Division of Cardiothoracic Surgery, University of Minnesota, Minneapolis, MN 55455, USA.
J Thorac Cardiovasc Surg. 2012 Apr;143(4 Suppl):S29-32. doi: 10.1016/j.jtcvs.2011.10.031. Epub 2011 Dec 6.
Congenital mitral and tricuspid valve abnormalities in unbalanced atrioventricular canal defects are complex. We designed procedures to both repair and induce growth of hypoplastic atrioventricular valves and ventricles to achieve 2-ventricle repairs. Midterm data were assessed for reliability of catch-up growth, resulting quality of atrioventricular valves, and adequacy of 2-ventricle repairs.
The 24 consecutive infants (14 female and 10 male) with unbalanced atrioventricular canal defects had significant hypoplasia of 1 atrioventricular valve and/or ventricle (an echocardiography-derived z value of ≤-3.0 standard errors of the mean below expected). Operative approaches included the following: (1) Staged repair was performed, with complete valve repair, partial closure of the atrial septal, and ventricular septal defects, and (usually) pulmonary artery banding. After adequate growth, repair was completed. A vestigial mitral valve (4-7 mm) in 3 patients led to partitioning the large tricuspid valve, creating a second mitral valve. (2) Repair with a shift in atrioventricular valve partitioning was performed to increase hypoplastic atrioventricular valve size. (3) Repair with snared atrial septal defects and ventricular septal defect was performed to allow intracardiac shunting. The hypoplastic atrioventricular valves and hypoplastic ventricles were reassessed on local follow-up (5-15 years).
The initial z scores were -2.8 to -7.4 for hypoplastic atrioventricular valves and -1.0 to -7.5 for hypoplastic ventricles. Follow-up z scores were -0.6 to -2.7 for hypoplastic atrioventricular valves and -2.0 to +1.8 for hypoplastic ventricles. Another 11 patients were also judged to be within normal limits. Three reoperations were for mitral valve regurgitation, and 1 reoperation was for mitral valve replacement. One patient died of central nervous system bleed just before extracorporeal membrane oxygenation weaning, and 2 patients died of late potassium overdose, for an 88% survival. Survivors are well with 2-ventricle repairs, and 15 of 19 patients are not taking cardiac medications.
Increasing atrioventricular valve flow reliably induced growth. Valve repair and growth achieved a 2-ventricle repair in all patients.
不平衡房室管缺损中的先天性二尖瓣和三尖瓣异常较为复杂。我们设计了既能修复又能诱导发育不良房室瓣和心室生长的手术方法,以实现双心室修复。评估中期数据以确定追赶生长的可靠性、房室瓣的质量和双心室修复的充分性。
24 例连续的不平衡房室管缺陷婴儿(女 14 例,男 10 例)存在 1 个房室瓣和/或心室发育不良(超声心动图衍生的 z 值≤-3.0 个均值标准差以下预期值)。手术方法包括:(1)分期修复,包括完全瓣膜修复、部分房间隔缺损和室间隔缺损,以及(通常)肺动脉带。在充分生长后完成修复。3 例患者存在残余的二尖瓣(4-7mm),导致大型三尖瓣分隔,形成第二个二尖瓣。(2)通过房室瓣分隔移位进行修复,以增大发育不良的房室瓣大小。(3)通过圈套房缺和室缺进行修复,以允许心内分流。在局部随访(5-15 年)中再次评估发育不良的房室瓣和发育不良的心室。
初始 z 值为发育不良的房室瓣为-2.8 至-7.4,发育不良的心室为-1.0 至-7.5。随访时的 z 值为发育不良的房室瓣为-0.6 至-2.7,发育不良的心室为-2.0 至+1.8。另外 11 例也被认为在正常范围内。3 例患者因二尖瓣反流行再次手术,1 例患者因二尖瓣置换行再次手术。1 例患者在体外膜氧合脱机前因中枢神经系统出血死亡,2 例患者因晚期钾过量死亡,存活率为 88%。存活者均行双心室修复,19 例中有 15 例未服用心脏药物。
增加房室瓣流量可可靠地诱导生长。瓣膜修复和生长使所有患者均实现双心室修复。