The limiation of staged repair in the surgical management of congenital complex heart anomalies with aortic arch obstruction
Objective: Severe aortic obstruction including an interrupted aortic arch in congenital complex heart anomalies remains a challenge in surgical management.Methods: Treatment and outcomes in 75 consecutive patients who underwent an aortic arch repair as the first step of the staged repair protocol be...
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Veröffentlicht in: | General thoracic and cardiovascular surgery 2003-07, Vol.51 (7), p.302-307 |
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creator | Aeba, Ryo Katogi, Toshiyuki Hashizume, Kenichi Iino, Yoshimi Koizumi, Kiyoshi Hotoda, Kentaro Inoue, Shinya Matayoshi, Hideki Yoshitake, Akihiro Yozu, Ryohei |
description | Objective: Severe aortic obstruction including an interrupted aortic arch in congenital complex heart anomalies remains a challenge in surgical management.Methods: Treatment and outcomes in 75 consecutive patients who underwent an aortic arch repair as the first step of the staged repair protocol between 1975 and 2000 were reviewed. Their ages at repair ranged from day to 8.5 months.Results: Cross-sectional postoperative follow-up data were available in all the patients. The follow-up period ranged from 0 to 27.6 years (mean 7.3±7.3 years). There were 20 postoperative hospital deaths (27%) and 7 late deaths. The Kaplan-Meier estimate of survival was 81.3%±4.5% at 1 month, 68.0%±5.4% at 1 years, 65.0%±5.5% at 5 years, 63.1%±5.7% at 10 years, 63.1%±5.7% at 20 years. By Cox regression analysis, body weight of 2.5 kg or less is the only independent determinant of postoperative mortality (p=0.04, multivariable odds ratio: 2.50, [95% confidence interval: 1.02–6.1]). The aortic arch morphology, the primary cardiac lesion, or date of operation did not reach a statistically significant level to show correlation with mortality. Reintervention to reconstruct the aortic arch was performed at 9 occasions in 8 of the 55 patients who survived the primary operation (14.5%). The Kaplan-Meier estimate of the reintervention-free rate was 91.3%±4.2% at 5 years, 85.5%±5.6% at 10 years, 75.6%±8.2% at 20 years. Using multivariable Cox regression analysis, interrupted aortic arch (versus aortic coarctation) was the only independent predictor of a shorter time to reintervention (p=0.001, multivariable odds ratio: 16.1, [95% confidence interval: 3.2–80.2].Conclusions: The staged repair protocol was associated with significant limitations in patient survival and with the development of recurrent aortic arch obstruction. Thus, a primary repair protocol may serve as an alternate approach, especially in patients with low weight or with an interrupted aortic arch. |
doi_str_mv | 10.1007/BF02719382 |
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Their ages at repair ranged from day to 8.5 months.Results: Cross-sectional postoperative follow-up data were available in all the patients. The follow-up period ranged from 0 to 27.6 years (mean 7.3±7.3 years). There were 20 postoperative hospital deaths (27%) and 7 late deaths. The Kaplan-Meier estimate of survival was 81.3%±4.5% at 1 month, 68.0%±5.4% at 1 years, 65.0%±5.5% at 5 years, 63.1%±5.7% at 10 years, 63.1%±5.7% at 20 years. By Cox regression analysis, body weight of 2.5 kg or less is the only independent determinant of postoperative mortality (p=0.04, multivariable odds ratio: 2.50, [95% confidence interval: 1.02–6.1]). The aortic arch morphology, the primary cardiac lesion, or date of operation did not reach a statistically significant level to show correlation with mortality. Reintervention to reconstruct the aortic arch was performed at 9 occasions in 8 of the 55 patients who survived the primary operation (14.5%). The Kaplan-Meier estimate of the reintervention-free rate was 91.3%±4.2% at 5 years, 85.5%±5.6% at 10 years, 75.6%±8.2% at 20 years. Using multivariable Cox regression analysis, interrupted aortic arch (versus aortic coarctation) was the only independent predictor of a shorter time to reintervention (p=0.001, multivariable odds ratio: 16.1, [95% confidence interval: 3.2–80.2].Conclusions: The staged repair protocol was associated with significant limitations in patient survival and with the development of recurrent aortic arch obstruction. Thus, a primary repair protocol may serve as an alternate approach, especially in patients with low weight or with an interrupted aortic arch.