This study is a prospective, multicenter, real world, observational study, which aims at evaluating the safety, efficacy and economic cost of endovascular treatments for endovascular therapies in chronic femoropopliteal occlusive disease with severe calcification. It is estimated that 400 subjects diagnosed with chronic femoropopliteal occlusive disease with severe calcification and receive endovascular treatments will be enrolled in eight centers nationwide from January 2021 to December 2022. All the subjects will be under follow-up for two years. There is no restriction on the endovascular techniques. The primary outcomes include the technical success rate of each endovascular techniques and the reintervention rate driven by lesions' clinical symptoms.
Arteriosclerosis obliterans (ASO) is a common disease in middle-aged and elderly people, which affects up to 30% people who are over 70 years in the general population. Its symptoms include claudication, rest pain and ischemic tissue loss depending on its severity. Nowadays, endovascular treatments have become the first-line therapy. If ASO is combined with severe calcification, the treatment will be much more challenging. The efficacy of plain old balloon angioplasty is limited. New devices including drug-coated balloon, intravascular Lithotripsy, directional atherectomy, Supera stent and drug-eluting stent offer another chance and better prognosis. The data of these new devices, however, are mainly from low quality evidence. Therefore, we start this prospective, multicenter, real world, observational study, providing new data on the safety, efficacy and health economics evaluation of endovascular treatments for endovascular therapies in chronic femoropopliteal occlusive disease with severe calcification.
Study Type
OBSERVATIONAL
Enrollment
600
The First Affliated Hospital, Zhejiang University, School of Medicine
Hangzhou, Zhejiang, China
RECRUITINGTechnical success rate
Successfully revascularize the target vessel. The residual stenosis is \<30% and there is no acute thrombosis occurred in the target vessel within 1 week post-operation.
Time frame: 1 week
The clinically driven target lesion revascularization(CD-TLR) rate at post-interventional
Any reintervention within the target lesion due to symptoms or drop of ≥20% ABI compared to baseline.
Time frame: 1 month
The clinically driven target lesion revascularization(CD-TLR) rate at post-interventional
Any reintervention within the target lesion due to symptoms or drop of ≥20% ABI compared to baseline.
Time frame: 6 months
The clinically driven target lesion revascularization(CD-TLR) rate at post-interventional
Any reintervention within the target lesion due to symptoms or drop of ≥20% ABI compared to baseline.
Time frame: 12 months
The clinically driven target lesion revascularization(CD-TLR) rate at post-interventional
Any reintervention within the target lesion due to symptoms or drop of ≥20% ABI compared to baseline.
Time frame: 18 months
The clinically driven target lesion revascularization(CD-TLR) rate at post-interventional
Any reintervention within the target lesion due to symptoms or drop of ≥20% ABI compared to baseline.
Time frame: 24 months
Vascular quality of life questionnaire(VascuQol)
The VascuQol was designed as a questionnaire containing five domains: pain (4 items), symptoms (4 items), activities (8 items), social (2 items), and emotional (7 items) to evaluate Health related quality of life (HRQL). Every item has seven response options, with scores ranging from 1 to 7. A total score is the sum of all 25 item scores divided by 25.And both the total score as well as the domain scores range from 1 (worst HRQL) to 7 (best HRQL).The lower the value, the poorer the quality of life.
Time frame: 1 month,6 months,12 months,18 months and 24 months
Incidence of severe adverse events
Severe adverse events include anyone of the following: Myocardial infarction, ischemic stroke, cardiovascular mortality, acute limb ischemia, and major amputation of a vascular etiology.
Time frame: 1 month,6 months,12 months,18 months and 24 months
Patency of the target vessel
The patency is assessed by the vascular ultrasound.
Time frame: Patency of the target vessel. [ Time Frame: 1 month,6 months,12 months,18 months and 24 months
Health economics evaluation
All the cost related to the target vessel and spent in the inpatient ward will be recorded and analyzed.
Time frame: 24 months
Wound, Ischemia, and foot infection(WIFI) classification system
The Wound, Ischemia, and foot Infection (WIfI) classification system is a composite outcome measure encompassing demographic changes and expanding techniques of revascularization to perform meaningful analyses of outcomes in the treatment of the threatened limb, including wound, ischemia and foot infection. Each index was evaluated by very low, low, moderate and high, the very low represents no risk, the high reveals high risk of amputation.
Time frame: 1 month,6 months,12 months,18 months and 24 months
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