Bypass surgery better than endovascular treatment in chronic limb-threatening Ischemia
A recent study published in the European Journal of Vascular & Endovascular Surgery suggests Bypass surgery shows better outcomes with some post-op complications than percutaneous transluminal angioplasty with/without stenting (PTA/S)in Chronic Limb Threatening Ischemia (CLTI) patients with long (GLASS grade III and IV) femoropopliteal disease.
Intermittent claudication is usually treated conservatively. However, if conservative treatment fails and the patient is strongly disabled, invasive treatment can be considered. Percutaneous transluminal angioplasty (PTA) or bypass surgery are the possible treatment options for patients with chronic limb-threatening Ischemia. A decision-analysis, based on the results of cohort studies, advised PTA for stenosis or short occlusions, whereas vein bypass surgery was recommended for long occlusions. However, this recommendation was based on heterogeneous patient groups and the optimal method of treatment remains controversial. For this purpose researchers of Clinic for Vascular & Endovascular surgery, Serbia conducted a study to compare short and long term outcomes between PTA/S and OSB in CLTI patients with long (GLASS grade III and IV) femoropopliteal disease.
It was a two-centre retrospective study including all consecutive patients with CLTI undergoing first time lower extremity intervention at two distinct vascular surgical centres between 1 January 2012 and 1 January 2018. A total of 1545 CLTI consecutive limbs were treated for femoropopliteal GLASS grade III and IV lesions at two vascular surgical centres and among which some patients were randomly assigned to either OSB (n=235) or PTA/S (n=235). Researchers calculated the propensity score for each limb using covariables from baseline and angiographic characteristics. The major outcome analyzed were freedom from re-intervention in the treated extremity and major amputation. Researchers also analyzed all hospital complications among the two patient groups.
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