TY - JOUR
T1 - First Report of Edge Vascular Response at 12 Months of Magmaris, A Second-Generation Drug-Eluting Resorbable Magnesium Scaffold, Assessed by Grayscale Intravascular Ultrasound, Virtual Histology, and Optical Coherence Tomography. A Biosolve-II Trial Sub-Study
AU - Hideo-Kajita, Alexandre
AU - Garcia-Garcia, Hector M.
AU - Haude, Michael
AU - Joner, Michael
AU - Koolen, Jacques
AU - Ince, Hüseyin
AU - Abizaid, Alexandre
AU - Toelg, Ralph
AU - Lemos, Pedro A.
AU - von Birgelen, Clemens
AU - Christiansen, Evald Høj
AU - Wijns, William
AU - Neumann, Franz Josef
AU - Kaiser, Christoph
AU - Eeckhout, Eric
AU - Teik, Lim Soo
AU - Escaned, Javier
AU - Azizi, Viana
AU - Kuku, Kayode O.
AU - Ozaki, Yuichi
AU - Dan, Kazuhiro
AU - Waksman, Ron
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Introduction and objective: The edge vascular response (EVR)remains unknown in second generation drug-eluting Resorbable Magnesium Scaffold (RMS), such as Magmaris. The aim of the study was to evaluate tissue modifications in the RMS edges over time, assessed by different invasive imaging modalities. Methods: The patients treated with the device were assessed by optical coherence tomography (OCT), grayscale intravascular ultrasound (IVUS), and virtual histology IVUS at baseline and 12 months. The EVR study performed a segment- and frame-level analysis of the 5 mm segments proximal and distal of the actual RMS. Results: The segment-level grayscale IVUS (n = 10), virtual histology IVUS (n = 10), and OCT (n = 18)analysis did not show any significant changes after 12 months, except for a fibrous plaque area (FPA)reduction of 0.5mm 2 (p = 0.017)in the proximal segment compared to baseline. In the frame-level analysis, IVUS evaluation revealed a vessel area decreased 2.80 ± 1.43 mm 2 (p = 0.012)and 2.49 ± 1.53 mm 2 (p = 0.022)in 2 proximal frames. This was accompanied by plaque area reduction of 0.88 ± 0.70 mm 2 (p = 0.048)and a FPA decreased by 0.63 ± 0.48 mm 2 (p = 0.004)in one proximal frame. In 1 distal frame, there was a dense calcium area reduction of 0.10 ± 0.12 mm 2 (p = 0.045), FPA and fibrous fatty plaque increased 0.54 ± 0.53 mm 2 (p = 0.023)and 0.17 ± 0.16 mm 2 (p = 0.016), respectively. By OCT, there was a lumen area decrease of 0.76 ± 1.51 mm 2 (p = 0.045)in a distal frame. Conclusion: At 12 months, Magmaris EVR assessment does not show overall significant changes, except for a fibrous plaque area reduction in the proximal segment. This could be translated as a benign healing process at the edges of the RMS. The edge vascular response (EVR)remains unknown in second generation drug-eluting absorbable metal scaffolds (RMS), such as Magmaris. Patients treated with the device were assessed by multi invasive imaging modalities [i.e. optical coherence tomography (OCT), grayscale intravascular ultrasound (IVUS), and virtual histology IVUS]evaluating the tissue changes over time in the segment- and frame-level analysis of the 5 mm segments proximal and distal of the actual RMS. As a result, after 12 months, Magmaris EVR assessment does not show overall significant changes, except for a fibrous plaque area reduction in the proximal segment, translating a benign healing process at the edges of the RMS.
AB - Introduction and objective: The edge vascular response (EVR)remains unknown in second generation drug-eluting Resorbable Magnesium Scaffold (RMS), such as Magmaris. The aim of the study was to evaluate tissue modifications in the RMS edges over time, assessed by different invasive imaging modalities. Methods: The patients treated with the device were assessed by optical coherence tomography (OCT), grayscale intravascular ultrasound (IVUS), and virtual histology IVUS at baseline and 12 months. The EVR study performed a segment- and frame-level analysis of the 5 mm segments proximal and distal of the actual RMS. Results: The segment-level grayscale IVUS (n = 10), virtual histology IVUS (n = 10), and OCT (n = 18)analysis did not show any significant changes after 12 months, except for a fibrous plaque area (FPA)reduction of 0.5mm 2 (p = 0.017)in the proximal segment compared to baseline. In the frame-level analysis, IVUS evaluation revealed a vessel area decreased 2.80 ± 1.43 mm 2 (p = 0.012)and 2.49 ± 1.53 mm 2 (p = 0.022)in 2 proximal frames. This was accompanied by plaque area reduction of 0.88 ± 0.70 mm 2 (p = 0.048)and a FPA decreased by 0.63 ± 0.48 mm 2 (p = 0.004)in one proximal frame. In 1 distal frame, there was a dense calcium area reduction of 0.10 ± 0.12 mm 2 (p = 0.045), FPA and fibrous fatty plaque increased 0.54 ± 0.53 mm 2 (p = 0.023)and 0.17 ± 0.16 mm 2 (p = 0.016), respectively. By OCT, there was a lumen area decrease of 0.76 ± 1.51 mm 2 (p = 0.045)in a distal frame. Conclusion: At 12 months, Magmaris EVR assessment does not show overall significant changes, except for a fibrous plaque area reduction in the proximal segment. This could be translated as a benign healing process at the edges of the RMS. The edge vascular response (EVR)remains unknown in second generation drug-eluting absorbable metal scaffolds (RMS), such as Magmaris. Patients treated with the device were assessed by multi invasive imaging modalities [i.e. optical coherence tomography (OCT), grayscale intravascular ultrasound (IVUS), and virtual histology IVUS]evaluating the tissue changes over time in the segment- and frame-level analysis of the 5 mm segments proximal and distal of the actual RMS. As a result, after 12 months, Magmaris EVR assessment does not show overall significant changes, except for a fibrous plaque area reduction in the proximal segment, translating a benign healing process at the edges of the RMS.
KW - Edge vascular response
KW - Grayscale intravascular ultrasound
KW - Magmaris
KW - Optical coherence tomography
KW - Virtual histology
UR - http://www.scopus.com/inward/record.url?scp=85065170289&partnerID=8YFLogxK
U2 - 10.1016/j.carrev.2019.02.019
DO - 10.1016/j.carrev.2019.02.019
M3 - Article
C2 - 31079817
AN - SCOPUS:85065170289
VL - 20
SP - 392
EP - 398
JO - Cardiovascular Revascularization Medicine
JF - Cardiovascular Revascularization Medicine
SN - 1553-8389
IS - 5
ER -