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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