Heart 1998;80:330-333 ( October )
Adenosine induced transient cardiac standstill in catheter interventional procedures for congenital heart disease
a Heart Unit, Birmingham Children's Hospital NHS Trust,
Ladywood Middleway, Birmingham B16 8ET, UK, b Department of Anaesthetics, Birmingham
Children's Hospital NHS Trust
Correspondence to: Dr De Giovanni.
Accepted for publication 18 June 1998
Objective
To describe the use of intravenous
adenosine to create transient cardiac standstill during balloon
dilatation procedures for congenital heart defects.
Setting
A tertiary paediatric cardiac centre.
Design and patients
This was a prospective pilot
study. Thirteen patients born with congenital heart disease and who had
stenotic lesions requiring relief were considered for the technique.
All were suitable for balloon dilatation. Their ages ranged from 2 months to 30 years, mean (SD) 9.9 (9.8) years. The dose of adenosine
varied from 0.125 mg/kg to 0.555 mg/kg, mean 0.33 (0.127).
Results
Two patients only developed sinus
bradycardia in response to adenosine, which may have been related to
the technique of administration. The other 11 experienced a period of
asystole, which ranged from 2.4 to 10.8 seconds, mean 4.99 (2.27), and
a total atrioventricular block period of 5.0 to 21.2 seconds, mean 9.47 (4.64). The interval between adenosine injection and the onset of
asystole varied from 2.4 to 15.8 seconds, mean 8.05 (3.6), depending on
cannula size, site of administration, and cardiac output. The peak
gradient across the stenotic lesions fell from 52.3 (23.7) to 17.8 (11.9) mm Hg (p < 0.001). Apart from one short episode of atrial
fibrillation there were no complications.
Conclusions
Intravenous adenosine is a safe and
effective agent for creating transient cardiac standstill during
balloon dilatation procedures for congenital heart disease. This
achieves stability which is likely to improve results and reduce
complications. It may have applications in other fields of cardiac
intervention where an immobile heart is desirable during the critical
phase of a procedure.
© 1998 by Heart
This article has been cited by other articles:
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