Transient ischemic attack: Difference between revisions
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imported>Robert Badgett m (Transient Ischemic Attack (TIA) moved to Transient ischemic attack: This matched MeSH entry term. Also, I think cz prefers this capitalization.) |
imported>Robert Badgett (Started diagnosis section) |
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A '''Transient Ischemic Attack''' ('''TIA''') is a ''brief'' loss of neurologic function. In a TIA, the affected [[brain]] cells were not killed, but only transiently deprived of blood supply and the signs of what seems to be a [[stroke]], (or black-out), pass quickly and ''completely''. A TIA is often a warning sign of an impending stroke, however, and like a true stroke, is a neurologic emergency. None the less, a TIA is ''not'' a true stroke. | A '''Transient Ischemic Attack''' ('''TIA''') is a ''brief'' loss of neurologic function. In a TIA, the affected [[brain]] cells were not killed, but only transiently deprived of blood supply and the signs of what seems to be a [[stroke]], (or black-out), pass quickly and ''completely''. A TIA is often a warning sign of an impending stroke, however, and like a true stroke, is a neurologic emergency. None the less, a TIA is ''not'' a true stroke. | ||
==Diagnosis== | |||
===History and physical examination=== | |||
The history and physical examination of patients with a possible TIA is difficult to interpret. Two neurologists interviewing the same patient have statistically 'substantial' but imperfect [[Kappa statistic|agreement]] about whether the patient had a TIA.<ref name="pmid6464066">{{cite journal |author=Kraaijeveld CL, van Gijn J, Schouten HJ, Staal A |title=Interobserver agreement for the diagnosis of transient ischemic attacks |journal=Stroke |volume=15 |issue=4 |pages=723–5 |year=1984 |pmid=6464066 |doi=}}</ref> Disagreement may occur even when a 'standardized' patient is trained to give identical histories to each neurologist.<ref name="pmid2919420">{{cite journal |author=Koudstaal PJ, Gerritsma JG, van Gijn J |title=Clinical disagreement on the diagnosis of transient ischemic attack: is the patient or the doctor to blame? |journal=Stroke |volume=20 |issue=2 |pages=300–1 |year=1989 |pmid=2919420 |doi=}}</ref> | |||
===Differential diagnosis=== | |||
Other disorders that may cause similar symptoms are syncope, seizure, migraine, vestibulopathy, and conversion disorder.<ref name="pmidpending-Johnston">S. Claiborne Johnston, “Transient Neurological Attack: A Useful Concept?,” JAMA 298, no. 24 (December 26, 2007), http://jama.ama-assn.org/cgi/content/full/298/24/2912 (accessed December 27, 2007).</ref> | |||
==Treatment== | ==Treatment== | ||
===Anti-platelet drugs=== | ===Anti-platelet drugs=== | ||
The most effective anti-platelet treatment is probably to combine aspirin, 25 mg twice a day with extended-release dipyridamole 200 mg twice a day according to the ESPRIT<ref name="pmid16714187">{{cite journal |author=Halkes PH, van Gijn J, Kappelle LJ, Koudstaal PJ, Algra A |title=Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial |journal=Lancet |volume=367 |issue=9523 |pages=1665–73 |year=2006 |pmid=16714187 |doi=10.1016/S0140-6736(06)68734-5 |issn=}}</ref> | The most effective anti-platelet treatment is probably to combine aspirin, 25 mg twice a day with extended-release dipyridamole 200 mg twice a day according to the ESPRIT<ref name="pmid16714187">{{cite journal |author=Halkes PH, van Gijn J, Kappelle LJ, Koudstaal PJ, Algra A |title=Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial |journal=Lancet |volume=367 |issue=9523 |pages=1665–73 |year=2006 |pmid=16714187 |doi=10.1016/S0140-6736(06)68734-5 |issn=}}</ref> | ||
Revision as of 07:29, 27 December 2007
Overview (summary)
A Transient Ischemic Attack (TIA) is a brief loss of neurologic function. In a TIA, the affected brain cells were not killed, but only transiently deprived of blood supply and the signs of what seems to be a stroke, (or black-out), pass quickly and completely. A TIA is often a warning sign of an impending stroke, however, and like a true stroke, is a neurologic emergency. None the less, a TIA is not a true stroke.
Diagnosis
History and physical examination
The history and physical examination of patients with a possible TIA is difficult to interpret. Two neurologists interviewing the same patient have statistically 'substantial' but imperfect agreement about whether the patient had a TIA.[1] Disagreement may occur even when a 'standardized' patient is trained to give identical histories to each neurologist.[2]
Differential diagnosis
Other disorders that may cause similar symptoms are syncope, seizure, migraine, vestibulopathy, and conversion disorder.[3]
Treatment
Anti-platelet drugs
The most effective anti-platelet treatment is probably to combine aspirin, 25 mg twice a day with extended-release dipyridamole 200 mg twice a day according to the ESPRIT[4]
The combination of aspirin and clopidogrel should probably be avoided according to the MATCH[5] and CHARISMA[6] studies.
Invasive treatment
Carotid endarterectomy may prevent stroke in patients with more than 70% stenosis of the carotid artery.[7]
Expedited care protocol
A before and after comparison study found reduced mortality fell from 10% to 2% with the following protocol started the day the patient presents for medical care:[8]
- "antiplatelet therapy: aspirin in patients not already on antiplatelet therapy (75 mg daily), or clopidogrel if aspirin was contraindicated" (loading dose of clopidogrel 300 mg).
