Why the study?
Does a consecutive high dose bolus and infusion of alteplase improve thrombolysis in a patient with acute massive pulmonary embolism?
Does a consecutive high dose bolus and infusion of alteplase improve thrombolysis in a patient with acute massive pulmonary embolism?
A novel alteplase regimen combining a 50 mg bolus and 50 mg infusion successfully treated massive acute pulmonary embolism without bleeding complications in a high-risk patient.
Single-case success with alteplase bolus-infusion in massive PE without bleeding; hypothesis-generating and leaves open efficacy versus standard regimens.
We describe the successful use of a novel dosage regimen of alteplase in a 77-year-old man with massive acute pulmonary embolism in the presence of a relative contraindication (recent cranial surgery). An intravenous alteplase bolus of 50 mg was administered, followed 40 min later by a 50 mg infusion over 2 h. Pulmonary arteriography showed a considerable increase in intraluminal filling of thrombotically occluded vessels as a result of alteplase administration, and was accompanied by marked clinical improvement. Peak alteplase plasma concentration after the bolus was 5.5 micrograms/ml, and the steady state concentration during infusion was 0.52 micrograms/ml. Detailed monitoring of haemostasis parameters showed elevated endogenous fibrinolytic activity at baseline, very high levels of fibrin degradation products during treatment resulting from lysis of an extensive thrombus mass, moderate fibrinogenolysis compared to fibrinolysis, long plasma half-lives of fibrin(ogen) degradation products (9.2-11.0 h), and increased thrombin generation. There were no bleeding side-effects. The regimen combines the advantages of rapid onset (bolus) and maintained potency (infusion) of thrombolytic effect in pulmonary embolism.
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Tebbe et al. (1992) studied this question.
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