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Case 5: Ms. LawCase 5: Ms. Law
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TerminologyTerminology
Myasthenia gravis (MG) Autoimmune & neuromuscular junction
disease, Characterized by rapid weakness of
muscle with use + improvement withrest Antibodies form against acetylcholine
(ACh) receptors less functioningreceptors at motor end plate weaker
muscle contraction Improvement with rest nerves can
replenish supply of ACh Signs - ptosis (drooping of eyelid),
flaccid dysarthria, dysphagia
(Duffy, 2005)
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TerminologyTerminology
MG crisis MG deterioration that necessitate
mechanical ventilation
Bulbar symptoms Bulbar muscles: oropharyngeal and
laryngeal muscles
Impairment difficulties withspeech, swallowing or both
(Bershad, Feen, & Suarez, 2008)
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TerminologyTerminology
Consolidation White shadowed areas reflected in
chest x-ray
Can be caused by bronchial infection
Yentis, Hirsch, & Smith (2009)
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Background informationBackground information
F / 60Diagnosis of myasthenia gravis in
2003
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Medical historyMedical history
20th Nov 2006 admitted ICUbecause of: Fever
Respiratory failureExaminations:
Physical examinationWorsening of bulbar symptoms
(dysphagia, dysarthria & ptosis) CXRBilateral lower zone patchy consolidation
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Medical historyMedical history
Diagnosis Influenza
Pneumonia
Acute MG crisisFeeding at ICU
R/T tube
28th Nov 2006 discharged togeneral ward
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History of treatmentHistory of treatment
Swallowing training since 23rdNov 2006
Re-assessment done on 10th Dec
2006
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Assessment resultsAssessment results
Satisfactory dental condition
Pre-requisite for mastication
Fair tongue strength and adequaterange of movement
food bolus formation
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Assessment resultsAssessment results
Reduced MPT
Fair cough effort
Weak vocal fold adduction
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Assessment resultsAssessment results
Diminished gag reflex
NOT indicative of swallowing reflex
Moderate degree of hypernasality Functional swallowing is possible withou
VP closure (Logemann, 1998)
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Assessment resultsAssessment results
Mild delay in swallowing
High consistency: rest at vallecula
Low consistency: splash into the airway
Moderately reduced laryngeal
elevation Reduced closure of airway by epiglottis
CP sphincter NOT opened adequately
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Assessment resultsAssessment results Multiple swallow per intake
Food remaining at valleculae andpyriform sinuses
Throat clearing with thin liquid, mildly
thick liquid, puree and biscuits Aspiration
Delay in swallowing increases withamount of food
Implication for tx planning
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Management planManagement plan
Compensatory strategies Postural modification
Diet modification
Improve oral sensory awarenessSwallowing therapies
Deep pharyngeal neuromuscular
stimulation
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Postural modificationPostural modification
Chin tuck (Logemann, 1998) Instructions: Bring your chin to chest
Rationale:
Push the base of tongue towardspharyngeal wall
Expands valleculae recesses
Narrows the entrance to laryngeal
vestibule by moving the epiglottisposteriorly
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Diet modificationDiet modification
10cc thin liquid Rationale: Scores 1 in 8-point Penetration/
aspiration Scale (Rosenbak et al., 1996)
No solid food Rationale: Scores 5 in 8-point
penetration/aspiration scale (Rosenbak etal., 1996) : penetration occurs!
Meal: pureed meat congee ( )
to Lydia: what is the rationale? Thevegetable and meat is a must to bepureed la, but how about the choicebetween congee/ soft rice/ pureed for
the
?
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Improve oral sensoryImprove oral sensory
awarenessawarenessSensory enhancement
techniques
Present a cold/ sour bolus
Rationale: to trigger the pharyngeal stageof swallowing more rapidly (Logemann,1998)
D h lD h l
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Deep pharyngealDeep pharyngeal
neuromuscular stimulationneuromuscular stimulation
(DPNS)(DPNS)Provide stimulations with icedlemon glycerin swabs to oral andpharyngeal areas
Rationale:To stimulate the contraction of
pharyngeal and lingual muscles
To stimulate the cranial nerve bytouching specific areas within themouth and tongue
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Swallowing maneuver?Swallowing maneuver?
Would not be implementedRationale:The patient is diagnosed to have MG
in which she would show muscleweakness on sustained effort (Webb& Adler, 2008)
these maneuvers require increasedmuscular effort and are notappropriate in patients who fatigueeasily (Logemann, 1998, pg. 215)
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ReferencesReferences
Bershad, E. M., Feen, E. S., & Suarez, J. I.(2008). Myasthenia gravis crisis. SouthernMedical Journal, 101 (1), 63-69
Duffy, J. R. (2005). Motor speech disorders:Substrates, differential diagnosis, and
management(2nd ed.). St. Louis: ElsevierMosby.Love, R. J., & Webb, W. G. (2008). Neurology
for the speech-language pathologist. St.Louis, MO: Mosby/Elsevier.
Yentis, S. M., Hirsch, N. P., & Smith, G. B.(2009). Anaesthensia and intensive care A-Z: An encyclopedia of principles andpractice (4th ed.). New York: ElsevierLimited.