Literature DB >> 9119809

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

M Nakazawa1, I Park, M Yamada, T Nakanishi, K Momma, S Hoshino, Y Takanashi, Y Imai.   

Abstract

We reviewed the clinical records of 185 patients who were possible candidates for Fontan operation. We did this to clarify whether all patients with suitable anomalies ultimately underwent a Fontan operation. Of the 152 patients with decreased pulmonary blood flow, 38 (26%) did not fulfill the criteria for Fontan operation, and 17 of the 33 patients (52%) with increased pulmonary blood flow (P < 0.01) were excluded as candidates. Of 48 non-candidate survivors, 19 had high pulmonary artery (PA) pressure or resistance and small PA (which we term "poor PA"), 17 had pulmonary hypertension, 6 had a markedly distorted PA, and 6 had severe ventricular dysfunction. A significant proportion of possible candidates with a suitable anomaly ultimately did not undergo a Fontan operation, because of "poor PA", a congenital condition that precluded Fontan operation.

Entities:  

Mesh:

Year:  1996        PMID: 9119809     DOI: 10.1007/bf02559992

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  28 in total

Review 1.  Ventricular performance in congenital heart disease.

Authors:  T P Graham
Journal:  Circulation       Date:  1991-12       Impact factor: 29.690

2.  Surgical experience with the modified Fontan procedure.

Authors:  J G Coles; S Kielmanowicz; R M Freedom; L N Benson; F Moes; P M Olley; M Rabinovitch; H Rosenberg; H Sherret; R D Rowe
Journal:  Circulation       Date:  1987-09       Impact factor: 29.690

3.  Asynchronous volume changes of the two ventricles after Fontan operation in patients with a biventricular heart.

Authors:  H Yamamura; M Nakazawa; I Park; T Nakanishi; K Momma; Y Imai
Journal:  Heart Vessels       Date:  1994       Impact factor: 2.037

4.  Lung biopsy with frozen section as a diagnostic aid in patients with congenital heart defects.

Authors:  M Rabinovitch; A R Castaneda; L Reid
Journal:  Am J Cardiol       Date:  1981-01       Impact factor: 2.778

5.  Total cavopulmonary connection: a logical alternative to atriopulmonary connection for complex Fontan operations. Experimental studies and early clinical experience.

Authors:  M R de Leval; P Kilner; M Gewillig; C Bull
Journal:  J Thorac Cardiovasc Surg       Date:  1988-11       Impact factor: 5.209

6.  Pulmonary vascular disease in transposition of the great vessels and intact ventricular septum.

Authors:  E A Newfeld; M H Paul; A J Muster; F S Idriss
Journal:  Circulation       Date:  1979-03       Impact factor: 29.690

7.  The modified Fontan operation for children less than 4 years old.

Authors:  D A Bartmus; D J Driscoll; K P Offord; R A Humes; D D Mair; H V Schaff; F J Puga; G K Danielson
Journal:  J Am Coll Cardiol       Date:  1990-02       Impact factor: 24.094

8.  A new method for the quantitative standardization of cross-sectional areas of the pulmonary arteries in congenital heart diseases with decreased pulmonary blood flow.

Authors:  S Nakata; Y Imai; Y Takanashi; H Kurosawa; K Tezuka; M Nakazawa; M Ando; A Takao
Journal:  J Thorac Cardiovasc Surg       Date:  1984-10       Impact factor: 5.209

9.  Pulmonary vascular disease after systemic-pulmonary arterial shunt operations.

Authors:  E A Newfeld; D Waldman; M H paul; A J Muster; R B Cole; F Idriss; W Riker
Journal:  Am J Cardiol       Date:  1977-05-04       Impact factor: 2.778

10.  The Fontan operation. Ventricular hypertrophy, age, and date of operation as risk factors.

Authors:  J K Kirklin; E H Blackstone; J W Kirklin; A D Pacifico; L M Bargeron
Journal:  J Thorac Cardiovasc Surg       Date:  1986-12       Impact factor: 5.209

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.