scholarly journals What constitutes a ‘Good’ recovery outcome in post-acute Guillain-Barré syndrome? Results of a Nationwide Survey of post-acute GBS sufferers in the United Kingdom

2009 ◽  
Vol 17 (5) ◽  
pp. 677-683 ◽  
Author(s):  
I. Davidson ◽  
C. Wilson ◽  
T. Walton ◽  
S. Brissenden ◽  
M. Campbell ◽  
...  
2006 ◽  
Vol 166 (12) ◽  
pp. 1301 ◽  
Author(s):  
Richard A. Hughes ◽  
Judith Charlton ◽  
Radoslav Latinovic ◽  
Martin C. Gulliford

2020 ◽  
Author(s):  
Rui-Di Sun ◽  
jun Jiang

Abstract Objectives To compare the clinical profile and long-term outcome of children with asymmetry weakness and symmetry weakness in Guillain-Barre syndrome(GBS). Methods We retrospective analysis the clinical parameters, auxiliary examinations and long-term outcome between asymmetry weakness and symmetry weakness in childhood GBS. Results A total of 72 children were included, 12 children had asymmetry weakness. Six children were transient asymmetry weakness and six children were persistent asymmetry weakness. Compared to symmetry weakness children, asymmetry weakness had more preschool children (75% vs 25%, P=0.005), longer days on hospital(26.5(15-37) days vs 11(9-15) days, p =0.000), more mechanical ventilation in children(50% vs 8.33%, p=0.000), higher Disease severity score(DSS)at nadir of disease(4(3-5) vs 3(1-4), p=0.010), more axonal subtypes(50% vs 15%, p=0.013) and more complications(58.33% vs 8.33%, p=0.000). Eight children had sequelae and sixty-four children had good recovery. Compared to good recovery group, sequelae group had more axonal subtypes(62.5% vs 15.63%, p=0.002) and more persistent asymmetry weakness(62.5% vs 4.69%, p=0.000). Conclusions In conclusion, asymmetry weakness had two types in GBS, namely transient and persistent asymmetry weakness. Asymmetry weakness in GBS indicated more complex condition during disease than symmetry weakness. Persistent asymmetry weakness and axonal subtypes in GBS related with sequelae. Anterior horn cells in the spinal cord involvement may be the possible function in persistent asymmetry weakness combined with axonal subtypes in GBS.


2016 ◽  
Vol 21 (4) ◽  
Author(s):  
Christopher J Williams ◽  
Rhys H Thomas ◽  
Trevor P Pickersgill ◽  
Marion Lyons ◽  
Gwen Lowe ◽  
...  

We report a cluster of atypical Guillain–Barré syndrome in 10 adults temporally related to a cluster of four children with acute flaccid paralysis, over a 3-month period in South Wales, United Kingdom. All adult cases were male, aged between 24 and 77 years. Seven had prominent facial diplegia at onset. Available electrophysiological studies showed axonal involvement in five adults. Seven reported various forms of respiratory disease before onset of neurological symptoms. The ages of children ranged from one to 13 years, three of the four were two years old or younger. Enterovirus testing is available for three children; two had evidence of enterovirus D68 infection in stool or respiratory samples. We describe the clinical features, epidemiology and state of current investigations for these unusual clusters of illness.


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