TY - JOUR
T1 - Tissue plasminogen activator for the treatment of thromboembolism in infants and children
AU - Levy, Maurice
AU - Benson, Lee N.
AU - Burrows, Patricia E.
AU - Bentur, Yedidia
AU - Strong, Dawn K.
AU - Smith, Joanne
AU - Johnson, David
AU - Jacobson, Sheila
AU - Koren, Gideon
N1 - Funding Information:
The degradation of fibrin (fibrinolysis) is controlled by a delicate interplay among fibrin, a2-antiplasmin, plasmino- Submitted for publication April 9, 1990; accepted Oct. 5, 1990. Reprint requests: Gideon Koren, MD, Division of Clinical Pharmacology, Hospital for Sick Children, 555 University Ave., Toronto, Ontario M5G 1X8, Canada. *Dr. Koren is a Career Scientist of the Ontario Ministry of Health.
PY - 1991/3
Y1 - 1991/3
N2 - We report our experience with the use of tissue plasminogen activator to treat 12 infants and children with various thromboembolic states after conventional thrombolytic agents had failed. The dosage range was between 0.1 to 0.5 mg/kg per hour. Complete clot dissolution occurred in seven cases after 2 hours to 3 days of therapy. Partial clot dissolution and clinical improvement were noted in another four patients. Bleeding complications were noted in 6 of the 12 patients and included bruising, oozing from various venipuncture sites, and bleeding; these complications were controlled by clinically available means. In all cases with bleeding the dose rate was in the higher range (0.46 to 0.50 mg/kg per hour). In one patient, restlessness, agitation, and screaming were noted during administration of tissue plasminogen activator and when it was reinstituted. We conclude that tissue plasminogen activator is effective in inducing clot lysis in children. Because the effective dose appears to overlap with those causing bleeding, we recommend that a dose of 0.1 mg/kg per hour be started and increased gradually if clot dissolution does not occur, with close monitoring for bleeding.
AB - We report our experience with the use of tissue plasminogen activator to treat 12 infants and children with various thromboembolic states after conventional thrombolytic agents had failed. The dosage range was between 0.1 to 0.5 mg/kg per hour. Complete clot dissolution occurred in seven cases after 2 hours to 3 days of therapy. Partial clot dissolution and clinical improvement were noted in another four patients. Bleeding complications were noted in 6 of the 12 patients and included bruising, oozing from various venipuncture sites, and bleeding; these complications were controlled by clinically available means. In all cases with bleeding the dose rate was in the higher range (0.46 to 0.50 mg/kg per hour). In one patient, restlessness, agitation, and screaming were noted during administration of tissue plasminogen activator and when it was reinstituted. We conclude that tissue plasminogen activator is effective in inducing clot lysis in children. Because the effective dose appears to overlap with those causing bleeding, we recommend that a dose of 0.1 mg/kg per hour be started and increased gradually if clot dissolution does not occur, with close monitoring for bleeding.
UR - http://www.scopus.com/inward/record.url?scp=0025969005&partnerID=8YFLogxK
U2 - 10.1016/S0022-3476(05)82170-5
DO - 10.1016/S0022-3476(05)82170-5
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C2 - 1900334
AN - SCOPUS:0025969005
SN - 0022-3476
VL - 118
SP - 467
EP - 472
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 3
ER -