Clinical presentation and symptomatology of Guillain-Barré syndrome: A literature review

Author:

Elendu Chukwuka1ORCID,Osamuyi Emmanuella I.2,Afolayan Ikeoluwa A.3,Opara Nnamdi C.4,Chinedu-Anunaso Nkeiruka A.5,Okoro Chinonso B.5,Nwankwo Augustine U.1,Ezidiegwu Dianne O.6,Anunaso Chinweike A.7,Ogbu Collins C.8,Aghahowa Samuel O.9,Atuchukwu Chibuzor S.6,Akpa Everister U.10,Peterson Jesse C.1

Affiliation:

1. Federal University Teaching Hospital, Owerri, Nigeria

2. Bingham University Teaching Hospital, Jos, Nigeria

3. Plateaumed Nigeria Limited, Lagos, Nigeria

4. Imo State University, Owerri, Nigeria

5. University of Nigeria Teaching Hospital, Ituku-Ozalla, Nigeria

6. Nnamdi Azikiwe University Teaching Hospital Nnewi, Nnewi, Nigeria

7. Alex Ekwueme Federal University Ndufu-Alike, Abakaliki, Nigeria

8. University of Port Harcourt Teaching Hospital, Choba, Nigeria

9. Nigerian Navy Reference Hospital, Ojo, Nigeria

10. Jos University Teaching Hospital, Jos, Nigeria.

Abstract

Guillain-Barré Syndrome (GBS) is a rare but potentially life-threatening neurological disorder characterized by acute onset ascending paralysis and sensory abnormalities. This article provides a comprehensive overview of GBS, covering its epidemiology, etiology, clinical presentation, diagnostic evaluation, management and treatment, prognosis, psychosocial impact, recent advances in research, public health implications, and ethical considerations. Epidemiological data reveal variations in GBS prevalence, incidence rates, and geographical distribution influenced by climate, infectious disease prevalence, and genetic susceptibility. Etiological factors include preceding infections, vaccinations, and autoimmune mechanisms, although the precise pathophysiology remains incomplete. Clinical presentation encompasses prodromal symptoms, motor deficits, sensory abnormalities, autonomic dysfunction, and variants such as Miller-Fisher Syndrome and Bickerstaff brainstem encephalitis. Neurological examination findings include weakness, paralysis, sensory deficits, and reflex changes, while autonomic dysfunction manifests as cardiovascular, respiratory, and gastrointestinal symptoms. Diagnostic evaluation relies on clinical criteria, laboratory tests (e.g., cerebrospinal fluid analysis, nerve conduction studies), and consideration of differential diagnoses. Management strategies encompass supportive care, immunomodulatory therapies (e.g., intravenous immunoglobulin, plasma exchange), and rehabilitation interventions to optimize functional outcomes and promote recovery. Prognosis varies depending on clinical features, treatment response, and complications such as respiratory failure and autonomic instability. Psychosocial impact encompasses psychological effects on patients and caregivers, highlighting the importance of coping strategies and support systems. Recent advances in research focus on emerging treatments, genetic predisposition, and biomarker discovery, offering promise for improving GBS outcomes. Public health implications include vaccination safety concerns and healthcare system considerations for GBS management. Ethical considerations encompass patient autonomy, resource allocation, and end-of-life decision-making.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference60 articles.

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