The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study

•A multicenter cohort of patients with acutely ruptured intracranial aneurysms treated stent-assisted coiling.•A lower rate of perioperative complications in the treatment within 24 h.•The LVIS stent achieved a high complete aneurysm occlusion.•Clinical outcomes and angiographic results did not diff...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical neurology and neurosurgery 2020-10, Vol.197, p.106117-106117, Article 106117
Hauptverfasser: Wang, Xianggan, Xing, Haixia, Cai, Jing, Jin, Dianshi, Chen, Yongchun, Cui, Yudi, Ding, Shenghao, Wan, Jieqing, Pan, Yaohua, Mao, Guohua, Zhao, Bing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 106117
container_issue
container_start_page 106117
container_title Clinical neurology and neurosurgery
container_volume 197
creator Wang, Xianggan
Xing, Haixia
Cai, Jing
Jin, Dianshi
Chen, Yongchun
Cui, Yudi
Ding, Shenghao
Wan, Jieqing
Pan, Yaohua
Mao, Guohua
Zhao, Bing
description •A multicenter cohort of patients with acutely ruptured intracranial aneurysms treated stent-assisted coiling.•A lower rate of perioperative complications in the treatment within 24 h.•The LVIS stent achieved a high complete aneurysm occlusion.•Clinical outcomes and angiographic results did not differ between the treatment of 24 h and that between 25−72 h. Stent-assisted coiling is increasingly used in the treatment of acutely ruptured intracranial aneurysms. However, the optimal timing of the stent-assisted coiling remains unknown. We aimed to investigate the safety and efficacy of the Low Profile Visualized Intraluminal Support (LVIS) stent for ruptured aneurysms treatment within 24 h comparing to the treatment between 25 and 72 h of symptom onset. We conducted a multicenter retrospective study on 110 consecutive patients with ruptured intracranial aneurysms. These patients were treated with LVIS stent within 72 h in four tertiary hospitals between January 2017 and December 2017. The timing of treatment was grouped into the treatment within 24 h and the treatment between 25 and 72 h. Baseline characteristics, periprocedural complications, angiographic results, and clinical outcomes were compared between the two groups. A total of 101 patients were included. 49 (48.5 %) patients were treated within 24 h and 52 (51.5 %) within between 25 and 72 h. Periprocedural complications occurred in 2 (4.1 %) patients treated within 24 h compared with those in 10 (19.2 %) treated between 25−72 h (P = 0.032). No early rebleeding occurred in both groups. 45 (91.8 %) of 49 aneurysms had complete occlusion on immediate angiography compared with 46 (88.5 %) of 52 aneurysms had complete occlusion. 2 (2.0 %) aneurysms were retreated. The clinical outcomes and angiographic results did not differ between the two groups. The LVIS stent-assisted coiling may be safe and effective in the treatment of selected patients with ruptured aneurysms within 24 h of symptom onset.
