Afp 30.07.2014
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1) Guillain-Barré syndrome (GBS) is an acute inflammatory demyelinating polyneuropathy that is a common cause of acute flaccid paralysis. 2) It is caused by an autoimmune attack against peripheral nerves following a viral or bacterial infection. Campylobacter jejuni is a frequent trigger that shares antigens with human nerves. 3) Clinical features include ascending limb weakness, diminished reflexes, and possible involvement of cranial nerves and respiratory muscles. Diagnosis involves CSF analysis showing elevated proteins with normal cell count and electrophysiology showing demyelination.
Afp 30.07.2014
- 1. Acute Flaccid Paralysis (AFP) Dr . AJAYAN.P JIPMER
- 2. digram of a cross section through the spinal cord The dorsal root on each side conveys sensory information to the spinal cord; the ventral root conveys motor commands to the muscles.
- 3. Differential Diagnosis of Acute Weakness: Cerebral: Bilateral strokes, Hysteria… Cerebellar : Acute cerebellar ataxia syndromes. Spinal: Compressive myolopathy , Transverse myelitis . Peripheral nerve: Acute inflammatory demyelinating neuropathy, Toxic neuropathy, Diphtheria, Tick paralysis
- 4. DD of Acute Weakness (cont): Neuromuscular junction: Botulism, Myasthenia Gravis… Muscle disease: Acute myositis. Acute inflammatory myopathies Metabolic myopathies , Periodic paralysis…
- 6. Acute Flaccid Paralysis WHO defines AFP syndrome as “ Rapid onset of weakness of an individual’s extremities, often including weakness of muscles of respiration & swallowing, progressing to maximum severity within 1-10 days. The term ‘flaccid’ indicates the absence of : Spasticity. Other signs of disordered CNS motor tracts such as : Hyperflexia, Clonus, Extensor plantar response .
- 7. Clinically spasticity is defined as velocity dependent resistance to stretch, where a lack of inhibition results in excessive contraction of the muscles, ultimately leading to hyperflexia (overly flexed joints).
- 8. AFP is an emergency in which management priorities are to support vital functions and reach a specific diagnosis in a timely manner with a focused history and physical examination.
- 9. DD of Acute Flaccid Paralysis Guillain-Barré Syndrome. Poliomyelitis. Transverse Myelitis.
- 10. Fever at onset - Polio or enteroviralmyelitis, Transverse myelitis, myositis, epidural abscess, and Koch spine (prolonged history) Trauma: head/neck Trivial trauma may lead to spinal compression in patients with cervical vertebral instability (Patients with Downs syndrome, congenital cervicovertebral anomalies or juvenile idiopathic arthritis)
- 11. Exposure Toxins: lead, arsenic Snake envenomation Dog bite: Rabies Preceding infectious prodrome/vaccination Guillain Barre syndrome or transverse myelitis Sore throat, neck swelling- diphtheretic polyneuropathy (non/partly immunized
- 12. Precipitating factors Diarrhea: Hypokalemia, enteroviral myelitis Exertion or post parandial: Hypokalemic periodic paralysis Intramuscular injection: Polio, traumatic sciatic neuritis Sensory loss/level -Compressive myelopathy, transverse myelitis
- 13. Early bowel/bladder involvement Compressive myelopathy, transverse myelitis Constipation in <1 y Botulism (H/o honey exposure) Prominent autonomic signs/symptoms Guillain Barre syndrome, Rabies, acute myelopathy
- 14. Ascending weakness Guillain Barre syndrome, Rabies, Varicella zoster virus, ascending myelitis Descending weakness ---Diphtheria, Botulism Prominent and earl ptosis Myasthenia Gravis, Botulism
- 15. Facial weakness Guillain Barre syndrome, Myasthenia Gravis, Botulism Fluctuating symptoms, fatigability Myasthenia Gravis Muscle tenderness ----Myositis, inflammatory myopathy, (myalgias may be severe in Guillain Barre syndrome
- 16. Muscle stretch reflexes Absent: Guillain Barre syndrome, Polio, Diphtheria, spinal shock, at level of spinal cord damage Preserved : Myasthenia Gravis, periodic paralysis, Botulism Exaggerated : Below level of spinal lesion, Upper motor neuron lesion
- 17. Spinal tenderness, painful spine movement Spinal trauma, epidural abscess
- 18. 1)Spinal cord -Compressive -Traumatic spinal injury, epidural abscess, hematoma, discitis inflammatory-- Transverse myelitis
- 19. 2)Anterior horn cell Viral - Poliomyelitis, vaccine associated poliomyelitis, Enteroviral myelitis, Japanese encephalitis Vascular ----Anterior spinal artery infarction
- 20. 3)Roots/nerves- Immune mediated-- Guillain Barre syndrome, Toxin-- Post diphtheritic, porphyria, arsenic Viral ------Rabies Trauma ----Injection related sciatic neuritis
- 21. 4)Neuromuscular junction Immune mediated--- Myasthenia Gravis Drugs, toxins-- Organophosphates, snake venom, drugs (aminoglycosides), Botulism Dyselectrolytemia ------Hypermagnesemia 5
- 22. 5) Muscle ----Infection Viral myositis Inflammation --nflammatory myopathy (polymyositis) Channelopathy ---Hypokalemic periodic paralysis Dyselectrolytemia -------------------Hypokalemia
- 24. Guillain-Barré Syndrome : • It is an acute idiopathic monophasic acquired inflammatory demyelinating polyradiculo-neuropathy. • Polyradiculopathy refers to damage to multiple nerve roots sufficient to produce neurologic symptoms & signs such as pain, weakness, and sensory affection. • GBS is the most common cause of acute flaccid paralysis in healthy infants and children.
