{"title":"婴儿房间隔切除术后继发性房间隔缺损并发顽固性心力衰竭1例","authors":"Z. Vassileva","doi":"10.19080/jocct.2019.14.555882","DOIUrl":null,"url":null,"abstract":"We present a case of resistant to medical treatment heart failure due to significant shunting through a secundum atrial septal defect by a 3-month old infant who underwent coarctectomy due to critical coarctation of the aorta at the age of 15 days. The tachydyspnea and failure to thrive persisted despite the successful resection of the coarctation and resolved very rapidly after subsequent operative closure of the atrial septal defect.","PeriodicalId":73635,"journal":{"name":"Journal of cardiology & cardiovascular therapy","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Rare Case of Secundum Atrial Septal Defect with Intractable Heart Failure after Coarctectomy by an Infant\",\"authors\":\"Z. Vassileva\",\"doi\":\"10.19080/jocct.2019.14.555882\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We present a case of resistant to medical treatment heart failure due to significant shunting through a secundum atrial septal defect by a 3-month old infant who underwent coarctectomy due to critical coarctation of the aorta at the age of 15 days. The tachydyspnea and failure to thrive persisted despite the successful resection of the coarctation and resolved very rapidly after subsequent operative closure of the atrial septal defect.\",\"PeriodicalId\":73635,\"journal\":{\"name\":\"Journal of cardiology & cardiovascular therapy\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of cardiology & cardiovascular therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.19080/jocct.2019.14.555882\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of cardiology & cardiovascular therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/jocct.2019.14.555882","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Rare Case of Secundum Atrial Septal Defect with Intractable Heart Failure after Coarctectomy by an Infant
We present a case of resistant to medical treatment heart failure due to significant shunting through a secundum atrial septal defect by a 3-month old infant who underwent coarctectomy due to critical coarctation of the aorta at the age of 15 days. The tachydyspnea and failure to thrive persisted despite the successful resection of the coarctation and resolved very rapidly after subsequent operative closure of the atrial septal defect.
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