TY - JOUR
T1 - Long-Term Outcomes of a Japanese Prospective Multicenter Registry Using a Heparin-Bonded Expanded Polytetrafluoroethylene Graft for Above-the-Knee Femoropopliteal Bypasses
AU - Japanese Bypass Registry Group
AU - Fujimura, Naoki
AU - Obara, Hideaki
AU - Matsubara, Kentaro
AU - Toya, Naoki
AU - Isogai, Naoko
AU - Ogino, Hidemitsu
AU - Fujii, Taku
AU - Kudo, Toshifumi
AU - Kanaoka, Yuji
AU - Harada, Hirohisa
AU - Uchiyama, Hidetoshi
AU - Guntani, Atsushi
AU - Shimogawara, Tatsuya
AU - Watada, Susumu
AU - Shibutani, Shintaro
AU - Ohki, Takao
N1 - Publisher Copyright:
© 2024 Japanese Circulation Society. All rights reserved.
PY - 2024/10
Y1 - 2024/10
N2 - Background: Despite the widespread use of PROPATEN®, a bioactive heparin-bonded expanded polytetrafluoroethylene graft, in bypass surgery, there are only a few reports of long-term results. We evaluated the long-term results of PROPATEN® use for above-knee femoropopliteal bypass (AKFPB). Methods and Results: After PROPATEN®-based AKFPB, patients were prospectively registered at 20 Japanese institutions between July 2014 and October 2017 to evaluate long-term results. During the median follow-up of 76 months (interquartile range 36–88 months) for 120 limbs (in 113 patients; mean [±SD] age 72.7±8.1 years; 66.7% male; ankle-brachial index [ABI] 0.45±0.27; lesion length 26.2±5.7 cm; chronic limb-threatening ischemia in 45 limbs), there were 8 major amputations; however, clinical improvement was sustained (mean [±SD] ABI 0.87±0.23) and the Rutherford classification grade improved in 105 (87.5%) limbs at the latest follow-up. At 8 years, the primary patency, freedom from target-lesion revascularization, secondary patency, survival, and amputation-free survival, as estimated by the Kaplan-Meier method, were 66.3±4.8%, 71.5±4.4%, 86.5±3.4%, 53.1±5.0%, and 47.4±5.3%, respectively. Conclusions: This multicenter prospective registry-based analysis showed sustained excellent clinical improvement and secondary patency for up to 8 years following PROPATEN®-based AKFPB. PROPATEN® constitutes a durable and good revascularization option for complex superficial femoral artery lesions, especially when endovascular treatment is inappropriate or an adequate venous conduit is unavailable.
AB - Background: Despite the widespread use of PROPATEN®, a bioactive heparin-bonded expanded polytetrafluoroethylene graft, in bypass surgery, there are only a few reports of long-term results. We evaluated the long-term results of PROPATEN® use for above-knee femoropopliteal bypass (AKFPB). Methods and Results: After PROPATEN®-based AKFPB, patients were prospectively registered at 20 Japanese institutions between July 2014 and October 2017 to evaluate long-term results. During the median follow-up of 76 months (interquartile range 36–88 months) for 120 limbs (in 113 patients; mean [±SD] age 72.7±8.1 years; 66.7% male; ankle-brachial index [ABI] 0.45±0.27; lesion length 26.2±5.7 cm; chronic limb-threatening ischemia in 45 limbs), there were 8 major amputations; however, clinical improvement was sustained (mean [±SD] ABI 0.87±0.23) and the Rutherford classification grade improved in 105 (87.5%) limbs at the latest follow-up. At 8 years, the primary patency, freedom from target-lesion revascularization, secondary patency, survival, and amputation-free survival, as estimated by the Kaplan-Meier method, were 66.3±4.8%, 71.5±4.4%, 86.5±3.4%, 53.1±5.0%, and 47.4±5.3%, respectively. Conclusions: This multicenter prospective registry-based analysis showed sustained excellent clinical improvement and secondary patency for up to 8 years following PROPATEN®-based AKFPB. PROPATEN® constitutes a durable and good revascularization option for complex superficial femoral artery lesions, especially when endovascular treatment is inappropriate or an adequate venous conduit is unavailable.
KW - Above-the-knee femoropopliteal bypass
KW - Bioactive heparin-bonded expanded polytetrafluoroethylene graft
KW - Lower extremity arterial disease
KW - PROPATEN
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UR - http://www.scopus.com/inward/citedby.url?scp=85198836217&partnerID=8YFLogxK
U2 - 10.1253/circj.CJ-24-0135
DO - 10.1253/circj.CJ-24-0135
M3 - Article
C2 - 38616124
AN - SCOPUS:85198836217
SN - 1346-9843
VL - 88
SP - 1656
EP - 1663
JO - Circulation Journal
JF - Circulation Journal
IS - 10
ER -