Lacour-Gayet F, Serraf A, Fermont L, Bruniaux J, Rey C, Touchot A, Petit J, Planché C
Pediatric Cardiac Surgery Department, Marie Lannelongue Hospital, Paris Sud Université, France.
J Thorac Cardiovasc Surg. 1992 Nov;104(5):1238-45.
The optimal Fontan-type operation greatly depends on appropriate initial palliation. Several surgical techniques have been used in infancy to palliate patients with univentricular hearts, ventriculoarterial discordance, and subaortic stenosis. The two most common are pulmonary artery banding and Damus-Norwood procedures. Palliative arterial switch operation is another surgical option that was used in this early series of seven infants. The principle of this operation is to "switch" the subaortic obstruction into a subpulmonary obstruction; the coronary artery relocation on the large pulmonary trunk creates a harmonious aortic root and the connection of the rudimentary ventricular chamber to the pulmonary artery trunk creates a natural protection of the pulmonary vascular bed through the restrictive bulboventricular foramen. Seven infants with univentricular hearts, ventriculoarterial discordance, and subaortic stenosis underwent a palliative arterial switch operation. All infants had an associated aortic arch obstruction of various degrees, including one with interrupted aortic arch, five with coarctation with severe arch hypoplasia, and one with isolated arch hypoplasia. There were three with double-inlet left ventricle, three with tricuspid atresia, and one with transposition of the great arteries with ventricular septal defect and severe right ventricular hypoplasia. The subaortic obstruction was patent at birth in five patients who underwent a palliative switch operation in the first 2 months of life, and rapidly occurred following a previous neonatal pulmonary artery banding associated with arch repair in two patients who underwent a switch operation at 5 and 8 months of age, respectively. The operation includes aortic arch repair without prosthetic material, an atrial septectomy, and the arterial switch. An associated pulmonary shunt was required in five patients and a pulmonary artery banding in one. There was one early death in a patient with [S,L,L] anatomy and congenital atrioventricular block, leading to an early mortality of 14% (95% confidence limits: 1% to 28%). There was one late death. Four survivors are waiting for a Fontan-type procedure, and one survivor had satisfactory right ventricular growth. Early palliative arterial switch operation offers several advantages: reconstruction of a harmonious aortic root, natural protection of the pulmonary bed through the restrictive bulboventricular foramen, prevention of deleterious myocardial hypertrophy, and arch reconstruction without the introduction of a foreign material. This aggressive technique may provide a satisfactory palliation in infants with univentricular hearts and ventriculoarterial discordance, when the bulboventricular foramen/aortic anulus ratio is less than 0.8 or when the subaortic stenosis is severe enough to be associated with an arch obstruction.(ABSTRACT TRUNCATED AT 400 WORDS)
最佳的Fontan类手术很大程度上取决于恰当的初始姑息治疗。婴儿期已采用多种手术技术来姑息治疗单心室心脏、心室动脉不协调及主动脉瓣下狭窄的患者。最常用的两种是肺动脉环扎术和达穆斯 - 诺伍德手术。姑息性动脉调转术是本系列7例婴儿早期采用的另一种手术选择。该手术的原则是将主动脉瓣下梗阻“转换”为肺动脉瓣下梗阻;在大的肺动脉干上重新定位冠状动脉可形成和谐的主动脉根部,而将未发育完全的心室腔与肺动脉干相连可通过限制性球室孔对肺血管床起到自然保护作用。7例患有单心室心脏、心室动脉不协调及主动脉瓣下狭窄的婴儿接受了姑息性动脉调转术。所有婴儿均伴有不同程度的主动脉弓梗阻,其中1例为主动脉弓中断,5例为伴有严重弓发育不全的缩窄,1例为孤立性弓发育不全。有3例为双入口左心室,3例为三尖瓣闭锁,1例为大动脉转位合并室间隔缺损及严重右心室发育不全。5例在出生时主动脉瓣下梗阻开放的患者在出生后2个月内接受了姑息性调转术,另外2例分别在5个月和8个月大时接受调转术的患者,在先前新生儿期肺动脉环扎术联合主动脉弓修复术后迅速出现主动脉瓣下梗阻。手术包括无人工材料的主动脉弓修复、房间隔切除术及动脉调转术。5例患者需要联合肺分流术,1例需要肺动脉环扎术。1例具有[S,L,L]解剖结构及先天性房室传导阻滞的患者早期死亡,早期死亡率为14%(95%可信区间:1%至28%)。有1例晚期死亡。4例幸存者正在等待Fontan类手术,1例幸存者右心室生长情况良好。早期姑息性动脉调转术具有多种优势:重建和谐的主动脉根部,通过限制性球室孔对肺床起到自然保护作用,预防有害的心肌肥厚,以及无需引入外来材料进行主动脉弓重建。当球室孔/主动脉瓣环比值小于0.8或主动脉瓣下狭窄严重到与主动脉弓梗阻相关时,这种积极的技术可能为患有单心室心脏和心室动脉不协调的婴儿提供满意的姑息治疗。(摘要截选至400字)