Overview
The best reperfusion strategy for medium-sized vessel occlusion (MeVO) is not well established. Given the proven treatment effect of intra-arterial thrombolysis in patients with large vessel occlusion (LVO), the investigators hypothesized that intra-arterial tenecteplase (TNK) could increase the recanalization rate of MeVO and thus improve clinical outcome. The current study aimed to explore the safety and efficacy of intra-arterial TNK in patients with MeVO.
Eligibility
Inclusion Criteria:
- Age ≥18 years;
- Medium vessel occlusion (MeVO), referring to M2-3 of MCA; A1-3 of ACA; P1-3 of PCA;
PICA, AICA or SCA (including primary, distal embolism in the same region after
thrombectomy or concurrent embolism in other regions).
- Primary MeVO as detected by the first DSA examination or secondary MeVO after mechanical thrombectomy for large vessel occlusion;
- MeVO causes neurological deficits in motor strength, language, vision etc;
- Endovascular mechanical thrombectomy cannot be performed as assessed by the investigator;
- Absence of parenchymal hematoma on CT images performed in the angio suite.
- Within 24 hours from symptom onset;
- Signed informed consent by patient or patient's legally authorized representative.
Exclusion Criteria:
- Patients with completed infarction in the territory of the MeVO on non-contrast CT;
- Patients with intracranial hemorrhage;
- Coagulation disorders, tendency for systemic hemorrhagic, thrombocytopenia (<100,000/mm3);
- Severe hepatic or renal dysfunction, increase in ALT or AST (more than 2 times of upper limit of normal value), increase in serum creatinine (more than 1.5 times of upper limit of normal value) or requiring dialysis;
- After mechanical thrombectomy, severe and sustained (> 5 minutes) uncontrolled hypertension (systolic blood pressure over 180mmHg or diastolic blood pressure over 105 mmHg);
- Patients with contraindication or allergy to any ingredient of study medication;
- Pregnancy, plan to get pregnant or active lactation;
- The estimated life expectancy is less than 6 months due to other serious diseases;
- Other conditions unsuitable for this clinical study as assessed by researcher.