Guilain Barre Syndrome

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Jump to: navigation, search Guillain-Barré syndrome Classification and external resources

ICD-10

G61.0

ICD-9

357.0

OMIM

139393

DiseasesDB 5465 MedlinePlus 000684 eMedicine emerg/222 neuro/7 pmr/48 neuro/598 MeSH

D020275

Guillain-Barré syndrome (GBS) (in French pronounced [ɡilɛ̃ baˈʁe][1][2], in English pronounced /ˈɡiːlæn ˈbɑreɪ/[3], /ɡiːˈæn bəˈreɪ/,[4] etc.[5]) is an acute inflammatory demyelinating polyneuropathy (AIDP), an autoimmune disease affecting the peripheral nervous system, usually triggered by an acute infectious process. It is included in the wider group of peripheral neuropathies. There are several types of GBS, but unless otherwise stated, GBS refers to the most common form, acute inflammatory demyelinating polyneuropathy (AIDP). It is frequently severe and usually exhibits as an ascending paralysis noted by weakness in the legs that spreads to the upper limbs and the face along with complete loss of deep tendon reflexes. With prompt treatment by plasmapheresis or intravenous immunoglobulins and supportive care, the majority of patients will regain full functional capacity. However, death may occur if severe pulmonary complications and dysautonomia are present.

Contents [hide]

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1 Pathophysiology 2 Signs and symptoms o 2.1 Clinical variants 3 Diagnosis o 3.1 Diagnostic criteria  3.1.1 Required  3.1.2 Supportive o 3.2 Differential diagnosis 4 Treatment 5 Prognosis 6 History 7 Notable sufferers 8 References

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9 External links

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[edit] Pathophysiology All forms of Guillain-Barré syndrome are due to an immune response to foreign antigens (such as infectious agents or vaccines) but mistargeted to host nerve tissues instead (a form of antigenic mimicry). The targets of such immune attack are thought to be gangliosides, which are complex glycosphingolipids present in large quantities on human nerve tissues, especially in the nodes of Ranvier. An example is the GM1 ganglioside, which can be affected in as many as 20-50% of cases, especially in those preceded by Campylobacter jejuni infections. Another example is the GQ1b ganglioside, which is the target in the Miller Fisher syndrome variant (see below). The end result of such autoimmune attack on the peripheral nerves is inflammation of myelin and conduction block, leading to a muscle paralysis that may be accompanied by sensory or autonomic disturbances. However, in mild cases, axonal function remains intact and recovery can be rapid if remyelination occurs. In severe cases, such as in the AMAN or AMSAN variants (see below), axonal degeneration occurs, and recovery depends on axonal regeneration. Recovery becomes much slower, and there is a greater degree of residual damage. Recent studies on the disease have demonstrated that approximately 80% of the patients have myelin loss, whereas, in the remaining 20%, the pathologic hallmark of the disease is indeed axon loss.

[edit] Signs and symptoms The disease is characterized by weakness which affects the lower limbs first, and rapidly progresses in an ascending fashion. Patients generally notice weakness in their legs, manifesting as "rubbery legs" or legs that tend to buckle, with or without dysesthesias

(numbness or tingling). As the weakness progresses upward, usually over periods of hours to days, the arms and facial muscles also become affected. Frequently, the lower cranial nerves may be affected, leading to bulbar weakness, (oropharyngeal dysphagia, that is difficulty with swallowing, drooling, and/or maintaining an open airway) and respiratory difficulties. Most patients require hospitalization and about 30% require ventilatory assistance. Facial weakness is also commonly a feature, but eye movement abnormalities are not commonly seen in ascending GBS, but are a prominent feature in the Miller Fisher variant (see below.) Sensory loss, if present, usually takes the form of loss of proprioception (position sense) and areflexia (complete loss of deep tendon reflexes), an important feature of GBS. Loss of pain and temperature sensation is usually mild. In fact, pain is a common symptom in GBS, presenting as deep aching pain usually in the weakened muscles, which patients compare to the pain from overexercising. These pains are self-limited and should be treated with standard analgesics. Bladder dysfunction may occur in severe cases but should be transient. If severe, spinal cord disease should be suspected. Fever should not be present, and if it is, another cause should be suspected. In severe cases of GBS, loss of autonomic function is common, manifesting as wide fluctuations in blood pressure, orthostatic hypotension, and cardiac arrhythmias. The symptoms are similar to those for progressive inflammatory neuropathy.[6]

