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dc.contributor.authorMcDougall, C. G.
dc.contributor.authorJohnston, S. Claiborne
dc.contributor.authorGholkar, A.
dc.contributor.authorBarnwell, S. L.
dc.contributor.authorVazquez Suarez, J. C.
dc.contributor.authorMasso Romero, J.
dc.contributor.authorChaloupka, J. C.
dc.contributor.authorBonafe, A.
dc.contributor.authorWakhloo, Ajay K.
dc.contributor.authorTampieri, D.
dc.contributor.authorDowd, C. F.
dc.contributor.authorFox, A. J.
dc.contributor.authorImm, S. J.
dc.contributor.authorCarroll, K.
dc.contributor.authorTurk, A. S.
dc.date2022-08-11T08:10:47.000
dc.date.accessioned2022-08-23T17:19:48Z
dc.date.available2022-08-23T17:19:48Z
dc.date.issued2014-05-01
dc.date.submitted2017-06-05
dc.identifier.citationAJNR Am J Neuroradiol. 2014 May;35(5):935-42. Epub 2014 Jan 30. <a href="https://doi.org/10.3174/ajnr.A3857">Link to article on publisher's site</a>
dc.identifier.issn0195-6108 (Linking)
dc.identifier.doi10.3174/ajnr.A3857
dc.identifier.pmid24481333
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48159
dc.description.abstractBACKGROUND AND PURPOSE: The ability of polymer-modified coils to promote stable aneurysm occlusion after endovascular treatment is not well-documented. Angiographic aneurysm recurrence is widely used as a surrogate for treatment failure, but studies documenting the correlation of angiographic recurrence with clinical failure are limited. This trial compares the effectiveness of Matrix(2) polyglycolic/polylactic acid biopolymer-modified coils with bare metal coils and correlates the angiographic findings with clinical failure (ie, target aneurysm recurrence), a composite end point that includes any incident of posttreatment aneurysm rupture, retreatment, or unexplained death. MATERIALS AND METHODS: This was a multicenter randomized noninferiority trial with blinded end point adjudication. We enrolled 626 patients, divided between Matrix(2) and bare metal coil groups. The primary outcome was target aneurysm recurrence at 12 +/- 3 months. RESULTS: At 455 days, at least 1 target aneurysm recurrence event had occurred in 14.6% of patients treated with bare metal coils and 13.3% of Matrix(2) (P = .76, log-rank test) patients; 92.8% of target aneurysm recurrence events were re-interventions for aneurysms that had not bled after treatment, and 5.8% of target aneurysm recurrence events resulted from hemorrhage or rehemorrhage, with or without retreatment. Symptomatic re-intervention occurred in only 4 (0.6%) patients. At 455 days, 95.8% of patients with unruptured aneurysms and 90.4% of those with ruptured aneurysms were independent (mRS ≤ 2). Target aneurysm recurrence was associated with incomplete initial angiographic aneurysm obliteration, presentation with rupture, and a larger aneurysmal dome and neck size. CONCLUSIONS: Tested Matrix(2) coils were not inferior to bare metal coils. Endovascular coiling of intracranial aneurysms was safe, and the rate of technical success was high. Target aneurysm recurrence is a promising clinical outcome measure that correlates well with established angiographic measurements.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=24481333&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.3174/ajnr.A3857
dc.subjectNervous System Diseases
dc.subjectNeurology
dc.subjectRadiology
dc.titleBioactive versus bare platinum coils in the treatment of intracranial aneurysms: the MAPS (Matrix and Platinum Science) trial
dc.typeJournal Article
dc.source.journaltitleAJNR. American journal of neuroradiology
dc.source.volume35
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/radiology_pubs/268
dc.identifier.contextkey10251729
html.description.abstract<p>BACKGROUND AND PURPOSE: The ability of polymer-modified coils to promote stable aneurysm occlusion after endovascular treatment is not well-documented. Angiographic aneurysm recurrence is widely used as a surrogate for treatment failure, but studies documenting the correlation of angiographic recurrence with clinical failure are limited. This trial compares the effectiveness of Matrix(2) polyglycolic/polylactic acid biopolymer-modified coils with bare metal coils and correlates the angiographic findings with clinical failure (ie, target aneurysm recurrence), a composite end point that includes any incident of posttreatment aneurysm rupture, retreatment, or unexplained death.</p> <p>MATERIALS AND METHODS: This was a multicenter randomized noninferiority trial with blinded end point adjudication. We enrolled 626 patients, divided between Matrix(2) and bare metal coil groups. The primary outcome was target aneurysm recurrence at 12 +/- 3 months.</p> <p>RESULTS: At 455 days, at least 1 target aneurysm recurrence event had occurred in 14.6% of patients treated with bare metal coils and 13.3% of Matrix(2) (P = .76, log-rank test) patients; 92.8% of target aneurysm recurrence events were re-interventions for aneurysms that had not bled after treatment, and 5.8% of target aneurysm recurrence events resulted from hemorrhage or rehemorrhage, with or without retreatment. Symptomatic re-intervention occurred in only 4 (0.6%) patients. At 455 days, 95.8% of patients with unruptured aneurysms and 90.4% of those with ruptured aneurysms were independent (mRS ≤ 2). Target aneurysm recurrence was associated with incomplete initial angiographic aneurysm obliteration, presentation with rupture, and a larger aneurysmal dome and neck size.</p> <p>CONCLUSIONS: Tested Matrix(2) coils were not inferior to bare metal coils. Endovascular coiling of intracranial aneurysms was safe, and the rate of technical success was high. Target aneurysm recurrence is a promising clinical outcome measure that correlates well with established angiographic measurements.</p>
dc.identifier.submissionpathradiology_pubs/268
dc.contributor.departmentDepartment of Radiology
dc.source.pages935-42


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