2006
DOI: 10.1016/j.jvs.2006.07.044
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Low-molecular-weight heparin for prevention of restenosis after femoropopliteal percutaneous transluminal angioplasty: A randomized controlled trial

Abstract: Treatment with 2500 IU dalteparin subcutaneously given for 3 months after femoropopliteal PTA failed to reduce restenosis/reocclusion at 12 months. However, dalteparin may be beneficial in the subgroup of patients with CLI at 12 months follow-up.

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Cited by 43 publications
(32 citation statements)
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“…Several trials have obtained similar results comparable with our study [20,35]. It still remains unclear why argatroban treatment does not provide a similar benefit in the prevention of restenosis.…”
Section: Discussionsupporting
confidence: 88%
“…Several trials have obtained similar results comparable with our study [20,35]. It still remains unclear why argatroban treatment does not provide a similar benefit in the prevention of restenosis.…”
Section: Discussionsupporting
confidence: 88%
“…Despite this interesting result, dalteparin 2500 UI, administered for 3 months after femoropopliteal angioplasty plus aspirin 100 mg/day versus aspirin alone, failed to reduce incidence of restenosis/reocclusion at 12 months. However, dalteparin appeared to be beneficial at the 12-month follow-up in the subgroup of patients with critical limb ischemia (Koppensteiner et al, 2006).…”
Section: Low Molecular Weight Heparinsmentioning
confidence: 87%
“…The median TVR time was 24 months with a well-known high rate of 40 % TVR in the fi rst 12 months [9]. One in fi ve patients is estimated to need an intervention on the opposite leg after 4 years.…”
Section: Discussionmentioning
confidence: 99%