Guillain-Barré Syndrome (GBS)

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Questions and Answers

In the context of Guillain-Barré Syndrome (GBS), if a patient's nerve conduction studies reveal a progressive deterioration specifically affecting the temporal dispersion of F-waves, which pathological mechanism is most likely contributing to this electrophysiological finding?

  • Preferential disruption of the nodes of Ranvier, resulting in complete conduction block and absent compound muscle action potentials (CMAPs).
  • Patchy demyelination along the motor nerve fibers, causing asynchronous conduction and prolonged distal motor latencies. (correct)
  • Uniform axonal loss across all nerve fibers, leading to diminished but consistently timed responses in both sensory and motor studies.
  • Selective degeneration of the dorsal root ganglia leading to impaired sensory action potential amplitudes.

A patient with Guillain-Barré Syndrome (GBS) presents with significant bulbar dysfunction, impacting their ability to protect their airway. Following intubation and mechanical ventilation, which of the following interventions is most crucial to prevent ventilator-associated pneumonia, considering the specific paralytic complications of GBS?

  • Frequent assessment of cuff pressure and adjustment to minimize aspiration risk, alongside kinetic therapy to mobilize secretions. (correct)
  • Implementation of a comprehensive oral care protocol, including chlorhexidine rinses, to reduce oral bacterial load
  • Strict adherence to sterile suctioning techniques, combined with regular oropharyngeal and endotracheal cultures.
  • Initiation of early enteral nutrition via a nasogastric tube to maintain caloric intake and gut motility.

A patient diagnosed with Guillain-Barré Syndrome (GBS) develops autonomic instability characterized by alternating episodes of severe hypertension and profound hypotension. What is the most appropriate initial pharmacological intervention to manage these labile blood pressure fluctuations while minimizing neurological compromise?

  • Administer short-acting beta-blockers, such as esmolol, to provide rapid control of hypertensive episodes without significantly affecting hypotensive periods.
  • Employ a combination of short-acting vasodilators for hypertension and intravenous fluids for hypotension, guided by continuous arterial pressure monitoring and frequent neurological assessments. (correct)
  • Implement a regimen of long-acting ACE inhibitors to provide sustained blood pressure control and prevent abrupt fluctuations.
  • Initiate a continuous infusion of norepinephrine to maintain a stable mean arterial pressure during hypotensive episodes, titrating to avoid hypertensive spikes.

In a patient with GBS undergoing plasmapheresis, which of the following hematological and biochemical parameters requires the most vigilant monitoring to promptly detect and manage potential complications associated with the procedure?

<p>Frequent monitoring of serum potassium and magnesium levels, coupled with continuous ECG monitoring, to detect and correct electrolyte imbalances and cardiac arrhythmias. (D)</p> Signup and view all the answers

Given the autoimmune pathophysiology of Guillain-Barré Syndrome (GBS), which of the following cellular mechanisms is primarily responsible for the characteristic demyelination observed in affected peripheral nerves?

<p>Macrophages infiltrating the peripheral nervous system and stripping myelin sheaths via phagocytosis, driven by opsonization with anti-myelin antibodies. (B)</p> Signup and view all the answers

Which of the following electrodiagnostic findings would be most indicative of Acute Motor Axonal Neuropathy (AMAN), a subtype of Guillain-Barré Syndrome (GBS), as opposed to the more common Acute Inflammatory Demyelinating Polyneuropathy (AIDP)?

<p>Normal motor nerve conduction velocities with significantly reduced compound muscle action potential (CMAP) amplitudes, particularly in distal muscles. (C)</p> Signup and view all the answers

Considering the diagnostic criteria for Miller Fisher Syndrome (MFS), a variant of Guillain-Barré Syndrome (GBS), which of the following clinical presentations would be most consistent with this diagnosis?

<p>Ophthalmoplegia, ataxia, and areflexia, with anti-GQ1b antibodies present in serum and minimal or absent limb weakness. (A)</p> Signup and view all the answers

A patient with Guillain-Barré Syndrome (GBS) exhibits significant dysphagia and is at high risk for aspiration. Prior to initiating enteral nutrition, which diagnostic test is most crucial to perform in order to guide the safest method of feeding and minimize the risk of pulmonary complications?

<p>A modified barium swallow study, with video fluoroscopy, to assess swallowing mechanics and identify the presence of aspiration. (A)</p> Signup and view all the answers

Which of the following pathophysiological mechanisms best explains the transient hypertension often observed in patients with Guillain-Barré Syndrome (GBS) during the acute phase of the illness?

<p>Dysregulation of the baroreceptor reflex and sympathetic nervous system hyperactivity, leading to increased peripheral vascular resistance. (D)</p> Signup and view all the answers

A patient with GBS is being considered for intravenous immunoglobulin (IVIG) therapy. Which of the following mechanisms of action is the primary basis for IVIG's therapeutic effect in this context?

