Thrombolytics

1992 ◽  
Vol 3 (2) ◽  
pp. 423-434
Author(s):  
C. Lynne Ostrow

Thrombolytic therapy is the most recent advance in the treatment of acute myocardial infarction. Several research trials have been conducted worldwide in the last decade that have established that thrombolytic therapy has reduced mortality 50%, reduces the size of the infarction, improves left ventricular function, and reduces the incidence and severity of congestive heart failure. The three most commonly used thrombolytic agents at this time arc streptokinase, tissue plasminogen activator, and anisoylated plasminogen-streptokinase activator complex. All three agents can be administered through a peripheral intravenous. Recent research results have reported similar efficacy on 5-week mortality of all three agents. Careful assessment of prospective patients is essential since bleeding complications arc the most serious side effect of this therapy. Nursing care of a patient undergoing thrombolytic therapy includes careful assessment of the patient for contraindications in the patient’s medical history, assessment of potential allergic and bleeding complications, and evaluation of the reperfusion markers. Patients are subsequently treated with anticoagulants, aspirin, or dipyridamole. It appears that thrombolytic therapy will become increasingly available to all patients with a diagnosis of suspected acute myocardial infarction. At present, treatment with thrombolytic agents is less available in the United States compared to Europe

Open Heart ◽  
2019 ◽  
Vol 6 (1) ◽  
pp. e000987 ◽  
Author(s):  
Brunilda Alushi ◽  
Andel Douedari ◽  
Georg Froehlig ◽  
Wulf Knie ◽  
Thomas H Wurster ◽  
...  

ObjectiveWe investigated the benefit of Impella, a modern percutaneous mechanical support (pMCS) device, versus former standard intra-aortic balloon pump (IABP) in acute myocardial infarction complicated by cardiogenic shock (AMICS).MethodsThis single-centre, retrospective study included patients with AMICS receiving pMCS with either Impella or IABP. Disease severity at baseline was assessed with the IABP-SHOCK II score. The primary outcome was all-cause mortality at 30 days. Secondary outcomes were parameters of shock severity at the early postimplantation phase. Adjusted Cox proportional hazards models identified independent predictors of the primary outcome.ResultsOf 116 included patients, 62 (53%) received Impella and 54 (47%) IABP. Despite similar baseline mortality risk (IABP-SHOCK II high-risk score of 18 % vs 20 %; p = 0.76), Impella significantly reduced the inotropic score (p < 0.001), lactate levels (p < 0.001) and SAPS II (p =0.02) and improved left ventricular ejection fraction (p = 0.01). All-cause mortality at 30 days was similar with Impella and IABP (52 % and 67 %, respectively; p = 0.13), but bleeding complications were more frequent in the Impella group (3 vs 4 units of transfused erythrocytes concentrates due to bleeding complications, p = 0.03). Previous cardiopulmonary resuscitation (HR 3.22, 95% CI 1.76 to 5.89; p < 0.01) and an estimated intermediate (HR 2.77, 95% CI 1.42 to 5.40; p < 0.01) and high (HR 4.32 95% CI 2.03 to 9.24; p = 0.01) IABP-SHOCK II score were independent predictors of all-cause mortality.ConclusionsIn patients with AMICS, haemodynamic support with the Impella device had no significant effect on 30-day mortality as compared with IABP. In these patients, large randomised trials are warranted to ascertain the effect of Impella on the outcome.


1993 ◽  
Vol 1 (4) ◽  
pp. 145-151 ◽  
Author(s):  
Roger L. White

Thrombolytic therapy has clearly become an established therapeutic modality to treat patients with acute myocardial infarction. Since there is no ideal agent at this time, we must evaluate the advantages and disadvantages of current therapy based on major clinical studies. Thrombolysis is the body's natural response to dissolving clots after they have served their purpose. Thrombolytic agents accelerate fibrinolysis by overwhelming the system. There are 4 thrombolytic agents currently available: streptokinase urokinase, anistreplase (APSAC), and rt-PA. Tissue plasminogen activator is a naturally occurring protein that can be created with genetic recombinant technology (rt-PA). It establishes higher patency rates (70–90%) than the other available thrombolytic agents. Recently published results of accelerated rt-PA infusion during acute myocardial infarction demonstrate that the infarct-related artery seems to open more quickly and provide greater blood flow. The use of intravenous heparin as adjunctive therapy along with aspirin seems to maintain patency at comparable levels to streptokinase. Not only is mortality reduced in the accelerated rt-PA group, but complications from myocardial infarction such as arrhythmia and heart failure are significantly reduced. rt-PA remains the drug of choice in the hypotensive patient and, because of potential allergy, in patients with previous exposure to streptokinase. Percutaneous transluminal coronary angioplasty is frequently needed to improve long-term patency and reduce ischemic episodes. Recent studies show that it may provide some advantage over thrombolytic therapy, because the artery can be opened faster, with higher flow rates.


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