Intra-Arterial Tenecteplase to Improve the Microvascular Hemodynamics After Mechanical Thrombectomy
brief summary
This is a prospective, single-arm, open-label study to evaluate the efficacy of intra-arterial tenecteplase in improving microvascular reperfusion following successful large vessel recanalization. Acute ischemic stroke patients with large anterior circulation large vessel occlusion will receive a single weight-based dose of intra-arterial tenecteplase after achieving successful large vessel recanalization (defined as TICI ≥ 2b) via standard of care mechanical thrombectomy. Microvascular flow will be assessed by quantitative angiography before and after the intra-arterial drug administration in order to quantify the impact of targeted thrombolysis on microvascular reperfusion. Reperfusion will be secondarily assessed with 24-hour imaging, final infarct volume will be quantified 72 hours following treatment, and functional outcome will be assessed in the short-term by the NIHSS and in the long-term by the 90-day modified Rankin Scale.
detailed description
This is a prospective, single-arm, open-label pilot trial to evaluate the efficacy of IA-TNK in improving microvascular reperfusion following successful large vessel recanalization. Acute ischemic stroke patients will receive IA-TNK after achieving mTICI ≥ 2b recanalization via standard of care mechanical thrombectomy (MT). Microvascular flow will be assessed by quantitative angiography before and after IA-TNK to quantify the impact of targeted thrombolysis on microvascular reperfusion. Reperfusion will be secondarily assessed with 24-hour imaging. Final infarct volume will be quantified 72 hours following treatment. Functional outcome will be assessed in the short-term by the NIHSS and at 90-days by the modified Rankin Scale.
N=20 acute stroke patients will be enrolled after successful recanalization of a proximal anterior circulation LVO (internal carotid artery or first segment of the middle cerebral artery). After standard of care MT, every patient will undergo a quantitative angiographic assessment with syngo iFLOW (Siemens Healthineers). More specifically, 2D angiographic images will be acquired with a 8 Fr catheter located in the extracranial C2-C4 segment of the internal carotid artery. 6 mLs of contrast agent will be injected at a flow rate of 4 mL/sec (standardized injection via power injector). The 2D imaging will be acquired at a rate of 4 frames per second to acquire images in anterior-posterior and lateral positions. Images will be transferred to the workstation at which syngo iFLOW software will enable quantification of the microvascular cerebral circulation time (mCCT). Post-processing via iFLOW requires 1-2 minutes. ROI selection to quantify mCCT requires approximately 2-5 minutes.
After post-MT mCCT is quantified, the catheter will be advanced to the distal M1 segment of the MCA (distal to lenticulostriates). 0.125 mg/kg (max 12.5mg) of TNK (i.e. 50% of the IV dose) will be administered via a 5-minute intraarterial infusion (using a programmable syringe pump). As described in section 3.3.1, the dose may be modified as clinical trial data become available, if the available data identify an alternative dose to be optimal.
10 minutes post-TNK, the quantitative angiographic assessment will be repeated to calculate the post-treatment mCCT. The primary objective of this trial is to quantify the change in mCCT associated with IA-TNK treatment.
Post-treatment clinical monitoring will continue as per institutional standard of care (post-MT and post-TNK monitoring). Standard of care NCCT, in addition to protocol CTA/CTP, will be performed 24 hours post-TNK to secondarily assess recanalization, reperfusion, and safety (i.e. hemorrhagic complications). Study protocol MRI of the brain will also be performed 72 hours post-TNK to quantify final infarct volume. Serial NIHSS will assess early functional outcome. Dramatic clinical recovery (DCR) will be defined as a ≥8 point improvement in NIHSS between baseline and 24 hours post-TNK. 90-day mRS will assess long-term functional outcome.