Early and Intermediate Term Results for Surgical Correction of Total Anomalous Pulmonary Venous Connection
Background: This retrospective study evaluated factors associated with mortality and morbidity in patients having functionally biventricular heart (FBH) and functionally univentricular heart (FUH) undergoing total anomalous pulmonary venous connection (TAPVC) repair. Methods: We reviewed medical rec...
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Veröffentlicht in: | Journal of cardiac surgery 2012-05, Vol.27 (3), p.376-380 |
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description | Background: This retrospective study evaluated factors associated with mortality and morbidity in patients having functionally biventricular heart (FBH) and functionally univentricular heart (FUH) undergoing total anomalous pulmonary venous connection (TAPVC) repair. Methods: We reviewed medical records retrospectively and identified 72 patients undergoing TAPVC repair between July 2002 and December 2010; and 62 patients had FBH and 10 patients had FUH. The median age and weight at repair was 9.1 months (range, 8 days–16 years) and 6.7 kg (range, 2.5–57 kg). The TAPVC anatomy was supracardiac in 41 (56.9%), cardiac in 18 (25%), infracardiac in eight (11.1%), and mixed in five patients (6.9%). Results: There were seven early deaths (2 FBH [25%] and 5 FUH [62.5%]) and one late death (FUH). Presence of FUH (p < 0.01), heterotaxy syndrome (p = 0.03), young age (p < 0.01), low weight (p < 0.01) and long CPB time (p = 0.04) at the time of surgery were statistically significant risk factors for mortality. Morbidity was related to long duration of postoperative mechanical ventilation, intensive care unit and hospital stay. Presence of FUH was the only significant risk factor for morbidity (p < 0.01). After a mean follow‐up of 52.1 months (range, 3–74 months), 59 (92%) of 64 survivors were asymptomatic without any medication, and five have mild symptoms with regular physical activity. Conclusion: Operative results of TAPVC have dramatically improved in recent years. However, patients having FUH (especially with concomitant palliative surgery), heterotaxy syndrome, low weight, early age, and long CPB time still have an increased operative mortality. (J Card Surg 2012;27:376‐380) |
doi_str_mv | 10.1111/j.1540-8191.2012.01435.x |
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Methods: We reviewed medical records retrospectively and identified 72 patients undergoing TAPVC repair between July 2002 and December 2010; and 62 patients had FBH and 10 patients had FUH. The median age and weight at repair was 9.1 months (range, 8 days–16 years) and 6.7 kg (range, 2.5–57 kg). The TAPVC anatomy was supracardiac in 41 (56.9%), cardiac in 18 (25%), infracardiac in eight (11.1%), and mixed in five patients (6.9%). Results: There were seven early deaths (2 FBH [25%] and 5 FUH [62.5%]) and one late death (FUH). Presence of FUH (p < 0.01), heterotaxy syndrome (p = 0.03), young age (p < 0.01), low weight (p < 0.01) and long CPB time (p = 0.04) at the time of surgery were statistically significant risk factors for mortality. Morbidity was related to long duration of postoperative mechanical ventilation, intensive care unit and hospital stay. Presence of FUH was the only significant risk factor for morbidity (p < 0.01). After a mean follow‐up of 52.1 months (range, 3–74 months), 59 (92%) of 64 survivors were asymptomatic without any medication, and five have mild symptoms with regular physical activity. Conclusion: Operative results of TAPVC have dramatically improved in recent years. However, patients having FUH (especially with concomitant palliative surgery), heterotaxy syndrome, low weight, early age, and long CPB time still have an increased operative mortality. (J Card Surg 2012;27:376‐380)</description><identifier>ISSN: 0886-0440</identifier><identifier>EISSN: 1540-8191</identifier><identifier>DOI: 10.1111/j.1540-8191.2012.01435.x</identifier><identifier>PMID: 22497245</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Abnormalities, Multiple - mortality ; Abnormalities, Multiple - surgery ; Adolescent ; Age Factors ; Body Weight ; Cardiopulmonary Bypass ; Child ; Child, Preschool ; Female ; Follow-Up Studies ; Heart Atria - abnormalities ; Heart Atria - surgery ; Heart Defects, Congenital - mortality ; Heart Defects, Congenital - surgery ; Humans ; Infant ; Infant, Newborn ; Male ; Postoperative Complications ; Proportional Hazards Models ; Pulmonary Veins - abnormalities ; Pulmonary Veins - surgery ; Retrospective Studies ; Risk Factors ; Scimitar Syndrome - mortality ; Scimitar Syndrome - surgery ; Survival Rate ; Treatment Outcome</subject><ispartof>Journal of cardiac surgery, 2012-05, Vol.27 (3), p.376-380</ispartof><rights>2012 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4085-852bb555eadfa101a76b960d25ddb6a39a0c23ed166d333470552f742a083493</citedby><cites>FETCH-LOGICAL-c4085-852bb555eadfa101a76b960d25ddb6a39a0c23ed166d333470552f742a083493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1540-8191.2012.01435.