Abstract

BackgroundCritical limb ischemia (CLI) is the clinical end stage of peripheral artery disease and is associated with high amputation, mortality rates and poor quality of life. For CLI patients with no revascularization options, venous arterialization could be an alternative technique for limb salvage. A systematic review and meta-analysis published in 2017 concluded that venous arterialization may be considered a viable alternative. A recent development, is the Percutaneous Deep Vein Arterialization (pDVA), that is CE-marked and currently under investigation of the FDA. This procedure, called LimFlow, is a novel, minimally invasive, endovascular approach to perform a venous arterialization procedure. The limited evidence for its use necessitates a scientific judgement of the pDVA. Therefore, we initiated a prospective clinical post market trial to investigate the outcome of the pDVA in no-option critical limb ischemia.Methods/designThe objective of this prospective study is to collect “real-life” clinical data among a population of patients treated with the pDVA in order to evaluate the clinical effectiveness and safety of the LimFlow System in patients with no-option critical limb ischemia. This study is a single-arm, open-label, prospective, post-market follow-up study to be conducted on up to fifty (50) eligible patients with a twelve-month follow-up period. The Primary endpoint is measured by amputation free survival. Secondary endpoints are complete wound healing, primary and secondary patency, limb salvage, renal function and technical and procedural success. Patients will be assessed at regular intervals during one year after the initial percutaneous deep vein arterialization procedure through clinical evaluation and self-completed questionnaires.DiscussionThe last decade several studies have been published with promising results and the number of treated patients has considerably grown. Venous arterialization could be a valuable treatment option in patients with often no other options than amputation of the affected limb.The first results in men are promising although more research and long term follow up is needed to establish the efficacy of this new treatment modality.With this prospective study, we evaluate the clinical effectiveness and safety in patients with no-option CLI treated with the pDVA (LimFlow System).Trial registrationNCT03321552.

Highlights

  • Critical limb ischemia (CLI) is the clinical end stage of peripheral artery disease and is associated with high amputation, mortality rates and poor quality of life

  • The first results in men are promising more research and long term follow up is needed to establish the efficacy of this new treatment modality

  • We evaluate the clinical effectiveness and safety in patients with no-option CLI treated with the Percutaneous Deep Vein Arterialization (pDVA) (LimFlow System)

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Summary

Discussion

Critical limb ischemia (CLI) is the end stage of peripheral artery disease (PAD) and is associated with high amputation and mortality rates. (Sprengers et al, 2010) The quality of life is poor and data of patients with no-option CLI is significantly worse than scores previously obtained in patients with cancer, chronic heart disease, and chronic kidney disease underlining the need for improved treatment of these patients. (Sprengers et al, 2010). When there is an absence of distal target vessels or only small artery’s (the “desert foot”) it often leads to failure of all revascularization attempts and culminates in major amputation. These are the nooption CLI patients where a venous arterialization can be a viable alternative. A meta-analysis of the venous arterialization in patients with no-option CLI, show a pooled limb salvage rate at 12 months of 75%. With this prospective study, we evaluate the clinical effectiveness and safety in patients with no-option CLI treated with the pDVA (LimFlow System)

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