24.3 Movement disorders Flashcards

1
Q

Define athetosis, dystonia, tics, chorea, tremor, restless leg syndrome and ataxia.

A
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2
Q

What is cerebral palsy?

A

An umbrella term for non-progressive neurological and physical disabilities caused by damage or a lesion to a child’s brain early in life or in utero.
It is the most common congenital cause of physical impairment.

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3
Q

What is the range of disability with regards to cerebral palsy?

A
  • Monoplegia: affects 1 limb
  • Paraplegia: affects 2 limbs
  • Quadriplegia: affects 4 limbs
  • Hemiplegia: affects limbs on one side
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4
Q

How is brain damage caused in cerebral palsy?

A

Mainly due to hypoxia, trauma or infection.
E.g. a long and difficult birth.

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5
Q

What are the risk factors for cerebral palsy?

A
  • Maternal age lower than 20 or above 35
  • Pre-eclampsia
  • Prenatal irradiation
  • Pre-natal infections e.g. rubella, syphilis, cytomegalovirus
  • Peri-natal risks (during birth) e.g. traumatic or breach birth, prolonged delivery
  • Post-natal infections e.g. meningitis, encephalitis
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6
Q

What are the 5 types of cerebral palsy?

A
  • Spastic CP (most common, 77%)
  • Athetoid cerebral palsy
  • Ataxic CP
  • Hypotonic CP
  • Mixed type
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7
Q

What are the features of cerebral palsy?

A
  • Visual, hearing and speech impairments
  • May have a learning disability
  • Weakness in one or more limbs, foot that drags as they walk
  • Non-progressive
  • Secondary complications can occur
  • Epilepsy may also be present
  • Dysphagia
  • Excessive drooling
  • Poor control over hand and arm movements
  • Abnormal gait
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8
Q

What secondary complications might someone with cerebral palsy experience?

A
  • Respiratory complications due to dysphagia
  • Gastric reflux
  • Constipation due to reduced muscle tone
  • Bladder and kidney infections
  • Pressure sores on the skin
  • Peri-oral skin issues due to drooling
  • Musculo-skeletal issues e.g. arthritis, dislocations, deformities
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9
Q

What dental considerations are there with regards to people with cerebral palsy?

A
  • Developmental abnormalities: maxillary arch often tapered, labially inclined incisors, malocclusion may be more common due to poor oromuscular co-ordination, lack of lip seal and tongue thrust
  • Uncontrolled movement: spacicity of TMJ musuclature, spontaneous jaw dislocation, spontaneous subluxation of TMJ, facial grimacing
  • Bruxism and tooth wear due to uncontrolled movement of TMJ muscles, may be exacerbated by reflux
  • Periodontal disease: mouth breathing, anti-epileptic medication can cause gingival enlargement, increased food retention, poor mobility so poor OH, if they are PEG fed they will have lots of calculus
  • Caries: food retention, struggle with OH, dietary supplements may be cariogenic
  • Truama: increased risk of falls and seizures
  • Xerostomia: reduced salivary flow rate and lower buffering capacity, medication may also cause xerosotmia
  • Sialorrhea: excessive drooling
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10
Q

How can sialorrhea be managed?

A
  • Anticholinergic drugs e.g. glycopyrronium bromide
  • Botox can be used, effects last 2-6 months
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11
Q

How may cerebral palsy affect dental treatment?

A
  • Setting depends on severity, some pts can be treated in primary care
  • Consider ability to consent, CP doesn’t mean someone doesn’t have the intellect to consent always
  • Sedation may be required, jerky movements can affect treatment
  • Support pts head with pillow
  • GA may be needed
  • Hoist in hospitals or specialist dental practice to get pt into chair
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12
Q

What is Huntington’s disease?

A

A hereditary neurodegenerative disorder.
- Huntington gene on chromosome 4
- Autosomal dominant
- Causes damage to the basal ganglia and cerebral cortex
- Symptoms develop aged 30-50

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13
Q

What are the signs and symptoms of Huntington’s?

A
  • Early symptoms include uncontrollable muscle movements, clumsiness, stumbling when walking, lack of concentration, mood and personality changes, depression, aggression, problems remembering new facts, difficulty making decisions and driving
  • As disease progresses, speech becomes slurred, swallowing and eating difficulties arise, walking becomes difficult and patient may require a wheelchair
  • Cognitive decline can result in dementia
  • Duration of disease is 10-30 years after diagnosis
  • Triad of symptoms: movement, cognition, mental health
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14
Q

What is the management for Huntington’s?

