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Long-term follow-up of homograft function after pulmonary valve replacement in patients with tetralogy of Fallot
To analyse the long-term outcomes after pulmonary valve replacement (PVR) in patients with a previous correction for tetralogy of Fallot. In a retrospective study, 158 adult patients with a diagnosis of tetralogy of Fallot, who had undergone a PVR after initial total correction in childhood, were id...
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Published in: | European heart journal 2006-06, Vol.27 (12), p.1478-1484 |
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container_title | European heart journal |
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creator | OOSTERHOF, Thomas MEIJBOOM, Folkert J VLIEGEN, Hubert W HAZEKAMP, Mark G ZWINDERMAN, Aeiko H BOUMA, Berto J VAN DIJK, Arie P. J MULDER, Barbara J. M |
description | To analyse the long-term outcomes after pulmonary valve replacement (PVR) in patients with a previous correction for tetralogy of Fallot.
In a retrospective study, 158 adult patients with a diagnosis of tetralogy of Fallot, who had undergone a PVR after initial total correction in childhood, were identified from the CONCOR (CONgenital CORvitia) registry. All patients underwent 175 PVRs between June 1986 and June 2005. To analyse the predictors for homograft dysfunction and adverse events (death, reoperations, balloon angioplasty), Cox-regression analysis was performed. Overall freedom from significant homograft dysfunction was 66% after 5 years and 47% after 10 years. We could not identify predictors for combined homograft dysfunction. Event-free survival was 78% at 10 years and 68% at 15 years after PVR. Both early significant pulmonary regurgitation (PR) (HR 6.8, P = 0.017) and pulmonary stenosis (PS) (HR 4.0, P = 0.037) after surgery were associated with adverse events. When analysing direct post-operative PR or PS, we observed that in patients with severe, pre-operative PR, right ventricular aneurysm/patch resection resulted in a lower post-operative PR (mean difference grade 0.38 +/- 0.14, P = 0.01). Less significant post-operative PS was associated with a higher diameter of the homograft (HR 0.37, P = 0.006).
While 47% of the patients in our study were free from homograft dysfunction at 10 years after PVR, event-free survival after PVR remained fairly good (78%). Significant residual lesions directly after surgery influenced event-free survival. A smaller diameter of the pulmonary homograft and severe pre-surgical PR were related to early homograft dysfunction after surgery. |
doi_str_mv | 10.1093/eurheartj/ehl033 |
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In a retrospective study, 158 adult patients with a diagnosis of tetralogy of Fallot, who had undergone a PVR after initial total correction in childhood, were identified from the CONCOR (CONgenital CORvitia) registry. All patients underwent 175 PVRs between June 1986 and June 2005. To analyse the predictors for homograft dysfunction and adverse events (death, reoperations, balloon angioplasty), Cox-regression analysis was performed. Overall freedom from significant homograft dysfunction was 66% after 5 years and 47% after 10 years. We could not identify predictors for combined homograft dysfunction. Event-free survival was 78% at 10 years and 68% at 15 years after PVR. Both early significant pulmonary regurgitation (PR) (HR 6.8, P = 0.017) and pulmonary stenosis (PS) (HR 4.0, P = 0.037) after surgery were associated with adverse events. When analysing direct post-operative PR or PS, we observed that in patients with severe, pre-operative PR, right ventricular aneurysm/patch resection resulted in a lower post-operative PR (mean difference grade 0.38 +/- 0.14, P = 0.01). Less significant post-operative PS was associated with a higher diameter of the homograft (HR 0.37, P = 0.006).
