Brassard M, Fouron J C, van Doesburg N H, Mercier L A, De Guise P
Department of Pediatrics, Ste-Justine Hospital, and Adult Congenital Heart Disease Clinic, Montreal Heart Institute, University of Montreal, Quebec, Canada.
Am J Cardiol. 1999 Jun 1;83(11):1552-5. doi: 10.1016/s0002-9149(99)00146-0.
There are few studies providing information on the natural course of hemodynamically insignificant atrial septal defect (ASD). To review the outcome of patients with secundum ASD, we retrospectively reviewed the charts of patients who had initially not been considered for surgical closure after age 1 year, and who had either a follow-up of at least 10 years or documented closure. Thirty patients, 22 females and 8 males, fulfilled our inclusion criteria. Mean age at diagnosis was 1.3 year and mean follow-up duration was 11.5 years. Seventeen patients had spontaneous closure of the ASD at a mean age of 8.4 years. There were 7 asymptomatic patients whose ASD was still patent at the last visit (mean age 14.1 years, mean follow-up 13.2), with defect dimensions on echocardiography ranging from 1 to 6 mm. The remaining 6 patients were considered to require surgical closure on the basis of an apparent increase in size of the ASD and secondary clinical and hemodynamic manifestations. These results (1) confirm that not all secundum ASDs need to be treated surgically because they can still spontaneously close past the age of 5, and (2) suggest that in a minority of cases the size of the defect could increase.
关于血流动力学无显著意义的房间隔缺损(ASD)自然病程的研究较少。为了回顾继发孔型ASD患者的转归,我们回顾性分析了1岁后最初未考虑手术闭合且随访至少10年或有闭合记录的患者病历。30例患者符合纳入标准,其中女性22例,男性8例。诊断时的平均年龄为1.3岁,平均随访时间为11.5年。17例患者ASD自发闭合,平均年龄为8.4岁。有7例无症状患者,其ASD在末次随访时仍未闭合(平均年龄14.1岁,平均随访13.2年),超声心动图显示缺损大小为1至6毫米。其余6例患者因ASD大小明显增加以及继发的临床和血流动力学表现而被认为需要手术闭合。这些结果(1)证实并非所有继发孔型ASD都需要手术治疗,因为它们在5岁后仍可自发闭合;(2)表明在少数情况下缺损大小可能会增加。