2003
DOI: 10.1016/s0002-9149(03)00666-0
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Transcutaneous ultrasound-facilitated coronary thrombolysis during acute myocardial infarction

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Cited by 53 publications
(33 citation statements)
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“…Extracorporeal ultrasound has been combined with thrombolytic drugs in clinical trials to treat both acute myocardial infarction [26] and acute middle cerebral artery stroke [27] with promising results. However, both of these treatment methods require further validation and optimisation.…”
Section: Discussionmentioning
confidence: 99%
“…Extracorporeal ultrasound has been combined with thrombolytic drugs in clinical trials to treat both acute myocardial infarction [26] and acute middle cerebral artery stroke [27] with promising results. However, both of these treatment methods require further validation and optimisation.…”
Section: Discussionmentioning
confidence: 99%
“…Therapeutic transcutaneous ultrasound has been investigated as an adjunct to intravenously administered thrombolytic drug therapy in an attempt to improve these outcomes [13,14], however recent human clinical trials using this technique in ST elevation myocardial infarction (PLUS Trial [unpublished data, 2003]), and acute ischemic stroke (TRUMBI Trial [15]), have failed to show efficacy or safety, probably due to the problematic high attenuation characteristics of the therapeutic ultrasound through lung or bone [16,17] plus ultrasound's propensity, especially at higher intensities, to lead to increased platelet adhesion [18], damage blood vessels [19][20][21][22][23][24] and burn the overlying skin of patients receiving therapy [22,23].…”
Section: Introductionmentioning
confidence: 99%
“…Recent clinical studies have demonstrated improved thrombolysis with the concomitant use of focused ultrasound and a thrombolytic agent for stroke and acute myocardial infarction [2][3][4]. Suggested mechanisms include acoustic streaming which promotes transport of drugs into the thrombus, radiation force which might facilitate reformation and opening of the fibrin matrix enhancing drug diffusion, cleaving of fibrin polymers to extend the surface for drug interaction, and direct effects on binding of the agent to fibrin [5].…”
mentioning
confidence: 99%