doi_str_mv 10.1016/j.clineuro.2020.106117
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2430370850</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0303846720304601</els_id><sourcerecordid>2449454394</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-a927da65ed3c387916b135a16c159ada208580b0ff72e561f01a3e43382d5ef63</originalsourceid><addsrcrecordid>eNqFkUtuFDEQhi0EIkPgCpElNmx68Kvd3ayIIh6RRmJBYGt57LLGo34MtjtR77gDB-FOnIQaJmHBhpWl8ld__VU_IRecrTnj-vV-7fo4wpymtWDiWNScN4_IireNqHSn28dkxSSTVat0c0ae5bxnjEmp26fkTIpG1U3HVuTHzQ5otgHKQu3oKYQQnXULnQIt-LX5ev2Z5gJjoWFKf0olgS3DsYJMmg9lTuBpHEuyLtkx2h6V0NmSh0zvYtnFkQr16_vP3TSn_IZe0mHuS3SoAIkmKGnKB3Al3qKTMvvlOXkSbJ_hxf17Tr68f3dz9bHafPpwfXW5qZzsdKlsJxpvdQ1eOtk2HddbLmvLteN1Z70VrK1btmUhNAJqzQPjVoKSshW-hqDlOXl10j2k6dsMuZghZgd9j_anORuh8H4NqjBEX_6D7nGZEd0hpTpVK9kppPSJcrhSThDMIcXBpsVwZo6xmb15iM0cYzOn2LDx4l5-3g7g_7Y95ITA2xMAeI_bCMlkF2F04GPC0xk_xf_N-A0m_q7-</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2449454394</pqid></control><display><type>article</type><title>The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study</title><source>Elsevier ScienceDirect Journals Complete</source><source>ProQuest Central UK/Ireland</source><creator>Wang, Xianggan ; Xing, Haixia ; Cai, Jing ; Jin, Dianshi ; Chen, Yongchun ; Cui, Yudi ; Ding, Shenghao ; Wan, Jieqing ; Pan, Yaohua ; Mao, Guohua ; Zhao, Bing</creator><creatorcontrib>Wang, Xianggan ; Xing, Haixia ; Cai, Jing ; Jin, Dianshi ; Chen, Yongchun ; Cui, Yudi ; Ding, Shenghao ; Wan, Jieqing ; Pan, Yaohua ; Mao, Guohua ; Zhao, Bing</creatorcontrib><description>•A multicenter cohort of patients with acutely ruptured intracranial aneurysms treated stent-assisted coiling.•A lower rate of perioperative complications in the treatment within 24 h.•The LVIS stent achieved a high complete aneurysm occlusion.•Clinical outcomes and angiographic results did not differ between the treatment of 24 h and that between 25−72 h. Stent-assisted coiling is increasingly used in the treatment of acutely ruptured intracranial aneurysms. However, the optimal timing of the stent-assisted coiling remains unknown. We aimed to investigate the safety and efficacy of the Low Profile Visualized Intraluminal Support (LVIS) stent for ruptured aneurysms treatment within 24 h comparing to the treatment between 25 and 72 h of symptom onset. We conducted a multicenter retrospective study on 110 consecutive patients with ruptured intracranial aneurysms. These patients were treated with LVIS stent within 72 h in four tertiary hospitals between January 2017 and December 2017. The timing of treatment was grouped into the treatment within 24 h and the treatment between 25 and 72 h. Baseline characteristics, periprocedural complications, angiographic results, and clinical outcomes were compared between the two groups. A total of 101 patients were included. 49 (48.5 %) patients were treated within 24 h and 52 (51.5 %) within between 25 and 72 h. Periprocedural complications occurred in 2 (4.1 %) patients treated within 24 h compared with those in 10 (19.2 %) treated between 25−72 h (P = 0.032). No early rebleeding occurred in both groups. 45 (91.8 %) of 49 aneurysms had complete occlusion on immediate angiography compared with 46 (88.5 %) of 52 aneurysms had complete occlusion. 2 (2.0 %) aneurysms were retreated. The clinical outcomes and angiographic results did not differ between the two groups. The LVIS stent-assisted coiling may be safe and effective in the treatment of selected patients with ruptured aneurysms within 24 h of symptom onset.