Epidemiological study of Guillain-Barré syndrome in south east England
a Department of Neurology, b Department of Public Health
Medicine, UMDS Guy's Hospital, St Thomas' Street, London, UK
Correspondence to: Professor R A C Hughes, Department of Neurology, UMDS Guy's Hospital, St Thomas' Street, London SE1 9RT, UK.
Received 25 March 1997 and in revised form 1
September 1997;
Accepted 17 September 1997
OBJECTIVES
To determine the incidence, treatment,
and outcome of Guillain-Barré syndrome in south east England.
METHODS
Patients presenting with confirmed
Guillain-Barré syndrome between 1 July 1993 and 30 June 1994 were
recruited via a voluntary reporting scheme coordinated by the British
Neurological Surveillance Unit, hospital activity data collected from
acute admitting hospitals within the South East and South West Thames
Regional Health Authorities, death certificates, and a contemporary
research study of Guillain-Barré syndrome and Campylobacter
jejuni infection. All patients were followed up for one year to
determine outcome.
RESULTS
Seventy nine patients were recruited, 35 (44%) male, 44 (56%) female, including three children (two boys, one
girl). The crude (95% confidence interval (95% CI)) annual incidence
was 1.2 (0.9-1.4) cases/100 000 population and 1.5 (1.3-1.8)/100 000 when adjusted for undetected cases. Twenty (25%) patients required
ventilation for an average (SD) of 42 (64) days. Thirty six (46%)
patients received intravenous human immunoglobulin, five (6%) received plasma exchange, 11 (14%) both treatments, three (4%) steroids, and
25 (32%) no immunomodulatory treatment. One year later, six patients
(8%) had died, all of whom were older than 60, three (4%) remained
bedbound or ventilator dependent, seven (9%) were unable to walk
unaided, 14 (17%) were unable to run, and 49 (62%) had made a
complete or almost complete recovery. Increasing age was significantly
associated with a poorer outcome at one year.
CONCLUSIONS
Despite the frequent use of modern
immunomodulatory treatments Guillain-Barré syndrome still carries
considerable morbidity and mortality.
© 1998 by Journal of Neurology, Neurosurgery, and Psychiatry
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