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Randomized Controlled Trial of Acotec Drug-Eluting Balloon Versus Plain Balloon for Below-the-Knee Angioplasty.
Liistro, Francesco; Angioli, Paolo; Ventoruzzo, Giorgio; Ducci, Kenneth; Reccia, Matteo Rocco; Ricci, Lucia; Falsini, Giovanni; Scatena, Alessia; Pieroni, Maurizio; Bolognese, Leonardo.
Affiliation
  • Liistro F; Cardiovascular Department, San Donato Hospital, Arezzo, Italy. Electronic address: francescoliistro@hotmail.com.
  • Angioli P; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Ventoruzzo G; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Ducci K; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Reccia MR; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Ricci L; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Falsini G; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Scatena A; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Pieroni M; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
  • Bolognese L; Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
JACC Cardiovasc Interv ; 13(19): 2277-2286, 2020 10 12.
Article in En | MEDLINE | ID: mdl-32950416
OBJECTIVES: The aim of this study was to investigate the efficacy and safety of the Litos drug-coated balloon (DCB) versus plain old balloon angioplasty (POBA) for reduction of late lumen loss (LLL) in patients with critical limb ischemia undergoing below-the-knee (BTK) intervention. BACKGROUND: Restenosis after balloon angioplasty of BTK arteries approximates 70%. Previous studies of DCBs in BTK arteries produced conflicting results. METHODS: ACOART-BTK (Evaluation of the Use of ACOTEC Drug-Eluting Balloon Litos® in Below-the-Knee Arteries to Treat Critical Limb Ischemia) is a randomized controlled single-center study. Inclusion criteria were critical limb ischemia (Rutherford class ≥4) and significant stenosis or occlusion >40 mm of at least 1 BTK vessel with distal runoff successfully treated with angioplasty. Six-month angiographic LLL was the primary endpoint. Occlusive restenosis at 6 months and clinically driven target lesion revascularization at 12 months were secondary endpoints. RESULTS: From January 2016 through January 2019, 105 patients with 129 BTK lesions were enrolled in the study. Mean lesion length was 168 ± 109 mm in the DCB group and 187 ± 113 mm in the POBA group (p = 0.30). Almost 70% of lesions were occluded at baseline in both groups. On 6-month angiography, mean LLL was 0.51 ± 0.60 mm in the DCB group and 1.31 ± 0.72 mm in the POBA group (p < 0.001); rates of occlusive restenosis were 8.6% and 48.4%, respectively (p < 0.001). Twelve-month clinically driven target lesion revascularization occurred in 6 of 62 DCB-treated lesions (10%) versus 27 of 66 POBA-treated lesions (41%) (p < 0.001). Complete healing at 12 months was observed in 42 of 47 DCB-treated limbs (89.4) versus 35 of 47 POBA-treated limbs (74.5%) (p = 0.05); no major amputations occurred. CONCLUSIONS: Litos DCBs strikingly reduced LLL, vessel reocclusion, and clinically driven target lesion revascularization compared with POBA in BTK angioplasty.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angioplasty, Balloon / Drug-Eluting Stents / Peripheral Arterial Disease Type of study: Clinical_trials Limits: Humans Language: En Journal: JACC Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angioplasty, Balloon / Drug-Eluting Stents / Peripheral Arterial Disease Type of study: Clinical_trials Limits: Humans Language: En Journal: JACC Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2020 Type: Article