An unusual presentation of prolonged delirium
BMJ 2021; 373 doi: https://doi.org/10.1136/bmj.n1423 (Published 16 June 2021) Cite this as: BMJ 2021;373:n1423- Richard Burne, specialty doctor in psychiatry1,
- Russell Birkett, academic clinical fellow in psychiatry2,
- William Bennet, consultant in endocrinology3,
- Abhi Shetty, consultant in liaison psychiatry1
- 1Sheffield Health and Social Care NHS Foundation Trust, Sheffield, UK
- 2Mental Health Research Unit, School of Health and Related Research (ScHARR), University of Sheffield, South Yorkshire, UK
- 3Department of Endocrinology and Metabolic Medicine, Sheffield Teaching Hospitals NHS Foundation Trust, Northern General Hospital, South Yorkshire, UK
- Correspondence to: A Shetty Abhijeeth.Shetty@shsc.nhs.uk
A woman in her 20s had a three week history of acute headaches, slurred speech, and unusual behaviour.
Neuropsychiatric symptoms were prominent, including confusion, confabulation, labile affect, persecutory beliefs, agitation, and aggression. No neurological deficits were present, her visual fields were normal, and she had no history of seizures.
Over the three weeks, her management had included: admission to neurology and discharge home; admission to psychiatry under the Mental Health Act and transfer back to neurology before discharge home again; readmission to psychiatry under the act.
Six months earlier she was investigated for hirsutism by her general practitioner: androgen levels were raised but pelvic ultrasonography did not show polycystic ovaries.
Moderate psychosocial stressors were present. She took no medication, had no psychiatric or substance misuse history, and had no relevant family history.
Routine delirium screen1—urinalysis, chest radiography, electrocardiogram, a computed tomography head scan, and blood tests (full blood count, …
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