- * "In patients seen within 48 h of their event, or those seen within 7 days who were thought to be at particularly high early risk", clopidogrel (75 mg daily, to be stopped after 30 days; loading dose of clopidogrel 300 mg) was recommended in addition to aspirin."[9]
- However, as noted above combining aspirin 25 mg twice a day with extended-release dipyridamole 200 mg twice a day might be a better choice than either aspirin alone or aspirin combined with clopidogrel.
- simvastatin 40 mg daily
- "blood pressure lowering unless systolic blood pressure was below 130 mm Hg on repeated measurement (either by increases in existing medication, or by commencement of perindopril 4 mg daily with or without indapamide 1·25 mg daily)"
- anticoagulation as required
- "Brain imaging was required before starting combination antiplatelet treatment or anticoagulation after a minor stroke"
Prognosis
A meta-analysis of 18 cohort studies found the risk of stroke after 7 days varies from 0% to 13%. The lowest rates were in studies of emergency treatment by specialist stroke services.[10]
The ABCD2 score can predict likelihood of subsequent stroke.[11][12]
The score is calculated as:
- Age ≥ 60 years = 1 point
- Blood pressure at presentation ≥ 140/90 mm Hg = 1 point
- Clinical features
- unilateral weakness = 2 points
- speech disturbance without weakness = 1 point
- Duration of attack
- ≥ 60 minutes = 2 points
- 10–59 minutes = 1 point
- Diabetes = 1 point
Interpretation of score, the risk for stroke:
- Score 0-3 (low)
- 2 day risk = 1.0%
- 7 day risk = 1.2%
- Score 4-5 (moderate)
- 2 day risk = 4.1%
- 7 day risk = 5.9%
- Score 6–7 (high)
- 2 day risk = 8.1%
- 7 day risk = 11.7%
References
- ↑ Kraaijeveld CL, van Gijn J, Schouten HJ, Staal A (1984). "Interobserver agreement for the diagnosis of transient ischemic attacks". Stroke 15 (4): 723–5. PMID 6464066. [e]
- ↑ Koudstaal PJ, Gerritsma JG, van Gijn J (1989). "Clinical disagreement on the diagnosis of transient ischemic attack: is the patient or the doctor to blame?". Stroke 20 (2): 300–1. PMID 2919420. [e]
- ↑ S. Claiborne Johnston, “Transient Neurological Attack: A Useful Concept?,” JAMA 298, no. 24 (December 26, 2007), http://jama.ama-assn.org/cgi/content/full/298/24/2912 (accessed December 27, 2007).
- ↑ Halkes PH, van Gijn J, Kappelle LJ, Koudstaal PJ, Algra A (2006). "Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial". Lancet 367 (9523): 1665–73. DOI:10.1016/S0140-6736(06)68734-5. PMID 16714187. Research Blogging.
- ↑ Diener HC, Bogousslavsky J, Brass LM, et al (2004). "Aspirin and clopidogrel compared with clopidogrel alone after recent ischaemic stroke or transient ischaemic attack in high-risk patients (MATCH): randomised, double-blind, placebo-controlled trial". Lancet 364 (9431): 331–7. DOI:10.1016/S0140-6736(04)16721-4. PMID 15276392. Research Blogging.
- ↑ Bhatt DL, Fox KA, Hacke W, et al (2006). "Clopidogrel and aspirin versus aspirin alone for the prevention of atherothrombotic events". N. Engl. J. Med. 354 (16): 1706–17. DOI:10.1056/NEJMoa060989. PMID 16531616. Research Blogging.
- ↑ (1991) "Beneficial effect of carotid endarterectomy in symptomatic patients with high-grade carotid stenosis. North American Symptomatic Carotid Endarterectomy Trial Collaborators". N. Engl. J. Med. 325 (7): 445–53. PMID 1852179. [e]
- ↑ Rothwell PM, Giles MF, Chandratheva A, et al (2007). "Effect of urgent treatment of transient ischaemic attack and minor stroke on early recurrent stroke (EXPRESS study): a prospective population-based sequential comparison". Lancet 370 (9596): 1432–42. DOI:10.1016/S0140-6736(07)61448-2. PMID 17928046. Research Blogging.
- ↑ Markus HS, Droste DW, Kaps M, et al (2005). "Dual antiplatelet therapy with clopidogrel and aspirin in symptomatic carotid stenosis evaluated using doppler embolic signal detection: the Clopidogrel and Aspirin for Reduction of Emboli in Symptomatic Carotid Stenosis (CARESS) trial". Circulation 111 (17): 2233–40. DOI:10.1161/01.CIR.0000163561.90680.1C. PMID 15851601. Research Blogging.
- ↑ Giles MF, Rothwell PM (2007). "Risk of stroke early after transient ischaemic attack: a systematic review and meta-analysis". Lancet Neurol 6 (12): 1063–72. DOI:10.1016/S1474-4422(07)70274-0. PMID 17993293. Research Blogging.
- ↑ Johnston SC, Rothwell PM, Nguyen-Huynh MN, et al (2007). "Validation and refinement of scores to predict very early stroke risk after transient ischaemic attack". Lancet 369 (9558): 283-92. DOI:10.1016/S0140-6736(07)60150-0. PMID 17258668. Research Blogging.
- ↑ Rothwell PM, Giles MF, Flossmann E, et al (2005). "A simple score (ABCD) to identify individuals at high early risk of stroke after transient ischaemic attack". Lancet 366 (9479): 29-36. DOI:10.1016/S0140-6736(05)66702-5. PMID 15993230. Research Blogging.