<p>Blockade of Fc receptors on macrophages, inhibiting their ability to phagocytose opsonized myelin and strip nerve fibers. (A)</p> Signup and view all the answers

In managing a patient with GBS who has developed respiratory failure and requires mechanical ventilation, which ventilator strategy is most appropriate to mitigate the risk of ventilator-induced lung injury (VILI) while ensuring adequate gas exchange?

<p>Low tidal volumes (6-8 mL/kg) with permissive hypercapnia, targeting a plateau pressure below 30 cm H2O and accepting a higher PaCO2. (D)</p> Signup and view all the answers

A patient with GBS undergoing rehabilitation demonstrates a motor strength of 2/5 (per the Medical Research Council scale) in the lower extremities. Which of the following interventions is most appropriate to incorporate into the patient's physical therapy plan to promote neuroplasticity and functional recovery?

<p>Task-specific training involving repetitive practice of functional movements, supplemented with orthotics to promote proper alignment and reduce compensatory strategies. (A)</p> Signup and view all the answers

A patient with GBS develops severe constipation secondary to autonomic dysfunction and immobility. Which of the following pharmacological interventions is most appropriate for managing their constipation while minimizing the risk of exacerbating autonomic instability?

<p>Daily use of osmotic laxatives, such as polyethylene glycol (PEG), to draw water into the colon and soften the stool. (B)</p> Signup and view all the answers

A pregnant patient presents with rapidly progressive ascending paralysis and is subsequently diagnosed with Guillain-Barré Syndrome (GBS). Which of the following considerations is most critical in managing this patient's care to ensure optimal outcomes for both mother and fetus?

<p>Prompt initiation of plasmapheresis or intravenous immunoglobulin (IVIG) therapy, irrespective of gestational age, to halt disease progression and prevent respiratory compromise. (D)</p> Signup and view all the answers

Which of the following outcome measures is most sensitive and specific for tracking functional recovery in patients with Guillain-Barré Syndrome (GBS) undergoing rehabilitation, particularly in the chronic phase of the illness?

<p>The Guillain-Barré Syndrome Disability Scale (GBS DS), providing a global assessment of disability ranging from 0 (healthy) to 7 (death). (B)</p> Signup and view all the answers

A patient with a confirmed diagnosis of Guillain-Barré Syndrome (GBS) is being discharged from the hospital. Which of the following long-term management strategies is most important to address with the patient and their family to optimize their ongoing recovery and quality of life?

<p>Regular aerobic exercise and strength training to improve cardiovascular fitness and muscle strength, consulting with a physical therapist to develop a personalized exercise program. (A)</p> Signup and view all the answers

A patient with a history of Guillain-Barré Syndrome secondary to Campylobacter jejuni infection is being evaluated for potential immunodeficiency. What specific immunological assay would provide the most direct evidence for the presence of an underlying humoral immune defect?

<p>Quantification of serum immunoglobulin levels (IgG, IgA, IgM) to identify potential deficiencies in antibody production. (A)</p> Signup and view all the answers

In a patient with GBS, which of the following clinical scenarios would warrant the most urgent initiation of mechanical ventilation?

<p>A FVC of 15 mL/kg and a rising PaCO2 (A)</p> Signup and view all the answers

A patient with Guillain-Barré Syndrome (GBS) reports experiencing severe neuropathic pain, described as burning and shooting sensations in their extremities. Which of the following pharmacological agents is most appropriate as a first-line treatment for this type of pain?

<p>Anticonvulsants, such as gabapentin or pregabalin, to stabilize neuronal excitability and reduce neuropathic pain signals. (D)</p> Signup and view all the answers

A previously healthy adult presents with rapidly progressive, ascending paralysis, areflexia, and facial diplegia over the course of one week. Lumbar puncture reveals albuminocytologic dissociation. Which of the following diagnostic tests would be most crucial to perform next to confirm the diagnosis and classify the subtype of Guillain-Barré Syndrome (GBS)?

<p>Electromyography (EMG) and nerve conduction studies (NCS) to assess the pattern and extent of peripheral nerve involvement, differentiating between demyelinating and axonal subtypes. (D)</p> Signup and view all the answers

In a patient with GBS experiencing significant orthostatic hypotension, which of the following non-pharmacological interventions should be prioritized to mitigate symptoms and prevent syncope?

<p>Applying sequential compression devices (SCDs) to the lower extremities to enhance venous return and prevent pooling of blood in the legs. (C)</p> Signup and view all the answers

Which of the following neuroimaging findings would be most suggestive of a diagnosis other than Guillain-Barré Syndrome (GBS) in a patient presenting with acute onset of ascending paralysis and areflexia?

