Arteriovenous fistula patency in the 3 years following vonapanitase and placebo treatment

被引:15
作者
Peden, Eric K. [1 ]
O'Connor, Timothy P. [2 ]
Browne, Barry J. [3 ]
Dixon, Bradley S. [4 ]
Schanzer, Andres S. [5 ]
Jensik, Stephen C. [6 ]
Sam, Albert D., II [7 ]
Burke, Steven K. [8 ]
机构
[1] Houston Methodist Hosp, Dept Cardiovasc Surg, Houston, TX USA
[2] Renal Care Associates, Peoria, IL USA
[3] Calif Inst Renal Res, San Diego, CA USA
[4] Univ Iowa Hosp & Clin, Dept Med, Iowa City, IA 52242 USA
[5] Univ Massachusetts, Sch Med, Div Vasc & Endovasc Surg, Worcester, MA USA
[6] Rush Univ, Med Ctr, Transplant Program, Chicago, IL 60612 USA
[7] Tulane Univ, Inst Heart & Vasc, New Orleans, LA 70118 USA
[8] Proteon Therapeut Inc, Res & Dev, Waltham, MA USA
关键词
I PANCREATIC ELASTASE; SMOOTH-MUSCLE CELLS; DIRECTED MIGRATION; HEMODIALYSIS; PEPTIDE; GRAFTS;
D O I
10.1016/j.jvs.2016.08.101
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: This study explored the long-term outcomes of arteriovenous fistulas treated with vonapanitase (recombinant human elastase) at the time of surgical creation. Methods: This was a randomized, double-blind, placebo-controlled trial of 151 patients undergoing radiocephalic or brachiocephalic arteriovenous fistula creation who were randomized equally to placebo, vonapanitase 10 mg, or vonapanitase 30 mg. The results after 1 year of follow-up were previously reported. The current analysis occurred when the last patient treated was observed for 3 years. For the current analysis, the primary end point was primary patency; the secondary end points included secondary patency, use of the fistula for hemodialysis, and rate of procedures to restore or to maintain patency. Results: There was no significant difference in the risk of primary patency loss with vonapanitase 10 mg or 30 mg vs placebo. When seven initial patency loss events related to cephalic arch and central vein balloon angioplasty were excluded, the risk of patency loss was reduced with vonapanitase overall (hazard ratio [HR], 0.63; P =.049) and 30 mg (HR, 0.51; P =.03). In patients with radiocephalic fistulas (n = 67), the risks of primary and secondary patency loss were reduced with 30 mg (HR, 0.37 [P =.02] and 0.24 [P =.046], respectively). The rate of procedures to restore or to maintain fistula patency was reduced with 30 mg vs placebo (0.23 vs 0.72 procedure days/patient/year; P =.03) and also reduced in patients with radiocephalic fistulas with 30 mg vs placebo (0.17 vs 0.85 procedure days/patient/year; P =.048). Conclusions: In this study, vonapanitase did not significantly improve primary patency in the primary analysis but did significantly improve primary patency in an analysis that excluded patency loss due to cephalic arch and central vein balloon angioplasty. In patients with radiocephalic fistulas, 30 mg significantly improved primary and secondary patency. Vonapanitase 30 mg decreased the rate of procedures to restore or to maintain patency in the analysis that included all patients and in the subset with radiocephalic fistulas.
引用
收藏
页码:1113 / 1120
页数:8
相关论文
共 19 条
[1]   Increasing arteriovenous fistulas in hemodialysis patients: Problems and solutions [J].
Allon, M ;
Robbin, ML .
KIDNEY INTERNATIONAL, 2002, 62 (04) :1109-1124
[2]   In vivo vascular engineering of vein grafts: Directed migration of smooth muscle cells by perivascular release of elastase limits neointimal proliferation [J].
Amabile, PG ;
Wong, H ;
Uy, M ;
Boroumand, S ;
Elkins, CJ ;
Yuksel, E ;
Waugh, JM ;
Dake, MD .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2002, 13 (07) :709-715
[3]   Studies of human pancreatic elastase treatment of rabbit and human vein rings to predict human therapeutic doses [J].
Burke, Steven K. ;
Bunton, David ;
Bingham, Karen ;
Moss, Emma ;
Bland, Kimberly S. ;
Starcher, Barry ;
Wong, Marco D. ;
Franano, F. Nicholas .
PHARMACOLOGY RESEARCH & PERSPECTIVES, 2016, 4 (03) :1-7
[4]   Recombinant Human Elastase Alters the Compliance of Atherosclerotic Tibial Arteries After Ex Vivo Angioplasty [J].
Burke, Steven K. ;
Bingham, Karen ;
Moss, Emma ;
Gottlieb, Daniel P. ;
Wong, Marco D. ;
Bland, Kimberly S. ;
Franano, F. Nicholas .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2016, 67 (04) :305-311
[5]   Superior Patency of Upper Arm Arteriovenous Fistulae in High Risk Patients [J].
Chiulli, Larissa C. ;
Vasilas, Penny ;
Dardik, Alan .
JOURNAL OF SURGICAL RESEARCH, 2011, 170 (01) :157-164
[6]   Why don't fistulas mature? [J].
Dixon, B. S. .
KIDNEY INTERNATIONAL, 2006, 70 (08) :1413-1422
[7]   ELASTIN FRAGMENTS ATTRACT MACROPHAGE PRECURSORS TO DISEASED SITES IN PULMONARY-EMPHYSEMA [J].
HUNNINGHAKE, GW ;
DAVIDSON, JM ;
RENNARD, S ;
SZAPIEL, S ;
GADEK, JE ;
CRYSTAL, RG .
SCIENCE, 1981, 212 (4497) :925-927
[8]   Human type I pancreatic elastase treatment of arteriovenous fistulas in patients with chronic kidney disease [J].
Hye, Robert J. ;
Peden, Eric K. ;
O'Connor, Timothy P. ;
Browne, Barry J. ;
Dixon, Bradley S. ;
Schanzer, Andres S. ;
Jensik, Stephen C. ;
Dember, Laura M. ;
Jaff, Michael R. ;
Burke, Steven K. .
JOURNAL OF VASCULAR SURGERY, 2014, 60 (02) :454-U174
[9]  
Kawashima I, 1992, DNA Seq, V2, P303, DOI 10.3109/10425179209030963
[10]   SUBSTRATUM-BOUND ELASTIN PEPTIDE INHIBITS AORTIC SMOOTH-MUSCLE CELL-MIGRATION INVITRO [J].
OOYAMA, T ;
FUKUDA, K ;
ODA, H ;
NAKAMURA, H ;
HIKITA, Y .
ARTERIOSCLEROSIS, 1987, 7 (06) :593-598