» Articles » PMID: 35860488

Clinical Features and Outcome of the Guillain-Barre Syndrome: A Single-Center 11-Year Experience

Abstract

Background: Clinical presentation, electrophysiological subtype, and outcome of the Guillain-Barre' Syndrome (GBS) may differ between patients from different geographical regions. This study aims to assess clinical-neurophysiological features of an adult, Italian GBS cohort over 11 years.

Methods: Retrospective (from 1 January 2011 to 31 December 2021) analysis was carried out on patients admitted to the Siena University Hospital who fulfilled the GBS diagnostic criteria. Demographic data, clinical characteristics, treatment, need of mechanical ventilation (MV), laboratory and electrophysiological tests, preceding infections/vaccination/other conditions, and comorbidities were collected for each patient.

Results: A total of 84 patients (51 men, median age of 61 years), were identified. GBS subtype was classified as acute inflammatory demyelinating polyneuropathy (AIDP) in the 66.6% of patients, acute motor/sensory axonal neuropathy (AMAN/AMSAN) in 20.2%, and the Miller Fisher syndrome in 5 (5.9%). Flu syndrome and gastrointestinal infection were the most common preceding conditions. In total, five (5.9%) subjects had concomitant cytomegalovirus (CMV) infection. Cranial nerve involvement occurred in 34.5% of subjects. Differences between the axonal and AIDP forms of GBS concerned the presence of anti-ganglioside antibodies. In total, seven (8.33%) patients required MV.

Discussion: The epidemiological and clinical characteristics of GBS in different countries are constantly evolving, especially in relation to environmental changes. This study provides updated clinical-epidemiological information in an Italian cohort.

Citing Articles

Predictors of respiratory failure in Guillain-Barré syndrome: a 22 year cohort study from a single Italian centre.

Galassi G, Mazzoli M, Ariatti A, Bedin R, Marzullo D, Bastia E Eur J Neurol. 2023; 31(1):e16090.

PMID: 37823704 PMC: 11235807. DOI: 10.1111/ene.16090.


COVID-19 as a trigger of Guillain-Barré syndrome: A review of the molecular mechanism.

Malekpour M, Khanmohammadi S, Meybodi M, Shekouh D, Rahmanian M, Kardeh S Immun Inflamm Dis. 2023; 11(5):e875.

PMID: 37249286 PMC: 10187022. DOI: 10.1002/iid3.875.


Triggers of Guillain-Barré Syndrome: Predominates.

Finsterer J Int J Mol Sci. 2022; 23(22).

PMID: 36430700 PMC: 9696744. DOI: 10.3390/ijms232214222.


Guillain-Barré Syndrome in Northern China: A Retrospective Analysis of 294 Patients from 2015 to 2020.

Zhai Q, Guo C, Xue F, Qiang J, Li C, Guo L J Clin Med. 2022; 11(21).

PMID: 36362550 PMC: 9658830. DOI: 10.3390/jcm11216323.

References
1.
Green C, Baker T, Subramaniam A . Predictors of respiratory failure in patients with Guillain-Barré syndrome: a systematic review and meta-analysis. Med J Aust. 2018; 208(4):181-188. DOI: 10.5694/mja17.00552. View

2.
Benedetti M, Pugliatti M, DAlessandro R, Beghi E, Chio A, Logroscino G . A Multicentric Prospective Incidence Study of Guillain-Barré Syndrome in Italy. The ITANG Study. Neuroepidemiology. 2015; 45(2):90-9. DOI: 10.1159/000438752. View

3.
McGrogan A, Madle G, Seaman H, de Vries C . The epidemiology of Guillain-Barré syndrome worldwide. A systematic literature review. Neuroepidemiology. 2008; 32(2):150-63. DOI: 10.1159/000184748. View

4.
Visser L, van der Meche F, Meulstee J, Rothbarth P, Jacobs B, Schmitz P . Cytomegalovirus infection and Guillain-Barré syndrome: the clinical, electrophysiologic, and prognostic features. Dutch Guillain-Barré Study Group. Neurology. 1996; 47(3):668-73. DOI: 10.1212/wnl.47.3.668. View

5.
Hughes R, Perkin G, PIERCE J . Controlled trial prednisolone in acute polyneuropathy. Lancet. 1978; 2(8093):750-3. DOI: 10.1016/s0140-6736(78)92644-2. View