2019
DOI: 10.1007/s00270-019-02385-5
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Cost-Effectiveness of Drug-Eluting Stents for Infrapopliteal Lesions in Patients with Critical Limb Ischemia: The PADI Trial

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Cited by 11 publications
(4 citation statements)
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“…Data from the PADI trial which included patients with CLI, were used. Detailed study design and results of this study have been published elsewhere [32][33][34][35]. In short, the PADI trial is a randomized controlled trial to investigate drug eluting stents (DES) for the treatment of infrapopliteal lesions in patients with CLI in comparison with the current reference treatment.…”
Section: Patientsmentioning
confidence: 99%
“…Data from the PADI trial which included patients with CLI, were used. Detailed study design and results of this study have been published elsewhere [32][33][34][35]. In short, the PADI trial is a randomized controlled trial to investigate drug eluting stents (DES) for the treatment of infrapopliteal lesions in patients with CLI in comparison with the current reference treatment.…”
Section: Patientsmentioning
confidence: 99%
“…22 Despite the poor long-term survival of this very high-risk cohort of patients, regardless of treatment option for critical limb ischaemia, treatment with PES is theorised to offer additional economic benefits, at least through 5 years, due to the increased incidence-and event-free survival associated with the PES. 23 The SAVAL trial is a recently completed multicentre trial studying a DES designed specifically for use in infrapopliteal critical limb ischaemia (NCT03551496). The SAVAL DES (Boston Scientific, Boston, MA, US) is a paclitaxel-coated self-expanding stent measuring 3.5 mm x 80 mm, longer than coronary artery stents, specifically engineered to be durable in infrapopliteal arteries.…”
Section: Drug-eluting Stentsmentioning
confidence: 99%
“…elsewhere [14][15][16][17]. Briefly, the PADI Trial was an investigator-initiated prospective, multicenter RCT in CLI patients due to infrapopliteal pathology to assess the value of drug eluting stents (DES) compared to the current reference treatment with bare-metal stents (BMS).…”
Section: Patientsmentioning
confidence: 99%