Clinical features and outcome of Guillain–Barre syndrome in Saudi Arabia: a multicenter, retrospective study
Mohammed H. Alanazy,
Sawsan S. Bakry,
Afnan Alqahtani,
Norah S. AlAkeel,
Naael Alazwary,
Afag M. Osman,
Rania A. Mustafa,
Talal M. Al-Harbi,
Sameeh O. Abdulmana,
Aimee C. Amper,
Yousef Aldughaythir,
Abdulrahman S. Ali,
Seraj Makkawi,
Alaa Maglan,
Loujen Alamoudi,
Feras Alsulaiman,
Majed Alabdali,
Aysha A. AlShareef,
Ahmad R. Abuzinadah,
Ahmed K. Bamaga
Affiliations
Mohammed H. Alanazy
Division of Neurology, Department of Internal Medicine, King Saud University Medical City and College of Medicine, King Saud University
Sawsan S. Bakry
Division of Neurology, Department of Internal Medicine, King Saud University Medical City and College of Medicine, King Saud University
Afnan Alqahtani
Division of Neurology, Department of Internal Medicine, King Saud University Medical City and College of Medicine, King Saud University
Norah S. AlAkeel
College of Medicine, King Saud University
Naael Alazwary
Department of Medicine, Security Forces Hospital Program
Afag M. Osman
Department of Neurology, Prince Sultan Military Medical City
Rania A. Mustafa
Department of Neurology, Prince Sultan Military Medical City
Talal M. Al-Harbi
Neurology Department, Neuroscience Center, King Fahad Specialist Hospital-Dammam
Sameeh O. Abdulmana
Neurology Department, Neuroscience Center, King Fahad Specialist Hospital-Dammam
Aimee C. Amper
Neurology Department, Neuroscience Center, King Fahad Specialist Hospital-Dammam
Yousef Aldughaythir
Neurology Department, National Neuroscience Institute, King Fahad Medical City
Abdulrahman S. Ali
Neurology Department, National Neuroscience Institute, King Fahad Medical City
Seraj Makkawi
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences
Alaa Maglan
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences
Loujen Alamoudi
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences
Feras Alsulaiman
Department of Neurology, King Fahad Hospital of the University, Imam Abdulrhman Bin Faisal University
Majed Alabdali
Department of Neurology, King Fahad Hospital of the University, Imam Abdulrhman Bin Faisal University
Aysha A. AlShareef
Internal Medicine Department, Neurology Division, Neuromuscular Medicine Unit, Faculty of Medicine and King Abdulaziz University Hospital, King Abdulaziz University
Ahmad R. Abuzinadah
Internal Medicine Department, Neurology Division, Neuromuscular Medicine Unit, Faculty of Medicine and King Abdulaziz University Hospital, King Abdulaziz University
Ahmed K. Bamaga
Pediatric department, Neuromuscular Medicine Unit, Faculty of Medicine and King Abdulaziz University Hospital, King Abdulaziz University
Abstract Background Guillain–Barre syndrome (GBS) is an inflammatory polyradiculoneuropathy characterized by rapidly evolving weakness and areflexia, reaching nadir within 4 weeks. Data on the characteristic of GBS in Saudi Arabia are limited. This study aimed to describe the clinical, electrophysiological, and laboratory characteristics and outcome of a multicenter cohort of patients with GBS. Methods This is a retrospective multicenter nationwide study. Patients who had GBS, identified through Brighton Criteria, between January 2015 and December 2019 were included. Data collected included demographics, clinical features, cerebrospinal fluid profile, reported electrophysiological patterns, treatment, and outcome. Reported GBS subtypes were compared using chi-square, Fisher's exact, or Mann–Whitney U tests, as appropriate. Results A total of 156 patients with GBS were included (men, 61.5%), with a median age of 38 (interquartile range, 26.25–53.5) years. The most commonly reported antecedent illnesses were upper respiratory tract infection (39.1%) and diarrhea (27.8%). All but two patients (98.7%) had weakness, 64.1% had sensory symptoms, 43.1% had facial diplegia, 33.8% had oropharyngeal weakness, 12.4% had ophthalmoplegia, and 26.3% needed mechanical ventilation. Cytoalbuminological dissociation was observed in 69.1% of the patients. GBS-specific therapy was administered in 96.8% of the patients, of whom 88.1% had intravenous immunoglobulin, and 11.9% had plasmapheresis. Approximately half of the patients were able to walk independently within 9 months after discharge, and a third regained the ability to walk independently thereafter. Death of one patient was caused by septicemia. Acute inflammatory demyelinating polyradiculoneuropathy was the most commonly reported GBS subtype (37.7%), followed by acute motor axonal neuropathy (29.5%), and acute motor-sensory axonal neuropathy (19.2%). Conclusion The clinical and laboratory characteristics and outcome of GBS in the Arab population of Saudi Arabia are similar to the international cohorts. The overall prognosis is favorable.