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Transient global amnesia

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Transient global amnesia
Classification and external resources
ICD-10 G45.4
ICD-9 437.7
DiseasesDB 13251
eMedicine neuro/380 
MeSH D020236

Transient global amnesia (TGA), is an anxiety-producing temporary loss of the ability to form new long-term memories that by definition resolves within 24 hours and most commonly affects the middle-aged or elderly.[1] During the episode, affected people remain alert and communicative, with no disturbance in their knowledge of personal identity. Specific neurological problems, such as epilepsy, are not present and other more general cognitive abilities are unaffected. Worldwide, its incidence is between approximately 3 and 35 cases per 100,000 people per year.[2]

Contents

[edit] Differential diagnosis

TGA is differentiated from stroke by the lack of other neurologic deficits.[3] Other differential diagnoses are transient epileptic amnesia (TEA), and amnesic strokes.[4]

[edit] Presentation

TGA does produce an inability to assimilate certain, generally current or recent, details while social skills and memories of distant past events or trivia is maintained.

The requirements for TGA include:[5]

  • The attack was witnessed and reported as being a definite loss of recent memory (anterograde amnesia).
  • There was an absence of clouding of consciousness.
  • There were no focal neurological signs or deficits during or after the attack.
  • There were no features of epilepsy, and the patient did not have any recent head injury or active epilepsy.
  • The attack resolved within 24 hours.

[edit] Causes

The underlying cause of TGA is unclear. One current hypothesis is that TGA may be due to venous congestion of the brain,[6] leading to ischemia of structures involved with memory, such as the hippocampus.[7] This may be triggered by performing a Valsalva maneuver in the context of various precipitating events such as immersion in cold water, sexual activity, severe emotional stress and vigorous exertion.[8][9]

[edit] Prognosis

The prognosis of TGA is very good. It does not affect mortality and has a small recurrence rate.

"The most important part of management after diagnosis is looking after the psychological needs of the patient and his or her relatives. Seeing a once competent and healthy partner, sibling or parent become incapable of remembering what was said only a minute ago is very distressing, and hence it is often the relatives who will require reassurance." [10]

[edit] See also

[edit] References

  1. ^ Hodges JR, Warlow CP. (1990) Syndromes of transient amnesia: towards a classification. A study of 153 cases. J Neurol Neurosurg Psychiatry, 53 (10), 834-43. PMID 2266362
  2. ^ Quinette P, Guillery-Girard B, Dayan J, et al. What does transient global amnesia really mean? Review of the literature and thorough study of 142 cases. Brain 2006;129 (Part 7):1640–58.
  3. ^ Monzani V, Rovellini A, Schinco G, et al. Transient global amnesia or subarachnoid haemorrhage? Clinical and laboratory findings in a particular type of acute global amnesia. Eur J Emerg Med 2000;7:291–3.
  4. ^ Engmann, Birk; Reuter, Mike: A case history of sudden memory dysfunction – caused by transient epileptic amnesia. Akt Neurol 2003;30:350–353
  5. ^ Hodges JR, Warlow CP Syndromes of transient amnesia: towards a classification; a study of 153 cases. Neurosurg Psychiatry 1990;53:834–43
  6. ^ Lewis SL Aetiology of transient global amnesia. Lancet.1998;352:397–399.
  7. ^ Chung CP, Hsu H, Chao A, et al. Detection of intracranial venous reflux in patients of transient global amnesia. Neurology 2006;66:1873–7.
  8. ^ "UCLA Department of Medicine - wfsection-Transient Global Amnesia". http://www.med.ucla.edu/modules/wfsection/article.php?articleid=38. Retrieved on 2007-07-25. 
  9. ^ Moreno-Lugris XC, Martinez-Alvarez J , Branas F , et al. Transient global amnesia. Case–control study of 24 cases. Rev Neurol 1996;24:554–7.
  10. ^ Magnus Harrison and Mark Williams (2007). "The diagnosis and management of transient global amnesia in the emergency department". Emerg Med J 24: 444–445. doi:10.1136/emj.2007.046565. 
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