Guillain-Barré Case Study: David: Difference between revisions

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# Unable to care for two young daughters (participation)  
# Unable to care for two young daughters (participation)  
# Inability to ambulate (activity)  
# Inability to ambulate (activity)  
# Lower extremity weakness: 3 or 3+/5 for quads, hamstrings, calves, dorsiflexors (body function)  
# Lower extremity weakness in all major muscle groups (body function)


==== '''Goals''' ====
==== '''Goals''' ====

Revision as of 01:20, 11 May 2023

Abstract[edit | edit source]

Introduction[edit | edit source]

Guillain-Barré Syndrome (GBS) is a rare autoimmune disease that affects the peripheral nervous system (PNS). The exact mechanism is unclear, but the majority of GBS cases are triggered following bacterial or viral infection[1]. GBS can also be triggered by trauma, surgery, cancer, or vaccination[2]. Following the triggering event, an autoimmune reaction takes place where the immune system targets and breaks down the myelin sheath surrounding peripheral nerves[3]. The first symptoms noticed are typically numbness, tingling, or pain (alone or in combination) beginning in the hands or feet. The over the course of days to weeks there is progressive muscle weakness in the extremities and potential paralysis[4]. Guillain-Barré Syndrome can also lead to weakening of the respiratory muscles and eventual respiratory failure[1]. Many complications can arise during the acute stage of GBS including: blood clots, heart attack, pneumonia, and infection. Death occurs in 7.5% of all cases of GBS.

Signs and Symptoms[edit | edit source]

  • Numbness, tingling, or pain (alone or in combination) that begins in the hands and feet
  • Progressive bilateral weakness of the extremities
  • Impaired gait and balance
  • Weakness of facial muscles
  • Difficulty with swallowing or speaking
  • Double vision
  • Severe pain that may worsen during the night
  • Changes to bowel/bladder control
  • Paralysis
  • Respiratory failure
  • Autonomic dysfunction (abnormal changes to heart rate and blood pressure)

Epidemiology[edit | edit source]

  • More common in men[5]
  • Risk increases with age[5]
  • 3,000 to 6,000 cases per year in the United States[6]
  • Incidence of subtypes varies between countries[2]

Subtypes[edit | edit source]

ImageGBS1.png

There are several subtypes of GBS, each presenting differently and affecting different populations. In North America, the most common form of GBS is Acute Inflammatory Demyelinating Polyradiculoneuropathy (AIDP)[2]. AIDP is characterized by the presence of sensory symptoms, muscle weakness, involvement of cranial nerves, and autonomic dysregulation. The focus of this case study is on the AIDP subtype.

Prognosis[edit | edit source]

GBS Scale 2023.png
GBSpicture2.jpg

Symptom severity can vary and as such, the degree of recovery and the timeline also varies. Many patients have chronic symptoms and changes to their functional status following their bout with GBS. The Guillain-Barré Syndrome (GBS) Disability Scale is used to measure the degree of recovery. Recovery can range from full recovery for some patients to significant functional impairment for others. The prognosis of GBS depends primarily on age of the patient and on the severity of symptoms two weeks after onset. Older individuals are more likely to have lasting effects following an episode of GBS.

Over 25% of GBS cases will lead to weakness of the respiratory muscles which may eventually lead to respiratory failure. If this occurs, the patient will have to be intubated and placed on mechanical ventilation. Mechanical ventilation can lead to complications such as pneumonia which can affect negatively affect recovery.

Client Characteristics[edit | edit source]

Patient Profile[edit | edit source]

  • Initials: D. A (David Atkin)
  • Preferred Name: Dave
  • Age: 35 years
  • DOB: 12 June 1987
  • Gender: Male
  • Height: 172cm
  • Weight: 90kgs  
  • Significant Presentation: Acute onset of symmetrical bilateral acroparesthesia and paralysis in lower extremities. Patient presented with areflexia and flaccidity bilaterally on testing.

