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首页> 外文期刊>The Annals of Thoracic Surgery: Official Journal of the Society of Thoracic Surgeons and the Southern Thoracic Surgical Association >Tracheostomy After Operations for Congenital Heart Disease: An Analysis of the Society of Thoracic Surgeons Congenital Heart Surgery Database
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Tracheostomy After Operations for Congenital Heart Disease: An Analysis of the Society of Thoracic Surgeons Congenital Heart Surgery Database

机译:先天性心脏病手术后气管切开术:胸外科医师学会先天性心脏病手术数据库的分析

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Audio/VideoDownload File (109.54 MB)Download File (109.54 MB)Need help playing this video?Try playing the flash (.flv) version of this videoYou may need to download the latest version of FlashUse the "Download File" link to play the source videoAuthor InterviewData SourceStudy PopulationData Collection and DefinitionsStatistical AnalysisSupplementary DataReferencesInformation concerning tracheostomy after operations for congenital heart disease has come primarily from single-center reports. We aimed to describe the epidemiology and outcomes associated with postoperative tracheostomy in a multi-institutional registry.MethodsThe Society of Thoracic Surgeons Congenital Heart Database (2000 to 2014) was queried for all index operations with the adverse event “postoperative tracheostomy” or “respiratory failure, requiring tracheostomy.” Patients with preoperative tracheostomy or weighing less than 2.5 kg undergoing isolated closure of patent ductus arteriosus were excluded. Trends in tracheostomy incidence over time from January 2000 to June 2014 were analyzed with a Cochran-Armitage test. The patient characteristics associated with operative mortality were analyzed for January 2010 to June 2014, including deaths occurring up to 6 months after transfer of patients to long-term care facilities.ResultsFrom 2000 to 2014, the incidence of tracheostomy after operations for congenital heart disease increased from 0.11% in 2000 to a high of 0.76% in 2012 (p?< 0.0001). From 2010 to 2014, 648 patients underwent tracheostomy. The median age at operation was 2.5 months (25th, 75th percentile: 0.4, 7). Prematurity (n?= 165, 26%), genetic abnormalities (n?= 298, 46%), and preoperative mechanical ventilation (n?= 275, 43%) were common. Postoperative adverse events were also common, including cardiac arrest (n?= 131, 20%), extracorporeal support (n?= 87, 13%), phrenic or laryngeal nerve injury (n?= 114, 18%), and neurologic deficit (n?= 51, 8%). The operative mortality was 25% (n?= 153).ConclusionsTracheostomy as an adverse event of operations for congenital heart disease remains rare but has been increasingly used over the past 15 years. This trend and the considerable mortality risk among patients requiring postoperative tracheostomy support the need for further research in this complex population.Congenital Heart Surgery:The Annals of Thoracic Surgery CME Program is located online at http://www.annalsthoracicsurgery.org/cme/home. To take the CME activity related to this article, you must have either an STS member or an individual non-member subscription to the journal.As the field of pediatric cardiovascular surgery has evolved, surgical repair or palliation in patients with?complex underlying cardiac lesions who often have?coexistent noncardiac comorbidities has become commonplace at most centers. Many of these patients have prolonged postoperative courses, including prolonged need for mechanical ventilation. In some cases, liberation from mechanical ventilation is not possible, and tracheostomy is considered. Several institutions have reported their experiences with pediatric patients requiring tracheostomy after cardiac operations [
机译:音频/视频下载文件(109.54 MB)下载文件(109.54 MB)需要帮助播放此视频吗?尝试播放此视频的Flash(.flv)版本您可能需要下载Flash的最新版本使用“下载文件”链接来播放来源视频作者InterviewData来源研究人口数据收集和定义统计分析补充数据参考文献有关先天性心脏病手术后气管切开术的信息主要来自单中心报告。我们旨在通过多机构注册表描述与术后气管切开术相关的流行病学和结果。方法对胸外科医师协会先天性心脏数据库(2000年至2014年)的所有指标操作进行查询,包括不良事件“术后气管切开术”或“呼吸衰竭”。 ,需要进行气管切开术。”术前气管切开术或体重少于2.5 kg的患者行单纯性动脉导管未闭的患者被排除在外。使用Cochran-Armitage测试分析了2000年1月至2014年6月期间气管切开术发生率的趋势。分析了2010年1月至2014年6月与手术死亡率相关的患者特征,包括在将患者转移至长期护理机构后6个月内发生的死亡。结果2000年至2014年,先天性心脏病手术后气管切开术的发生率增加了从2000年的0.11%上升到2012年的0.76%(p <0.0001)。从2010年到2014年,共有648例患者进行了气管切开术。手术中位年龄为2.5个月(25、75%:0.4、7)。早产(n = 165、26%),遗传异常(298 = 46%)和术前机械通气(n = 275、43%)是常见的。术后不良事件也很常见,包括心脏骤停(n = 131,20%),体外支持(n = 87、13%),或喉神经损伤(n = 114、18 ) %)和神经功能缺损(n?= 51,8%)。手术死亡率为25%(n = 153)。结论气管切开术作为先天性心脏病手术的不良事件仍然很少见,但在过去的15年中已得到越来越多的使用。这种趋势以及需要进行气管切开术的患者中相当大的死亡风险支持了这一复杂人群的进一步研究。先天性心脏病手术:《胸外科史》 CME计划可在线访问http://www.annalsthoracicsicsryry.org/cme/家。要从事与本文相关的CME活动,您必须是该期刊的STS会员或非会员个人。随着儿科心血管外科领域的发展,患有复杂的基础心脏病变的患者的手术修复或缓解谁经常患有非心脏合并症在大多数中心已经变得司空见惯。这些患者中的许多患者术后病程延长,包括长期需要机械通气。在某些情况下,不可能从机械通气中解放出来,因此考虑进行气管切开术。一些机构已经报告了他们在心脏手术后需要气管切开术的小儿患者的经历[

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