</description><identifier>ISSN: 1344-4964</identifier><identifier>ISSN: 1863-6705</identifier><identifier>EISSN: 1863-2092</identifier><identifier>EISSN: 1863-6713</identifier><identifier>DOI: 10.1007/BF02719382</identifier><language>eng</language><publisher>Tokyo: Springer Nature B.V</publisher><subject>Mortality ; Regression analysis</subject><ispartof>General thoracic and cardiovascular surgery, 2003-07, Vol.51 (7), p.302-307</ispartof><rights>Japanese Association for Thoracic Surgery 2003.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c635-880abe31d3194d4a2b424c55b83d5f3ffaff66af5ce7bc78f7ecd51e563f4173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2918733185?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,21368,21369,27903,27904,33509,33723,43638,43784,64361,64365,72215</link.rule.ids></links><search><creatorcontrib>Aeba, Ryo</creatorcontrib><creatorcontrib>Katogi, Toshiyuki</creatorcontrib><creatorcontrib>Hashizume, Kenichi</creatorcontrib><creatorcontrib>Iino, Yoshimi</creatorcontrib><creatorcontrib>Koizumi, Kiyoshi</creatorcontrib><creatorcontrib>Hotoda, Kentaro</creatorcontrib><creatorcontrib>Inoue, Shinya</creatorcontrib><creatorcontrib>Matayoshi, Hideki</creatorcontrib><creatorcontrib>Yoshitake, Akihiro</creatorcontrib><creatorcontrib>Yozu, Ryohei</creatorcontrib><title>The limiation of staged repair in the surgical management of congenital complex heart anomalies with aortic arch obstruction</title><title>General thoracic and cardiovascular surgery</title><description>Objective: Severe aortic obstruction including an interrupted aortic arch in congenital complex heart anomalies remains a challenge in surgical management.Methods: Treatment and outcomes in 75 consecutive patients who underwent an aortic arch repair as the first step of the staged repair protocol between 1975 and 2000 were reviewed. Their ages at repair ranged from day to 8.5 months.Results: Cross-sectional postoperative follow-up data were available in all the patients. The follow-up period ranged from 0 to 27.6 years (mean 7.3±7.3 years). There were 20 postoperative hospital deaths (27%) and 7 late deaths. The Kaplan-Meier estimate of survival was 81.3%±4.5% at 1 month, 68.0%±5.4% at 1 years, 65.0%±5.5% at 5 years, 63.1%±5.7% at 10 years, 63.1%±5.7% at 20 years. By Cox regression analysis, body weight of 2.5 kg or less is the only independent determinant of postoperative mortality (p=0.04, multivariable odds ratio: 2.50, [95% confidence interval: 1.02–6.1]). The aortic arch morphology, the primary cardiac lesion, or date of operation did not reach a statistically significant level to show correlation with mortality. Reintervention to reconstruct the aortic arch was performed at 9 occasions in 8 of the 55 patients who survived the primary operation (14.5%). The Kaplan-Meier estimate of the reintervention-free rate was 91.3%±4.2% at 5 years, 85.5%±5.6% at 10 years, 75.6%±8.2% at 20 years. Using multivariable Cox regression analysis, interrupted aortic arch (versus aortic coarctation) was the only independent predictor of a shorter time to reintervention (p=0.001, multivariable odds ratio: 16.1, [95% confidence interval: 3.2–80.2].Conclusions: The staged repair protocol was associated with significant limitations in patient survival and with the development of recurrent aortic arch obstruction. Thus, a primary repair protocol may serve as an alternate approach, especially in patients with low weight or with an interrupted aortic arch.</description><subject>Mortality</subject><subject>Regression analysis</subject><issn>1344-4964</issn><issn>1863-6705</issn><issn>1863-2092</issn><issn>1863-6713</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpFkMFKxDAYhIMouK5efIKAN6GaNEnTHnVxVVjw4N7L3zTZZmmTmqSo4MPbZQVPMzAfMzAIXVNyRwmR949rkktasTI_QQtaFizLSZWfzp5xnvGq4OfoIsY9IVwKWS3Qz7bTuLeDhWS9w97gmGCnWxz0CDZg63CaiTiFnVXQ4wHcHA_apQOrvNtpZ9McKD-Mvf7CnYaQMDg_QG91xJ82dRh8SFZhCKrDvokpTOowd4nODPRRX_3pEr2vn7arl2zz9vy6ethkqmAiK0sCjWa0ZbTiLYe84TlXQjQla4VhxoAxRQFGKC0bJUsjtWoF1aJghlPJlujm2DoG_zHpmOq9n4KbB-u8oqVkjJZipm6PlAo-xqBNPQY7QPiuKakP39b_37Jf609uSA</recordid><startdate>200307</startdate><enddate>200307</enddate><creator>Aeba, Ryo</creator><creator>Katogi, Toshiyuki</creator><creator>Hashizume, Kenichi</creator><creator>Iino, Yoshimi</creator><creator>Koizumi, Kiyoshi</creator><creator>Hotoda, Kentaro</creator><creator>Inoue, Shinya</creator><creator>Matayoshi, Hideki</creator><creator>Yoshitake, Akihiro</creator><creator>Yozu, Ryohei</creator><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>200307</creationdate><title>The