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10.2176/nmc.oa.2017-0145 http://scihub22266oqcxt.onion/10.2176/nmc.oa.2017-0145 C5929914!5929914 !29526881     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29526881 &cmd=llinks): Failed to open stream: HTTP request failed! 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Efficacy and Safety of REVIVE SE Thrombectomy Device for Acute Ischemic Stroke: River JAPAN (Reperfuse Ischemic Vessels with Endovascular Recanalization Device in Japan) |pdf=|usr=}}{{29526881 }} gab.com Text Efficacy and Safety of REVIVE SE Thrombectomy Device for Acute Ischemic Stroke: River JAPAN (Reperfuse Ischemic Vessels with Endovascular Recanalization Device in Japan) JO: Neurol Med Chir (Tokyo) http://www.kidney.de/pget.php?&tw=1&pmid=29526881 #FOAvip REVIVE SE (REVIVE) is a closed-ended, self-expanding stent retriever used in the RIVER JAPAN study. We present our early experience with REVIVE for revascularization of acute ischemic stroke (AIS) in patients who have failed or are ineligible for intravenous recombinant tissue plasminogen activator treatment. This prospective, single-arm, non-randomized, multicenter registry study followed up patients undergoing mechanical thrombectomy with REVIVE for 90 days. The primary endpoint was a post-procedure Thrombolysis in Cerebral Infarction (TICI) score ?2a. Secondary endpoints were clot migration/embolization; recanalization without symptomatic intracranial hemorrhage (ICH) at 24 h; symptomatic ICH; good neurological outcome (modified Rankin Scale score ?2 National Institute of Health Stroke Scale (NIHSS) score decrease ?10) at day 90; device- or procedure-related serious adverse events (SAEs) and mortality at day 90. To confirm non-inferiority of REVIVE, results were compared with historical data of the Merci Retriever. About 49 patients were enrolled (median age 73 years; males 46.9%; middle cerebral artery (MCA) occlusion 83.7%; median NIHSS score 17). A post-procedure TICI score ?2a was observed in 73.5% (36/49, 95% confidence interval [CI] 58.9-85.1) of patients. No post-procedural clot migration/embolization events occurred. Successful recanalization without symptomatic ICH was observed in 62.5% (30/48, 95% CI 47.4-76.0). The good neurological outcome was achieved in 66.7% (32/48) patients. Symptomatic ICH and device- or procedure-related SAEs were reported in 6.3% and 12.2% of patients, respectively. Two deaths were reported. REVIVE demonstrated equivalent efficacy and safety as the Merci Retriever. Results suggest that REVIVE is effective and safe in recanalizing occluded intracranial arteries in AIS. Twit Text FOAVip Efficacy and Safety of REVIVE SE Thrombectomy Device for Acute Ischemic Stroke: River JAPAN (Reperfuse Ischemic Vessels with Endovascular Recanalization Device in Japan) ????Neurol Med Chir (Tokyo) http://www.kidney.de/pget.php?&tw=1&pmid=29526881 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29526881 #FOAvip English Wikipedia <ref>{{Cite pmid|29526881 }}</ref> Efficacy and Safety of REVIVE SE Thrombectomy Device for Acute Ischemic Stroke: River JAPAN (Reperfuse Ischemic Vessels with Endovascular Recanalization Device in Japan) #MMPMID29526881 Sakai N ; Ota S ; Matsumoto Y ; Kondo R ; Satow T ; Kubo M ; Tsumoto T ; Enomoto Y ; Kataoka T ; Imamura H ; Todo K ; Hayakawa M ; Yamagami H ; Toyoda K ; Ito Y ; Sugiu K ; Matsumaru Y ; Yoshimura S Neurol Med Chir (Tokyo) 2018[Apr]; 58 (4 ): 164-172 PMID29526881 show ga REVIVE SE (REVIVE) is a closed-ended, self-expanding stent retriever used in the RIVER JAPAN study. We present our early experience with REVIVE for revascularization of acute ischemic stroke (AIS) in patients who have failed or are ineligible for intravenous recombinant tissue plasminogen activator treatment. This prospective, single-arm, non-randomized, multicenter registry study followed up patients undergoing mechanical thrombectomy with REVIVE for 90 days. The primary endpoint was a post-procedure Thrombolysis in Cerebral Infarction (TICI) score ?2a. Secondary endpoints were clot migration/embolization; recanalization without symptomatic intracranial hemorrhage (ICH) at 24 h; symptomatic ICH; good neurological outcome (modified Rankin Scale score ?2 National Institute of Health Stroke Scale (NIHSS) score decrease ?10) at day 90; device- or procedure-related serious adverse events (SAEs) and mortality at day 90. To confirm non-inferiority of REVIVE, results were compared with historical data of the Merci Retriever. About 49 patients were enrolled (median age 73 years; males 46.9%; middle cerebral artery (MCA) occlusion 83.7%; median NIHSS score 17). A post-procedure TICI score ?2a was observed in 73.5% (36/49, 95% confidence interval [CI] 58.9-85.1) of patients. No post-procedural clot migration/embolization events occurred. Successful recanalization without symptomatic ICH was observed in 62.5% (30/48, 95% CI 47.4-76.0). The good neurological outcome was achieved in 66.7% (32/48) patients. Symptomatic ICH and device- or procedure-related SAEs were reported in 6.3% and 12.2% of patients, respectively. Two deaths were reported. REVIVE demonstrated equivalent efficacy and safety as the Merci Retriever. Results suggest that REVIVE is effective and safe in recanalizing occluded intracranial arteries in AIS. |Adult [MESH] |Aged [MESH] |Aged, 80 and over [MESH] |Brain Ischemia/complications/*surgery [MESH] |Endovascular Procedures/*instrumentation [MESH] |Female [MESH] |Humans [MESH] |Japan [MESH] |Male [MESH] |Middle Aged [MESH] |Prospective Studies [MESH] |Stents [MESH] |Stroke/etiology/*surgery [MESH] |Thrombectomy/*instrumentation [MESH]Efficacy and Safety of REVIVE SE Thrombectomy Device for Acute Ischemi(epmc).pdf DeepDyve Pubget Overpricing