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Page 43

allied

academies

August 16-17, 2018 | Paris, France

Primary Healthcare

12

th

International Conference on

International Conference and Medicare Expo on

&

Pediatrics Health Care

Joint Event

Journal of Current Pediatric Research | Volume: 22

Introduction:

StudiescomparingtheDemyelinatingGBS(Dmy-

GBS) and axonal GBS (Ax-GBS) subtype in children are lacking.

Methods:

Inthishospitalbased,prospectiveandobservational

study, consecutive childrenwithGBSwere studied to compare

the clinical profile and outcome among the subtypes.

Results:

Among 9847 children admitted to the emergency,

95 had acute flaccid paralysis, 57 of whom had GBS.

Electrophysiologic studies were completed in 56, of whom

20 each had Dmy-GBS and Ax-GBS(19 motor axonal), 12 had

non-reactive nerves, and 5 unclassifiable findings. Mean age

of onset in Dmy-GBS was 55 months while Ax-GBS occurred

later at 84 months. More children in Ax-GBS group had

preceding gastroenteritis (4 vs 2), while Dmy-GBS had upper

respiratory infections (12 vs 7). Mean time from onset of

symptoms to hospital admission was more in Dmy-GBS 18

days to 8 days in Ax-GBS. Ataxia was only seen in Dmy-GBS

while wrist drop, foot drop and hyperreflexia were seen only

with Ax-GBS. Asymmetry of motor findings was more likely in

Ax-GBS(10vs4 P=0.048).Respiratorymuscle involvement (6 vs

3) and artificial ventilation (5 vs 2) was more in Ax-GBS. The

average duration of hospital stay was more in Ax-GBS 16 days

to 11 days in Dmy-GBS. Children with Ax-GBS less likely to be

non-ambulant at discharge (12 vs 6, p=0.036). Mean disability

scores at hospital discharge (4.9±1.2 vs 4±0.9, p=0.015)

and at last follow up (0.7±1.01 vs 0.05±0.2, p=0.016) were

higher in Ax-GBS. Children with Dmy-GBS were more likely to

achieve normalcy on follow up (19 vs 12, p=0.023). IVIg was

the treatment modality and was tolerated well with no side

effects reportedwithno relapseof symptoms after treatment.

Conclusion:

Axonal and demyelinating subtypes of GBS are

equally common in children of North India. Children with

axonal GBS have severe clinical course and more short term

morbidity and slower recovery.

e:

drpradeepgupta87@gmail.com

How different is demyelinating and axonal subtypes of Guillain-Barré syndrome (GBS) in children? A

study from tertiary care centre in Northern India

Pradeep Kumar Gupta, Naveen Sankhyan, Pratibha Singhi

and

Sunit Singhi

Siddhi Memorial Hospital, Bhaktapur, Nepal

Pediatrics & Primary HealthCare 2018, Volume 22

DOI: 10.4066/0971-9032-C1-003