Jacobs Jeffrey Phillip, Pasquali Sara K, Morales David L S, Jacobs Marshall Lewis, Mavroudis Constantine, Chai Paul Jubeong, Tchervenkov Christo I, Lacour-Gayet Francois G, Walters Hal, Quintessenza James Anthony
The Congenital Heart Institute of Florida (CHIF), All Children's Hospital and Children's Hospital of Tampa, University of South Florida College of Medicine, Cardiac Surgical Associates of Florida (CSAoF), Saint Petersburg and Tampa, FL, USA.
World J Pediatr Congenit Heart Surg. 2011 Apr;2(2):278-86. doi: 10.1177/2150135110397670.
According to The International Society for Nomenclature of Pediatric and Congenital Heart Disease (ISNPCHD), "Heterotaxy is synonymous with 'visceral heterotaxy' and 'heterotaxy syndrome'. Heterotaxy is defined as an abnormality where the internal thoraco-abdominal organs demonstrate abnormal arrangement across the left-right axis of the body. By convention, heterotaxy does not include patients with either the expected usual or normal arrangement of the internal organs along the left-right axis, also known as 'situs solitus', or patients with complete mirror-imaged arrangement of the internal organs along the left-right axis also known as `situs inversus'." or patients with complete mirror-image arrangement of the internal organs along the left-right axis, also known as situs inversus. The purpose of this article is to review the data about heterotaxy in the Society of Thoracic Surgeons (STS) Congenital Heart Surgery Database. The investigators examined all index operations in the STS Congenital Heart Surgery Database over 12 years from January 1, 1998 to December 31, 2009, inclusive. This analysis resulted in a cohort of 77 153 total index operations. Of these, 1505 operations (1.95%) were performed in patients with heterotaxy. Of the 1505 index operations performed in patients with heterotaxy, 1144 were in patients with asplenia and 361 were in patients with polysplenia. In every STS -EACTS Congenital Heart Surgery Mortality Category, discharge mortality is higher in patients with heterotaxy compared with patients without heterotaxy (EACTS = European Association for Cardio-Thoracic Surgery). Discharge mortality after systemic to pulmonary artery shunt is 6.6% in a cohort of all single-ventricle patients except those with heterotaxy, whereas it is 10.8% in single-ventricle patients with heterotaxy. Discharge mortality after Fontan is 1.8% in a cohort of all single-ventricle patients except those with heterotaxy, whereas it is 4.2% in single-ventricle patients with heterotaxy. The STS Congenital Heart Surgery Database is largest congenital heart surgery database in North America. This review of data from the STS Congenital Heart Surgery Database allows for unique documentation of practice patterns and outcomes. From this analysis, it is clear that heterotaxy is a challenging problem with increased discharge mortality in most subgroups.
根据国际小儿及先天性心脏病命名学会(ISNPCHD)的定义,“内脏异位与‘内脏异位症’和‘异位症综合征’同义。内脏异位被定义为一种异常情况,即胸腹部内部器官在身体的左右轴线上呈现异常排列。按照惯例,内脏异位不包括内脏器官沿左右轴线呈预期的正常排列(即‘正位’)的患者,也不包括内脏器官沿左右轴线呈完全镜像排列(即‘镜像右位心’)的患者。” 本文的目的是回顾胸外科医师协会(STS)先天性心脏病手术数据库中有关内脏异位的数据。研究人员检查了1998年1月1日至2009年12月31日(含)这12年间STS先天性心脏病手术数据库中的所有索引手术。该分析得出总共77153例索引手术的队列。其中,1505例手术(1.95%)是在内脏异位患者中进行的。在内脏异位患者进行的1505例索引手术中,1144例是无脾患者,361例是多脾患者。在每个STS-EACTS先天性心脏病手术死亡率类别中,内脏异位患者的出院死亡率高于无内脏异位的患者(EACTS = 欧洲心胸外科学会)。在除内脏异位患者之外的所有单心室患者队列中,体肺分流术后的出院死亡率为6.6%,而在内脏异位的单心室患者中为10.8%。在除内脏异位患者之外的所有单心室患者队列中,Fontan术后的出院死亡率为1.8%,而在内脏异位的单心室患者中为4.2%。STS先天性心脏病手术数据库是北美最大的先天性心脏病手术数据库。对STS先天性心脏病手术数据库数据的回顾使得能够独特地记录实践模式和结果。从该分析中可以清楚地看出,内脏异位是一个具有挑战性的问题,在大多数亚组中出院死亡率都有所增加。