Caldwell James, McGuinness Ben, Lee Shane S, Barber P Alan, Holden Andrew, Wu Teddy, Krauss Martin, Laing Andrew, Collecutt Wayne, Liebeskind David S, Hetts Steven W, Brew Stefan
Neuroradiology, Auckland City Hospital, Auckland, New Zealand
Neuroradiology, Auckland City Hospital, Auckland, New Zealand.
J Neurointerv Surg. 2022 Dec;14(12):1239-1243. doi: 10.1136/neurintsurg-2021-018318. Epub 2021 Dec 14.
We describe the first-in-human experience using the Route 92 Medical Aspiration System to perform thrombectomy in the initial 45 consecutive stroke patients enrolled in the SUMMIT NZ trial. This aspiration system includes a specifically designed delivery catheter which enables delivery of 0.070 inch and 0.088 inch aspiration catheters.
The SUMMIT NZ trial is a prospective, multicenter, single-arm study with core lab imaging adjudication. Patients presenting with acute ischemic stroke from large vessel occlusion are eligible to enrol. The study has had three phases which transitioned from use of the 0.070 inch to the 0.088 inch catheter.
Vessel occlusions were located in the internal carotid artery (27%), M1 (60%) and M2 (13%). Median baseline National Institutes of Health Stroke Scale (NIHSS) was 16 (IQR 10). Across the three phases, the first-pass reperfusion rate of modified Thrombolysis In Cerebral Infarction (mTICI) ≥2b was 62% using the Route 92 Medical system; this rate was 29% in phase 1, 56% in phase 2, and 80% in phase 3. The first-pass reperfusion rate of mTICI ≥2c was 42% overall, 29% in phase 1, 33% in phase 2, and 55% in phase 3. A final reperfusion rate of mTICI ≥2b was achieved in 96% of cases, with 36% of cases using adjunctive devices. Patients had an average improvement of 6.7 points in NIHSS from baseline at 24 hours, and at 90 days 48% were functionally independent (modified Rankin Scale 0-2).
In this early experience, the Route 92 Medical Aspiration System has been effective and safe. The system has design features that improve catheter deliverability and have the potential to increase first-pass reperfusion rates in aspiration thrombectomy.
我们描述了在新西兰SUMMIT试验中最初连续纳入的45例中风患者中,使用92号路线医疗抽吸系统进行血栓切除术的首例人体经验。该抽吸系统包括一个专门设计的输送导管,可输送0.070英寸和0.088英寸的抽吸导管。
新西兰SUMMIT试验是一项前瞻性、多中心、单臂研究,由核心实验室进行影像判定。因大血管闭塞导致急性缺血性中风的患者有资格入组。该研究有三个阶段,从使用0.070英寸导管过渡到使用0.088英寸导管。
血管闭塞位于颈内动脉(27%)、M1段(60%)和M2段(13%)。基线时美国国立卫生研究院卒中量表(NIHSS)中位数为16(四分位间距10)。在三个阶段中,使用92号路线医疗系统时,改良脑梗死溶栓(mTICI)≥2b级的首次通过再灌注率为62%;在第1阶段为29%,第2阶段为56%,第3阶段为80%。mTICI≥2c级的首次通过再灌注率总体为42%,第1阶段为29%,第2阶段为33%,第3阶段为55%。96%的病例最终实现了mTICI≥2b级的再灌注率,其中36%的病例使用了辅助装置。患者在24小时时NIHSS较基线平均改善6.7分,在90天时48%的患者功能独立(改良Rankin量表0 - 2级)。
在这一早期经验中,92号路线医疗抽吸系统有效且安全。该系统具有改善导管输送性的设计特点,有可能提高抽吸血栓切除术中的首次通过再灌注率。