Siegler James E, Koneru Manisha, Shaikh Hamza, Salim Hamza Adel, Musmar Basel, Adeeb Nimer, Yedavalli Vivek, Daraghma Motaz, Naamani Kareem El, Henninger Nils, Sundararajan Sri Hari, Kühn Anna Luisa, Ghozy Sherief, Scarcia Luca, Tan Benjamin Yq, Heit Jeremy J, Regenhardt Robert W, Morsi Rami Z, Kass-Hout Tareq, Vigilante Nicholas, Cancelliere Nicole M, Bernstock Joshua D, Rouchaud Aymeric, Fiehler Jens, Sheth Sunil A, Essibayi Muhammed Amir, Puri Ajit S, Dyzmann Christian, Colasurdo Marco, Barreau Xavier, Renieri Leonardo, Filipe João Pedro, Harker Pablo, Radu Răzvan Alexandru, Marotta Thomas R, Spears Julian, Ota Takahiro, Mowla Ashkan, Jabbour Pascal, Biswas Arundhati, Clarençon Frédéric, Klein Piers, Abdalkader Mohamad, Nguyen Thanh N, Varela Ricardo, Baker Amanda, Altschul David, Gonzalez Nestor R, Möhlenbruch Markus A, Costalat Vincent, Gory Benjamin, Stracke Christian Paul, Hecker Constantin, Griessenauer Christoph J, Liebeskind David S, Pedicelli Alessandro, Alexandre Andrea M, Tancredi Illario, Faizy Tobias D, Kalsoum Erwah, Lubicz Boris, Patel Aman B, Pereira Vitor Mendes, Khalife Jane, Rana Ankit, Guenego Adrien, Dmytriw Adam A
Cooper Neurological Institute, Cooper University Hospital, Cooper Medical School of Rowen University, Camden, NJ, USA.
Department of Neurology, University of Chicago, Chicago, IL, USA.
Interv Neuroradiol. 2025 May 21:15910199251341603. doi: 10.1177/15910199251341603.
BackgroundEndovascular therapy (EVT) for stroke due to distal or medium vessel occlusion (DMVO) is safe. Due to the distinct anatomical characteristics of DMVOs, further evaluation of EVT is crucial to determine which devices may yield better outcomes.MethodsA retrospective analysis of adults with DMVO treated in 37 centers (11 countries) was queried. The primary outcome of favorable shift in 90-day modified Rankin Scale (mRS) was compared between patients treated with Trevo versus other devices on first pass using 1:1 propensity score matching (PSM) with multivariable adjustment. Secondary outcomes included the number of pass attempts, final thrombolysis in cerebral infarction (TICI) score 2b-3, symptomatic intracranial hemorrhage (sICH), improvement in National Institutes of Health Stroke Scale (NIHSS) at 24h, and 90-day mortality.ResultsOf the 1115 included patients, 264 (24%) were treated with Trevo (PSM cohort of 261 per group). Trevo use was not associated with a favorable 90-day mRS shift (proportional odds ratio [OR] 1.10, 95% confidence interval [CI] 0.80-1.51). Trevo was associated with fewer passes (adjusted β=-0.25, 95% CI -0.48 - -0.03), higher odds of TICI 2b-3 (adjusted OR 1.97, 95% CI 1.11-3.49), and a greater 24h NIHSS improvement (adjusted β= -1.74, 95% CI -3.11 - -0.36), with no difference in sICH or mortality (p>0.05). Results were similar in sensitivity analyses.ConclusionsWe observed no safety concerns with Trevo as compared to other EVT devices for DMVO recanalization. There was a signal of better technical efficacy and early clinical improvement.
背景
对于由远端或中间血管闭塞(DMVO)导致的中风,血管内治疗(EVT)是安全的。由于DMVO独特的解剖学特征,对EVT进行进一步评估对于确定哪种器械可能产生更好的治疗效果至关重要。
方法
对在37个中心(11个国家)接受治疗的成年DMVO患者进行回顾性分析。使用1:1倾向评分匹配(PSM)并进行多变量调整,比较首次通过时使用Trevo与其他器械治疗的患者在90天改良Rankin量表(mRS)上的良好转变这一主要结局。次要结局包括通过尝试次数、最终脑梗死溶栓(TICI)评分2b - 3、有症状颅内出血(sICH)、24小时时美国国立卫生研究院卒中量表(NIHSS)的改善情况以及90天死亡率。
结果
在纳入的1115例患者中,264例(24%)接受了Trevo治疗(每组PSM队列261例)。使用Trevo与90天mRS良好转变无关(比例优势比[OR] 1.10,95%置信区间[CI] 0.80 - 1.51)。Trevo与较少的通过次数相关(调整后的β = -0.25,95% CI -0.48 - -0.03),TICI 2b - 3的几率更高(调整后的OR 1.97,95% CI 1.11 - 3.49),以及24小时NIHSS改善更大(调整后的β = -1.74,95% CI -3.11 - -0.36),sICH或死亡率无差异(p>0.05)。敏感性分析结果相似。
结论
与用于DMVO再通的其他EVT器械相比我们观察到使用Trevo没有安全问题。有技术疗效更好和早期临床改善的迹象。