- 25. )1865-1826( Georges Charles Guillain, neurologist (1876-1961), André Strohl, physicien (1887- 1977) Jean-Alexandre Barré, neurologist (1880- 1967) French neurologists and physicians first started describing Guillain-Barré Syndrome in 1859
- 26. Epidemiology : • The annual incidence 0.6 to 2.4 cases / 100,000 population and occurs at all ages and in both sexes. • The incidence is lower in children, 0.38 and 0.91 cases / 100,000 in two reports. • Occurs rarely in children younger than 2 years of age, but can occur in infants. • Males are affected 1.5 times <females in all ages.
- 27. GBS.Pathophysiology : • Immune mediated disease. • There is no known genetic factors. • 2/3 of cases follow a respiratory or GI infection. • Campylobacter infection is the most common, but other organisms include CMV, EBV, HSV, Enteroviruses,… • Guillain-Barré syndrome has been reported to follow : – vaccinations . – epidural anesthesia. – thrombolytic agents.
- 28. The pathophysiologic mechanism of an antecedent illness and of GBS can be typified by Campylobacter jejuni infections. The virulence of C jejuni is thought to be based on the presence of specific antigens in its capsule that are shared with nerves. Immune responses directed against lipopolysaccharide antigens in the capsule of C jejuni result in antibodies that cross-react with ganglioside GM1 in myelin, resulting in the immunologic damage to the peripheral nervous system. This process has been termed molecular mimicry.
- 29. GBS.Pathophysiology : • The main lesions are acute inflammatory demyelinating polyradiculopathy, with acute axonal degeneration in some cases, particularly those following campylobacter infection. • A variety of auto-antibodies to gangliosides have been identified especially with axonal forms of the disease.
- 30. Pathologic findings in GBS include : lymphocytic infiltration of spinal roots and peripheral nerves (cranial nerves may be involved as well), followed by macrophage-mediated, multifocal stripping of myelin. This phenomenon results in defects in the propagation of electrical nerve impulses, with eventual absence or profound delay in conduction, causing flaccid paralysis. Recovery is typically associated with remyelination.
- 32. Hypothetical mechanism of immune response in Guillain-Barré syndrome Inflammatory infiltrates
- 33. Clinical Features of GBS : Usually 2 - 4 weeks following respiratory or GI infection. • The classic presentation: * Fine paresthesias in the toes and fingertips. * Lower extremity weakness: symmetric & ascending. * Gait unsteadiness. * Inability to walk. * Respiratory muscles involvement. * Neuropathic pain… low back pain. • Cranial Neuropathy: Facial nerve is most commonly affected, resulting in bilateral facial weakness.
- 34. Clinical Features… cont : By the peak of the illness, the frequency of symptoms was as follows: - 79% had neuropathic pain. - 60% could not walk . - 51% had autonomic dysfunction. - 46% had cranial nerve involvement. - 24% could not use their arms. - 13% required mechanical ventilation.
- 35. 46% had cranial nerve involve ment.
- 37. Physical Examination : • Symmetric limb weakness. • diminished or absent reflexes. • Vibration and position sensation are affected in 40% of cases. • Autonomic dysfunction: * Cardiac dysrhythmias. * Orthostatic hypotension, * Hypertension. * Paralytic ileus . * Bladder dysfunction.
- 38. A reflex is an involuntary and nearly immediate movement in response to a stimulus mediated via the reflex arc. reflexes = peripheral problem. reflexes = central problem.
- 39. Human reflexes :Stretch reflexes • Jaw jerk reflex: (CN V) • Biceps reflex (C5, C6) • Brachio-radialis reflex (C5, C6, C7) • Extensor digitorum reflex (C6, C7) • Triceps reflex (C6, C7, C8) • Patellar reflex or knee-jerk reflex L2, L3, L4) • Ankle jerk reflex (Achilles reflex) (S1, S2) While the reflexes above are stimulated mechanically, the term H-reflex refers to the analogous reflex stimulated electrically, and Tonic vibration reflex for those stimulated to vibration.
- 40. Name Sensory Motor Pupillary light reflex II III Accommodation reflex II III Jaw jerk reflex V V Corneal reflex, also known as the blink reflex V VII Vestibulo-ocular reflex VIII III, IV, VI + Gag reflex IX X
- 42. Clinical Course : • >90% of patients reach the lowest point of their function within 2 - 4 weeks, with return of function occurring slowly over the course of weeks to months. • The clinical course of GBS in children is shorter than in adults and recovery is more complete. • In patients who did not require mechanical ventilation, the median time to recovery of independent walking was 43 to 52 days in children compared to 85 days in adults.
