Department of Pediatrics, Division of Pediatric Cardiology, The University of Texas-Houston Medical School/Children's Memorial Hermann Hospital, Houston, TX, USA.
Indian J Pediatr. 2013 Jan;80(1):32-8. doi: 10.1007/s12098-012-0833-6. Epub 2012 Jun 30.
The purpose of this review/editorial is to discuss how and when to treat the most common acyanotic congenital heart defects (CHD); the discussion of cyanotic heart defects will be presented in a subsequent editorial. By and large, the indications and timing of intervention are decided by the severity of the lesion. Balloon pulmonary valvuloplasty is the treatment of choice for valvar pulmonary stenosis and the indication for intervention is peak-to-peak systolic pressure gradient >50 mmHg across the pulmonary valve. For aortic valve stenosis, balloon aortic valvuloplasty appears to be the first therapeutic procedure of choice; the indications for balloon dilatation of aortic valve are peak-to-peak systolic pressure gradient across the aortic valve in excess of 70 mmHg irrespective of the symptoms or a gradient ≥ 50 mmHg with either symptoms or electrocardiographic ST-T wave changes indicative of myocardial perfusion abnormality. The indications for intervention in coarctation of the aorta are significant hypertension and/or congestive heart failure along with a pressure gradient in excess of 20 mmHg across the coarctation; the type of intervention varies with age at presentation and the anatomy of coarctation: surgical intervention for neonates and young infants, balloon angioplasty for discrete native coarctation in children, and stents in adolescents and adults. Long segment coarctations or those associated with hypoplasia of the isthmus or transverse aortic arch require surgical treatment in younger children and stents in adolescents and adults. For post-surgical aortic recoarctation, balloon angioplasty in young children and stents in adolescents and adults are treatment options. Transcatheter closure methods are currently preferred for ostium secundum atrial septal defects (ASDs); the indications for occlusion are right ventricular volume overload by echocardiogram. Ostium primum, sinus venosus and coronary sinus ASDs require surgical closure. For all ASDs elective closure around age 4 to 5 y is recommended or as and when detected beyond that age. For the more common perimembraneous ventricular septal defects (VSDs) of large size, surgical closure should be performed prior to 6 to 12 mo of age. Muscular VSDs may be closed with devices. Patent ductus arteriosus (PDA) may be closed with Amplatzer Duct Occluder if they are moderate to large and Gianturco coils if they are small. Surgical and video-thoracoscopic closure are the available options at some centers. In the presence of pulmonary hypertension appropriate testing to determine suitability for closure should be undertaken. The treatment of acyanotic CHD with currently available medical, transcatheter and surgical methods is feasible, safe and effective and should be performed at an appropriate age in order to prevent damage to cardiovascular structures.
本文的目的是讨论如何以及何时治疗最常见的非发绀型先天性心脏病(CHD);发绀型心脏病的讨论将在后续的社论中呈现。总的来说,介入的适应证和时机取决于病变的严重程度。球囊肺动脉瓣成形术是瓣叶型肺动脉瓣狭窄的治疗选择,介入的适应证是肺动脉瓣跨瓣收缩期压力阶差>50mmHg。对于主动脉瓣狭窄,球囊主动脉瓣成形术似乎是首选的治疗方法;主动脉瓣球囊扩张的适应证是主动脉瓣跨瓣收缩期压力阶差>70mmHg,无论症状如何,或压力阶差>50mmHg,同时伴有症状或心电图 ST-T 波改变提示心肌灌注异常。主动脉缩窄的介入适应证是严重高血压和/或充血性心力衰竭,以及缩窄处压力阶差>20mmHg;介入的类型取决于就诊时的年龄和缩窄的解剖结构:新生儿和婴儿采用手术干预,儿童采用球囊血管成形术治疗单纯性缩窄,青少年和成年人采用支架。长段缩窄或伴有峡部或升主动脉横弓发育不良的缩窄需要在年幼的儿童中进行手术治疗,而在青少年和成年人中则需要支架。对于主动脉缩窄术后再狭窄,儿童采用球囊血管成形术,青少年和成年人采用支架治疗。目前,经导管封堵方法是治疗继发孔房间隔缺损(ASD)的首选方法;封堵的适应证是超声心动图显示右心室容量超负荷。原发孔、窦房结和冠状窦 ASD 需要手术闭合。对于所有 ASD,建议在 4 至 5 岁左右进行择期封堵,或在该年龄后发现时进行封堵。对于较大的膜周室间隔缺损(VSD),应在 6 至 12 个月之前进行手术闭合。肌部 VSD 可使用器械闭合。中等至大型动脉导管未闭(PDA)可使用 Amplatzer 导管封堵器,小型 PDA 可使用 Gianturco 线圈。一些中心有外科和胸腔镜下闭合的选择。在存在肺动脉高压的情况下,应进行适当的检查以确定是否适合封堵。目前可用的医学、经导管和手术方法治疗非发绀型 CHD 是可行的、安全的和有效的,并且应在适当的年龄进行,以防止心血管结构受损。