One-year outcomes of the U.S. and Japanese regulatory trial of the Misago stent for treatment of superficial femoral artery disease (OSPREY study)

The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease. The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between...

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Published inJournal of vascular surgery Vol. 63; no. 2; pp. 370 - 376.e1
Main Authors Ohki, Takao, Angle, John F., Yokoi, Hiroyoshi, Jaff, Michael R., Popma, Jeffrey, Piegari, Guy, Kanaoka, Yuji, Angle, J. Fritz, Feiring, Andrew, Nelson, Brian, Glickman, Marc, Guimaraes, Marcelo, Hall, Patrick, Johnson, Sarah, Jordan, William, Khoudoud, Omran, Leung, Daniel, McGarvey, Joseph, McKinsey, James, Nowygrod, Roman, Shammas, Nicolas, Carey, Daniel, Iyengar, Srinivas, Isenbarger, Daniel, Ali, Vaqar, Ashchi, Majdi, Rivera, Ernesto, Moursi, Mohammed, Bachinsky, William, Metzger, Christopher, Aronow, Herbert, Wiechmann, Bret, Callicutt, Christopher, Gordon, Ian, Chaille, Peter, Espinoza, Andrey, Foster, Malcolm, Sharafuddin, Mel, Shah, Rakesh, Bunch, Frank, Harlin, Stuart, Iwabuchi, Masashi, Ando, Kenji, Kichikawa, Kimihiko, Muramatsu, Toshiya, Urasawa, Kazushi, Yokoi, Yoshiaki, Uematsu, Masaaki, Lo, Ping-Han, Huang, Chi-Hung, Kao, Hsien-Li, Jae, HwanJun
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.02.2016
Subjects
Online AccessGet full text
ISSN0741-5214
1097-6809
1097-6809
DOI10.1016/j.jvs.2015.08.093

