“…In the prospective, multinational randomized controlled Zilver PTX trial, the 2-year safety and efficacy of a paclitaxel-coated drug-eluting stent (DES) was compared with PTA in patients with superficial femoral artery lesions. In patients who received the paclitaxel-coated DES, 2-year outcomes showed statistically significant differences in terms of event-free survival, primary patency, and clinical benefits ( 122 ).…”
Section: Surgical Revascularization In Patients With CLI (
mentioning
(2014) Systematic reviews and meta-analyses for more profitable strategies in peripheral artery disease, Annals of Medicine, 46:7,[475][476][477][478][479][480][481][482][483][484][485][486][487][488][489]
“…In the prospective, multinational randomized controlled Zilver PTX trial, the 2-year safety and efficacy of a paclitaxel-coated drug-eluting stent (DES) was compared with PTA in patients with superficial femoral artery lesions. In patients who received the paclitaxel-coated DES, 2-year outcomes showed statistically significant differences in terms of event-free survival, primary patency, and clinical benefits ( 122 ).…”
Section: Surgical Revascularization In Patients With CLI (
mentioning
(2014) Systematic reviews and meta-analyses for more profitable strategies in peripheral artery disease, Annals of Medicine, 46:7,[475][476][477][478][479][480][481][482][483][484][485][486][487][488][489]
“…Bei der Verwendung frischer venöser Homografts fehlen Ergebnisse im Zusammenhang mit Infektionen. Die prinzipielle Anwendbarkeit wurde jedoch durch eine Düsseldorfer Arbeitsgruppe gezeigt [17], wobei analog zu den arteriellen Gefäßen die aktuelle Gesetzeslage eine Anwendung unmöglich macht [15]. Kommerziell erhältliche kryokonservierte Venen (CryoVein) wurden hinsichtlich ihrer Verwendung in der Bypasschirurgie ausgedehnt untersucht, jedoch fehlen auch hier Ergebnisse im Kontext mit Infektionen [18].…”
unclassified
“…Eine akzeptable Datenlage scheint hinsichtlich der Verwendung arterieller bzw. venöser Homografts vorzuliegen[14,[16][17][18]. Dennoch sind die hohen Anschaffungskosten sowie die immer schlechter werdende Verfügbarkeit nicht zuletzt aufgrund gesetzlicher Anforderungen für den Routineeinsatz problematisch[15].…”
Treatment of vascular graft infections in peripheral bypass surgery in the absence of endogenous material necessitates the use of infection-resistant materials. The present study showed promising results using a collagen-biosynthetic prosthesis. Due to a lack of long-term results, the graft should be used only after detailed informed consent is obtained from the patient. The expenses incurred by using the biosynthetic graft should be covered adequately by revenues from these patients.
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