While 47% of the patients in our study were free from homograft dysfunction at 10 years after PVR, event-free survival after PVR remained fairly good (78%). Significant residual lesions directly after surgery influenced event-free survival. A smaller diameter of the pulmonary homograft and severe pre-surgical PR were related to early homograft dysfunction after surgery.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/ehl033</identifier><identifier>PMID: 16707545</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; Biological and medical sciences ; Blood Pressure - physiology ; Cardiology. Vascular system ; Congenital heart diseases. Malformations of the aorta, pulmonary vessels and vena cava ; Disease-Free Survival ; Electrocardiography ; Endocardial and cardiac valvular diseases ; Female ; Follow-Up Studies ; Graft Survival - physiology ; Heart ; Heart Valve Prosthesis ; Humans ; Male ; Medical sciences ; Pregnancy ; Pregnancy Complications, Cardiovascular - etiology ; Pulmonary Valve ; Pulmonary Valve Insufficiency - complications ; Pulmonary Valve Insufficiency - surgery ; Pulmonary Valve Stenosis - complications ; Pulmonary Valve Stenosis - surgery ; Reoperation ; Retrospective Studies ; Tetralogy of Fallot - complications ; Transplantation, Homologous</subject><ispartof>European heart journal, 2006-06, Vol.27 (12), p.1478-1484</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Jun 15, 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-92cf990326cdb2d0070151adffcfff113dda7d119cbb166b4434b92952e964463</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17859446$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16707545$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OOSTERHOF, Thomas</creatorcontrib><creatorcontrib>MEIJBOOM, Folkert J</creatorcontrib><creatorcontrib>VLIEGEN, Hubert W</creatorcontrib><creatorcontrib>HAZEKAMP, Mark G</creatorcontrib><creatorcontrib>ZWINDERMAN, Aeiko H</creatorcontrib><creatorcontrib>BOUMA, Berto J</creatorcontrib><creatorcontrib>VAN DIJK, Arie P. J</creatorcontrib><creatorcontrib>MULDER, Barbara J. M</creatorcontrib><title>Long-term follow-up of homograft function after pulmonary valve replacement in patients with tetralogy of Fallot</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>To analyse the long-term outcomes after pulmonary valve replacement (PVR) in patients with a previous correction for tetralogy of Fallot.
In a retrospective study, 158 adult patients with a diagnosis of tetralogy of Fallot, who had undergone a PVR after initial total correction in childhood, were identified from the CONCOR (CONgenital CORvitia) registry. All patients underwent 175 PVRs between June 1986 and June 2005. To analyse the predictors for homograft dysfunction and adverse events (death, reoperations, balloon angioplasty), Cox-regression analysis was performed. Overall freedom from significant homograft dysfunction was 66% after 5 years and 47% after 10 years. We could not identify predictors for combined homograft dysfunction. Event-free survival was 78% at 10 years and 68% at 15 years after PVR. Both early significant pulmonary regurgitation (PR) (HR 6.8, P = 0.017) and pulmonary stenosis (PS) (HR 4.0, P = 0.037) after surgery were associated with adverse events. When analysing direct post-operative PR or PS, we observed that in patients with severe, pre-operative PR, right ventricular aneurysm/patch resection resulted in a lower post-operative PR (mean difference grade 0.38 +/- 0.14, P = 0.01). Less significant post-operative PS was associated with a higher diameter of the homograft (HR 0.37, P = 0.006).
While 47% of the patients in our study were free from homograft dysfunction at 10 years after PVR, event-free survival after PVR remained fairly good (78%). Significant residual lesions directly after surgery influenced event-free survival. A smaller diameter of the pulmonary homograft and severe pre-surgical PR were related to early homograft dysfunction after surgery.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Cardiology. Vascular system</subject><subject>Congenital heart diseases. Malformations of the aorta, pulmonary vessels and vena cava</subject><subject>Disease-Free Survival</subject><subject>Electrocardiography</subject><subject>Endocardial and cardiac valvular diseases</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Graft Survival - physiology</subject><subject>Heart</subject><subject>Heart Valve Prosthesis</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Cardiovascular - etiology</subject><subject>Pulmonary Valve</subject><subject>Pulmonary Valve Insufficiency - complications</subject><subject>Pulmonary Valve Insufficiency - surgery</subject><subject>Pulmonary Valve Stenosis - complications</subject><subject>Pulmonary Valve Stenosis - surgery</subject><subject>Reoperation</subject><subject>Retrospective Studies</subject><subject>Tetralogy of Fallot - complications</subject><subject>Transplantation, Homologous</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpdkc1r3DAQxUVJabZJ7z0FEWhuTiTrw9axLE1aWMilhdyMLI92vciSK8kJ-e-rZZcEepoZ-M1j3jyEvlJyS4lid7DEHeiY93ewc4SxD2hFRV1XSnJxhlaEKlFJ2T6do88p7QkhraTyEzqnsiGN4GKF5k3w2ypDnLANzoWXaplxsHgXprCN2mZsF2_yGDwuA0Q8L24KXsdX_KzdM-AIs9MGJvAZjx7POo-lTfhlzDucIUftwvb1IHmvi36-RB-tdgm-nOoF-nP_4_f6Z7V5fPi1_r6pDFMyV6o2VinCammGvh4IaQgVVA_WGmstpWwYdDNQqkzfUyl7zhnvVa1EDcU8l-wC3Rx15xj-LpByN43JgHPaQ1hSJ1vCBaMH8Po_cB-W6MttXU0FV4S3tEDkCJkYUopguzmOU_lCR0l3iKJ7i6I7RlFWrk66Sz_B8L5w-n0Bvp0AnYx2NmpvxvTONa1QByf_AIhaluw</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>OOSTERHOF, Thomas</creator><creator>MEIJBOOM, Folkert J</creator><creator>VLIEGEN, Hubert W</creator><creator>HAZEKAMP, Mark G</creator><creator>ZWINDERMAN, Aeiko H</creator><creator>BOUMA, Berto J</creator><creator>VAN DIJK, Arie P. 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Malformations of the aorta, pulmonary vessels and vena cava</topic><topic>Disease-Free Survival</topic><topic>Electrocardiography</topic><topic>Endocardial and cardiac valvular diseases</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Graft Survival - physiology</topic><topic>Heart</topic><topic>Heart Valve Prosthesis</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Cardiovascular - etiology</topic><topic>Pulmonary Valve</topic><topic>Pulmonary Valve Insufficiency - complications</topic><topic>Pulmonary Valve Insufficiency - surgery</topic><topic>Pulmonary Valve Stenosis - complications</topic><topic>Pulmonary Valve Stenosis - surgery</topic><topic>Reoperation</topic><topic>Retrospective Studies</topic><topic>Tetralogy of Fallot - complications</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OOSTERHOF, Thomas</creatorcontrib><creatorcontrib>MEIJBOOM, Folkert J</creatorcontrib><creatorcontrib>VLIEGEN, Hubert W</creatorcontrib><creatorcontrib>HAZEKAMP, Mark G</creatorcontrib><creatorcontrib>ZWINDERMAN, Aeiko H</creatorcontrib><creatorcontrib>BOUMA, Berto J</creatorcontrib><creatorcontrib>VAN DIJK, Arie P. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term follow-up of homograft function after pulmonary valve replacement in patients with tetralogy of Fallot</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>27</volume><issue>12</issue><spage>1478</spage><epage>1484</epage><pages>1478-1484</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>To analyse the long-term outcomes after pulmonary valve replacement (PVR) in patients with a previous correction for tetralogy of Fallot.
In a retrospective study, 158 adult patients with a diagnosis of tetralogy of Fallot, who had undergone a PVR after initial total correction in childhood, were identified from the CONCOR (CONgenital CORvitia) registry. All patients underwent 175 PVRs between June 1986 and June 2005. To analyse the predictors for homograft dysfunction and adverse events (death, reoperations, balloon angioplasty), Cox-regression analysis was performed. Overall freedom from significant homograft dysfunction was 66% after 5 years and 47% after 10 years. We could not identify predictors for combined homograft dysfunction. Event-free survival was 78% at 10 years and 68% at 15 years after PVR. Both early significant pulmonary regurgitation (PR) (HR 6.8, P = 0.017) and pulmonary stenosis (PS) (HR 4.0, P = 0.037) after surgery were associated with adverse events. When analysing direct post-operative PR or PS, we observed that in patients with severe, pre-operative PR, right ventricular aneurysm/patch resection resulted in a lower post-operative PR (mean difference grade 0.38 +/- 0.14, P = 0.01). Less significant post-operative PS was associated with a higher diameter of the homograft (HR 0.37, P = 0.006).
While 47% of the patients in our study were free from homograft dysfunction at 10 years after PVR, event-free survival after PVR remained fairly good (78%). Significant residual lesions directly after surgery influenced event-free survival. A smaller diameter of the pulmonary homograft and severe pre-surgical PR were related to early homograft dysfunction after surgery.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>16707545</pmid><doi>10.1093/eurheartj/ehl033</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences Blood Pressure - physiology Cardiology. Vascular system Congenital heart diseases. Malformations of the aorta, pulmonary vessels and vena cava Disease-Free Survival Electrocardiography Endocardial and cardiac valvular diseases Female Follow-Up Studies Graft Survival - physiology Heart Heart Valve Prosthesis Humans Male Medical sciences Pregnancy Pregnancy Complications, Cardiovascular - etiology Pulmonary Valve Pulmonary Valve Insufficiency - complications Pulmonary Valve Insufficiency - surgery Pulmonary Valve Stenosis - complications Pulmonary Valve Stenosis - surgery Reoperation Retrospective Studies Tetralogy of Fallot - complications Transplantation, Homologous |
title | Long-term follow-up of homograft function after pulmonary valve replacement in patients with tetralogy of Fallot |
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