<p>Focal lesions in the brainstem or spinal cord on MRI, suggesting a central nervous system process such as multiple sclerosis or transverse myelitis. (C)</p> Signup and view all the answers

In a patient with GBS, which of the following mechanisms accounts for the albuminocytologic dissociation observed in the cerebrospinal fluid (CSF)?

<p>Increased permeability of the blood-brain barrier, allowing albumin to leak into the CSF without a corresponding increase in cell count. (D)</p> Signup and view all the answers

Which clinical finding is most indicative of impending respiratory failure in a patient with GBS, requiring immediate intervention?

<p>Decreasing Inspiratory pressure (D)</p> Signup and view all the answers

Which of the following is the most appropriate goal for nutritional support in a patient with severe GBS and prolonged paralysis:

<p>Providing adequate calories and protein to maintain lean body mass and support respiratory muscle function. (A)</p> Signup and view all the answers

A patient with GBS develops deep vein thrombosis (DVT) in the lower extremity. Which anticoagulant is most appropriate, considering potential complications?

<p>Low-molecular-weight heparin (LMWH). (C)</p> Signup and view all the answers

When educating caregivers of a patient with GBS, what is the most critical instruction regarding skin care?

<p>Reposition the patient every two hours and inspect skin for breakdown. (D)</p> Signup and view all the answers

A patient with GBS exhibits emotional lability and anxiety due to their condition. Which intervention is most appropriate in this circumstance?

<p>Providing supportive counseling, relaxation techniques, and involving family members. (B)</p> Signup and view all the answers

A patient with GBS is being managed with mechanical ventilation. Which nursing intervention is essential to prevent corneal damage?

<p>Taping the eyelids closed and applying artificial tears regularly. (D)</p> Signup and view all the answers

For a patient with GBS who has difficulty clearing secretions, which intervention is most important to prevent pneumonia?

<p>Performing chest physiotherapy and suctioning as needed (B)</p> Signup and view all the answers

Which intervention is most important to address the risk of contractures in a patient with GBS and prolonged paralysis?

<p>Performing range-of-motion exercises regularly. (A)</p> Signup and view all the answers

When monitoring a patient with GBS, which assessment finding is most indicative of autonomic nervous system dysfunction?

<p>Hypertension (A)</p> Signup and view all the answers

What is the primary focus of rehabilitation interventions during the plateau phase of GBS?

<p>Preventing complications and managing pain. (A)</p> Signup and view all the answers

Which predisposing factor is most closely associated with the development of GBS?

<p>Recent viral or bacterial infection. (D)</p> Signup and view all the answers

Which type of paralysis is the most common manifestation of GBS?

<p>Ascending paralysis (D)</p> Signup and view all the answers

What is the recommended frequency for checking individual muscle groups in a patient with GBS?

<p>Every 2 hours (D)</p> Signup and view all the answers

Which diagnostic finding is most consistent with GBS in cerebrospinal fluid (CSF)?

<p>Elevated protein levels (B)</p> Signup and view all the answers

Flashcards

Guillain-Barré Syndrome (GBS)

An acute infectious neuritis of the cranial and peripheral nerves caused by an overreaction of the immune system, resulting in destruction of myelin sheaths.

What is another name for GBS?

Also known as Landry's Paralysis. Rare; affects 1-2 out of 100,000. It is the most common cause of rapidly acquired paralysis.

What usually precedes GBS?

GBS is usually preceded by a mild upper respiratory infection or gastroenteritis. Recovery may take up to a year.

What are the predisposing factors of GBS?

The cause of of GBS is Unknown, but predisposing factors include antecedent viral infection, immunization and autoimmune disorders.

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What is AIDP?

Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP). The most common sign of AIDP is muscle weakness that starts in the lower part of the body and spreads upward.

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Miller Fisher Syndrome (MFS)

Paralysis starts in the eyes, associated with unsteady gait. MFS occurs in about 5 percent of people with Guillain-Barre syndrome in the U.S. but is more common in Asia.

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Pathophysiology of GBS?

Segmental demyelination of peripheral nerves causes inflammation and degeneration in sensory and motor nerve roots.

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What are the manifestations of GBS?

Generalized muscle weakness (starts from lower extremities), muscle weakness of the legs, and persistent pain in the back, calves of the legs and may progress to upper extremities & trunk

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What are the autonomic disturbances of GBS?

Paralysis of the ocular, facial, glossal and esopharyngeal muscles (dysphagia & dysarthria), disturbance of heart rate and rhythm, transient HTN. orthostatic hypotension, and paralytic ileus.

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Diagnostics for GBS?

CSF studies - elevated CHON levels; EMG - diminishes electrical activity of skeletal muscles; Nerve Conduction Studies - progressive deterioration of nerve conduction velocity

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CSF CHON levels in GBS

Elevated protein levels in cerebrospinal fluid (CSF).