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Abstract The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease. The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial. The Misago stent was implanted in 261subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P = .829), stent fracture rate (1.3% vs 0.0%; P = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P = 1.000). OSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.
AbstractList The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease.OBJECTIVEThe purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease.The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial.METHODSThe safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial.The Misago stent was implanted in 261 subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P = .829), stent fracture rate (1.3% vs 0.0%; P = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P = 1.000).RESULTSThe Misago stent was implanted in 261 subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P = .829), stent fracture rate (1.3% vs 0.0%; P = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P = 1.000).OSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.CONCLUSIONSOSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.
The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease. The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial. The Misago stent was implanted in 261subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P = .829), stent fracture rate (1.3% vs 0.0%; P = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P = 1.000). OSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.
The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease. The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial. The Misago stent was implanted in 261 subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P = .829), stent fracture rate (1.3% vs 0.0%; P = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P = 1.000). OSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.
Objective The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral artery (SFA) disease. Methods The safety and efficacy of the Misago SFA stent were evaluated prospectively in this initial collaboration trial between Japan and the United States. Because this trial enrolled patients mainly from Japan and the United States and because there is a question as to whether a race difference exists in SFA stent performance, the race difference on outcome was also analyzed. In addition, results were compared with a prior SFA stent trial. Results The Misago stent was implanted in 261subjects with TransAtlantic Inter-Society Consensus (TASC) type A and type B SFA lesions (201 subjects in the United States, 50 in Japan, 9 in Taiwan, 1 in South Korea). The mean age of the patients was 69.3 ± 10.0 years, and the mean lesion length was 83.8 ± 41.3 mm. The overall 12-month primary patency rate and clinically driven target lesion revascularization were 82.9% and 13.0%, respectively. Regional differences within the Occlusive/Stenotic Peripheral Artery Revascularization Study (OSPREY) and outcomes between U.S. and Asian patients were similar, including primary patency (82.9% vs 83.0%; P  = .889), clinically driven target lesion revascularization (13.4% vs 11.7%; P  = .829), stent fracture rate (1.3% vs 0.0%; P  = 1.000), and stent thrombosis rate (0.5% vs 0.0%; P  = 1.000). Conclusions OSPREY 12-month data showed satisfactory outcome of the Misago stent for the treatment of TASC type A and type B SFA lesions and appears to be comparable to recent stent trials. In addition, the lack of difference in outcome among races supports the value of international trials.
Author McKinsey, James
Rivera, Ernesto
Yokoi, Hiroyoshi
McGarvey, Joseph
Bachinsky, William
Aronow, Herbert
Piegari, Guy
Wiechmann, Bret
Sharafuddin, Mel
Ohki, Takao
Foster, Malcolm
Angle, J. Fritz
Jae, HwanJun
Ando, Kenji
Muramatsu, Toshiya
Angle, John F.
Johnson, Sarah
Nowygrod, Roman
Metzger, Christopher
Jaff, Michael R.
Hall, Patrick
Isenbarger, Daniel
Moursi, Mohammed
Popma, Jeffrey
Iyengar, Srinivas
Nelson, Brian
Yokoi, Yoshiaki
Leung, Daniel
Callicutt, Christopher
Guimaraes, Marcelo
Espinoza, Andrey
Lo, Ping-Han
Carey, Daniel
Shammas, Nicolas
Khoudoud, Omran
Iwabuchi, Masashi
Ashchi, Majdi
Shah, Rakesh
Urasawa, Kazushi
Harlin, Stuart
Uematsu, Masaaki
Jordan, William
Kao, Hsien-Li
Kichikawa, Kimihiko
Glickman, Marc
Huang, Chi-Hung
Gordon, Ian
Bunch, Frank
Ali, Vaqar
Kanaoka, Yuji
Chaille, Peter
Feiring, Andrew
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ContentType Journal Article
Contributor Leung, Daniel
McKinsey, James
Callicutt, Christopher
Rivera, Ernesto
Guimaraes, Marcelo
McGarvey, Joseph
Espinoza, Andrey
Lo, Ping-Han
Carey, Daniel
Shammas, Nicolas
Angle, J Fritz
Bachinsky, William
Aronow, Herbert
Piegari, Guy
Wiechmann, Bret
Sharafuddin, Mel
Khoudoud, Omran
Iwabuchi, Masashi
Ohki, Takao
Ashchi, Majdi
Foster, Malcolm
Jae, HwanJun
Ando, Kenji
Shah, Rakesh
Muramatsu, Toshiya
Urasawa, Kazushi
Harlin, Stuart
Johnson, Sarah
Nowygrod, Roman
Metzger, Christopher
Uematsu, Masaaki
Jordan, William
Kao, Hsien-Li
Kichikawa, Kimihiko
Hall, Patrick
Isenbarger, Daniel
Glickman, Marc
Huang, Chi-Hung
Gordon, Ian
Bunch, Frank
Moursi, Mohammed
Ali, Vaqar
Iyengar, Srinivas
Nelson, Brian
Chaille, Peter
Feiring, Andrew
Yokoi, Yoshiaki
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Snippet The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial femoral...
Objective The purpose of this study was to assess the safety and efficacy of the Misago stent (Terumo Corp, Tokyo, Japan) in occlusive and stenotic superficial...
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SubjectTerms Aged
Constriction, Pathologic
Endovascular Procedures - adverse effects
Endovascular Procedures - instrumentation
Female
Femoral Artery - physiopathology
Humans
Japan - epidemiology
Male
Middle Aged
Peripheral Arterial Disease - diagnosis
Peripheral Arterial Disease - ethnology
Peripheral Arterial Disease - physiopathology
Peripheral Arterial Disease - therapy
Prospective Studies
Prosthesis Design
Prosthesis Failure
Republic of Korea
Risk Factors
Stents
Surgery
Taiwan
Thrombosis - etiology
Time Factors
Treatment Outcome
United States - epidemiology
Vascular Patency
Title One-year outcomes of the U.S. and Japanese regulatory trial of the Misago stent for treatment of superficial femoral artery disease (OSPREY study)
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https://dx.doi.org/10.1016/j.jvs.2015.08.093
https://www.ncbi.nlm.nih.gov/pubmed/26483003
https://www.proquest.com/docview/1760921121
Volume 63
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