Balloon angioplasty (PTA) is an established treatment modality for stenosis in dysfunctional arteriovenous fistulae (AVF), although most studies showing efficacy have been retrospective, uncontrolled, and nonrandomized. In addition, it is unknown whether correction of stenosis not associated with significant hemodynamic, functional, and clinical abnormality may improve survival in AVF. This study was a prospective controlled open trial to evaluate whether prophylactic PTA of stenosis not associated with access dysfunction improves survival in native, virgin, radiocephalic forearm AVF. Sixty-two stenotic, functioning AVF, i.e., able to provide adequate dialysis, were enrolled in the study: 30 were allocated to control and 32 to PTA. End poin...
Background: Native or prosthetic arteriovenous (AV) fistulas are preferred for permanent haemodialys...
Purpose: This study aimed to evaluate the post-intervention target primary patency of drug-coated ba...
BackgroundThe aim of this pilot study was to evaluate the safety and efficacy of the MagicTouch™ sir...
AbstractPurpose: Maintenance of hemodialysis access grafts represents an enormous social and clinica...
Use of a covered stent after percutaneous transluminal angioplasty (PTA) was compared to PTA alone f...
PURPOSEWe aimed to determine the predictors of technical success and patency after percutaneous tran...
BACKGROUND: Stenosis is the main cause of arteriovenous fistula (AVF) failure. It is unclear, howeve...
ObjectiveThe aim of this trial was to compare the rates of patency achieved by cutting and conventio...
Randomized controlled trial of prophylactic repair of hemodialysis arteriovenous graft stenosis.Back...
AbstractPurposeTo assess the safety and efficacy of an expanded polytetrafluoroethylene stent graft ...
Objective: to conduct comprehensive comparative analysis of the patency rate of native arteriovenous...
Background: Preemptive correction of a stenosis in an arteriovenous (AV) access (fistula or graft) t...
Background and Aims: Stenosis due to intimal hyperplasia and restenosis after initially successful p...
AbstractEndovascular treatment of the malfunctioning fistula can involve a combination of angioplast...
Background: Reliable vascular access is essential for patients receiving haemodialysis. An arteriove...
Background: Native or prosthetic arteriovenous (AV) fistulas are preferred for permanent haemodialys...
Purpose: This study aimed to evaluate the post-intervention target primary patency of drug-coated ba...
BackgroundThe aim of this pilot study was to evaluate the safety and efficacy of the MagicTouch™ sir...
AbstractPurpose: Maintenance of hemodialysis access grafts represents an enormous social and clinica...
Use of a covered stent after percutaneous transluminal angioplasty (PTA) was compared to PTA alone f...
PURPOSEWe aimed to determine the predictors of technical success and patency after percutaneous tran...
BACKGROUND: Stenosis is the main cause of arteriovenous fistula (AVF) failure. It is unclear, howeve...
ObjectiveThe aim of this trial was to compare the rates of patency achieved by cutting and conventio...
Randomized controlled trial of prophylactic repair of hemodialysis arteriovenous graft stenosis.Back...
AbstractPurposeTo assess the safety and efficacy of an expanded polytetrafluoroethylene stent graft ...
Objective: to conduct comprehensive comparative analysis of the patency rate of native arteriovenous...
Background: Preemptive correction of a stenosis in an arteriovenous (AV) access (fistula or graft) t...
Background and Aims: Stenosis due to intimal hyperplasia and restenosis after initially successful p...
AbstractEndovascular treatment of the malfunctioning fistula can involve a combination of angioplast...
Background: Reliable vascular access is essential for patients receiving haemodialysis. An arteriove...
Background: Native or prosthetic arteriovenous (AV) fistulas are preferred for permanent haemodialys...
Purpose: This study aimed to evaluate the post-intervention target primary patency of drug-coated ba...
BackgroundThe aim of this pilot study was to evaluate the safety and efficacy of the MagicTouch™ sir...