McMahon C J, Feltes T F, Fraley J K, Bricker J T, Grifka R G, Tortoriello T A, Blake R, Bezold L I
The LillieFrank Abercrombie Division of Pediatric Cardiology, Texas Children's Hospital and Baylor College of Medicine, Houston, 6621 Fannin, Texas 77030, USA.
Heart. 2002 Mar;87(3):256-9. doi: 10.1136/heart.87.3.256.
To investigate the natural history of secundum atrial septal defects (ASDs) over several years using serial echocardiographic studies.
All patients with isolated secundum ASDs who had serial transthoracic echocardiograms at Texas Children's Hospital, Houston, Texas, from January 1991 to December 1998 were identified. Patients with fenestrated or multiple ASDs, other congenital heart defects, or less than a six month interval between echocardiograms were excluded. There were 104 patients eligible for inclusion in the study. Studies were reviewed by two echocardiographers (blinded) and the maximal diameter was recorded. Defects were defined as small (> 3 mm to < 6 mm), moderate (> or = 6 mm to < 12 mm), or large (> or = 12 mm). ASDs that grew > or = 20 mm were defined as having outgrown transcatheter closure with the device available to the authors' institution.
ASD diameter increased in 68 of 104 patients (65%), including 31 patients (30%) with a > 50% increase in diameter. Spontaneous closure occurred in four patients (4%). Thirteen defects (12%) increased to > or = 20 mm. One fifth of the patients studied had an insufficient atrial rim by transthoracic echocardiogram to hold an atrial septal occluder. The only factor associated with significant growth of ASDs was initial size of the defect. ASD growth was independent both of age at diagnosis and when indexed to body surface area.
Two thirds of secundum ASDs may enlarge with time and there is the potential for secundum ASDs to outgrow transcatheter closure with specific devices. Further development in devices and general availability of devices capable of closing larger ASDs should circumvent this problem.
通过系列超声心动图研究,探讨继发孔型房间隔缺损(ASD)多年的自然病史。
确定1991年1月至1998年12月在德克萨斯州休斯顿市德克萨斯儿童医院接受系列经胸超声心动图检查的所有孤立性继发孔型ASD患者。排除有筛孔状或多发性ASD、其他先天性心脏缺陷或超声心动图检查间隔少于6个月的患者。有104例患者符合纳入本研究的条件。由两名超声心动图医生(盲法)复查研究资料并记录最大直径。缺损被定义为小(>3mm至<6mm)、中(≥6mm至<12mm)或大(≥12mm)。直径增长≥20mm的ASD被定义为已长大到无法使用作者所在机构可用的装置进行经导管封堵。
104例患者中有68例(65%)ASD直径增大,其中31例(30%)直径增大超过50%。4例患者(4%)出现自然闭合。13个缺损(12%)增大至≥20mm。经胸超声心动图显示,五分之一的研究患者心房边缘不足,无法容纳房间隔封堵器。与ASD显著生长相关的唯一因素是缺损的初始大小。ASD的生长与诊断时的年龄以及根据体表面积进行指数化均无关。
三分之二的继发孔型ASD可能随时间增大,继发孔型ASD有可能长大到无法使用特定装置进行经导管封堵。封堵更大ASD的装置的进一步研发以及这些装置的普遍可得性应能解决这一问题。