DeGroff C G
University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, 3705 Fifth Avenue, Pittsburgh, PA 15213, USA.
Pediatr Cardiol. 2008 Jan;29(1):3-12. doi: 10.1007/s00246-007-9104-0. Epub 2007 Oct 5.
The Fontan procedure and its subsequent modifications over the past 30 years can be described as a class of surgical procedures for patients born with complex congenital heart disease exhibiting a single-ventricle physiology. The long-term outcome for children currently undergoing a Fontan procedure remains worrisome because of multiple late morbidities observed. Despite significant modeling efforts spanning three decades, improvements to the Fontan procedure have occurred without comprehensive validation from these modeling studies. Careful examination shows that modeling studies to date offer only a "glimpse through a keyhole" into understanding and modeling a representative range of the variations in anatomy and physiology that exist in Fontan patients. Suggestions for future investigations are provided.
在过去30年中,Fontan手术及其后续改良手术可被描述为针对患有表现为单心室生理的复杂先天性心脏病的患者的一类外科手术。由于观察到多种晚期并发症,目前接受Fontan手术的儿童的长期预后仍然令人担忧。尽管经过了三十年的大量建模努力,但Fontan手术的改进并未得到这些建模研究的全面验证。仔细研究表明,迄今为止的建模研究只是“透过钥匙孔瞥见”,用于理解和模拟Fontan患者中存在的解剖学和生理学变化的代表性范围。文中还提供了对未来研究的建议。