</description><identifier>ISSN: 0303-8467</identifier><identifier>EISSN: 1872-6968</identifier><identifier>DOI: 10.1016/j.clineuro.2020.106117</identifier><identifier>PMID: 32745790</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Aneurysm ; Aneurysms ; Angiography ; Blood clots ; Clinical outcomes ; Coiling ; Complications ; Endovascular coiling ; Hemorrhage ; Implants ; Ischemia ; Medical imaging ; Neurology ; Occlusion ; Patients ; Prognosis ; Ruptured intracranial aneurysm ; Statistical analysis ; Stent-assisted coiling ; Stents</subject><ispartof>Clinical neurology and neurosurgery, 2020-10, Vol.197, p.106117-106117, Article 106117</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><rights>2020. Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-a927da65ed3c387916b135a16c159ada208580b0ff72e561f01a3e43382d5ef63</citedby><cites>FETCH-LOGICAL-c396t-a927da65ed3c387916b135a16c159ada208580b0ff72e561f01a3e43382d5ef63</cites><orcidid>0000-0002-2341-1959</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2449454394?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32745790$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xianggan</creatorcontrib><creatorcontrib>Xing, Haixia</creatorcontrib><creatorcontrib>Cai, Jing</creatorcontrib><creatorcontrib>Jin, Dianshi</creatorcontrib><creatorcontrib>Chen, Yongchun</creatorcontrib><creatorcontrib>Cui, Yudi</creatorcontrib><creatorcontrib>Ding, Shenghao</creatorcontrib><creatorcontrib>Wan, Jieqing</creatorcontrib><creatorcontrib>Pan, Yaohua</creatorcontrib><creatorcontrib>Mao, Guohua</creatorcontrib><creatorcontrib>Zhao, Bing</creatorcontrib><title>The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study</title><title>Clinical neurology and neurosurgery</title><addtitle>Clin Neurol Neurosurg</addtitle><description>•A multicenter cohort of patients with acutely ruptured intracranial aneurysms treated stent-assisted coiling.•A lower rate of perioperative complications in the treatment within 24 h.•The LVIS stent achieved a high complete aneurysm occlusion.•Clinical outcomes and angiographic results did not differ between the treatment of 24 h and that between 25−72 h. Stent-assisted coiling is increasingly used in the treatment of acutely ruptured intracranial aneurysms. However, the optimal timing of the stent-assisted coiling remains unknown. We aimed to investigate the safety and efficacy of the Low Profile Visualized Intraluminal Support (LVIS) stent for ruptured aneurysms treatment within 24 h comparing to the treatment between 25 and 72 h of symptom onset. We conducted a multicenter retrospective study on 110 consecutive patients with ruptured intracranial aneurysms. These patients were treated with LVIS stent within 72 h in four tertiary hospitals between January 2017 and December 2017. The timing of treatment was grouped into the treatment within 24 h and the treatment between 25 and 72 h. Baseline characteristics, periprocedural complications, angiographic results, and clinical outcomes were compared between the two groups. A total of 101 patients were included. 49 (48.5 %) patients were treated within 24 h and 52 (51.5 %) within between 25 and 72 h. Periprocedural complications occurred in 2 (4.1 %) patients treated within 24 h compared with those in 10 (19.2 %) treated between 25−72 h (P = 0.032). No early rebleeding occurred in both groups. 45 (91.8 %) of 49 aneurysms had complete occlusion on immediate angiography compared with 46 (88.5 %) of 52 aneurysms had complete occlusion. 2 (2.0 %) aneurysms were retreated. The clinical outcomes and angiographic results did not differ between the two groups. The LVIS stent-assisted coiling may be safe and effective in the treatment of selected patients with ruptured aneurysms within 24 h of symptom onset.