History of Present Illness[edit | edit source]

  • Date of Admission: 30th March 2023
  • Type of Admission: Self- referral. Patient woke up and was unable to move his lower limbs. Patient brought in an ambulance to Kingston General hospital (KGH).
  • Initial Diagnosis: Acute inflammatory demyelinating polyneuropathy (AIDP) a sub-type of Guillain-Barré syndrome. The patient was admitted in KGH on 14th March 2023 with a gastrointestinal infection (caused by Campylobacter Jejuni[1]) which is one of the significant diagnostic indicators.  
  • Date of Onset: 30th March 2023
  • Treatment to Date (20th April 2023): Intravenous immunoglobulin therapy and plasmapheresis, the previous PT and PTA worked on bed mobility.
  • Present Status: Alert and oriented. Minimal regain of motor and sensory loss bilaterally on both extremities. (Note: On 15th April 2023, patient was transferred to ICU and intubated after acute bradycardia, bilateral facial paralysis and acute respiratory distress. Patient had shown progressive bilateral symmetrical sensory and motor loss in both upper and lower extremities.)
  • Precautions / Contraindications: Patient may exhibit occasional orthostatic hypotension if they are assisted out of recumbent position.  

Past Medical History[edit | edit source]

  • Allergies: Peanuts and tree nuts

Medication[edit | edit source]

  • Venus thromboembolic prophylactics to prevent Deep Vein Thrombosis and Pulmonary Embolism.
  • Amlodipine 5mg per day for hypertension.

Health Habits[edit | edit source]

  • Smokes one pack every day since he was 30 years old (5 pack-years) and reports drinking 1 beer (3 times a week).

Social History[edit | edit source]

  • Patient works as a manager at a software development firm in Kingston.
  • The patient lives in a 2-story independent house that has 12 stairs with his wife and 2 daughters (age 9 and 6).  

Functional History[edit | edit source]

  • Patient did resistance training at GoodLife fitness twice a week.
  • Patient was independent with BADLs and IADLs
  • Patient fell once while skateboarding and fractured his left wrist in December 2019.

Current Functional Status[edit | edit source]

  • Patient has independent bed mobility.  
  • Patient can maintain seated posture alone but needs assist x1 to transition from laying to sitting and assist x2 to stand.
  • Patient unable to ambulate due to balance impairments combined weakness in extremities.

Examination Findings[edit | edit source]

Observation[edit | edit source]

Mobility[edit | edit source]

  • Bed mobility: independent to slide up, down, sideways, roll onto side
  • Lie to sit: minimal Ax1
  • Sit-to-stand: unable to stand on own requires max Ax2
  • Transfers: moderate Ax2 required for pivot transfer

Personal Care/ADLs[edit | edit source]

  • Assistance needed for dressing and bathing
  • Currently utilizing a urinary catheter
  • Independent to feed oneself

Gait[edit | edit source]

  • Currently unable to ambulate due to lower extremity weakness
  • Need fitting for gait aid when required

Range of Motion[edit | edit source]

Muscle group AROM PROM Muscle Group AROM PROM
All shoulder movements WNL WNL Hip flexion 45 WNL
All elbow movements WNL WNL Hip extension 10 WNL
All wrist movements WNL WNL Hip adduction WNL WNL
Hip abduction WNL WNL
Knee extension WNL WNL
Knee flexion 100 WNL
Dorsiflexion WNL WNL
Plantar flexion WNL WNL

Muscle Strength[edit | edit source]

Muscle group Right Left Muscle Group Right Left
All shoulder movements 4 4 Hip flexion 3- 3-
Elbow flexion 4- 4- Hip extension 3- 3-
Elbow extension 4 4 Hip adduction 4 4
Wrist flexion 4- 4- Hip abduction 3 3
Wrist extension 4- 4- Knee extension 3+ 3+
Knee flexion 3- 3-
Dorsiflexion 3+ 3+
Plantar flexion 3+ 3+

Balance[edit | edit source]

  • Seated: patient can maintain a seated posture independently once positioned, with SBA
  • Standing: unable to independently stand, requires max Ax2

Common Comorbidities[edit | edit source]

  • Hypertension
  • Diabetes
  • Hyperlipidemia

Outcome Measures[edit | edit source]

  • Functional Independence Measure (FIM)
    • The FIM is a common outcome measure used to determine the ability to perform activities of daily living. It is made up of 18 individual items consisting of motor and cognitive functioning, that are scored from 1 (total assistance) to 7 (independent). Each item is added together to get an overall level of independence between 18-1126. The FIM is considered time-consuming but an easy to use, valid and reliable method that can be trusted in clinical settings to assess patients with various disabilities.
  • Medical Research Council Sumscore
    • The Medical Research Council Sumscore is the most common tool used to measure muscle strength in individuals with neurological conditions including GBS. This tool considers six main muscle groups (bilaterally) and assesses their strength using a scale of 0-5. These six scores can then be added together to create a total sum ranging from 0 to 60. It has shown to be a clinically useful tool for physiotherapists.
  • 10-Meter Walk Test
    • The 10-meter walk test is a useful tool to measure gait speed and functional mobility. The tool uses the amount of time a patient takes to walk 10 meters, to provide a speed in m/sec. This can be compared to normative data to determine risk of falls and if a gait aid is indicated. The 10-meter walk test is a common tool used by clinicians and is seen as reliable and valid for a number of neurological conditions.  

