Literature DB >> 2441896

Childhood systemic-pulmonary shunts: subsequent suitability for Fontan operation.

M Mietus-Snyder, P Lang, J E Mayer, R A Jones, A R Castaneda, J E Lock.   

Abstract

We investigated whether or not a systemic arteriopulmonary shunt (SAPS) after 1 year of age affects a child's chances for a successful Fontan procedure. From 1967 to 1986, 50 patients more than 1 year old with tricuspid atresia or other complex lesions amenable to a Fontan operation received a SAPS. Follow-up was incomplete in six patients. Two patients died within 1 week of surgery, and two died within 9 months for a total mortality of 8%. Each of the 40 remaining patients was catheterized 6 months to 10.8 years (mean 4.9 years) after placement of a SAPS. By the criteria of Choussat and Fontan, there were one or more adverse SAPS-induced changes in nine patients (23%). Three developed pulmonary hypertension, one with associated elevation of pulmonary arteriolar resistance and pulmonary artery distortion, and one in conjunction with severe congestive heart failure. Six additional patients developed isolated distortion of the ipsilateral pulmonary artery. Of these nine patients, three had successful Fontan operations (33%), two died after the Fontan operation, and four are no longer candidates. In contrast, of 31 patients without documented SAPS-induced complications, 27 have undergone Fontan operations, 23 successfully (74%). Palliation with a SAPS after 1 year of age can place children at increased risk for a subsequent Fontan operation.

Entities:  

Mesh:

Year:  1987        PMID: 2441896

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  3 in total

1.  When should pulmonary artery angioplasty be performed for Fontan candidates with pulmonary coarctation? Two cases of pulmonary artery angioplasty with the Blalock-Taussig shunt on pump in neonates.

Authors:  Nobuyuki Ishibashi; Masaaki Koide; Shunji Uchita; Masashi Seguchi
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2004-04

2.  A congenitally "poor" pulmonary artery is a major reason for exclusion from Fontan operation.

Authors:  M Nakazawa; I Park; M Yamada; T Nakanishi; K Momma; S Hoshino; Y Takanashi; Y Imai
Journal:  Heart Vessels       Date:  1996       Impact factor: 2.037

3.  Transcatheter closure of ventriculopulmonary artery communications in staged Fontan procedures.

Authors:  Tarak Desai; John Wright; Rami Dhillon; Oliver Stumper
Journal:  Heart       Date:  2006-12-12       Impact factor: 5.994

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.