BMJ 2005;330:406-409 (19 February), doi:10.1136/bmj.330.7488.406
Clinical review
Locked-in syndrome
Eimear Smith, specialist registrar in rehabilitation medicine1,
Mark Delargy, consultant in rehabilitation medicine1
1 National Rehabilitation Hospital, Dun Laoghaire, County Dublin, Ireland
Correspondence to: E Smith eimear.smith@nrh.ie
| The first 150 words of the full text of this article appear below. |
Introduction
The locked-in syndrome is caused by an insult to the ventral
pons, most commonly an infarct, haemorrhage, or trauma. The
characteristics of the syndrome are quadriplegia and anarthria
with preservation of consciousness. Patients retain vertical
eye movement, facilitating non-verbal communication. Ten year
survival rates as high as 80% have been reported. Even limited
physical recovery can improve quality of life and enable patients
to return to live with their families. Early referral to a specialist
rehabilitation service for specialist care and technology is
therefore important.
Sources and selection criteria
We gathered information for this article through searches in
Medline and Taylor and Francis Health Sciences, identifying
relevant case series reviews on the locked-in syndrome and other
brain stem strokes. Our own experience is also incorporated.
Clinical features
Locked-in syndrome was first defined in 1966 as quadriplegia,
lower cranial nerve paralysis, and mutism with preservation
of consciousness, vertical gaze, and upper eyelid movement.
1 It was redefined in
. . . [Full text of this article]
Classification
Diagnosis and early management
Recovery and prognosis
Development of communication devices
Quality of life for patients and carers

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