0 months (mean 8.8 months) with no mortality, and two of these patients have now had their modified Fontan operation at 23.0 to 46.7 months of age with no mortality (four are still awaiting surgery). Two patients have undergone a two-ventricle repair with a Rastelli procedure, with no mortality at 7.4 and 14.1 months of age. Early in our experience, infants undergoing the Norwood operation had a high early mortality most often related to sudden hemodynamic instability. After we instituted a protocol that adds carbon dioxide to the inspired gas during postoperative mechanical ventilation, the postoperative course became more stable and there have been no operative deaths. In summary, the operative mortality for the Norwood operation continues to improve. A subsequent Fontan operation can be performed with excellent clinical results. (J T HORAC C ARDIOVASC S URG 1995;109:654-62)
doi_str_mv 10.1016/S0022-5223(95)70346-2
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77221320</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022522395703462</els_id><sourcerecordid>77221320</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-af99ed37dff44f73dda11fce68e9c84e1d754ed7a2c62d7509ea5029e52c61a53</originalsourceid><addsrcrecordid>eNqFkV1rHCEUhqWkpJu0PyHgVdNcTKrOOK5XJSz5gtBeNIXeidFjxjCjW3W7yb-Pm11C7gLCEd_n6OERoSNKTimh_fffhDDWcMbab5KfCNJ2fcM-oBklUjT9nP_dQ7NX5BM6yPmBECIIlftoXwjKGWUz5G4HwD9jWsdocVxC0sXHgHWwOK_uMvxbQSj4Ioaiw5vcb5bToWS89mXAJk7LER5rDfcQfNEjHkCngq3PoDN8Rh-dHjN82dVD9Ofi_HZx1dz8urxenN00pmtlabSTEmwrrHNd50RrrabUGejnIM28A2oF78AKzUzP6p5I0JwwCbweUM3bQ_R1e-8yxTp6Lmry2cA46gBxlZUQjNGWkQryLWhSzDmBU8vkJ52eFCVq41e9-FUbeUpy9eJXsdp3tHtgdTeBfe3aCa358TYf_P2w9glUnvQ4Vpqqh2Jy_R3VqZ53lfyxJaH6-O8hqWw8BAO2dpmibPTvzPIMso2aKQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77221320</pqid></control><display><type>article</type><title>The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EZB Electronic Journals Library</source><creator>Weldner, Paul W. ; Myers, John L. ; Gleason, Marie M. ; Cyran, Stephen E. ; Weber, Howard S. ; White, Michael G. ; Baylen, Barry G.</creator><creatorcontrib>Weldner, Paul W. ; Myers, John L. ; Gleason, Marie M. ; Cyran, Stephen E. ; Weber, Howard S. ; White, Michael G. ; Baylen, Barry G.</creatorcontrib><description>From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome ( n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation ( n = 7), complex single right ventricle with subaortic stenosis ( n = 8), critical aortic stenosis with endocardial fibroelastosis ( n = 2), and malaligned primum atrial septal defect with coarctation ( n = 2). Age at operation ranged from 1 day to 3.9 months (mean 9 days, median 3.5 days). The operative mortality (&lt; 30 days) was 33% (20 patients). Late mortality was 17% (10 patients). Nine of the 20 (45%) operative deaths occurred during the first 2 days after the operation as a result of sudden hemodynamic instability. All four infants with premature closure of the foramen ovale had pulmonary lymphangiectasia and died of pulmonary failure. Seven operative deaths have occurred in 36 patients since 1990 (19%); in the past 2 years, no operative deaths have occurred in 22 patients. Overall, there are 30 long-term survivors (50%). Twenty-one of these 30 infants have undergone a two-stage repair with a modified Fontan operation at 7.3 to 27.6 months of age (mean 18.1 months) with no mortality. Six patients have entered a three-stage repair strategy by undergoing a hemi-Fontan procedure at 6.8 to 23.0 months (mean 8.8 months) with no mortality, and two of these patients have now had their modified Fontan operation at 23.0 to 46.7 months of age with no mortality (four are still awaiting surgery). Two patients have undergone a two-ventricle repair with a Rastelli procedure, with no mortality at 7.4 and 14.1 months of age. Early in our experience, infants undergoing the Norwood operation had a high early mortality most often related to sudden hemodynamic instability. After we instituted a protocol that adds carbon dioxide to the inspired gas during postoperative mechanical ventilation, the postoperative course became more stable and there have been no operative deaths. In summary, the operative mortality for the Norwood operation continues to improve. A subsequent Fontan operation can be performed with excellent clinical results. (J T HORAC C ARDIOVASC S URG 1995;109:654-62)</description><identifier>ISSN: 0022-5223</identifier><identifier>EISSN: 1097-685X</identifier><identifier>DOI: 10.1016/S0022-5223(95)70346-2</identifier><identifier>PMID: 7715212</identifier><language>eng</language><publisher>United States: Mosby, Inc</publisher><subject>Cardiac Surgical Procedures - methods ; Cardiac Surgical Procedures - mortality ; Female ; Fontan Procedure ; Heart Defects, Congenital - mortality ; Heart Defects, Congenital - physiopathology ; Heart Defects, Congenital - surgery ; Hemodynamics ; Humans ; Infant ; Infant, Newborn ; Male ; Survival Rate</subject><ispartof>The Journal of thoracic and cardiovascular surgery, 1995-04, Vol.109 (4), p.654-662</ispartof><rights>1995 Mosby, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-af99ed37dff44f73dda11fce68e9c84e1d754ed7a2c62d7509ea5029e52c61a53</citedby><cites>FETCH-LOGICAL-c439t-af99ed37dff44f73dda11fce68e9c84e1d754ed7a2c62d7509ea5029e52c61a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022522395703462$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7715212$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weldner, Paul W.