» Articles » PMID: 3306267

Adverse Reactions to Thrombolytic Agents. Implications for Coronary Reperfusion Following Myocardial Infarction

Overview
Specialty Toxicology
Date 1987 Jul 1
PMID 3306267
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The use of thrombolytic agents to dissolve coronary artery thrombi causing acute transmural myocardial infarctions has been shown to decrease short term mortality, and improve left ventricular function, in patients with acute transmural myocardial infarction. Several thrombolytic agents are currently available which differ mainly in cost, antigenicity, and mechanism of action. Current investigations are being directed at finding safer, more effective thrombolytic agents and at developing optimal therapy following thrombolysis. The complications of thrombolytic therapy are for the most part minor and reversible. Immediate and delayed hypersensitivity to streptokinase is rare. Hypotension and arrhythmias commonly accompany myocardial reperfusion and are usually benign and self-limited. Haemorrhagic complications are the most frequent and serious problems following the use of thrombolytic agents. They can be lessened by the proper selection of patients to avoid those at high risk of bleeding. The avoidance of unnecessary arterial and venous punctures will decrease the incidence of minor but annoying local bleeding. Those agents which are activated at the site of thrombi will hopefully cause fewer bleeding episodes, but early experience with these agents has not been able to demonstrate a lower rate. With careful attention to patient selection and follow-up, thrombolytic agents can be safely and effectively used in the management of patients with acute myocardial infarction.

Citing Articles

Efficacy of Low-Dose Streptokinase Infusion in Late-Onset Permanent Tunnel Catheter Dysfunction: A Single-Center Interventional Study.

Gadekar K, Kibriya S, Kulkarni P, Balasubramanian S Cureus. 2024; 16(4):e58028.

PMID: 38738061 PMC: 11088470. DOI: 10.7759/cureus.58028.


Unveiling the Potent Fibrino(geno)lytic, Anticoagulant, and Antithrombotic Effects of Papain, a Cysteine Protease from Latex Using κ-Carrageenan Rat Tail Thrombosis Model.

Yang H, Zahan M, Yoon Y, Kim K, Hwang D, Kim W Int J Mol Sci. 2023; 24(23).

PMID: 38069092 PMC: 10706441. DOI: 10.3390/ijms242316770.


Biomimetic nanoparticle technology for cardiovascular disease detection and treatment.

Park J, Dehaini D, Zhou J, Holay M, Fang R, Zhang L Nanoscale Horiz. 2020; 5(1):25-42.

PMID: 32133150 PMC: 7055493. DOI: 10.1039/c9nh00291j.


Thrombolytic Potential of Novel Thiol-Dependent Fibrinolytic Protease from Bacillus cereus RSA1.

Sharma C, Salem G, Sharma N, Gautam P, Singh R Biomolecules. 2019; 10(1).

PMID: 31861284 PMC: 7022875. DOI: 10.3390/biom10010003.


Paramedics beliefs and attitudes towards pre-hospital thrombolysis.

Alanazi A, Alrashidi Q, Aljerian N Int J Appl Basic Med Res. 2014; 4(1):11-5.

PMID: 24600571 PMC: 3931206. DOI: 10.4103/2229-516X.125672.


References
1.
ASTRUP T, Stage A . Isolation of a soluble fibrinolytic activator from animal tissue. Nature. 1952; 170(4335):929. DOI: 10.1038/170929a0. View

2.
Kasper W, Meinertz T, Wollschlager H, Bonzel T, Wolff P, Drexler H . Coronary thrombolysis during acute myocardial infarction by intravenous BRL 26921, a new anisoylated plasminogen-streptokinase activator complex. Am J Cardiol. 1986; 58(6):418-21. DOI: 10.1016/0002-9149(86)90006-8. View

3.
Wei J, Markis J, Malagold M, Braunwald E . Cardiovascular reflexes stimulated by reperfusion of ischemic myocardium in acute myocardial infarction. Circulation. 1983; 67(4):796-801. DOI: 10.1161/01.cir.67.4.796. View

4.
Smith R, Dupe R, English P, Green J . Fibrinolysis with acyl-enzymes: a new approach to thrombolytic therapy. Nature. 1981; 290(5806):505-8. DOI: 10.1038/290505a0. View

5.
Alderman E, Jutzy K, Berte L, Miller R, FRIEDMAN J, CREGER W . Randomized comparison of intravenous versus intracoronary streptokinase for myocardial infarction. Am J Cardiol. 1984; 54(1):14-9. DOI: 10.1016/0002-9149(84)90297-2. View