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1540-8191.2012.01435.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22497245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karaci, Ali Riza</creatorcontrib><creatorcontrib>Harmandar, Bugra</creatorcontrib><creatorcontrib>Aydemir, Numan Ali</creatorcontrib><creatorcontrib>Sasmazel, Ahmet</creatorcontrib><creatorcontrib>Balci, Ahmet Yavuz</creatorcontrib><creatorcontrib>Saritas, Turkay</creatorcontrib><creatorcontrib>Yekeler, Ibrahim</creatorcontrib><creatorcontrib>Bilal, Mehmet Salih</creatorcontrib><title>Early and Intermediate Term Results for Surgical Correction of Total Anomalous Pulmonary Venous Connection</title><title>Journal of cardiac surgery</title><addtitle>J Card Surg</addtitle><description>Background: This retrospective study evaluated factors associated with mortality and morbidity in patients having functionally biventricular heart (FBH) and functionally univentricular heart (FUH) undergoing total anomalous pulmonary venous connection (TAPVC) repair. Methods: We reviewed medical records retrospectively and identified 72 patients undergoing TAPVC repair between July 2002 and December 2010; and 62 patients had FBH and 10 patients had FUH. The median age and weight at repair was 9.1 months (range, 8 days–16 years) and 6.7 kg (range, 2.5–57 kg). The TAPVC anatomy was supracardiac in 41 (56.9%), cardiac in 18 (25%), infracardiac in eight (11.1%), and mixed in five patients (6.9%). Results: There were seven early deaths (2 FBH [25%] and 5 FUH [62.5%]) and one late death (FUH). Presence of FUH (p < 0.01), heterotaxy syndrome (p = 0.03), young age (p < 0.01), low weight (p < 0.01) and long CPB time (p = 0.04) at the time of surgery were statistically significant risk factors for mortality. Morbidity was related to long duration of postoperative mechanical ventilation, intensive care unit and hospital stay. Presence of FUH was the only significant risk factor for morbidity (p < 0.01). After a mean follow‐up of 52.1 months (range, 3–74 months), 59 (92%) of 64 survivors were asymptomatic without any medication, and five have mild symptoms with regular physical activity. Conclusion: Operative results of TAPVC have dramatically improved in recent years. However, patients having FUH (especially with concomitant palliative surgery), heterotaxy syndrome, low weight, early age, and long CPB time still have an increased operative mortality. (J Card Surg 2012;27:376‐380)</description><subject>Abnormalities, Multiple - mortality</subject><subject>Abnormalities, Multiple - surgery</subject><subject>Adolescent</subject><subject>Age Factors</subject><subject>Body Weight</subject><subject>Cardiopulmonary Bypass</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Heart Atria - abnormalities</subject><subject>Heart Atria - surgery</subject><subject>Heart Defects, Congenital - mortality</subject><subject>Heart Defects, Congenital - surgery</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Postoperative Complications</subject><subject>Proportional Hazards Models</subject><subject>Pulmonary Veins - abnormalities</subject><subject>Pulmonary Veins - surgery</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Scimitar Syndrome - mortality</subject><subject>Scimitar Syndrome - surgery</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><issn>0886-0440</issn><issn>1540-8191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtP3DAURi3UqgzQv4C87Cap30k2lVDEDIxQeY1gaTmJgzI4NrUTMfPv6xA663pzrevvHl8dACBGKY7n5zbFnKEkxwVOCcIkRZhRnu6OwOLw8AUsUJ6LBDGGjsFJCFuECGEUfQPHsRYZYXwBtpfKmz1UtoHXdtC-102nBg038QofdBjNEGDrPHwc_UtXKwNL572uh85Z6Fq4cUPsXVjXK-PGAO9G0zur_B4-aTs1SmftHD8DX1tlgv7-WU_BZnm5Ka-Sm9vVdXlxk9QM5TzJOakqzrlWTaswwioTVSFQQ3jTVELRQqGaUN1gIRpKKcsQ56TNGFEop6ygp-DHjH3z7s-owyD7LtTaGGV1XEhGpBAZETyL0XyO1t6F4HUr33zXx-VjSE6i5VZOPuXkU06i5YdouYuj55-_jFV0dhj8ZzYGfs2B987o_X-D5fq2fJyuEZDMgC4MencAKP8qRUYzLp9_r-T9cv10Vyyv5Jr-BT3um_Q</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>Karaci, Ali Riza</creator><creator>Harmandar, Bugra</creator><creator>Aydemir, Numan Ali</creator><creator>Sasmazel, Ahmet</creator><creator>Balci, Ahmet Yavuz</creator><creator>Saritas, Turkay</creator><creator>Yekeler, Ibrahim</creator><creator>Bilal, Mehmet Salih</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</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>201205</creationdate><title>Early and Intermediate Term Results for Surgical Correction of Total Anomalous Pulmonary Venous Connection</title><author>Karaci, Ali Riza ; Harmandar, Bugra ; Aydemir, Numan Ali ; Sasmazel, Ahmet ; Balci, Ahmet Yavuz ; Saritas, Turkay ; Yekeler, Ibrahim ; Bilal, Mehmet Salih</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4085-852bb555eadfa101a76b960d25ddb6a39a0c23ed166d333470552f742a083493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Abnormalities, Multiple - mortality</topic><topic>Abnormalities, Multiple - surgery</topic><topic>Adolescent</topic><topic>Age Factors</topic><topic>Body Weight</topic><topic>Cardiopulmonary Bypass</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Heart Atria - abnormalities</topic><topic>Heart Atria - surgery</topic><topic>Heart Defects, Congenital - mortality</topic><topic>Heart Defects, Congenital - surgery</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Postoperative Complications</topic><topic>Proportional Hazards Models</topic><topic>Pulmonary Veins - abnormalities</topic><topic>Pulmonary Veins - surgery</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Scimitar Syndrome - mortality</topic><topic>Scimitar Syndrome - surgery</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karaci, Ali Riza</creatorcontrib><creatorcontrib>Harmandar, Bugra</creatorcontrib><creatorcontrib>Aydemir, Numan Ali</creatorcontrib><creatorcontrib>Sasmazel, Ahmet</creatorcontrib><creatorcontrib>Balci, Ahmet Yavuz</creatorcontrib><creatorcontrib>Saritas, Turkay</creatorcontrib><creatorcontrib>Yekeler, Ibrahim</creatorcontrib><creatorcontrib>Bilal, Mehmet Salih</creatorcontrib><collection>Istex</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>Journal of cardiac surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karaci, Ali Riza</au><au>Harmandar, Bugra</au><au>Aydemir, Numan Ali</au><au>Sasmazel, Ahmet</au><au>Balci, Ahmet Yavuz</au><au>Saritas, Turkay</au><au>Yekeler, Ibrahim</au><au>Bilal, Mehmet Salih</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early and Intermediate Term Results for Surgical Correction of Total Anomalous Pulmonary Venous Connection</atitle><jtitle>Journal of cardiac surgery</jtitle><addtitle>J Card Surg</addtitle><date>2012-05</date><risdate>2012</risdate><volume>27</volume><issue>3</issue><spage>376</spage><epage>380</epage><pages>376-380</pages><issn>0886-0440</issn><eissn>1540-8191</eissn><abstract>Background: This retrospective study evaluated factors associated with mortality and morbidity in patients having functionally biventricular heart (FBH) and functionally univentricular heart (FUH) undergoing total anomalous pulmonary venous connection (TAPVC) repair. Methods: We reviewed medical records retrospectively and identified 72 patients undergoing TAPVC repair between July 2002 and December 2010; and 62 patients had FBH and 10 patients had FUH. The median age and weight at repair was 9.1 months (range, 8 days–16 years) and 6.7 kg (range, 2.5–57 kg). The TAPVC anatomy was supracardiac in 41 (56.9%), cardiac in 18 (25%), infracardiac in eight (11.1%), and mixed in five patients (6.9%). Results: There were seven early deaths (2 FBH [25%] and 5 FUH [62.5%]) and one late death (FUH). Presence of FUH (p < 0.01), heterotaxy syndrome (p = 0.03), young age (p < 0.01), low weight (p < 0.01) and long CPB time (p = 0.04) at the time of surgery were statistically significant risk factors for mortality. Morbidity was related to long duration of postoperative mechanical ventilation, intensive care unit and hospital stay. Presence of FUH was the only significant risk factor for morbidity (p < 0.01). After a mean follow‐up of 52.1 months (range, 3–74 months), 59 (92%) of 64 survivors were asymptomatic without any medication, and five have mild symptoms with regular physical activity. Conclusion: Operative results of TAPVC have dramatically improved in recent years. However, patients having FUH (especially with concomitant palliative surgery), heterotaxy syndrome, low weight, early age, and long CPB time still have an increased operative mortality. (J Card Surg 2012;27:376‐380)</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>22497245</pmid><doi>10.1111/j.1540-8191.2012.01435.x</doi><tpages>5</tpages></addata></record> |
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subjects | Abnormalities, Multiple - mortality Abnormalities, Multiple - surgery Adolescent Age Factors Body Weight Cardiopulmonary Bypass Child Child, Preschool Female Follow-Up Studies Heart Atria - abnormalities Heart Atria - surgery Heart Defects, Congenital - mortality Heart Defects, Congenital - surgery Humans Infant Infant, Newborn Male Postoperative Complications Proportional Hazards Models Pulmonary Veins - abnormalities Pulmonary Veins - surgery Retrospective Studies Risk Factors Scimitar Syndrome - mortality Scimitar Syndrome - surgery Survival Rate Treatment Outcome |
title | Early and Intermediate Term Results for Surgical Correction of Total Anomalous Pulmonary Venous Connection |
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