Progressive Supranuclear Palsy Rating Scale (PSP-RS): Difference between revisions

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# The limb motor area six items with a maximum score of 16.  
# The limb motor area six items with a maximum score of 16.  
# The Gait area: five items with  a maximum score of 20.
# The Gait area: five items with  a maximum score of 20.
Item name and score definitions Comments, instructions
{| class="wikitable"
 
! colspan="2" |Item name and score definitions Comments, instructions
I. History
|-
 
|I. History
1.Withdrawal
|1.Withdrawal
 
0 None
0 None


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7. Sleep difficulty
7. Sleep difficulty


0 Neither 1 nor 2� insomnia
0 Neither primary nor secondary insomnia
 
1 Either 1� or 2� insomnia; averages 55 h sleep nightly
 
2 Both 1� and 2� insomnia; averages 55 h sleep nightly
 
3 Either 1� or 2� insomnia; averages55 h sleep nightly


4 Both 1� and 2� insomnia; averages55 h sleep nightly
1 Either  primary or secondary insomnia; averages <5 h sleep nightly


1� insomnia is difficulty falling asleep
2 Both  primary and secondary insomnia; averages <5 h sleep nightly


2� is difficulty remaining asleep
3 Either  primary or secondary insomnia; averages <5 h sleep nightly


Ignore trips to bathroom after which pt. returns to sleep easily
4 Both  primary and secondary insomnia; averages <5 h sleep nightly


II. Mentation
primary insomnia is difficulty falling asleep


Items 8 ^11 use this scale:
secondary is difficulty remaining asleep
|-
|II. Mentation
Items 8 -11 use this scale:


0 Clearly absent
0 Clearly absent
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1 Equivocal or minimal
1 Equivocal or minimal


2 Clearly present, but does not interfere with activities of
2 Clearly present, but does not interfere with activities of daily living (ADL)
 
daily living (ADL)


3 Interferes mildly with ADL
3 Interferes mildly with ADL


4 Interferes markedly with ADL
4 Interferes markedly with ADL
 
|8. Disorientation ; Use MMSE items 1^-10 or history to estimate interference in ADLs
Estimate the degree to which each deficit would interfere with
 
performance of daily cognitive tasks
 
8. Disorientation  Use MMSE items 1^10 or history to estimate interference in ADLs
 
9. Bradyphrenia   
9. Bradyphrenia   


10. Emotional incontinence  If there is a history of inappropriate laughing or crying but none
10. Emotional incontinence   
 
at the time of the examination, rate a ‘1’ or ‘2’, depending on its
 
frequency
 
11. Grasping/imitatative/utilizing behaviour  If none is displayed spontaneously (e.g. grabbing your coat or arm, or the wheelchair arm), ask patient to rest hands on thighs,
 
III. Bulbar
 
12. Dysarthria


11. Grasping/imitative /utilizing behaviour 
|-
|III. Bulbar
|12. Dysarthria
0 None
0 None


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4 Requires artificial measures (oral suctioning, tracheostomy or feeding gastrostomy) to avoid aspiration
4 Requires artificial measures (oral suctioning, tracheostomy or feeding gastrostomy) to avoid aspiration
 
|-
IV. Ocular motor
|IV. Ocular motor
 
Items 14 -16 use this scale:
Items 14 -16 use this scale:


0 Saccades not slow or hypometric; 86 -100% of normal
0 Saccades not slow or hypometric; 86 -100% of normal excursion
 
excursion


1 Saccades slow or hypometric; 86 - 100% of normal excursion
1 Saccades slow or hypometric; 86 - 100% of normal excursion
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4 <15% of normal excursion or worse
4 <15% of normal excursion or worse
 
|14.Voluntary upward command movement
14.Voluntary upward command movement
 
15.Voluntary downward command movement
15.Voluntary downward command movement


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4 Functional blindness or near-blindness because of involuntary eyelid closure
4 Functional blindness or near-blindness because of involuntary eyelid closure
 
|-
V. Limb motor
|V. Limb motor
 
|18. Limb rigidity
18. Limb rigidity
 
0 Absent
0 Absent


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1 Impaired (6 -14 taps/5 s or moderate loss of amplitude
1 Impaired (6 -14 taps/5 s or moderate loss of amplitude


