Thrombolysis with recombinant tissue plasminogen activator (rt-PA) in 13 children

Citation
E. Schermer et al., Thrombolysis with recombinant tissue plasminogen activator (rt-PA) in 13 children, WIEN KLIN W, 112(21), 2000, pp. 927-933
Citations number
30
Categorie Soggetti
General & Internal Medicine
Journal title
WIENER KLINISCHE WOCHENSCHRIFT
ISSN journal
00435325 → ACNP
Volume
112
Issue
21
Year of publication
2000
Pages
927 - 933
Database
ISI
SICI code
0043-5325(20001110)112:21<927:TWRTPA>2.0.ZU;2-E
Abstract
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.