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The Journal of Thoracic and Cardiovascular Surgery, Vol 98, 214-216, Copyright © 1989 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
IM Mitchell, DW Goh and LD Abrams
Since 1984 five patients who had previously had cavopulmonary shunts for
cyanotic congenital heart disease have returned to the Birmingham
Childrens' Hospital with increasing breathlessness and cyanosis. Two had
had a classic Glenn (unidirectional) cavopulmonary shunt and three, a
bidirectional shunt; all shunts had been performed 5 to 18 years earlier.
Each patient was reinvestigated and underwent creation of a brachial
artery-basilic vein fistula. This procedure is known to have good patency
rates when used in other situations (for example, for hemodialysis), but it
has not been previously described for use in this context. Of the five
patients, four had a considerable and sustained symptomatic improvement on
follow-up of 12 to 49 months (mean 31 months), but the condition of one
continued to deteriorate; that child has subsequently undergone a Fontan
procedure, also with no improvement. Only one patient complained of
coldness of the arm, and there were no other complications. We believe a
brachial artery-basilic vein fistula has considerable advantages in terms
of ease of operation and postoperative complications when compared with an
axillary arteriovenous fistula, used as a supplement to an inadequate
cavopulmonary shunt.
ARTICLES
Creation of brachial artery-basilic vein fistula. A supplement to the cavopulmonary shunt
Department of Cardiothoracic Surgery, Birmingham Childrens' Hospital, Ladywood, Birmingham, England.
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