[edit] Clinical variants Although ascending paralysis is the most common form of spread in GBS, other variants also exist. •

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Miller Fisher Syndrome (MFS) is a rare variant of GBS and manifests as a descending paralysis, proceeding in the reverse order of the more common form of GBS. It usually affects the ocular muscles first and presents as ophthalmoplegia, ataxia, and areflexia. Anti-GQ1b antibodies are present in 90% of cases. Acute motor axonal neuropathy (AMAN)[7], aka. Chinese Paralytic Syndrome, attacks motor nodes of Ranvier and is prevalent in China and Mexico. The disease may be seasonal and recovery can be rapid. Anti-GD1a antibodies[8] are present. Anti-GD3 antibodies are found more frequently in AMAN Acute motor sensory axonal neuropathy (AMSAN) is similar to AMAN but also affects sensory nerves with severe axonal damage. Recovery is slow and often incomplete.[9]

[edit] Diagnosis The diagnosis of GBS usually depends on findings such as rapid development of muscle paralysis, areflexia, absence of fever, and a likely inciting event. CSF and ECD is used

almost every time to verify symptoms, but because of the acute nature of the disease, they may not become abnormal until after the first week of onset of signs and symptoms. •

CSF typical CSF findings include albumino-cytological dissociation, this is, an elevated protein level (100 - 1000 mg/dL) without an accompanying pleocytosis (increased cell count), as opposed to infectious causes. A sustained pleocytosis may indicate an alternative diagnosis such as infection.

Researchers speculate as to why protein is elevated without pleocytosis in the CSF. Infilitration of WBCs in the myelin are responsible for demyelination in the peripheral nerves. Specific, 2D gel electrophoresis showed proteins unspecifically affected in different inflammatory as well as non-inflammatory neurological diseases and may be of limited value as disease-related biochemical markers in GBS. [Proteome analysis of cerebrospinal fluid in Guillain–Barré syndrome]

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Electrodiagnostics electromyography (EMG) and nerve conduction study (NCS) may show prolonged distal latencies, conduction slowing, conduction block, and temporal dispersion of compound action potential in demyelinating cases. In primary axonal damage, the findings include reduced amplitude of the action potentials without conduction slowing.

[edit] Diagnostic criteria [edit] Required • • • •

Progressive, relatively symmetrical weakness of 2 or more limbs due to neuropathy Areflexia Disease course < 4 weeks Exclusion of other causes (see below)

[edit] Supportive • • • • • •

relatively symmetric weakness accompanied by numbness and/or tingling mild sensory involvement facial nerve or other cranial nerve involvement absence of fever typical CSF findings obtained from lumbar puncture electrophysiologic evidence of demyelination from electromyogram

[edit] Differential diagnosis • • • • • • • • • • • • • •

acute myelopathies with chronic back pain and sphincter dysfunction botulism with early loss of pupillary reactivity diphtheria with early oropharyngeal dysfunction Lyme disease polyradiculitis and other tick-borne paralyses porphyria with abdominal pain, seizures, psychosis vasculitis neuropathy poliomyelitis with fever and meningeal signs CMV polyradiculitis in immunocompromised patients critical illness neuropathy myasthenia gravis poisonings with organophosphate, poison hemlock, thallium, or arsenic paresis caused by West Nile Virus spinal astrocytoma Motor Neurone Disease

