Lower limb atherosclerosis can lead to blocked blood vessels causing pain on walking (intermittent claudication) or, if more severe, pain at rest, ulceration and gangrene (critical limb ischaemia).
Surgery to bypass the blockage uses either a piece of vein from another part of the person’s body or a synthetic graft. The bypass may help improve blood supply to the leg but the graft can also become blocked, even in the first year. To help prevent this, people are given aspirin (an antiplatelet drug) or a vitamin K antagonist (anti-blood clotting or antithrombotic drug), or both, to try to stop loss of blood flow through the graft (patency). The review of trials found that patients undergoing venous grafts were more likely to benefit from treatment with vitamin K antagonists than platelet inhibitors. Patients receiving an artificial graft may benefit from platelet inhibitors (aspirin). However, the evidence is not conclusive. Although a total of 14 randomised, controlled trials involving 4970 patients were included in the review, trials with larger patient numbers are needed. This is because there was considerable variation between the included trials in whether patients received both types of drugs, anticoagulation levels and how they were measured, and the indications for surgery, intermittent claudication or critical limb ischaemia.
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Peripheral arterial disease (PAD) is frequently treated by either an infrainguinal autologous (using the patient's own veins) or synthetic graft bypass. The rate of occlusion of the graft after one year is between 12% and 60%. To prevent occlusion, patients are treated with an antiplatelet or antithrombotic drug, or a combination of both. Little is known about which drug is optimal to prevent infrainguinal graft occlusion. This is an update of a Cochrane review first published in 2003.
Задачи
To evaluate whether antithrombotic treatment improves graft patency, limb salvage and survival in patients with chronic PAD undergoing infrainguinal bypass surgery.
Методы поиска
The Cochrane Peripheral Vascular Diseases Group searched their Specialised Register (last searched August 2010) and the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2010, Issue 3).
Критерии отбора
Randomised, controlled trials; two review authors independently assessed the methodological quality of each trial using a standardised checklist.
Сбор и анализ данных
Data collected included patient details, inclusion and exclusion criteria, type of graft, antithrombotic therapy, outcomes, and side effects.
Основные результаты
A total of 14 trials were included in this review; 4970 patient results were analysed. Four trials evaluating vitamin K antagonists (VKA) versus no VKA suggested that oral anticoagulation may favour autologous venous, but not artificial, graft patency as well as limb salvage and survival. Two other studies comparing VKA with aspirin (ASA) or aspirin and dipyridamole provided evidence to support a positive effect of VKA on the patency of venous but not artificial grafts. Three trials comparing low molecular weight heparin (LMWH) to unfractionated heparin (UFH) failed to demonstrate a significant difference on patency. One trial comparing LMWH with placebo found no significant improvement in graft patency over the first postoperative year in a population receiving aspirin. One trial showed an advantage for LMWH versus aspirin and dipyridamol at one year for patients undergoing limb salvage procedures. Perioperative administration of ancrod showed no greater benefit when compared to unfractionated heparin. Dextran 70 showed similar graft patency rates to LMWH but a significantly higher proportion of patients developed heart failure with dextran.
Выводы авторов
Patients undergoing infrainguinal venous graft are more likely to benefit from treatment with VKA than platelet inhibitors. Patients receiving an artificial graft benefit from platelet inhibitors (aspirin). However, the evidence is not conclusive. Randomised controlled trials with larger patient numbers are needed in the future to compare antithrombotic therapies with either placebo or antiplatelet therapies.
