PARKINSONS <3

Create an informative and visually appealing image depicting the human brain with highlighted areas associated with Parkinson's Disease, surrounded by medical symbols and illustrations of healthy and affected neurons. Include elements like a silhouette of a patient, and visual cues of symptoms like tremors or gait disturbances.

Parkinson's Disease Quiz

Test your knowledge about Parkinson's Disease with this comprehensive quiz! This quiz covers a wide range of topics regarding symptoms, types, and other neurological disorders that relate to Parkinsonism.

Challenge yourself and learn key facts with questions such as:

  • What are the primary motor symptoms?
  • What distinguishes Parkinson's from other similar disorders?
  • What are the various stages of the disease?
61 Questions15 MinutesCreated by LearningLeaf305
AKA “shaking palsy” It is a progressive disorder of the central nervous system (CNS) with both motor and nonmotor symptoms
PARKINSON’S DISEASE
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Age onset:
51-66 years old
40-67 years old
50-65 years old
51-67 years old
Refers to those cases where the etiology is idiopathic or unknown. - The first group symptoms are postural instability and gait difficulties.
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
This case occurs during the epidemics of an Influenza virus that occured from 1917 to 1926
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
Exposure to certain industrial & poisons, most common of which is manganese which clearly present a serious occupational hazard to miners.
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
Neuroleptics powerful tranquilizers & blood pressure medications can produce parkinsonian symptoms as a side effect.
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
Caused by repetitive micro traumas in the head. The MC type is Punch drunk Syndrome (Dementia Pugilistica) which is the case of Muhammad Ali.
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
Caused by metabolic conditions that result in Basal Ganglia calcification. (wilson’s dse, Hepatocerebral degeneration, Hallervorden-Spatz disease, Hypoparathyroidism)
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
This type of Parkinson’s disease is secondary to a group of neurodegenerative diseases that affect the substantia nigra and produce Parkinsonism symptoms along with their other neurological signs
Primary or Idiopathic Parkinsonism
Postencepalitic Parkinsonism
Toxic Parkinsonism
Pharmacologic Parkinsonism
Post traumatic parkinsonism
Metabolic Parkinsonism
Parkinson - Plus Syndrome
The substantia nigra contains pigmented cells which give it a characteristic ‘black appearance’. These cells are lost in PD and the substantia nigra becomes pale.
Neuromelonin
Neuromelanin
Neuromelime
Neuromelanine
Most common symptom gone when sleep and inactivity; Aggravated by emotional stress, fatigue or excitement "pill-rolling"
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
Increase in muscle tone during passive limb Takes two forms: 1. Lead pipe 2. Cogwheel - trunk rotation severely decreased
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
Dominance of progravity flexor muscles
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
€ Slowness of movement, masked facies, decreased eye blinking, inability to move •Fatigue •EMG: delayed motor unit recruitment, pauses once recruited, inability to increase firing rate
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
Predispose to falls; Weakness in anti-gravity muscles and balance Most disabling(DE LISA)
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
Transient inability to move
Tremor
Rigidity
Flexed Posture
Bradykinesia
Postural instability
Freezing Phenomenon
OTHER SYMPTOMS OF PD Except:
Gait & movement disturbances
Speech, voice & swallowing disorder
Sensory changes
Motor changes
Gastrointestinal changes
Cognitive & behavioral
Minimal or absent; unilateral if present
Stage 1
Stage 2
Stage 3
Stage 4
Stage 5
Minimal bilateral or midline involvement; balance not impaired
Stage 1
Stage 2
Stage 3
Stage 4
Stage 5
Impaired righting reflexes, unsteadiness when turning or rising from chair; some activities are restricted but pt is independent.
Stage 1
Stage 2
Stage 3
Stage 4
Stage 5
All symptoms are present & severe
Stage 1
Stage 2
Stage 3
Stage 4
Stage 5
Confined to bed or wheelchair
Stage 1
Stage 2
Stage 3
Stage 4
Stage 5
Defines as loss of neurons in caudate nucleus and putamen. - Autosomal dominant disease. - 4.1-8.4 in 100 000 / 30-40 y/o - Late stage: bradykinesia, rigidity, Postural Instability - Chorea is the hallmark - Depression-MC psychological dysfunction - Pneumonia and cardiovascular disease-MC mortality - language is okay
Huntington’s Disease
Heriditary Ataxia
Heriditary Spastic Paraparesis (Strumpell-Lorrain Syndrome)
Ourette Syndrome (Gilles De La Tourette Syndrome)
Progressive disorder with the presentation of limb and gait ataxia with diminished muscle stretch reflexes, joint position and vibratory appreciation
Huntington’s Disease
Heriditary Ataxia
Heriditary Spastic Paraparesis (Strumpell-Lorrain Syndrome)
Ourette Syndrome (Gilles De La Tourette Syndrome)
inherited disorder in which the primary symptoms are progressive bilateral lower limb spasticity & weakness - spasm in night or in cold weathee (weakness in hamstring, Tibialis Anterior, Iliopsoas muscles) - Difficulty in walking
Huntington’s Disease
Heriditary Ataxia
Heriditary Spastic Paraparesis (Strumpell-Lorrain Syndrome)
Ourette Syndrome (Gilles De La Tourette Syndrome)
Tic is the hallmark TYPES: Motor tic + Vocal tic Coprolalia - bad mouthing Copropraxia - bad gesture
Huntington’s Disease
Heriditary Ataxia
Heriditary Spastic Paraparesis (Strumpell-Lorrain Syndrome)
Ourette Syndrome (Gilles De La Tourette Syndrome)
Small step with increase speed secondary to displacement of COG; advanced stages. Progressive increase in speed with a shortening stride.
Festinating gait
Shuffling gait
Anteropulsive
Retropulsive