</creatorcontrib><creatorcontrib>Myers, John L.</creatorcontrib><creatorcontrib>Gleason, Marie M.</creatorcontrib><creatorcontrib>Cyran, Stephen E.</creatorcontrib><creatorcontrib>Weber, Howard S.</creatorcontrib><creatorcontrib>White, Michael G.</creatorcontrib><creatorcontrib>Baylen, Barry G.</creatorcontrib><title>The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease</title><title>The Journal of thoracic and cardiovascular surgery</title><addtitle>J Thorac Cardiovasc Surg</addtitle><description>From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome ( n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation ( n = 7), complex single right ventricle with subaortic stenosis ( n = 8), critical aortic stenosis with endocardial fibroelastosis ( n = 2), and malaligned primum atrial septal defect with coarctation ( n = 2). Age at operation ranged from 1 day to 3.9 months (mean 9 days, median 3.5 days). The operative mortality (&lt; 30 days) was 33% (20 patients). Late mortality was 17% (10 patients). Nine of the 20 (45%) operative deaths occurred during the first 2 days after the operation as a result of sudden hemodynamic instability. All four infants with premature closure of the foramen ovale had pulmonary lymphangiectasia and died of pulmonary failure. Seven operative deaths have occurred in 36 patients since 1990 (19%); in the past 2 years, no operative deaths have occurred in 22 patients. Overall, there are 30 long-term survivors (50%). Twenty-one of these 30 infants have undergone a two-stage repair with a modified Fontan operation at 7.3 to 27.6 months of age (mean 18.1 months) with no mortality. Six patients have entered a three-stage repair strategy by undergoing a hemi-Fontan procedure at 6.8 to 23.0 months (mean 8.8 months) with no mortality, and two of these patients have now had their modified Fontan operation at 23.0 to 46.7 months of age with no mortality (four are still awaiting surgery). Two patients have undergone a two-ventricle repair with a Rastelli procedure, with no mortality at 7.4 and 14.1 months of age. Early in our experience, infants undergoing the Norwood operation had a high early mortality most often related to sudden hemodynamic instability. After we instituted a protocol that adds carbon dioxide to the inspired gas during postoperative mechanical ventilation, the postoperative course became more stable and there have been no operative deaths. In summary, the operative mortality for the Norwood operation continues to improve. A subsequent Fontan operation can be performed with excellent clinical results. (J T HORAC C ARDIOVASC S URG 1995;109:654-62)</description><subject>Cardiac Surgical Procedures - methods</subject><subject>Cardiac Surgical Procedures - mortality</subject><subject>Female</subject><subject>Fontan Procedure</subject><subject>Heart Defects, Congenital - mortality</subject><subject>Heart Defects, Congenital - physiopathology</subject><subject>Heart Defects, Congenital - surgery</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Survival Rate</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1rHCEUhqWkpJu0PyHgVdNcTKrOOK5XJSz5gtBeNIXeidFjxjCjW3W7yb-Pm11C7gLCEd_n6OERoSNKTimh_fffhDDWcMbab5KfCNJ2fcM-oBklUjT9nP_dQ7NX5BM6yPmBECIIlftoXwjKGWUz5G4HwD9jWsdocVxC0sXHgHWwOK_uMvxbQSj4Ioaiw5vcb5bToWS89mXAJk7LER5rDfcQfNEjHkCngq3PoDN8Rh-dHjN82dVD9Ofi_HZx1dz8urxenN00pmtlabSTEmwrrHNd50RrrabUGejnIM28A2oF78AKzUzP6p5I0JwwCbweUM3bQ_R1e-8yxTp6Lmry2cA46gBxlZUQjNGWkQryLWhSzDmBU8vkJ52eFCVq41e9-FUbeUpy9eJXsdp3tHtgdTeBfe3aCa358TYf_P2w9glUnvQ4Vpqqh2Jy_R3VqZ53lfyxJaH6-O8hqWw8BAO2dpmibPTvzPIMso2aKQ</recordid><startdate>19950401</startdate><enddate>19950401</enddate><creator>Weldner, Paul W.</creator><creator>Myers, John L.</creator><creator>Gleason, Marie M.</creator><creator>Cyran, Stephen E.</creator><creator>Weber, Howard S.</creator><creator>White, Michael G.</creator><creator>Baylen, Barry G.</creator><general>Mosby, Inc</general><general>AATS/WTSA</general><scope>6I.