Heart 1998;79:576-581 ( June )
Fetal tachycardias: management and outcome of 127 consecutive cases
Department of
Fetal Cardiology, 15th Floor, Guy's Hospital, London SE1 9RT, UK
Correspondence to: Dr Simpson.
Accepted for publication 3 February 1998
Objective
To review the management and outcome of
fetal tachycardia, and to determine the problems encountered with
various treatment protocols.
Study design
Retrospective analysis.
Subjects
127 consecutive fetuses with a
tachycardia presenting between 1980 and 1996 to a single tertiary
centre for fetal cardiology. The median gestational age at presentation
was 32 weeks (range 18 to 42).
Results
105 fetuses had a supraventricular
tachycardia and 22 had atrial flutter. Overall, 52 fetuses were
hydropic and 75 non-hydropic. Prenatal control of the tachycardia was
achieved in 83% of treated non-hydropic fetuses compared with 66% of
the treated hydropic fetuses. Digoxin monotherapy converted most (62%)
of the treated non-hydropic fetuses, and 96% survived through the
neonatal period. First line drug treatment for hydropic fetuses was
more diverse, including digoxin (n = 5), digoxin plus verapamil
(n = 14), and flecainide (n = 27). The response rates to these
drugs were 20%, 57%, and 59%, respectively, confirming that digoxin
monotherapy is a poor choice for the hydropic fetus. Response to
flecainide was faster than to the other drugs. Direct fetal treatment
was used in four fetuses, of whom two survived. Overall, 73%
(n = 38) of the hydropic fetuses survived. Postnatally, 4% of the
non-hydropic group had ECG evidence of pre-excitation, compared with
16% of the hydropic group; 57% of non-hydropic fetuses were treated
with long term antiarrhythmics compared with 79% of hydropic fetuses.
Conclusions
Non-hydropic fetuses with
tachycardias have a very good prognosis with transplacental treatment.
Most arrhythmias associated with fetal hydrops can be controlled with
transplacental treatment, but the mortality in this group is 27%. At
present, there is no ideal treatment protocol for these fetuses and a
large prospective multicentre trial is required to optimise treatment
of both hydropic and non-hydropic fetuses.
© 1998 by Heart
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