2 Barely able to perform (0 -5 taps/5 s or severe loss of
2 Barely able to perform (0 -5 taps/5 s or severe loss of amplitude)
 
amplitude)


22. Apraxia of hand movement
22. Apraxia of hand movement
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2 Impairing most functions
2 Impairing most functions
 
|-
VI.Gait and midline
|VI. Gait and midline
 
|24. Neck rigidity or dystonia
24. Neck rigidity or dystonia
 
0 Absent
0 Absent


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4 Unable to test because of severe postural instability
4 Unable to test because of severe postural instability
|}


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Revision as of 09:43, 12 December 2020

Original Editor - Rucha Gadgil
Top Contributors - Rucha Gadgil

Introduction[edit | edit source]

The Progressive Supranuclear Palsy Rating Scale (PSPRS) is a disease specific measure of severity in patients with progressive supranuclear palsy (PSP). It measures disability across 28 items in six domains: daily activities (by history), behaviour, bulbar, ocular motor, limb motor and gait/midline. It was devised by Golbe and Strickland.

It is a quantitative measure of disability and attempts to include all of the important areas of clinical impairment in PSP.

Intended Population[edit | edit source]

This scale is targeted toward measuring the severity of clinical impairments in patients with Progressive supranuclear Palsy (PSP).

Method Of Use[edit | edit source]

Equipment:[edit | edit source]

Scale, Pen, Paper.

Cup of water

Training Required:[edit | edit source]

some examination item require prior clinical training

Time Required:[edit | edit source]

10 min

Instrument and Scoring[edit | edit source]

It is a Clinician reported measuring disability across six domains giving a maximum score of 100. It comprises of 28 items in six areas. Six items are rated on a 3-point scale (0–2) and 22 are rated on a 5-point scale (0–4).

  1. The History/Daily Activities area: seven items with a total maximum score of 24,
  2. The Mentation area: four items with a maximum score of 16,
  3. The Bulbar area: two items with a maximum score of 8,
  4. the ocular motor area four items with a maximum score of 16 points,
  5. The limb motor area six items with a maximum score of 16.
  6. The Gait area: five items with a maximum score of 20.
Item name and score definitions Comments, instructions
I. History 1.Withdrawal

0 None

1 Follows conversation in a group, may respond spontaneously, but rarely if ever initiates exchanges

2 Rarely or never follows conversation in a group

2. Irritability

0 No increase in irritability

1 Increased, but not interfering with family interactions

2 Interfering with family interactions

3. Dysphagia for solids

0 Normal; no difficulty with full range of food textures

1 Tough foods must be cut up into small pieces

2 Requires soft solid diet

3 Requires pureed or liquid diet

4 Tube feeding required for some or all feeding

4.Using knife and fork, buttoning clothes, washing hands and face

0 Normal

1 Somewhat slow but no help required

2 Extremely slow; or occasional help needed

3 Considerable help needed but can do some things alone

4 Requires total assistance

5. Falls

0 None in the past year

1 <1 per month; gait may otherwise be normal

2 1-4 per month

3 5-30 per month

4 >30 per month (or chairbound)

6. Urinary incontinence

0 None or a few drops less than daily

1 A few drops staining clothes daily

2 Large amounts, but only when asleep; no pad required during day

3 Occasional large amounts in daytime; pad required

4 Consistent, requiring diaper or catheter awake and asleep

7. Sleep difficulty

0 Neither primary nor secondary insomnia

1 Either primary or secondary insomnia; averages <5 h sleep nightly

2 Both primary and secondary insomnia; averages <5 h sleep nightly

3 Either primary or secondary insomnia; averages <5 h sleep nightly

4 Both primary and secondary insomnia; averages <5 h sleep nightly

primary insomnia is difficulty falling asleep

secondary is difficulty remaining asleep

II. Mentation

Items 8 -11 use this scale:

0 Clearly absent

1 Equivocal or minimal

2 Clearly present, but does not interfere with activities of daily living (ADL)

3 Interferes mildly with ADL

4 Interferes markedly with ADL

8. Disorientation ; Use MMSE items 1^-10 or history to estimate interference in ADLs

9. Bradyphrenia 

10. Emotional incontinence 

11. Grasping/imitative /utilizing behaviour 

III. Bulbar 12. Dysarthria

0 None

1 Minimal; all or nearly all words easily comprehensible

2 Definite, moderate; most words comprehensible

3 Severe; may be fluent but most words incomprehensible

4 Mute; or a few poorly comprehensible words

13. Dysphagia

0 None

1 Single sips, or fluid pools in mouth or pharynx, but no choking/coughing

2 Occasionally coughs to clear fluid; no frank aspiration

3 Frequently coughs to clear fluid; may aspirate slightly; may expectorate frequently rather than swallow secretions

4 Requires artificial measures (oral suctioning, tracheostomy or feeding gastrostomy) to avoid aspiration

IV. Ocular motor

Items 14 -16 use this scale:

0 Saccades not slow or hypometric; 86 -100% of normal excursion

1 Saccades slow or hypometric; 86 - 100% of normal excursion

2 51- 85% of normal excursion

3 16- 50% of normal excursion

4 <15% of normal excursion or worse

14.Voluntary upward command movement

15.Voluntary downward command movement

16.Voluntary left and right command movement

17. Eyelid dysfunction

0 None

1 Blink rate decreased (515/min) but no other abnormality

2 Mild inhibition of opening or closing or mild blepharospasm; no visual disability

3 Moderate lid-opening inhibition or blepharospasm causing partial visual disability

4 Functional blindness or near-blindness because of involuntary eyelid closure

V. Limb motor 18. Limb rigidity

0 Absent

1 Slight or detectable only on activation

2 Definitely abnormal, but full range of motion possible

3 Only partial range of motion possible

4 Little or no passive motion possible

19. Limb dystonia

0 Absent

1 Subtle or present only when activated by other movement

2 Obvious but not continuous

3 Continuous but not disabling

4 Continuous and disabling

20. Finger tapping

0 Normal ( <14 taps/5 s with maximal amplitude)

1 Impaired (6 -14 taps/5 s or moderate loss of amplitude

2 Barely able to perform (0 -5 taps/5 s or severe loss of amplitude)

21. Toe tapping

0 Normal (<14 taps/5 s with maximal amplitude)

1 Impaired (6 -14 taps/5 s or moderate loss of amplitude

2 Barely able to perform (0 -5 taps/5 s or severe loss of amplitude)

22. Apraxia of hand movement

0 Absent

1 Present, not impairing most functions

2 Impairing most functions

23. Tremor in any part

0 Absent

1 Present, not impairing most functions

2 Impairing most functions

VI. Gait and midline 24. Neck rigidity or dystonia

0 Absent

1 Slight or detectable only when activated by other movement

2 Definitely abnormal, but full range of motion possible

3 Only partial range of motion possible

4 Little or no passive motion possible

25. Arising from chair

0 Normal

1 Slow but arises on first attempt

2 Requires more than one attempt, but arises without using hands

3 Requires use of hands

4 Unable to arise without assistance

26. Gait

0 Normal

1 Slightly wide-based or irregular or slight pulsion on turns

2 Must walk slowly or occasionally use walls or helper to avoid falling, especially on turns

3 Must use assistance all or almost all the time

4 Unable to walk, even with walker; may be able to transfer

27. Postural stability

0 Normal (shifts neither foot or one foot)

1 Must shift each foot at least once but recovers unaided

2 Shifts feet and must be caught by examiner

3 Unable to shift feet; must be caught, but does not require assistance to stand still

4 Tends to fall without a pull; requires assistance to stand still

28. Sitting down

0 Normal

1 Slightly stiff or awkward

2 Easily positions self before chair, but descent into chair is uncontrolled

3 Has difficulty finding chair behind him/her and descent is uncontrolled

4 Unable to test because of severe postural instability


Management / Interventions[edit | edit source]

add text here relating to management approaches to the condition

Differential Diagnosis[edit | edit source]

add text here relating to the differential diagnosis of this condition

Resources[edit | edit source]

add appropriate resources here

References[edit | edit source]