Since thromboembolic events (TE) are rare among children there is only limi
ted information on the optimal choice of antithrombotic agents, dose and du
ration of antithrombotic therapy. Recombinant tissue plasminogen activator
(rt-PA) is increasingly used for thrombolytic therapy of organ- and limb th
reatening thrombosis in children. We investigated retrospectively the effic
acy and safety of rt-PA in 13 children treated consecutively between 1996-1
999, following the same protocol. The median age was 3.9 years (3 days to 1
6 years). All children suffered from underlying diseases. In addition, 7 ch
ildren had cardiac catheters and central venous catheters and two children
suffered from Factor V Leiden mutation. Seven children presented with a TE
in the arterial system, 6 with one in the venous system. All children were
treated with continuous infusion of rt-PA (median dose 0.05; 0.0125-0.2 mg/
kg/h) together with low-dose standard heparin (median dose 8; 5-15 IU/kg/h)
. Thrombolysis was performed for a median time period of 102 hours (6 hours
to 16 days). Treatment effects on the thrombus were regularly confirmed by
ultrasound. Plasma levels of fibrinogen and haemoglobin decreased moderate
ly during treatment. No cumulative effect or increased dose requirement of
rt-PA was detected during extended treatment. Patency of obstructed vessels
was achieved in all children. One child developed severe gastrointestinal
bleeding. Six children (46%) developed minor bleeding at the site of cathet
er puncture. One child developed rethrombosis at the site of the previous t
hrombus 2 weeks after completion of rt-PA treatment. Under rigorous laborat
ory and ultrasound control, our protocol using low dose rt-PA over a prolon
ged period of time was effective and safe.