Giant cell arteritis Flashcards
Define giant cell arteritis
Granulomatous inflammation of large arteries, particularly branches of the external carotid artery, most commonly the TEMPORAL ARTERY
Explain the aetiology/risk factors of giant cell arteritis
UNKNOWN
More common with increasing age
Some associations with ethnic background and infections
Associated with HLA-DR4 and HLA-DRB1
Associated with polymyalgia rheumaticia
Summarise the epidemiology of giant cell arteritis
More common in FEMALES
Peak age of onset: 65-70 yr
Recognise the presenting symptoms of giant cell arteritis
Subacute onset (usually over a few weeks)
Headache Scalp tenderness Jaw claudication Blurred vision Sudden blindness in one eye
Systemic: malaise, low-grade fever, lethargy,
weight loss, depression
Symptoms of polymyalgia rheumatica -
early morning pain and stiffness of muscles of the shoulder and pelvic girdle
NOTE: 40 - 60% of GCA has polymyalgia rheumaticia
Recognise the signs of giant cell arteritis on physical examination
Swelling and erythema overlying the temporal artery
Scalp and temporal tenderness
Thickened non-pulsatile temporal artery
Reduced visual acuity
Identify appropriate investigations for giant cell arteritis
Bloods
High ESR
FBC - normocytic anaemia of chronic disease
Temporal Artery Biopsy
Must be performed within 48 hrs of starting corticosteroids
Negative biopsy doesn’t necessarily rule out GCA
Generate a management plan for giant cell arteritis
High dose oral prednisolone IMMEDIATELY to prevent visual loss
Reduce the dose of prednisolone gradually
Many patients will need to be kept on a maintenance dose of prednisolone for 1-2 yrs
Low dose aspirin (with PPIs and gastroprotection) - reduces risk of visual loss, TIAs and stroke
Annual CXR for up to 10 yrs to look for thoracic aortic aneurysms
Identify possible complications of giant cell arteritis
Carotid artery aneurysms
Aortic aneurysms
Thrombosis
Embolism to the ophthalmic artery leading to visual disturbance and loss of vision
Summarise the prognosis for patients with giant cell arteritis
In most cases the condition will last for around 2 years before complete remission