Drug-Coated Balloons for Dysfunctional Dialysis Arteriovenous Fistulas

التفاصيل البيبلوغرافية
العنوان: Drug-Coated Balloons for Dysfunctional Dialysis Arteriovenous Fistulas
المؤلفون: Robert A. Lookstein, Stephanie Cihlar, Ido Weinberg, Kenneth Ouriel, Andrew Holden, In.Pact Av Access Investigators, Hiroaki Haruguchi, Lanyu Lei
المصدر: The New England journal of medicine. 383(8)
سنة النشر: 2020
مصطلحات موضوعية: Male, medicine.medical_specialty, Percutaneous, Drug coated balloon, Paclitaxel, medicine.medical_treatment, Dysfunctional family, Constriction, Pathologic, 030204 cardiovascular system & hematology, law.invention, Upper Extremity, 03 medical and health sciences, 0302 clinical medicine, Arteriovenous Shunt, Surgical, Randomized controlled trial, Coated Materials, Biocompatible, law, Renal Dialysis, Angioplasty, medicine, Vascular Patency, Humans, Single-Blind Method, 030212 general & internal medicine, Prospective Studies, Dialysis, Aged, business.industry, Cardiovascular Agents, General Medicine, Middle Aged, Surgery, Female, Hemodialysis, business, Angioplasty, Balloon, Vascular Access Devices
الوصف: Standard percutaneous transluminal angioplasty is the current recommended treatment for dysfunctional hemodialysis fistulas, yet long-term outcomes of this treatment are poor. Drug-coated balloons delivering the antirestenotic agent paclitaxel may improve outcomes.In this prospective, single-blinded, 1:1 randomized trial, we enrolled 330 participants at 29 international sites. Patients with new or restenotic lesions in native upper-extremity arteriovenous fistulas were eligible for participation. After successful high-pressure percutaneous transluminal angioplasty, participants were randomly assigned to receive treatment with a drug-coated balloon or a standard balloon. The primary effectiveness end point was target-lesion primary patency, defined as freedom from clinically driven target-lesion revascularization or access-circuit thrombosis during the 6 months after the index procedure. The primary safety end point, serious adverse events involving the arteriovenous access circuit within 30 days, was assessed in a noninferiority analysis (margin of noninferiority, 7.5 percentage points). The primary analyses included all participants with available end-point data. Additional sensitivity analyses were performed to assess the effect of missing data.A total of 330 participants underwent randomization; 170 were assigned to receive treatment with a drug-coated balloon, and 160 were assigned to receive treatment with a standard balloon. During the 6 months after the index procedure, target-lesion primary patency was maintained more often in participants who had been treated with a drug-coated balloon than in those who had been treated with a standard balloon (82.2% [125 of 152] vs. 59.5% [88 of 148]; difference in risk, 22.8 percentage points; 95% confidence interval [CI], 12.8 to 32.8; P0.001). Drug-coated balloons were noninferior to standard balloons with respect to the primary safety end point (4.2% [7 of 166] and 4.4% [7 of 158], respectively; difference in risk, -0.2 percentage points; 95% CI, -5.5 to 5.0; P = 0.002 for noninferiority). Sensitivity analyses confirmed the results of the primary analyses.Drug-coated balloon angioplasty was superior to standard angioplasty for the treatment of stenotic lesions in dysfunctional hemodialysis arteriovenous fistulas during the 6 months after the procedure and was noninferior with respect to access circuit-related serious adverse events within 30 days. (Funded by Medtronic; IN.PACT AV Access Study ClinicalTrials.gov number, NCT03041467.).
تدمد: 1533-4406
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26baa313c1443cfd094b8f58430eedf4
https://pubmed.ncbi.nlm.nih.gov/33761219
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....26baa313c1443cfd094b8f58430eedf4
قاعدة البيانات: OpenAIRE