limiation of staged repair in the surgical management of congenital complex heart anomalies with aortic arch obstruction</title><author>Aeba, Ryo ; Katogi, Toshiyuki ; Hashizume, Kenichi ; Iino, Yoshimi ; Koizumi, Kiyoshi ; Hotoda, Kentaro ; Inoue, Shinya ; Matayoshi, Hideki ; Yoshitake, Akihiro ; Yozu, Ryohei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635-880abe31d3194d4a2b424c55b83d5f3ffaff66af5ce7bc78f7ecd51e563f4173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Mortality</topic><topic>Regression analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aeba, Ryo</creatorcontrib><creatorcontrib>Katogi, Toshiyuki</creatorcontrib><creatorcontrib>Hashizume, Kenichi</creatorcontrib><creatorcontrib>Iino, Yoshimi</creatorcontrib><creatorcontrib>Koizumi, Kiyoshi</creatorcontrib><creatorcontrib>Hotoda, Kentaro</creatorcontrib><creatorcontrib>Inoue, Shinya</creatorcontrib><creatorcontrib>Matayoshi, Hideki</creatorcontrib><creatorcontrib>Yoshitake, Akihiro</creatorcontrib><creatorcontrib>Yozu, Ryohei</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>General thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aeba, Ryo</au><au>Katogi, Toshiyuki</au><au>Hashizume, Kenichi</au><au>Iino, Yoshimi</au><au>Koizumi, Kiyoshi</au><au>Hotoda, Kentaro</au><au>Inoue, Shinya</au><au>Matayoshi, Hideki</au><au>Yoshitake, Akihiro</au><au>Yozu, Ryohei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The limiation of staged repair in the surgical management of congenital complex heart anomalies with aortic arch obstruction</atitle><jtitle>General thoracic and cardiovascular surgery</jtitle><date>2003-07</date><risdate>2003</risdate><volume>51</volume><issue>7</issue><spage>302</spage><epage>307</epage><pages>302-307</pages><issn>1344-4964</issn><issn>1863-6705</issn><eissn>1863-2092</eissn><eissn>1863-6713</eissn><abstract>Objective: Severe aortic obstruction including an interrupted aortic arch in congenital complex heart anomalies remains a challenge in surgical management.Methods: Treatment and outcomes in 75 consecutive patients who underwent an aortic arch repair as the first step of the staged repair protocol between 1975 and 2000 were reviewed. Their ages at repair ranged from day to 8.5 months.Results: Cross-sectional postoperative follow-up data were available in all the patients. The follow-up period ranged from 0 to 27.6 years (mean 7.3±7.3 years). There were 20 postoperative hospital deaths (27%) and 7 late deaths. The Kaplan-Meier estimate of survival was 81.3%±4.5% at 1 month, 68.0%±5.4% at 1 years, 65.0%±5.5% at 5 years, 63.1%±5.7% at 10 years, 63.1%±5.7% at 20 years. By Cox regression analysis, body weight of 2.5 kg or less is the only independent determinant of postoperative mortality (p=0.04, multivariable odds ratio: 2.50, [95% confidence interval: 1.02–6.1]). The aortic arch morphology, the primary cardiac lesion, or date of operation did not reach a statistically significant level to show correlation with mortality. Reintervention to reconstruct the aortic arch was performed at 9 occasions in 8 of the 55 patients who survived the primary operation (14.5%). The Kaplan-Meier estimate of the reintervention-free rate was 91.3%±4.2% at 5 years, 85.5%±5.6% at 10 years, 75.6%±8.2% at 20 years. Using multivariable Cox regression analysis, interrupted aortic arch (versus aortic coarctation) was the only independent predictor of a shorter time to reintervention (p=0.001, multivariable odds ratio: 16.1, [95% confidence interval: 3.2–80.2].Conclusions: The staged repair protocol was associated with significant limitations in patient survival and with the development of recurrent aortic arch obstruction. Thus, a primary repair protocol may serve as an alternate approach, especially in patients with low weight or with an interrupted aortic arch.</abstract><cop>Tokyo</cop><pub>Springer Nature B.V</pub><doi>10.1007/BF02719382</doi><tpages>6</tpages></addata></record> |
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title | The limiation of staged repair in the surgical management of congenital complex heart anomalies with aortic arch obstruction |
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