BMJ 2000;320:483 ( 19 February )
Papers
Drug points
Clopidogrel associated with acute arthritis
Anu Garg,
Johannes Radvan,
Neil Hopkinson.
Department of
Cardiology, Royal Bournemouth Hospital, Bournemouth, Dorset BH8
8DH
Clopidogrel is a new ADP receptor antagonist used in the
prevention of myocardial infarction, stroke, and vascular death. We
report two cases of acute arthritis and tendonitis after clopidogrel use.
Case 1
A 76 year old woman was referred with a six year history of angina
pectoris. She was stabilised on treatment but began to develop further
symptoms at rest two months before referral. She had a long history of
hypertension. She took atenolol 100 mg once daily, diltiazem 90 mg
twice daily, isosorbide mononitrate 20 mg twice daily, and aspirin 75 mg daily.
Significant two vessel coronary artery disease was found at cardiac
catheterisation. She underwent percutaneous transluminal coronary
angioplasty and stent insertion of the right coronary artery. She was
prescribed diltiazem 120 mg twice daily, clopidogrel 75 mg once daily,
and aspirin 150 mg once daily.
Two weeks later she developed widespread pruritus, with no obvious
rash, and intense pain and swelling of the metacarpophalangeal joints.
The joints were red and hot, and there was synovitis. Other joints were
unaffected. Her erythrocyte sedimentation rate and C reactive protein
concentration were increased to 86 mm in the first hour and 81 mg/l
respectively. Uric acid concentration was normal and
x ray films showed soft tissue swelling only with no
chondrocalcinosis. Clopidogrel was stopped.
One week later the pruritus had settled and the joint pain had
improved. Repeat testing of inflammatory markers confirmed the improvement.
Case 2
A 63 year old man was referred with three episodes of chest
discomfort on exertion. He was an ex-smoker and had a six year history
of mild type 2 diabetes mellitus. In 1984 he had an uncomplicated
subarachnoid haemorrhage. He took lisinopril 20 mg once daily and long
acting diltiazem 200 mg once daily.
Severe coronary artery disease in a left dominant system was found
at cardiac catheterisation. He underwent coronary artery bypass
grafting. He was allergic to aspirin so was prescribed clopidogrel 75 mg once daily in addition to lisinopril.
Three weeks later he presented to his doctor with severe pain of
his right knee. The knee was tender, and he was unable to bear weight
on the leg. There was tenderness, heat, and swelling over the
quadriceps tendon proximal to the patella. His erythrocyte sedimentation rate was mildly increased to 47 mm in the first hour. His
serum urate concentration was normal. Clopidogrel was discontinued, and
the symptoms resolved.
To our knowledge arthritis has not been described as a side effect of
clopidogrel, and the manufacturer knows of only one case. The two cases
we describe had acute musculoskeletal inflammation and increased
concentrations of inflammatory markers. We recommend that
clopidogrel be considered as a potential cause of arthritis.
© BMJ 2000