Literature DB >> 8678634

Partial atrioventricular canal with congestive heart failure in the first year of life: surgical options.

A Giamberti1, B Marino, D di Carlo, F S Iorio, R Formigari, A de Zorzi, C Marcelletti.   

Abstract

BACKGROUND: An important subgroup of patients with partial atrioventricular canal require an operation in the first year of life because of refractory congestive heart failure.
METHODS: From June 1982 to April 1995, of 128 patients with partial atrioventricular canal, 35 patients (27%) underwent surgical treatment at less than 1 year of life. Associated cardiac anomalies were present in 22 patients. Only 7 patients (20%) had Down's syndrome. Five patients with left ventricular hypoplasia underwent aortic coarctectomy (3 patients) or Norwood operation (2 patients). The other 30 patients underwent anatomic repair in 24 cases and aortic coarctectomy in 6. The surgical results of patients submitted for anatomic repair were retrospectively correlated with the echocardiographic mitral valve diameter.
RESULTS: There were 7 deaths (29%) after anatomic repair, 2 (22%) after aortic coarctectomy, and 2 (100%) after Norwood operation. Infants with a mitral valve diameter less than 2.5 x 10-2 m/m2 died at repair. In a mean follow-up of 73.5 months there were five secondary mitral valve plasties and three repairs after aortic coarctectomy.
CONCLUSIONS: Among patients with partial atrioventricular canal, there is an important subgroup with clinical signs of heart failure in the first year of life. Left-sided obstructive lesions and complex mitral valve anomalies seem to play a fundamental role in the clinical evolution and prognosis of these patients. The echocardiographic mitral valve diameter may be useful for determining the correct surgical indication.

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Year:  1996        PMID: 8678634     DOI: 10.1016/0003-4975(96)00262-7

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  5 in total

1.  Atrioventricular Canal Defects.

Authors:  D J Murphy
Journal:  Curr Treat Options Cardiovasc Med       Date:  1999-12

2.  Early and late results of total correction of congenital cardiac anomalies in infancy.

Authors:  M Masuda; H Kado; N Kajihara; T Onzuka; K Kurisu; S Morita; Y Shiokawa; Y Imoto; R Tominaga; H Yasui
Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2001-08

3.  Aortic arch obstruction neonates with biventricular physiology: left-open compared to closed inter-atrial communication during primary repair--a retrospective study.

Authors:  André Rüffer; Caroline Bechtold; Ariawan Purbojo; Okan Toka; Martin Glöckler; Sven Dittrich; Robert Anton Cesnjevar
Journal:  J Cardiothorac Surg       Date:  2015-04-17       Impact factor: 1.637

Review 4.  Genetics of atrioventricular canal defects.

Authors:  Flaminia Pugnaloni; Maria Cristina Digilio; Carolina Putotto; Enrica De Luca; Bruno Marino; Paolo Versacci
Journal:  Ital J Pediatr       Date:  2020-05-13       Impact factor: 2.638

5.  Challenges in the Surgical Treatment of Atrioventricular Septal Defect in Children With and Without Down Syndrome in Romania-A Developing Country.

Authors:  Ioana-Cristina Olariu; Anca Popoiu; Andrada-Mara Ardelean; Raluca Isac; Ruxandra Maria Steflea; Tudor Olariu; Adela Chirita-Emandi; Ramona Stroescu; Mihai Gafencu; Gabriela Doros
Journal:  Front Pediatr       Date:  2021-07-07       Impact factor: 3.418

  5 in total

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