Janatuinen M J, Vänttinen E A, Saraste M K, Ingberg M V
Department of Surgery, University Central Hospital, Turku, Finland.
Scand J Thorac Cardiovasc Surg. 1989;23(3):219-24. doi: 10.3109/14017438909105998.
The surgical management of congenital aortic stenosis in 33 patients (age 2-20, mean 11 years) is described. The stenosis was valvular in 19 cases, subvalvular in eight and supravalvular in six. The primary procedures in valvular stenosis were valvotomy (12 cases), valve replacement (6) and exploration (1). Subvalvular stenosis was treated with resection of muscle (4), membrane (2) or both (2), and all six supravalvular lesions with patch aortoplasty. One death occurred during primary operation. Follow-up averaged 11.5 years. Of the 12 valvotomized patients, five required valve replacement after on average 10.6 years because of restenosis. Aortic regurgitation developed in six of the seven surviving patients treated for subvalvular stenosis, requiring reoperation in four. No mortality was associated with reoperation. All patients without valve replacement were reinvestigated. Of the seven with valvotomy, four had restenosis and three valves were in good condition. In supravalvular stenosis the gradients were low. Valvotomy and subvalvular resection can give effective palliation of aortic stenosis until the patient is old enough for definitive repair.
本文描述了33例(年龄2 - 20岁,平均11岁)先天性主动脉狭窄患者的手术治疗情况。其中瓣膜性狭窄19例,瓣下狭窄8例,瓣上狭窄6例。瓣膜性狭窄的主要手术方式为瓣膜切开术(12例)、瓣膜置换术(6例)和探查术(1例)。瓣下狭窄采用肌肉切除术(4例)、隔膜切除术(2例)或两者均切除(2例)进行治疗,所有6例瓣上病变均采用补片主动脉成形术。1例患者在初次手术期间死亡。随访平均11.5年。在12例行瓣膜切开术的患者中,5例因再狭窄平均在10.6年后需要进行瓣膜置换。在接受瓣下狭窄治疗的7例存活患者中,6例出现主动脉反流,其中4例需要再次手术。再次手术无死亡病例。所有未进行瓣膜置换的患者均再次接受检查。在7例行瓣膜切开术的患者中,4例出现再狭窄,3例瓣膜状况良好。在瓣上狭窄患者中,压力阶差较低。瓣膜切开术和瓣下切除术可有效缓解主动脉狭窄,直至患者年龄足够大能够进行确定性修复。