Clinical Hypothesis[edit | edit source]

Analysis Statement

35 y/o male admitted to Kingston General Hospital (KGH) via ambulance on March 30th, 2023, due to inability to move lower limbs after waking up. Pt presents with bilateral acroparesthesia and paralysis in lower extremities, with bilateral areflexia and flaccidity; diagnosed with acute inflammatory demyelinating polyneuropathy (AIDP) a sub-type of Guillain-Barre syndrome. Pt currently unable to ambulate due to impaired strength, sensory, and balance in lower extremities. This patient's prognosis tends to be positive with a variety of factors that favour his recovery including young age, previously active, and a relatively high MRC Sumscore on initial assessment. However, the patient has several negative factors affecting his prognosis as well, these include having to take care of two daughters, being a current smoker, and inability to ambulate. This patient would benefit from physiotherapy treatment focused on strengthening the lower extremities, improving balance, and increasing mobility.

Problem List[edit | edit source]

  1. Unable to care for two young daughters (participation)
  2. Inability to ambulate (activity)
  3. Lower extremity weakness in all major muscle groups (body function)

Goals[edit | edit source]

Long-Term Goal 1:

  • To be able to pick up and hold daughters safely within the next 4 months

Short-Term Goal:

  • To be able to sit up independently to read and interact with daughters within the next week

Long-Term Goal 2:

  • To be able to walk independently with a 2WW to get to the bathroom within the next 3 months

Short-Term Goal:

  • Achieve a sit-to-stand and be able to stand with minimal support and a 2WW within the next 3 weeks.

Long-Term Goal 3:

  • Gain the lower extremity strength to be able to perform 10 arm-supported squats within the next 2 months

Short-Term Goal:

  • To be able to complete 10 repetitions of in-bed resistance exercises (glute bridge, quad-over-roll), twice a day within the next 2 weeks

Intervention[edit | edit source]

Treatment Plan

Innovative Technology - IMPORTANT, 15 marks

Outcome[edit | edit source]

Response to Adverse Event

Discharge

Referrals - IMPORTANT, 15 marks

Discussion[edit | edit source]

References[edit | edit source]

Govoni V, Granieri E. Epidemiology of the Guillain-Barré syndrome. Current opinion in neurology. 2001 Oct 1;14(5):605-13.

GBS (Guillain-Barré Syndrome) and vaccines [Internet]. Centers for Disease Control and Prevention; 2023 [cited 2023 May 10]. Available from: https://www.cdc.gov/vaccinesafety/concerns/guillain-barre-syndrome.html

Hughes RA, Cornblath DR. Guillain-barre syndrome. The Lancet. 2005 Nov 5;366(9497):1653-66.

Ropper AH. The Guillain–Barré syndrome. New England journal of medicine. 1992 Apr 23;326(17):1130-6.

  1. 1.0 1.1 1.2 Willison HJ, Jacobs BC, van Doorn PA. Guillain-barre syndrome. The Lancet. 2016 Aug 13;388(10045):717-27.
  2. 2.0 2.1 2.2 Hughes RA, Cornblath DR. Guillain-barre syndrome. The Lancet. 2005 Nov 5;366(9497):1653-66.
  3. Ropper AH. The Guillain–Barré syndrome. New England journal of medicine. 1992 Apr 23;326(17):1130-6.
  4. Van den Berg B, Walgaard C, Drenthen J, Fokke C, Jacobs BC, Van Doorn PA. Guillain–Barré syndrome: pathogenesis, diagnosis, treatment and prognosis. Nature Reviews Neurology. 2014 Aug;10(8):469-82.
  5. 5.0 5.1 Govoni V, Granieri E. Epidemiology of the Guillain-Barré syndrome. Current opinion in neurology. 2001 Oct 1;14(5):605-13.
  6. 1. GBS (Guillain-Barré Syndrome) and vaccines [Internet]. Centers for Disease Control and Prevention; 2023 [cited 2023 May 10]. Available from: https://www.cdc.gov/vaccinesafety/concerns/guillain-barre-syndrome.html