A pilot randomized clinical safety study of sonothrombolysis augmentation with ultrasound-activated perflutren-lipid microspheres for acute ischemic stroke

Stroke. 2008 May;39(5):1464-9. doi: 10.1161/STROKEAHA.107.505727. Epub 2008 Mar 20.

Abstract

Background and purpose: Ultrasound transiently expands perflutren-lipid microspheres (muS), transmitting energy momentum to surrounding fluids. We report a pilot safety/feasibility study of ultrasound-activated muS with systemic tissue plasminogen activator (tPA).

Methods: Stroke subjects treated within 3 hours had abnormal Thrombolysis in Brain Ischemia (TIBI) residual flow grades 0 to 3 before tPA on transcranial Doppler (TCD). Randomization included Controls (tPA+TCD) or Target (tPA+TCD+2.8 mL microS). The primary safety end point was symptomatic intracranial hemorrhage (sICH) with worsening by >or=4 NIHSS points within 72 hours.

Results: Fifteen subjects were randomized 3:1 to Target, n=12 or Control, n=3. After treatment, asymptomatic ICH occurred in 3 Target and 1 Control, and sICH was not seen in any study subject. muS reached MCA occlusions in all Target subjects at velocities higher than surrounding residual red blood cell flow: 39.8+/-11.3 vs 28.8+/-13.8 cm/s, P<0.001. In 75% of subjects, microS permeated to areas with no pretreatment residual flow, and in 83% residual flow velocity improved at a median of 30 minutes from start of microS infusion (range 30 s to 120 minutes) by a median of 17 cm/s (118% above pretreatment values). To provide perspective, current study recanalization rates were compared with the tPA control arm of the CLOTBUST trial: complete recanalization 50% versus 18%, partial 33% versus 33%, none 17% versus 49%, P=0.028. At 2 hours, sustained complete recanalization was 42% versus 13%, P=0.003, and NIHSS scores 0 to 3 were reached by 17% versus 8%, P=0.456.

Conclusions: Perflutren microS reached and permeated beyond intracranial occlusions with no increase in sICH after systemic thrombolysis suggesting feasibility of further microS dose-escalation studies and development of drug delivery to tissues with compromised perfusion.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Aged
  • Aged, 80 and over
  • Brain Ischemia / diagnostic imaging*
  • Brain Ischemia / drug therapy
  • Cerebral Arteries / diagnostic imaging
  • Cerebral Arteries / drug effects
  • Cerebral Arteries / physiopathology
  • Cerebral Hemorrhage / etiology
  • Cerebral Hemorrhage / physiopathology
  • Cerebral Hemorrhage / prevention & control
  • Cerebrovascular Circulation / drug effects
  • Cerebrovascular Circulation / physiology
  • Contrast Media / therapeutic use
  • Female
  • Fibrinolytic Agents / therapeutic use
  • Fluorocarbons / therapeutic use*
  • Humans
  • Lipids / therapeutic use
  • Male
  • Microspheres*
  • Middle Aged
  • Pilot Projects
  • Stroke / diagnostic imaging*
  • Stroke / drug therapy
  • Thrombolytic Therapy / methods*
  • Tissue Plasminogen Activator / therapeutic use
  • Treatment Outcome
  • Ultrasonography, Doppler, Transcranial / adverse effects
  • Ultrasonography, Doppler, Transcranial / methods*

Substances

  • Contrast Media
  • Fibrinolytic Agents
  • Fluorocarbons
  • Lipids
  • perflutren
  • Tissue Plasminogen Activator