[edit] Treatment Supportive care with monitoring of all vital functions is the cornerstone of successful management in the acute patient. Of greatest concern is respiratory failure due to paralysis of the diaphragm. Early intubation should be considered in any patient with a vital capacity (VC) <20 ml/kg, a Negative Inspiratory Force (NIF) <-25 cmH2O, more than 30% decrease in either VC or NIF within 24 hours, rapid progression of disease, or autonomic instability. Once the patient is stabilized, treatment of the underlying condition should be initiated as soon as possible. Either high-dose intravenous immunoglobulins (IVIg) at 400mg/kg for 5 days or plasmapheresis can be administered, as they are equally effective and a combination of the two is not significantly better than either alone. Therapy is no longer effective after 2 weeks after the first motor symptoms appear, so treatment should be instituted as soon as possible. IVIg is usually used first because of its ease of administration and safety profile, with a total of five daily infusions for a total dose of 2 g/kg body weight (.4kg each day). The use of intravenous immunoglobulins is not without risk, occasionally causing hepatitis, or in rare cases, renal failure if used for longer than five days. Glucocorticoids have NOT been found to be effective in GBS. If plasmapheresis is chosen, a dose of 40-50 mL/kg plasma exchange (PE) is administered four times over a week. Following the acute phase, the patient may also need rehabilitation to regain lost functions. This treatment will focus on improving ADL (activities of daily living) functions such as brushing teeth, washing and getting dressed. Depending on the local structuring on health care, there will be established a team of different therapists and nurses according to patient needs. An occupational therapist can offer equipment (such as wheel chair and cutlery) to help the patient achieve ADL independence. A physiotherapist

would plan a progressive training programme, and guide the patient to correct, functional movement, avoiding harmful compensations which might have a negative effect in the long run. A Speech and Language Therapist would be essential in the patient regaining speaking and swallowing ability if they were intubated and received a tracheostomy. The Speech and Language Therapist would also offer advice to the medical team regarding the swallowing abilities of the patient and would help the patient regain their communication ability pre- Dysarthria. There would also be a doctor,nurse and other team members involved depending on the needs of the patient. This team contribute with their knowledge to guide the patient towards his or her goals, and it is important that all goals set by the separate team members are relevant for the patient's own priorities. After rehabilitation the patient should be able to function in his or her own home and attend necessary training as needed.

[edit] Prognosis Most of the time recovery starts after 4th week from the onset of the disease. Approximately 80% of patients have a complete recovery within a few months to a year, although minor findings may persist, such as areflexia. About 5–10% recover with severe disability, with most of such cases involving severe proximal motor and sensory axonal damage with inability of axonal regeneration. However, this is a grave disease and despite all improvements in treatment and supportive care, the death rate among patients with this disease is still about 2–3% even in the best intensive care units. Worldwide, the death rate runs slightly higher (4%), mostly from a lack of availability of life support equipment during the lengthy plateau lasting 4 to 6 weeks, and in some cases up to 1 year, when a ventilator is needed in the worst cases. About 5–10% of patients have one or more late relapses, in which case they are then classified as having chronic inflammatory demyelinating polyneuropathy (CIDP).

[edit] History The disease was first described by the French physician Jean Landry in 1859. In 1916, Georges Guillain, Jean Alexandre Barré, and Andre Strohl diagnosed two soldiers with the illness and discovered the key diagnostic abnormality of increased spinal fluid protein production, but normal cell count.[10] GBS is also known as acute inflammatory demyelinating polyneuropathy, acute idiopathic polyradiculoneuritis, acute idiopathic polyneuritis, French Polio, Landry's ascending paralysis and Landry Guillain Barre syndrome.

[edit] Notable sufferers • •

Andy Griffith, actor on Andy Griffith Show, and Matlock. He contracted GuillainBarré in 1983. [11] Rachel Chagall, actress, contracted GBS in 1982. In 1987 she portrayed Gabriela Brimmer, a notable disabilities activist. [12]

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Joseph Heller, author, contracted GBS in 1981. This episode in his life is recounted in the autobiographical No Laughing Matter, which contains alternating chapters by Heller and his good friend Speed Vogel.[13] Franklin D. Roosevelt, U.S. president. In 2003, a peer-reviewed study[14] found that it was more likely that Roosevelt's paralysis--long attributed to poliomyelitis--was actually Guillain-Barré syndrome. Markus Babbel, former international footballer, contracted GBS in 2001, following a period suffering from the Epstein-Barr virus. He lost almost an entire year of his footballing career between the two illnesses and never again demonstrated the same level of ability that won him over 50 caps for Germany. [1] Serge Payer, Canadian-born professional hockey player. After battling and overcoming the syndrome, He set up the Serge Payer foundation, which is dedicated to raising money for research into new treatments and cures for Guillain-Barré syndrome[15].

[edit] References 1. 2. 3. 4.

