Second-generation Magnesium Scaffold Magmaris, Device Design, and Preclinical Evaluation in a Porcine Coronary Artery Model. (Record no. 2144)

MARC details
000 -LEADER
fixed length control field 02528nam a22003017a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170428s20172017 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1774-024X
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 28262623
245 ## - TITLE STATEMENT
Title Second-generation Magnesium Scaffold Magmaris, Device Design, and Preclinical Evaluation in a Porcine Coronary Artery Model.
251 ## - Source
Source Eurointervention. , 2017 Mar 07
252 ## - Abbreviated Source
Abbreviated source EuroIntervention. , 2017 Mar 07
253 ## - Journal Name
Journal name EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2017
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Manufacturer FY2017
266 ## - Date added to catalog
Date added to catalog 2017-05-06
520 ## - SUMMARY, ETC.
Abstract AIMS: The second-generation drug-eluting absorbable magnesium scaffold Magmaris, recently introduced for treatment of obstructive coronary atherosclerotic lesions, suggests a good safety profile, but preclinical assessment is important for predicting clinical performance.
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Abstract CONCLUSIONS: Preclinical results suggest Magmaris has a favourable safety profile with advanced healing relative to benchmark, low acute thrombogenicity, and absence of excessive lumen loss up to 2 years and support clinical application of Magmaris for human use.
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Abstract METHODS AND RESULTS: Ninety Magmaris scaffolds were implanted into non-diseased porcine and rabbit models. A bioresorbable vascular scaffold (Absorb) and the permanent drugeluting stent (Xience Xpedition) served as controls. Scanning electron microscopy showed increased endothelialisation and decreased thrombus formation at 3 and 28 days in the Magmaris group compared with the Absorb group. In the Xience group, inflammation exceeded the level in the Magmaris group at 365 and 720 days. Neointimal growth was greater in the Magmaris group than in the Xience group. Late lumen loss decreased over time in both groups. Optical coherence tomography (OCT) showed stable luminal dimensions in both the Magmaris and Xience groups. Pharmacokinetic studies demonstrated a retarded elution profile in the Magmaris group with 69.4 % of sirolimus released at 90 days.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Heart & Vascular Institute
657 ## - INDEX TERM--FUNCTION
Medline publication type Journal Article
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors Waksman, Ron
790 ## - Authors
All authors Haude M, Joner M, Lapointe-Corriveau C, Leclerc G, Pritsch M, Waksman R, Wittchow E, Zumstein P
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.4244/EIJ-D-16-00915">https://dx.doi.org/10.4244/EIJ-D-16-00915</a>
Public note https://dx.doi.org/10.4244/EIJ-D-16-00915
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 05/06/2017   28262623 28262623 05/06/2017 05/06/2017 Journal Article

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