Cohen M I, Bush D M, Ferry R J, Spray T L, Moshang T, Wernovsky G, Vetter V L
Division of Cardiology, The Children' Hospital of Philadelphia and The University of Pennsylvania School of Medicine, 19104, USA.
Cardiol Young. 2000 Sep;10(5):447-57. doi: 10.1017/s1047951100008118.
Our study was designed to characterize the patterns of growth, in the medium term, of children with functionally univentricular hearts managed with a hemi-Fontan procedure in infancy, followed by a modified Fontan operation in early childhood. Failure of growth is common in patients with congenital cardiac malformations, and may be related to congestive heart failure and hypoxia. Repair of simple lesions appears to reverse the retardation in growth. Palliation of the functionally single ventricular physiology with a staged Fontan operation reduces the adverse effects of hypoxemia and prolonged ventricular volume overload. The impact of this approach on somatic growth is unknown. Retrospectively, we reviewed the parameters of growth of all children with functionally univentricular hearts followed primarily at our institution who had completed a staged construction of the Fontan circulation between January 1990 and December 1995. Measurements were available on all children prior to surgery, and annually for three years following the Fontan operation. Data was obtained on siblings and parents for comparative purposes. The criterions of eligibility for inclusion were satisfied by 65 patients. The mean Z score for weight was -1.5 +/- 1.2 at the time of the hemi-Fontan operation. Weight improved by the time of completion of the Fontan circulation (-0.91 +/- 0.99), and for the first two years following the Fontan operation, but never normalized. The mean Z scores for height at the hemi-Fontan and Fontan operations were -0.67 +/- 1.1 and -0.89 +/- 1.2 respectively. At most recent follow-up, with a mean age of 6.1 +/- 1.3 years, and a mean time from the Fontan operation of 4.4 +/- 1.4 years, the mean Z score for height was -1.15 +/- 1.2, and was significantly less than comparable Z scores for parents and siblings. In our experience, children with functionally univentricular hearts who have been palliated with a Fontan operation are significantly underweight and shorter than the general population and their siblings.
我们的研究旨在描述婴儿期接受半Fontan手术、幼儿期接受改良Fontan手术治疗的功能性单心室患儿的中期生长模式。先天性心脏畸形患者生长发育不良很常见,可能与充血性心力衰竭和缺氧有关。简单病变的修复似乎可以逆转生长发育迟缓。分期Fontan手术姑息治疗功能性单心室生理状态可减少低氧血症和长期心室容量超负荷的不良影响。这种方法对身体生长的影响尚不清楚。我们回顾性分析了1990年1月至1995年12月在我们机构接受主要随访、完成分期Fontan循环构建的所有功能性单心室患儿的生长参数。所有患儿术前均有测量数据,Fontan手术后每年测量一次,持续三年。为了进行比较,还获取了患儿兄弟姐妹和父母的数据。65例患者符合纳入标准。半Fontan手术时体重的平均Z值为-1.5±1.2。Fontan循环完成时体重有所改善(-0.91±0.99),Fontan手术后的前两年体重也有所改善,但从未恢复正常。半Fontan手术和Fontan手术时身高的平均Z值分别为-0.67±1.1和-0.89±1.2。在最近一次随访中,平均年龄为6.1±1.3岁,距Fontan手术的平均时间为4.4±1.4年,身高的平均Z值为-1.15±1.2,显著低于其父母和兄弟姐妹的可比Z值。根据我们的经验,接受Fontan手术姑息治疗的功能性单心室患儿明显体重过轻,身高低于一般人群及其兄弟姐妹。