Efficacy and safety of low-dose streptokinase plus desmopressin in acute myocardial infarction: A pilot study |
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Authors: | Dr. Raul Altman Enrique Gurfinkel Alejandra Scazziota Jorge Rouvier Luis de la Fuente Branco Mautner |
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Affiliation: | (1) Centro de Estudios Medicos y Bioquimicos, Viamonte 2008, 1056 Buenos Aires, Argentina;(2) Coronary Care Unit, Division of Cardiology, Hospital Fernandez, Argentina;(3) Hemodinamic Laboratory, Sanatorio Guemes, Buenos Aires, Argentina |
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Abstract: | In this pilot study the combined use of desmopressin, which releases tissue plasminogen activator from vascular endothelium, and a low dose of streptokinase as a new thrombolytic regimen for acute myocardial infarction is proposed. Eighteen patients with acute myocardial infarction were treated intravenously with 150,000 U (4 patients) or 250,000 U (14 patients) of streptokinase infused over 10 minutes, followed by 24 g of desmopressin infused over 5–10 minutes. Aspirin and beta-blockers were administered at admission, and heparin and oral anticoagulants were started at the end of the thrombolytic regimen. Hemostatic parameters were studied before and 30, 60, 120, and 240 minutes after starting thrombolytic therapy. Fifteen patients (83.3%) had evidence of clinical reperfusion. Angiography was performed with a mean delay of 8.8 hours (range 1.5–22 hours) from the start of thrombolytic therapy. Fourteen patients (77.8%) had patency of the infarct-related artery: 10 patients (55.6%) achieved TIMI grade 3, and 4 patients (22%) achieved TIMI grade 2. Two patients (one TIMI grade 1 and one TIMI grade 2) underwent coronary angioplasty. No patient died during the in-hospital period. At 18 months follow-up, all patients are alive. No major or minor bleeding was detected. The significant decline in plasma fibrinogen and in the euglobulin lysis time, and the increase in fibrinogen/fibrin degradation products, indicate a plasma lytic state. Crosslinked fibrin degradation products increased from 310±120 ng/ml to 670 ±310 ng/ml (p=0.009), suggesting that fibrin digestion occurred in vivo. This pilot study provides data supporting the feasibility and efficacy of a new and more economic thrombolytic treatment of acute myocardial infarction without hemorrhagic complications. |
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Keywords: | thrombolytic therapy acute myocardial infarction desmopressin streptokinase |
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