Intermittent claudication in patients without rest pain
and no peripheral tissue necrosis
▶BY MOUTH
▶Adult: 100 mg twice daily, to be taken 30 minutes
before food, cilostazol should be initiated by those
experienced in the management of intermittent
claudication, patients receiving cilostazol should be
assessed for improvement after 3 months; consider
discontinuation of treatment if there is no clinically
relevant improvement in walking distance
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DUE TO INTERACTIONS
▶Manufacturer advises reduce dose to 50 mg twice daily
with concurrent use of potent inhibitors of CYP3A4,
potent inhibitors of CYP2C19, omeprazole and
erythromycin.
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Active peptic ulcer. congestive
heart failure. coronary intervention in previous 6 months.
haemorrhagic stroke in previous 6 months. history of
severe tachyarrhythmia. myocardial infarction in previous
6 months. poorly controlled hypertension. predisposition
to bleeding. proliferative diabetic retinopathy.
prolongation of QT interval. unstable angina. ventricular
arrhythmia
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Atrial fibrillation. atrial flutter. atrial or
ventricular ectopy. diabetes mellitus (higher risk of
intraocular bleeding). stable coronary disease. surgery
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NICE decisions
▶Cilostazol, naftidrofuryl oxalate, pentoxifylline and inositol
nicotinate for the treatment of intermittent claudication in
people with peripheral arterial disease (May 2011) NICE TA223
Cilostazol is not recommended for the treatment of
intermittent claudication in patients with peripheral
arterial disease; patients currently receiving this treatment
should have the option to continue until they and their
clinician consider it appropriate to stop.
www.nice.org.uk/guidance/ta223
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