TY - JOUR
T1 - Ultrasound enhanced prehospital thrombolysis using microbubbles infusion in patients with acute st elevation myocardial infarction
T2 - Pilot of the sonolysis study
AU - Slikkerveer, Jeroen
AU - Kleijn, Sebastiaan A.
AU - Appelman, Yolande
AU - Porter, Thomas R.
AU - Veen, Gerrit
AU - van Rossum, Albert C.
AU - Kamp, Otto
PY - 2012/2
Y1 - 2012/2
N2 - In animal studies, transthoracic ultrasound and microbubbles have shown to dissolve thrombi in ST elevation myocardial infarction (STEMI). To examine this effect in patients, we have initiated the Sonolysis trial. In this pilot study of 10 patients with a first acute STEMI, we investigated the safety and feasibility of this trial. After pretreatment in the ambulance, five patients were randomized to receive microbubbles with three-dimensional (3-D) guided high mechanical index impulses (1.18) for 15 min, whereas the control group received placebo without ultrasound. Subsequently, primary percutaneous coronary intervention (PPCI) was performed, if indicated. All patients successfully underwent study treatment and PPCI. No significant difference between treatment and control group in safety (minor adverse events 2/5 vs. 2/5, p= NS) and outcome (TIMI III flow 3/5 vs. 1/5 respectively, p= 0.23) was recorded. These results demonstrate that the study protocol is feasible in the acute cardiac care setting and safe during treatment and follow-up.
AB - In animal studies, transthoracic ultrasound and microbubbles have shown to dissolve thrombi in ST elevation myocardial infarction (STEMI). To examine this effect in patients, we have initiated the Sonolysis trial. In this pilot study of 10 patients with a first acute STEMI, we investigated the safety and feasibility of this trial. After pretreatment in the ambulance, five patients were randomized to receive microbubbles with three-dimensional (3-D) guided high mechanical index impulses (1.18) for 15 min, whereas the control group received placebo without ultrasound. Subsequently, primary percutaneous coronary intervention (PPCI) was performed, if indicated. All patients successfully underwent study treatment and PPCI. No significant difference between treatment and control group in safety (minor adverse events 2/5 vs. 2/5, p= NS) and outcome (TIMI III flow 3/5 vs. 1/5 respectively, p= 0.23) was recorded. These results demonstrate that the study protocol is feasible in the acute cardiac care setting and safe during treatment and follow-up.
KW - Facilitated PCI
KW - Microbubbles
KW - STEMI
KW - Ultrasound
UR - http://www.scopus.com/inward/record.url?scp=84855493224&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84855493224&partnerID=8YFLogxK
U2 - 10.1016/j.ultrasmedbio.2011.11.001
DO - 10.1016/j.ultrasmedbio.2011.11.001
M3 - Article
C2 - 22178160
AN - SCOPUS:84855493224
SN - 0301-5629
VL - 38
SP - 247
EP - 252
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 2
ER -