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EMG results in GBS

EMG diminishes electrical activity of skeletal muscles

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Nerve Conduction Study result in GBS

Progressive deterioration of nerve conduction velocity

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Complications of GBS?

ARF, Cardiac dysrhythmia, DVT and pulmonary embolism, paralysis, pressure ulcers, contractures, muscle wasting, and aspiration.

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Medical Management of GBS?

Mechanical ventilation if respiratory problems are present, plasmapheresis, and continuous ECG monitoring.

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Drugs for GBS?

Propranolol for HTN, Atropine – for bradycardia, Corticosteroids- suppress immune response, and antiarrhythmic agents.

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Maintaining adequate ventilation

Monitor rate and depth of respirations; serial vital capacities, observe for ventilatory insufficiency, and maintain mechanical ventilation as needed

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Interventions required for cranial nerve function

Check gag reflex and swallowing activity, ability to handle secretions and voice.

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More interventions requiered by nurses

Prevent complications of immobility ROMs, anticoagulants, anti-embolism stockings, promote optimum nutrition, and provide psychological support and encouragement to client/significant

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Study Notes

  • Guillain-Barré Syndrome (GBS) is an acute infectious neuritis affecting cranial and peripheral nerves.
  • GBS is caused by the immune system overreacting to an infection and destroying myelin sheaths.
  • Landry’s Paralysis is another name for GBS.
  • GBS is rare, affecting 1-2 out of 100,000 individuals.
  • GBS is the most common cause of rapidly acquired paralysis.
  • GBS is usually preceded by mild upper respiratory infection or gastroenteritis.
  • Recovery from GBS can take up to a year after the initial and plateau periods.
  • GBS can cause residual effects and even death due to complications.
  • A major concern with GBS is difficulty of breathing.
  • The exact cause of GBS is unknown.

Predisposing Factors for GBS:

  • Antecedent viral infection can occur 2 weeks before symptom onset, from Campylobacter Jejuni, Cytomegalovirus, or Epstein-Barr Virus.
  • Immunization.
  • Autoimmune disorders.

Types of GBS:

  • Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP) is characterized by muscle weakness that starts in the lower body and spreads upward.
  • Miller Fisher Syndrome (MFS) is characterized by paralysis starting in the eyes and is associated with unsteady gait, it occurs in about 5% of GBS cases in the U.S. but is more common in Asia.
  • Acute Motor Axonal Neuropathy (AMAN) and Acute Motor-Sensory Axonal Neuropathy (AMSAN) are less common in the U.S. but more frequent in China, Japan, and Mexico.

Pathophysiology of GBS:

  • Segmental demyelination of peripheral nerves causes inflammation and degeneration in sensory and motor nerve roots.
  • Most clients experience spontaneous and complete recovery, but mild deficits may persist.

Manifestations of GBS:

  • Paresthesia.
  • Generalized muscle weakness starts from lower extremities and ascends.
  • Muscle weakness of the legs (Dyskinesia).
  • Persistent pain in the back, calves of the legs, and may progress to upper extremities & trunk.

Autonomic Disturbances in GBS:

  • Paralysis of ocular, facial, glossal, and esopharyngeal muscles, leading to dysphagia & dysarthria.
  • Disturbance of heart rate and rhythm.
  • Transient HTN.
  • Orthostatic Hypotension.
  • Paralytic ileus.

Diagnostics for GBS:

  • CSF studies show elevated CHON levels.
  • EMG diminishes electrical activity of skeletal muscles.
  • Nerve Conduction Studies show a progressive deterioration of nerve conduction velocity.

Complications of GBS:

  • ARF, or Acute Renal Failure.
  • Cardiac dysrhythmia.
  • DVT and pulmonary embolism.
  • Paralysis.
  • Pressure ulcers.
  • Contractures.
  • Muscle wasting.
  • Aspiration.

Medical Management of GBS:

  • Mechanical ventilation is required if respiratory problems are present.
  • Plasmapheresis decreases circulating antibodies.
  • Continuous ECG monitoring is needed
  • Drugs:
    • Propranolol for HTN.
    • Atropine for bradycardia.
    • Corticosteroids to suppress immune response.
    • Antiarrhythmic agents.

Nursing Interventions for GBS:

  • Maintain adequate ventilation by monitoring rate and depth of respirations, observing for ventilatory insufficiency, and maintaining mechanical ventilation as needed.
  • Check individual muscle groups every 2 hours.
  • Assess cranial nerve function by checking gag reflex,swallowing activity, ability to handle secretions, and monitoring voice.
  • Monitor vital signs and observe for signs of autonomic dysfunction.
  • Prevent complications of immobility with ROM exercises, anticoagulants, and anti-embolism stockings.
  • Promote comfort.
  • Promote optimum nutrition (TPN/Gastrostomy).
  • Provide psychological support and encouragement.

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