- 43. Forms of GBS : • Acute inflammatory demyelinating polyneuropathy (AIDP): the most common form in developed countries. • Acute motor axonal neuropathy: more common in developing countries. More severe with common respiratory involvement. Strong association with campylobacter. • Acute motor-sensory axonal neuropathy. • Miller Fisher syndrome: triad of external ophthalmo-plegia, Ataxia, areflexia with muscle weakness. • Polyneuritis cranialis: associated with CMV infection.
- 45. Diagnosis : Cerebrospinal Fluid: - After the first week of symptoms typically reveals: normal pressure, normal cell count. elevated proteins (greater than 50 mg/dL) - Early in the course (less than one week), protein levels may not yet be elevated, ( rarely remain persistently normal) .
- 46. Diagnosis: Electro-physiologic studies: - Most specific and sensitive tests for diagnosis. - Evidence evolving multifocal demyelination. - A normal study after several days of symptoms, makes the diagnosis of Guillain-Barré syndrome unlikely.
- 48. Doubt the Diagnosis of GBS IF: • Marked persistent asymmetry of weakness. • Persistent bladder or bowel dysfunction. • Bladder or bowel dysfunction at the onset. • Mononuclear leukocytosis in the CSF > 50. • Sharp sensory level. • Pupillary abnormalities are not seen in GBS.
- 49. GBS Management
- 50. GBS Management: • Critical care monitoring for autonomic and respiratory dysfunction. • Children with the following should be admitted to PICU: a. Flaccid quadriparesis. b. Rapidly progressive weakness. c. Reduced vital capacity (≤20 mL/kg) d. Bulbar palsy. e. Autonomic cardiovascular instability. N.B: Sedation and neuromuscular blockade should be avoided in ventilated patients because they obscure the course of the illness.
- 51. GBS Management: Risk factors for respiratory failure in GBS: Cranial nerve involvement. Short time from preceding respiratory illness. Rapid progression over less than 7 days. Elevated CSF protein in the first week. Severe weakness: unable to lift elbows above the bed unable to lift head above the bed unable to stand. 20% of children with GBS require mechanical ventilation for respiratory failure.
- 52. Special Therapy : Immune modulatory therapy: Intravenous Immunoglobulins. Plasmapheresis. • Both therapies have been shown to shorten recovery time by as much 50%. • Combining plasma exchange and IVIG neither improved outcomes nor shortened the duration of illness.
- 54. I V. IMMUNE GLOBULIN : • IVIG is preferred to plasma exchange in children because of the relative safety and ease of administration, although it has not been shown to have better results. • Randomized trials in severe disease show that IVIG started within 4 weeks from onset hastens recovery as much as plasmapheresis. • Long-term outcome, however, may not be affected. • Studies have demonstrated that one effect of the IVIG is to neutralize neuromuscular blocking antibodies.
- 55. IVIG Regimens : • Several IVIG regimens have been utilized. One regimen includes daily IVIG for 5 days at a dose of 0.4 gm/kg /day, which results in an improvement within a mean of 2 to 3 days after the start of therapy. Other authors use 2 gm/kg of IVIG given as a single dose or 1gm/kg/day for 2 days. • One study compared the outcome of 0.4 gm/kg/day given for 3 days versus 6 days. In that study, the 6 days of IVIG was superior when “time to walking” was used as an endpoint. • When comparing treatments of 1gm/kg for 2 days versus 0.4gm/kg over 5 days, no significant difference in the effectiveness was noted in the 2 treatment regimens. However, early “relapses” were more frequently observed in the shorter treatment group.
- 56. Plasmapheresis : • Studies in children indicate that plasmapheresis may decrease the severity and shorten the duration of GBS. • It is most beneficial when started within 7 days of the onset of symptoms but is still beneficial in patients treated up to 30 days after disease onset.
- 57. Management…cont : • Corticosteroids are not effective and not indicated • Interferon-ß reported to be beneficial in individual cases, but its safety and efficacy have not been established in clinical trials.
- 58. Prognosis
- 59. Prognosis : • In general, the prognosis in affected children is better than adults. • Recurrences are uncommon but can occur in children. Some may have a chronic progressive course, whereas others may show recurrences or relapses.
- 60. Prognosis : At long-term follow up, 93% were free of symptoms, and the remainder were able to walk unaided. 50% are ambulatory by 6 mo, 70% walk within ayear of onset of the disease. Mortality is approximately 3 to 4%, and usually is secondary to autonomic dysfunction and respiratory failure.
- 62. Please don’t miss the diagnosis of GBS. By noting: Symptoms begin 2 - 4 weeks following respiratory or GI infection. Diminished or absent reflexes. Symmetric & ascending lower extremity weakness. Sensations intact : Fine paresthesias in the toes and fingertips. No bladder or bowel dysfunction at the onset.