</description><subject>Aneurysm</subject><subject>Aneurysms</subject><subject>Angiography</subject><subject>Blood clots</subject><subject>Clinical outcomes</subject><subject>Coiling</subject><subject>Complications</subject><subject>Endovascular coiling</subject><subject>Hemorrhage</subject><subject>Implants</subject><subject>Ischemia</subject><subject>Medical imaging</subject><subject>Neurology</subject><subject>Occlusion</subject><subject>Patients</subject><subject>Prognosis</subject><subject>Ruptured intracranial aneurysm</subject><subject>Statistical analysis</subject><subject>Stent-assisted coiling</subject><subject>Stents</subject><issn>0303-8467</issn><issn>1872-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUtuFDEQhi0EIkPgCpElNmx68Kvd3ayIIh6RRmJBYGt57LLGo34MtjtR77gDB-FOnIQaJmHBhpWl8ld__VU_IRecrTnj-vV-7fo4wpymtWDiWNScN4_IireNqHSn28dkxSSTVat0c0ae5bxnjEmp26fkTIpG1U3HVuTHzQ5otgHKQu3oKYQQnXULnQIt-LX5ev2Z5gJjoWFKf0olgS3DsYJMmg9lTuBpHEuyLtkx2h6V0NmSh0zvYtnFkQr16_vP3TSn_IZe0mHuS3SoAIkmKGnKB3Al3qKTMvvlOXkSbJ_hxf17Tr68f3dz9bHafPpwfXW5qZzsdKlsJxpvdQ1eOtk2HddbLmvLteN1Z70VrK1btmUhNAJqzQPjVoKSshW-hqDlOXl10j2k6dsMuZghZgd9j_anORuh8H4NqjBEX_6D7nGZEd0hpTpVK9kppPSJcrhSThDMIcXBpsVwZo6xmb15iM0cYzOn2LDx4l5-3g7g_7Y95ITA2xMAeI_bCMlkF2F04GPC0xk_xf_N-A0m_q7-</recordid><startdate>202010</startdate><enddate>202010</enddate><creator>Wang, Xianggan</creator><creator>Xing, Haixia</creator><creator>Cai, Jing</creator><creator>Jin, Dianshi</creator><creator>Chen, Yongchun</creator><creator>Cui, Yudi</creator><creator>Ding, Shenghao</creator><creator>Wan, Jieqing</creator><creator>Pan, Yaohua</creator><creator>Mao, Guohua</creator><creator>Zhao, Bing</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2341-1959</orcidid></search><sort><creationdate>202010</creationdate><title>The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study</title><author>Wang, Xianggan ; Xing, Haixia ; Cai, Jing ; Jin, Dianshi ; Chen, Yongchun ; Cui, Yudi ; Ding, Shenghao ; Wan, Jieqing ; Pan, Yaohua ; Mao, Guohua ; Zhao, Bing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-a927da65ed3c387916b135a16c159ada208580b0ff72e561f01a3e43382d5ef63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aneurysm</topic><topic>Aneurysms</topic><topic>Angiography</topic><topic>Blood clots</topic><topic>Clinical outcomes</topic><topic>Coiling</topic><topic>Complications</topic><topic>Endovascular coiling</topic><topic>Hemorrhage</topic><topic>Implants</topic><topic>Ischemia</topic><topic>Medical imaging</topic><topic>Neurology</topic><topic>Occlusion</topic><topic>Patients</topic><topic>Prognosis</topic><topic>Ruptured intracranial aneurysm</topic><topic>Statistical analysis</topic><topic>Stent-assisted coiling</topic><topic>Stents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xianggan</creatorcontrib><creatorcontrib>Xing, Haixia</creatorcontrib><creatorcontrib>Cai, Jing</creatorcontrib><creatorcontrib>Jin, Dianshi</creatorcontrib><creatorcontrib>Chen, Yongchun</creatorcontrib><creatorcontrib>Cui, Yudi</creatorcontrib><creatorcontrib>Ding, Shenghao</creatorcontrib><creatorcontrib>Wan, Jieqing</creatorcontrib><creatorcontrib>Pan, Yaohua</creatorcontrib><creatorcontrib>Mao, Guohua</creatorcontrib><creatorcontrib>Zhao, Bing</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical neurology and neurosurgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xianggan</au><au>Xing, Haixia</au><au>Cai, Jing</au><au>Jin, Dianshi</au><au>Chen, Yongchun</au><au>Cui, Yudi</au><au>Ding, Shenghao</au><au>Wan, Jieqing</au><au>Pan, Yaohua</au><au>Mao, Guohua</au><au>Zhao, Bing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study</atitle><jtitle>Clinical neurology and neurosurgery</jtitle><addtitle>Clin Neurol Neurosurg</addtitle><date>2020-10</date><risdate>2020</risdate><volume>197</volume><spage>106117</spage><epage>106117</epage><pages>106117-106117</pages><artnum>106117</artnum><issn>0303-8467</issn><eissn>1872-6968</eissn><abstract>•A multicenter cohort of patients with acutely ruptured intracranial aneurysms treated stent-assisted coiling.