Forward festinating gait
Festinating gait
Shuffling gait
Anteropulsive
Retropulsive
Backward festinating gait (less common)
Festinating gait
Shuffling gait
Anteropulsive
Retropulsive
Early gait of PD; Decrease step length & velocity. Decrease cadence & velocity. Movement initiation & execution impairment.
Festinating gait
Shuffling gait
Anteropulsive
Retropulsive
(Anosmia) (100%)
Olfactory
Paresthesia
Dysphagia
Sialorrhea
Hypokinetic dysarthria
(50%)
Olfactory
Paresthesia
Dysphagia
Sialorrhea
Hypokinetic dysarthria
Often first symptoms; impaired swallowing; can lead to choking
Olfactory
Paresthesia
Dysphagia
Sialorrhea
Hypokinetic dysarthria
Increase in saliva & decrease spontaneous swallowing; common in sleeping & initiating speech.
Olfactory
Paresthesia
Dysphagia
Sialorrhea
Hypokinetic dysarthria
Decrease in voice volume & can lead to mutism (speak in whisper)
Olfactory
Paresthesia
Dysphagia
Sialorrhea
Hypokinetic dysarthria
Muscle contraction that leads to repetitive twisting movements of variable speed and abnormal posture
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Involuntary movement that is brief, rapid, forceful and rhytmic
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Writhing, snakelike involuntary movement.
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Large amplitude, movement often comes on suddenly with no clear pattern.
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Intermittent, stereotypical, jerky movement; eye blinking and throat clearing
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Purposeless, uniformly repetitive, voluntary movement of the whole body; head banging and seen with mental retardation
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
Inner restlessness and compulsion to move out;
Dystonia
Chorea
Athetosis
Ballismus
Tic
Stereotypy
Akathisia
A key feature of Parkinsons may detect low levels of dopamine in the brain,
Magnetic resonance imaging (MRI)
Positron Emission Tomography (PET)
A computerized tomography (CT)
Improve metabolism of intracerebral dopamine
Monoamine Oxidase Inhibitors
Levodopa
Dopamine agonists
Anticholinergic agents
To correct the essential neurochemical imbalance
Monoamine Oxidase Inhibitors
Levodopa
Dopamine agonists
Anticholinergic agents
Reducing rigidity & bradykinesia; also used to reduce motor fluctuations
Monoamine Oxidase Inhibitors
Levodopa
Dopamine agonists
Anticholinergic agents
Block cholinergic function & have the most benefir moderating tremor & rigidity; they have little or no effect on bradykinesia, & postural instability
Monoamine Oxidase Inhibitors
Levodopa
Dopamine agonists
Anticholinergic agents
For disabling tremor, effectively reduce longstanding tremor that is unresponsive to drug tx & may offer some improvement in rigidity.
Stereotaxic Thalamotomy
Transplantation to the corpus striatum
Discectomy
NOTA
In patients with advanced PD is highly experimental and is currently under intense research investigation. Only a very limited number of patients have undergone these procedures and they are not available for routine care.
Stereotaxic Thalamotomy
Transplantation to the corpus striatum
Discectomy
NOTA
Improve movement speed and consistency (e.g. walking patterns with focused instructions of “swing your arms”, walk fast” or “take large steps”)
Structured instructional sets
Visual cues
Rhythmic auditory stimulation (RAS)
Pulsed cues
Multisensory cueing
Include stationary floor markings & dynamic transportable cues
Structured instructional sets
Visual cues
Rhythmic auditory stimulation (RAS)
Pulsed cues
Multisensory cueing
Use of a metronome beat or a steady beat from a musical listening device
Structured instructional sets
Visual cues
Rhythmic auditory stimulation (RAS)
Pulsed cues
Multisensory cueing
To the earlobe or the hand
Structured instructional sets
Visual cues
Rhythmic auditory stimulation (RAS)
Pulsed cues
Multisensory cueing
Use of both visual and auditory cueing
Structured instructional sets
Visual cues
Rhythmic auditory stimulation (RAS)
Pulsed cues
Multisensory cueing
1. Optimal management involves a coordinated interdisciplinary team to oversee a comprehensive plan of care. 2. The therapist must prioritize the problems and interpret the goals in terms of what is efficacious. 3. Interventions are restorative, preventive, and compensatory.
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
Gentle rocking can be used to produce generalized relaxation of excessive muscle tension due to rigidity. Reduces anxiety associated with movement difficulties and prolonged times required to complete basic functional tasks
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
Improve flexibility and restores range in the neck & trunk and can be performed in combination with rotational exercises to promote relaxation. Combined with joint mobilization techniques, it
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
Indicated for patients with primary muscle weakness and insufficient central activation of the motor unit as well as for disuse weakness associated with prolonged inactivity. - Patient should consistently exercise at the same time after a medication dose on alternate days.
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
The overall emphasis is on improving mobility function with specific emphasis on improving mobility of axial structures, the head, trunk, hips, and shoulders.
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
Relaxation Breathing exercises Passive muscle stretching and positioning AROM and postural alignment Weight shifting Balance responses Gait activities Patient home exercises
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
Directed to reteach heel strike, improve weight transference, increase motion of the hip and knee, and prevent stiffness of the lower extremity
Objective of care
RELAXATION EXERCISES
FLEXIBILITY EXERCISES
STRENGTH TRAINING
FUNCTIONAL TRAINING
SCHENKMAN’S APPROACH
FLEWITT-HANFORD EXERCISES
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