A
  • No specific treatment
  • Medicines can help to improve quality of life
  • Antipsychotic/neuroleptic medicines help muscle movement and mood changes
  • Antidepressants can stabilise the mood e.g. fluoxetine, sertraline, citalopram, quetiapine, olanzapine, risperidone
  • Speech and language therapy to help speech and swallowing issues
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15
Q

What are the dental considerations with regards to patient’s with Huntington’s?

A
  • Oral hygiene affected by poor manual dexterity and cognitive decline
  • As condition progresses, capacity to consent may be lost
  • Communication difficulties, struggle to understand complex sentences
  • Mobility, will eventually require a wheelchair
  • PEG feeding = calculus
  • Trauma to soft tissues
  • Medications can cause xerostomia, xerostomia can lead to candida
  • Open mouth posture can exacerbate xerostomia
  • Vomiting and reflux can damage dentition and cause ulcers
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16
Q

How may Huntington’s affect dental treatment?

A
  • May be treated by GDP but could require referral to community dental services
  • Dentate patients should be prescribed high fluoride toothpastes and have increased prevention e.g. fluoride varnish, saliva replacement gels
  • Advanced complex treatments (implants, crowns and bridges) may be best tx planned with a specialist due to more complex long term maintenance requirements
  • Aspiration pneumonia is a risk at later stages (use good suction, rubber dam)
  • Simple treatments may be able to be provided in an electric wheelchair
  • If movements cause risk to practitioners and patients during treatment, referral is warranted for sedation/GA
17
Q

What is Parkinson’s disease?

A
  • A progressive movement disease.
  • The 2nd most common neurodegenerative condition in the UK (1st is Alzheimer’s).
  • No specific cause, but there are risk factors including age (usually older than 50), gender (male), head trauma. Generally not hereditary.
18
Q

What are the 3 types of Parkinson’s?

A
  • Idiopathic
  • Vascular
  • Drug-induced Parkinsonism (caused by drugs which block dopamine)
19
Q

What is the pathophysiology of Parkinson’s?

A

Degeneration and death of dopamine producing neurons in the substantia nigra (part of the basal ganglia).

20
Q

What are the symptoms of Parkinson’s?

A
  • Tremor
  • Rigidity
  • Shuffling
  • Stooped posture
  • Expressionless face
  • Difficult initiating movements
  • Depression
  • Dementia
  • Sleep disturbances
  • Difficulty smelling
21
Q

How is Parkinson’s managed?

A

Management of symptoms:
- Medicine to increase doapmine signalling in the brain, or to stimulate dopamine receptors e.g. Levodopa
- Deep brain stimulation, implanted device which generates pulse to stimulate parts of the brain affected by PD
- Occupational therapy
- Speech and language therapy
- Physio to aid muscle stiffness and joint pain
- Dietician to maintain weight due to dysphagia

22
Q

Name the medications used to treat Parkinson’s and their possible side effects.

A

May be helpful to tip chair and then pt lies down instead of laying them back as the chair moves due to dizziness.

23
Q

What are the dental considerations with regards to patients with Parkinson’s?

A
  • Speech disorder
  • Dysphagia
  • Drooling due to poor muscular control
  • Loss of smell/taste (early symptom)- may add lots of sugar to food for taste
  • Bruxism- muscle rigidity and poor coordination
  • Orofacial pain
  • Dentures are often poorly tolerated
  • Increased rate of caries and periodontal disease
  • Repetitive tongue movements
  • Xerostomia (reduced quantity and quality)
  • Burning mouth
24
Q

How may Parkinson’s affect dental treatment?

A
  • Heavy emphasis on prevention: high fluoride toothpaste, for dysphagia SLS-free toothpaste can help (no frothing) - Oranurse
  • Ensure messages between dieticians and dentists don’t conflict
  • May have slow speech, don’t rush the pt and give them plenty of time to communicate
  • Later stages of disease may be more suited towards community dental services
  • Sedation may help with movements but need to ensure airway is protected
  • Minimise risk of aspiration, especially in pts with dysphagia- 45 degree angle of chair, good suction, rubber dam, hand instruments instead of ultrasonic
  • Consider accessibility of surgery e.g. stairs