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Prevalence and development of additional cardiac abnormalities in 1448 patients with congenital ventricular septal defects

机译:1448例先天性室间隔缺损患者中额外心脏异常的发生和发展

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Objective: To determine by modern echocardiographic techniques the prevalence and development of cardiac abnormalities associated with ventricular septal defect (VSD). Methods: Consecutive patients referred to a tertiary centre for paediatric cardiology and attenders at an adult congenital heart disease clinic had details of clinical outcome prospectively recorded. Patients with VSD in association with conotruncal abnormalities, atrioventricular septal defects, and univentricular heart were not included in the study. Results: 1448 patients with VSD were assessed between 1991 and 1998. 1127 (78%) patients had isolated defects; of these 862 (76%) were perimembranous and 265 (24%) were muscular. Of the remainder, 284 (19.6% of the total population) patients had VSD associated with one other significant cardiac abnormality: 35 (2.4%) with two and two (0.1 %) with three other abnormalities. The most common associated cardiac abnormalities were infundibular pulmonary stenosis (5.8%), aortic valve prolapse (3.6%), pulmonary valvar stenosis (2.7%), osteum secundum atrial septal defect (2.2%), persistent ductus arteriosus (1.9%), and coarctation of the aorta (1.5%). In the cohort of 743 patients followed up from birth, cumulative mortality was 4% by the age of 8 years and most deaths occurred within the first year of life in infants with associated genetic abnormalities such as trisomy 13 or 18. Of the 594 patients attending the adult congenital clinic with VSD, aortic regurgitation due to aortic root prolapse developed in 45 (7.6%) patients. Most of these cases were detected before the patient was 30 years old. Conclusions: In 22% of patients with congenital VSD there were significant associated cardiac abnormalities. Some of these abnormalities, such as aortic prolapse and regurgitation or infundibular pulmonary stenosis, may develop or progress subsequently and therefore should be sought during the initial assessment and monitored during follow up. Follow up to the age of 30 years allows the detection of most cases of aortic regurgitation. The prognosis from VSD is excellent and the risk of endocarditis in a population informed of the need for antibiotic prophylaxis is small.
机译:目的:通过现代超声心动图技术确定与室间隔缺损(VSD)相关的心脏异常的发生率和发展。方法:转诊至小儿心脏病学三级中心的连续患者,以及成年先天性心脏病诊所的服务人员均已预先记录了临床结局的详细信息。伴有锥周异常,房室间隔缺损和单心室心脏病的VSD患者未纳入研究。结果:在1991年至1998年之间评估了1448例VSD患者。1127例(78%)患者具有孤立的缺损;在这862名(76%)的患者中,其周围是膜质,而265名(24%)的则是肌肉。在其余的284名(占总人口的19.6%)患者中,VSD伴有另一种严重的心脏异常:35例(2.4%)伴有两个严重的心脏异常,另外2例(0.1%)伴有其他三个心脏异常。最常见的相关心脏异常是漏斗性肺动脉狭窄(5.8%),主动脉瓣脱垂(3.6%),肺动脉瓣狭窄(2.7%),次发性房间隔缺损(2.2%),持续性动脉导管未闭(1.9%)和主动脉缩窄(1.5%)。在743例从出生开始随访的患者中,到8岁时的累积死亡率为4%,并且大多数死亡发生在具有相关遗传异常(如13三体或18三体性)的婴儿的出生后第一年。在具有VSD的成人先天性诊所中,有45名(7.6%)患者因主动脉根部脱垂而发生主动脉瓣关闭不全。这些病例大多数在患者30岁之前被发现。结论:22%的先天性VSD患者存在明显的相关心脏异常。这些异常中的一些,例如主动脉脱垂和反流或漏斗状肺动脉狭窄,可能随后发生或发展,因此应在初次评估中寻求并在随访期间进行监测。随访到30岁可以发现大多数主动脉瓣关闭不全的情况。 VSD的预后极好,并且知道需要预防抗生素的人群患心内膜炎的风险很小。

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