Transient global amnesia (TGA) is a clinical syndrome of reversible anterograde amnesia. It is an isolated disorder of memory function, generally resolving within 24 hours with a benign prognosis.

There is no specific treatment for TGA. The diagnosis is clinical, with investigations primarily focused on excluding alternative causes.

History
  • 1879 – The term ictus apoplectiques was first used by Jean–Alfred Fournier in 1879 to describe amnesic episodes in patients with neurosyphilis.
  • 1909 – Earliest clearly documented case resembling modern TGA was reported by Raoul Benon under the term ictus amnésique.” He described a 66-year-old woman with a 4–5 hour episode of amnesia, repetitive questioning, and a retrograde amnesia of 30 years, without other neurological signs—hallmarks of TGA. Benon distinguished these cases from amnesia due to general paresis.
  • 1954, Tormod Hauge reported three cases of transient memory loss following vertebral angiography, now retrospectively recognised as TGA.
  • 1956 – American neuroscientist, Morris Bender (1905-1983) described 12 patients with isolated amnestic episodes featuring confusion, repetitive questioning, and no recurrence—attributed to transient cerebral circulatory disturbance. Simultaneously, French neurologist Jean Antoine Courjon (1918-2017) and neuropsychiatrist Jean Alfred Marie Guyotat (1920-2017) described 16 patients with ictus amnésique, defined as transient retrograde amnesia without broader cognitive impairment. Unlike Bender’s cohort, six of their cases were recurrent.
  • 1958 – The modern term Transient Global Amnesia was introduced by Charles Miller Fisher (1913-2012) and Raymond D. Adams (1911–2008)
Epidemiology
  • Most cases occur between 50 and 80 years, with mean onset at 60-65 years.
Pathophysiology
  • Etiology remains unknown.
  • Likely site of disturbance: medial temporal lobe, especially the hippocampus.
  • No association with atherosclerotic risk factors.
  • No epileptic discharges on EEG.
  • Psychogenic stressors may act as triggers.
  • Theories include:
    • Migraine variant: vasospasm causing transient ischemia.
    • Venous congestion: Valsalva-associated cerebral venous hypertension.
Clinical Features
  • Typically in patients >50 years.
  • Abrupt onset and resolution.
  • Prominent anterograde amnesia:
    • Repetitive questioning
    • Inability to retain new information
    • Retrograde amnesia may also be present
  • Other cognitive functions intact:
    • Normal behaviour, language, and self-awareness
  • May perform complex tasks during episode
  • Duration: typically 1-12 hours, resolving within 24 hours
  • No increased risk of mortality, epilepsy or stroke
  • Recurrence rates: 3–25%
Differential Diagnosis
  • Seizure/post-ictal states
  • Drugs/toxins (e.g. alcohol blackouts)
  • Electrolyte disturbances (e.g. hypoglycaemia)
  • Wernicke encephalopathy
  • Stroke or TIA
  • Migraine
  • Head trauma
  • CNS infection/encephalitis
  • Psychogenic amnesia
Investigations

No definitive test. Aim: exclude other causes.

Bloods:

  • FBC
  • CRP
  • U&Es / glucose
  • LFTs

ECG:

  • Especially to exclude AF

EEG:

  • Typically normal

CT/CTA/CT Perfusion:

  • To rule out vascular pathology

MRI/MRA:

  • May show punctate hippocampal lesions on DWI; these are transient and non-specific

Urine drug screen:

  • Consider in younger patients
Management
  • Supportive care and reassurance
  • No specific therapy required
Disposition
  • Admit to Neurology Unit
  • Observe until resolution of symptoms

References

Publications

FOAMed

Fellowship Notes

MBBS DDU (Emergency) CCPU. Adult/Paediatric Emergency Medicine Advanced Trainee in Melbourne, Australia. Special interests in diagnostic and procedural ultrasound, medical education, and ECG interpretation. Co-creator of the LITFL ECG Library. Twitter: @rob_buttner

Dr James Hayes LITFL author

Educator, magister, munus exemplar, dicata in agro subitis medicina et discrimine cura | FFS |

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