•A lower rate of perioperative complications in the treatment within 24 h.•The LVIS stent achieved a high complete aneurysm occlusion.•Clinical outcomes and angiographic results did not differ between the treatment of 24 h and that between 25−72 h. Stent-assisted coiling is increasingly used in the treatment of acutely ruptured intracranial aneurysms. However, the optimal timing of the stent-assisted coiling remains unknown. We aimed to investigate the safety and efficacy of the Low Profile Visualized Intraluminal Support (LVIS) stent for ruptured aneurysms treatment within 24 h comparing to the treatment between 25 and 72 h of symptom onset. We conducted a multicenter retrospective study on 110 consecutive patients with ruptured intracranial aneurysms. These patients were treated with LVIS stent within 72 h in four tertiary hospitals between January 2017 and December 2017. The timing of treatment was grouped into the treatment within 24 h and the treatment between 25 and 72 h. Baseline characteristics, periprocedural complications, angiographic results, and clinical outcomes were compared between the two groups. A total of 101 patients were included. 49 (48.5 %) patients were treated within 24 h and 52 (51.5 %) within between 25 and 72 h. Periprocedural complications occurred in 2 (4.1 %) patients treated within 24 h compared with those in 10 (19.2 %) treated between 25−72 h (P = 0.032). No early rebleeding occurred in both groups. 45 (91.8 %) of 49 aneurysms had complete occlusion on immediate angiography compared with 46 (88.5 %) of 52 aneurysms had complete occlusion. 2 (2.0 %) aneurysms were retreated. The clinical outcomes and angiographic results did not differ between the two groups. The LVIS stent-assisted coiling may be safe and effective in the treatment of selected patients with ruptured aneurysms within 24 h of symptom onset.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32745790</pmid><doi>10.1016/j.clineuro.2020.106117</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-2341-1959</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0303-8467
ispartof Clinical neurology and neurosurgery, 2020-10, Vol.197, p.106117-106117, Article 106117
issn 0303-8467
1872-6968
language eng
recordid cdi_proquest_miscellaneous_2430370850
source Elsevier ScienceDirect Journals Complete; ProQuest Central UK/Ireland
subjects Aneurysm
Aneurysms
Angiography
Blood clots
Clinical outcomes
Coiling
Complications
Endovascular coiling
Hemorrhage
Implants
Ischemia
Medical imaging
Neurology
Occlusion
Patients
Prognosis
Ruptured intracranial aneurysm
Statistical analysis
Stent-assisted coiling
Stents
title The safety and efficacy of the LVIS stent for the treatment of ruptured intracranial aneurysms within 24 hours: A multicenter retrospective study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T07%3A21%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20safety%20and%20efficacy%20of%20the%20LVIS%20stent%20for%20the%20treatment%20of%20ruptured%20intracranial%20aneurysms%20within%2024%E2%80%AFhours:%20A%20multicenter%20retrospective%20study&rft.jtitle=Clinical%20neurology%20and%20neurosurgery&rft.au=Wang,%20Xianggan&rft.date=2020-10&rft.volume=197&rft.spage=106117&rft.epage=106117&rft.pages=106117-106117&rft.artnum=106117&rft.issn=0303-8467&rft.eissn=1872-6968&rft_id=info:doi/10.1016/j.clineuro.2020.106117&rft_dat=%3Cproquest_cross%3E2449454394%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2449454394&rft_id=info:pmid/32745790&rft_els_id=S0303846720304601&rfr_iscdi=true