</scope><scope>AAFTH</scope><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>19950401</creationdate><title>The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease</title><author>Weldner, Paul W. ; Myers, John L. ; Gleason, Marie M. ; Cyran, Stephen E. ; Weber, Howard S. ; White, Michael G. ; Baylen, Barry G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-af99ed37dff44f73dda11fce68e9c84e1d754ed7a2c62d7509ea5029e52c61a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Cardiac Surgical Procedures - methods</topic><topic>Cardiac Surgical Procedures - mortality</topic><topic>Female</topic><topic>Fontan Procedure</topic><topic>Heart Defects, Congenital - mortality</topic><topic>Heart Defects, Congenital - physiopathology</topic><topic>Heart Defects, Congenital - surgery</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weldner, Paul W.</creatorcontrib><creatorcontrib>Myers, John L.</creatorcontrib><creatorcontrib>Gleason, Marie M.</creatorcontrib><creatorcontrib>Cyran, Stephen E.</creatorcontrib><creatorcontrib>Weber, Howard S.</creatorcontrib><creatorcontrib>White, Michael G.</creatorcontrib><creatorcontrib>Baylen, Barry G.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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 Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weldner, Paul W.</au><au>Myers, John L.</au><au>Gleason, Marie M.</au><au>Cyran, Stephen E.</au><au>Weber, Howard S.</au><au>White, Michael G.</au><au>Baylen, Barry G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>1995-04-01</date><risdate>1995</risdate><volume>109</volume><issue>4</issue><spage>654</spage><epage>662</epage><pages>654-662</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><abstract>From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome ( n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation ( n = 7), complex single right ventricle with subaortic stenosis ( n = 8), critical aortic stenosis with endocardial fibroelastosis ( n = 2), and malaligned primum atrial septal defect with coarctation ( n = 2). Age at operation ranged from 1 day to 3.9 months (mean 9 days, median 3.5 days). The operative mortality (&lt; 30 days) was 33% (20 patients). Late mortality was 17% (10 patients). Nine of the 20 (45%) operative deaths occurred during the first 2 days after the operation as a result of sudden hemodynamic instability. All four infants with premature closure of the foramen ovale had pulmonary lymphangiectasia and died of pulmonary failure. Seven operative deaths have occurred in 36 patients since 1990 (19%); in the past 2 years, no operative deaths have occurred in 22 patients. Overall, there are 30 long-term survivors (50%). Twenty-one of these 30 infants have undergone a two-stage repair with a modified Fontan operation at 7.3 to 27.6 months of age (mean 18.1 months) with no mortality. Six patients have entered a three-stage repair strategy by undergoing a hemi-Fontan procedure at 6.8 to 23.0 months (mean 8.8 months) with no mortality, and two of these patients have now had their modified Fontan operation at 23.0 to 46.7 months of age with no mortality (four are still awaiting surgery). Two patients have undergone a two-ventricle repair with a Rastelli procedure, with no mortality at 7.4 and 14.1 months of age. Early in our experience, infants undergoing the Norwood operation had a high early mortality most often related to sudden hemodynamic instability. After we instituted a protocol that adds carbon dioxide to the inspired gas during postoperative mechanical ventilation, the postoperative course became more stable and there have been no operative deaths. In summary, the operative mortality for the Norwood operation continues to improve. A subsequent Fontan operation can be performed with excellent clinical results. (J T HORAC C ARDIOVASC S URG 1995;109:654-62)</abstract><cop>United States</cop><pub>Mosby, Inc</pub><pmid>7715212</pmid><doi>10.1016/S0022-5223(95)70346-2</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-5223
ispartof The Journal of thoracic and cardiovascular surgery, 1995-04, Vol.109 (4), p.654-662
issn 0022-5223
1097-685X
language eng
recordid cdi_proquest_miscellaneous_77221320
source MEDLINE; Elsevier ScienceDirect Journals Complete; EZB Electronic Journals Library
subjects Cardiac Surgical Procedures - methods
Cardiac Surgical Procedures - mortality
Female
Fontan Procedure
Heart Defects, Congenital - mortality
Heart Defects, Congenital - physiopathology
Heart Defects, Congenital - surgery
Hemodynamics
Humans
Infant
Infant, Newborn
Male
Survival Rate
title The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T20%3A05%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Norwood%20operation%20and%20subsequent%20Fontan%20operation%20in%20infants%20with%20complex%20congenital%20heart%20disease&rft.jtitle=The%20Journal%20of%20thoracic%20and%20cardiovascular%20surgery&rft.au=Weldner,%20Paul%20W.&rft.date=1995-04-01&rft.volume=109&rft.issue=4&rft.spage=654&rft.epage=662&rft.pages=654-662&rft.issn=0022-5223&rft.eissn=1097-685X&rft_id=info:doi/10.1016/S0022-5223(95)70346-2&rft_dat=%3Cproquest_cross%3E77221320%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77221320&rft_id=info:pmid/7715212&rft_els_id=S0022522395703462&rfr_iscdi=true