^ "John Wells's phonetic blog, 23rd February, 2007". ^ "See also, in the same blog, the entry of October 20th, 2008". ^ Recommended by the "GBS Support Group". ^ "Guillain-Barre Syndrome". Dictionary.com Unabridged (v 1.1). Random House. 5. ^ In English, Guillain may be pronounced with an L sound as in French, but it is common to pronounce it without one, originally based on the mistaken assumption that the French pronunciation of the ll is IPA [ j ] and not [ l ]. In English, both Guillain and Barré may be pronounced with the stress on either the first or the last syllable. The nasal vowel [ɛ̃]at the end of Guillain is either kept in English or replaced by a sequence of an oral vowel and a nasal consonant such as [æn]. 6. ^ David Brown (2008-02-04). "Inhaling Pig Brains May Be Cause of New Illness". The Washington Post. Retrieved on 2008-02-04. 7. ^ McKhann GM, Cornblath DR, Ho T, et al (1991). "Clinical and electrophysiological aspects of acute paralytic disease of children and young adults in northern China". Lancet 338 (8767): 593–7. doi:10.1016/01406736(91)90606-P. PMID 1679153. 8. ^ Ho TW, Mishu B, Li CY, et al (1995). "Guillain-Barré syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies". Brain 118 ( Pt 3): 597–605. PMID 7600081. 9. ^ Griffin JW, Li CY, Ho TW, et al (1995). "Guillain-Barré syndrome in northern China. The spectrum of neuropathological changes in clinically defined cases". Brain 118 ( Pt 3): 577–95. PMID 7600080. 10. ^ Guillain-Barré-Strohl syndrome and Miller Fisher's syndrome at Who Named It 11. ^ "Andy in Guideposts Magazine". 12. ^ "Gaby, A True Story (1987)". Films involving Disabilities.

13. ^ Vogel, Speed; Heller, Joseph (2004). No Laughing Matter. New York: Simon & Schuster. ISBN 0-7432-4717-5. 14. ^ Goldman AS, Schmalstieg EJ, Freeman DH, Goldman DA, Schmalstieg FC (2003). "What was the cause of Franklin Delano Roosevelt's paralytic illness?". J Med Biogr 11 (4): 232–40. PMID 14562158. 15. ^ Serge Payer Foundation, Serge Payer Foundation Mission.

[edit] External links • • • •

GBS/CIDP Foundation International Information from the Guillain-Barré Syndrome Support Group (UK) Information from GBS Association of New South Wales (AU) miller_fisher at NINDS

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Multiple sclerosis

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Nervous system pathology, primarily PNS (G50-G99, 350-359) V (Trigeminal neuralgia) - VII (Facial nerve paralysis, Cranial nerve diseaseBell's palsy, Melkersson-Rosenthal syndrome, Central seven) - XI (Accessory nerve disorder) Brachial plexus lesion - Thoracic outlet syndrome Radiculopathy, plexopathy Phantom limb upper limb (Carpal tunnel syndrome, Ulnar nerve entrapment, Radial neuropathy) Mono- neuropathylower limb (Meralgia paraesthetica, Tarsal tunnel syndrome, Morton's neuroma) Causalgia - Mononeuritis multiplex Charcot-Marie-Tooth disease - Dejerine Sottas syndrome HMSN - Refsum's disease autoimmune (Guillain-Barré syndrome, Chronic Polyradiculoneuropathyinflammatory demyelinating polyneuropathy) - Alcoholic polyneuropathy Neuromuscular junction disease

autoimmune (Myasthenia gravis, Lambert-Eaton myasthenic syndrome)

Congenital - dystrophin (Becker's, Duchenne) Distal - Emery-Dreifuss - Facioscapulohumeral Muscular dystrophy Limb-girdle muscular dystrophy - Myotonic Oculopharyngeal Myotonic dystrophy - Myotonia congenita MyotoniaThomsen disease - Neuromyotonia Paramyotonia congenita Bethlem myopathy - Central core disease Congenital myopathyCentronuclear myopathy - Nemaline myopathy Zaspopathy Mitochondrial myopathyMELAS - MERRF - KSS - PEO Periodic paralysisHypokalemic - Hyperkalemic

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Immune disorders: Hypersensitivity and autoimmune diseases

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