Bradley Scott M, Simsic Janet M, Atz Andrew M, Dorman B Hugh
Division of Cardiothoracic Surgery, Medical University of South Carolina, Charleston 29425, USA.
Ann Thorac Surg. 2002 Sep;74(3):805-10; discussion 810. doi: 10.1016/s0003-4975(02)03836-5.
The infant with a single ventricle and excessive pulmonary blood flow requires early protection of the pulmonary vascular bed to insure suitability for a subsequent Fontan procedure. The traditional approach, pulmonary artery banding, has had disappointing results. We have pursued an alternate strategy: division of the pulmonary artery, and placement of a systemic-to-pulmonary artery shunt. Potential sites of systemic outflow tract obstruction are simultaneously bypassed, by either a Damus-Kaye-Stansel, or modified Norwood procedure.
From January 1996 to June 2001, 22 infants were treated by this strategy. Patients with hypoplastic left heart syndrome were excluded. Median age was 18 days (range 2 days to 6 months). In addition to pulmonary artery division and shunt, 3 of 22 patients underwent a Damus-Kaye-Stansel procedure, and 13 of 22 patients underwent a modified Norwood procedure.
There were no operative deaths, and one late death. Actuarial survival beyond 30 months was 90%. At follow-up catheterization in 22 patients, median transpulmonary gradient was 7 mmHg (range 4 to 18), and median pulmonary vascular resistance 1.9 Wood units (range 0.9 to 3.3). Twenty-one patients have undergone a subsequent bidirectional superior cavopulmonary connection, and 6 a Fontan procedure, with no deaths. No patient developed subaortic stenosis, or aortic arch obstruction. Neoaortic insufficiency was none or trivial in 12 patients, mild in 3, and moderate in 1.
In patients with a functional single ventricle and excessive pulmonary flow, a strategy of pulmonary artery division and shunt, along with prophylactic bypass of systemic outflow obstruction, carries low operative and midterm mortality. It provides consistent protection of the pulmonary vascular bed, avoids subaortic stenosis and aortic arch obstruction, minimizes neoaortic insufficiency, and ensures suitability for progression along a Fontan pathway. These results provide a comparison for alternate strategies, including pulmonary artery banding.
患有单心室且肺血流量过多的婴儿需要早期保护肺血管床,以确保适合后续的Fontan手术。传统方法,即肺动脉环扎术,效果并不理想。我们采用了另一种策略:肺动脉离断,并进行体肺分流术。同时,通过Damus-Kaye-Stansel手术或改良Norwood手术绕过潜在的体循环流出道梗阻部位。
1996年1月至2001年6月,22例婴儿采用此策略进行治疗。排除左心发育不全综合征患者。中位年龄为18天(范围2天至6个月)。除肺动脉离断和分流外,22例患者中有3例接受了Damus-Kaye-Stansel手术,22例患者中有13例接受了改良Norwood手术。
无手术死亡病例,1例晚期死亡。30个月后的精算生存率为90%。22例患者随访时行心导管检查,经肺动脉平均压差为7 mmHg(范围4至18),肺血管阻力中位数为1.9 Wood单位(范围0.9至3.3)。21例患者随后接受了双向腔肺连接术,6例接受了Fontan手术,均无死亡。无一例患者发生主动脉瓣下狭窄或主动脉弓梗阻。12例患者新主动脉瓣关闭不全无或轻微,3例轻度,1例中度。
对于功能性单心室且肺血流量过多的患者,肺动脉离断和分流策略,以及预防性绕过体循环流出道梗阻,手术和中期死亡率较低。它能持续保护肺血管床,避免主动脉瓣下狭窄和主动脉弓梗阻,使新主动脉瓣关闭不全最小化,并确保适合沿着Fontan路径进展。这些结果为包括肺动脉环扎术在内的其他策略提供了比较依据。