GeriQBank · Paper II · Q5
Transient Ischaemic Attack
- Topic
- Stroke & Neurology
- Chapter
- Cerebrovascular Disease
- Years asked
- Not recorded in the source
- Frequency
- No university frequency data for this paper yet
Detailed answer
Pro · free in betaAttempt it firstOutline your answer as a 7-mark answer before revealing it — definition, causes, evaluation, management and the geriatric angle.Reveal answer
Cerebrovascular Disease
Question 5. Transient Ischaemic Attack 7 MARKS • ASKED ×2 Answer Textbook Core – 6 Points
Definition. A transient episode of neurological dysfunction caused by focal brain, spinal cord or retinal ischaemia, without acute infarction on imaging (tissue-based definition). The old time-based definition of “deficit resolving within 24 hours” is obsolete, because up to one-third of clinically transient events show a diffusion-weighted MRI lesion — and are therefore strokes.
Clinical features by territory. Carotid — contralateral hemiparesis, hemisensory loss, dysphasia, and amaurosis fugax (a curtain descending over one eye). Vertebrobasilar — vertigo with other brainstem signs, diplopia, dysarthria, dysphagia, ataxia, bilateral or crossed deficits, drop attacks. Isolated vertigo, syncope, confusion, generalised weakness or a “funny turn” are NOT a TIA.
Risk stratification — ABCD2 score. Age ≥60 = 1; Blood pressure ≥140/90 = 1; Clinical features: unilateral weakness = 2, speech disturbance without weakness = 1; Duration ≥60 min = 2, 10–59 min = 1; Diabetes = 1. A score of 4 or more is high risk. Stroke risk is greatest in the first 48 hours — roughly 5% at 7 days and 10% at 90 days if untreated. A TIA is a medical emergency, not an outpatient problem.
Investigations — all within 24 hours. MRI with diffusion-weighted imaging is the investigation of choice (CT if MRI is unavailable); carotid Doppler, CT angiography or MR angiography; ECG with prolonged cardiac monitoring (Holter or implantable loop recorder) — occult atrial fibrillation is a major and treatable cause in the elderly; echocardiography; glucose and HbA1c, lipids, full blood count, renal function, and ESR if amaurosis fugax (giant cell arteritis).
Acute antithrombotic treatment. For high-risk TIA (ABCD2 ≥4) of non-cardioembolic origin, give dual antiplatelet therapy — aspirin plus clopidogrel for 21 days, then a single agent (loading aspirin 300 mg and clopidogrel 300 mg; CHANCE and POINT trials). Add a high-intensity statin, control blood pressure and glycaemia, and stop smoking. If atrial fibrillation is present, the treatment is anticoagulation, not antiplatelets — a DOAC is preferred over warfarin in older adults.
Pathway and secondary prevention. Assess in a TIA clinic within 24 hours for high-risk patients; carotid revascularisation within 2 weeks for symptomatic 70–99% stenosis; treat the whole vascular risk profile; give driving advice (in India, cease driving for at least one month and reassess); and screen for cognitive impairment, depression and falls, since a TIA in an older person is a sentinel event for both vascular dementia and frailty.
Latest Update – 1 Point
INSPIRES trial (NEJM 2023; subgroup analyses 2024) — the DAPT window extends to 72 hours. In 6,100 patients with mild ischaemic stroke or high-risk TIA of presumed atherosclerotic cause, clopidogrel plus aspirin started within 72 hours reduced new stroke at 90 days compared with aspirin alone, at the cost of a small excess of moderate-to-severe bleeding; efficacy was similar whether treatment began before 24 hours or between 24 and 72 hours. This widens the previous 24-hour window to 72 hours — a change of real practical value in India, where patients frequently present late. The AHA/ASA 2026 guideline likewise supports dual antiplatelet therapy for non-disabling stroke and high-risk TIA.
Extra Points to Remember (repeated question)
Crescendo TIA (increasing frequency or duration) and TIA while already on an antiplatelet both mandate immediate admission.
TIA mimics to exclude: migraine aura, focal seizure with Todd’s paresis, hypoglycaemia, syncope, transient global amnesia, subdural haematoma, brain tumour, multiple sclerosis, peripheral vestibular disease. The ABCD2 score does not detect atrial fibrillation or carotid stenosis, so a low score never justifies omitting vascular and cardiac imaging.
Limb-shaking TIA — brief involuntary jerking of the contralateral limb on standing — indicates critical carotid stenosis with haemodynamic failure and is often misdiagnosed as a focal seizure.
ESUS (embolic stroke of undetermined source): routine anticoagulation is not beneficial (NAVIGATE-ESUS, RE-SPECT ESUS) — look harder for atrial fibrillation instead.
Examiner’s Tip — Verbatim Mark-Earning Lines
“A TIA is defined by absence of infarction on imaging, not by duration of symptoms.” “A TIA is a warning shot — the highest risk of stroke is in the first 48 hours.” “Antiplatelets for atherothrombotic TIA; anticoagulation for atrial fibrillation — never confuse the two.”
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References
- PAPERS-2-3-4_COMBINED.pdf — page 272
- GeriQBank source PDF — p. 272
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