MS Flashcards

1
Q

Multiple Sclerosis is a ______ disease

A

Demyelinating

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2
Q

What do demyelinating dis’s do and what is the MOST COMMON form?

A
  • DEC speed and quality of impulse conduction (saltatory conduction)
  • MS is most common form
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3
Q

Demyelination can occur due to:

A
  • Systemic disease
  • Malnutrition
  • Toxic exposure
  • Infection
  • Anoxia→ deprivation of O2
  • Ischemia→ local
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4
Q

MS Defined:

A

Demyelinating dis. characterized by a course of demyelination relapses & remissions, superimposed upon gradual neurologic deterioration

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5
Q

Keep in mind w/ MS:

A

ANY CNS white matter can be affected→ presentation will vary

*episodic AND chronic

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6
Q

MS Prevalence

A

Female > Male; 2:1 ratio

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7
Q

MS High Risk Areas

A

FURTHER AWAY FROM EQUATOR

  • Northern US, Northern Europe, Southern Canada, New Zealand, Southern Australia
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8
Q

MS Etiology:

A

Interaction b/w genetic predisposition & an inciting environmental antigen→ produces autoimmune demyelinating response in susceptible host

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9
Q

Theory of autoimmune response in MS:

A

CNS myelin becomes infected by virus and is perceived as antigen

*immune system then targets the “antigen” aka destroys myelin

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10
Q

Stress and MS

A

Stress does NOT HELP MS!

not proven*

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11
Q

Pathophysiology of MS:

A
  • Demyelinating lesions→ Plaques
    • sharply delineated lesions viewed on MRI
  • Inflammation may result in Mass Effect (obj in skull that pushes brain)
    • acute exacerb’s tx’d w/ steroids
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12
Q

More pathophys MS:

A
  • IF oligodendrocytes survive→ remyelination may occur
    • later stages→ if few remain, remyelination partial @ best
  • End Stage Patho:
    • myelin replaced by fibrous scarring (gliosis)→ inhibits impulse transmission
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13
Q

*Types of MS:

4:

A
  1. Relapsing-Remitting (most common)
    1. aka Exacerbating-Remitting
  2. Relapsing-Progressive
    1. aka Exacerbating-Progressive
  3. Primary-Progressive
    1. aka Chronic-Progressive
  4. Secondary-Progressive
    1. the one that begins as Relapse-Remitting then Chronic-progressive
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14
Q

Types of MS:

Relapsing-Remitting

aka Exacerbating-Remitting

A
  • Ep’s of rapid, abrupt deterioration w/ variable degrees of recovery over time
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15
Q

Types of MS:

Relapsing-Progressive

aka Exacerbating-Progressive

A
  • Relapses w/ lg degrees of residual impairs
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16
Q

Types of MS:

Primary-Progressive

aka Chronic-Progressive

A
  • Steady, progressive deterioration
  • Pace of deterioration may be steady OR varied
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17
Q

Types of MS:

Secondary-Progressive

aka the one that BEGINS as relapse-remitting THEN becomes chronic (primary)-progressive

A

one that BEGINS as relapse-remitting THEN becomes chronic (primary)-progressive

  • Sometimes Full recovery
  • Sometimes Partial recovery
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18
Q

MS:

Definitive Dx requires WHAT?

A
  • Requires clinical or para-clinical evidence of 2 or more spatially & temporally distinct lesions
    • aka 2 diff areas @ 2 diff times***
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19
Q

MS Dx and MRI Findings:

A
  • Lesions may NOT correlate w/ s/s
  • Lesions may BE PRESENT in absence of s/s
  • CSF via Lumbar Puncture
    • elevated IgG→ immune system elevation
    • Oligoclonal bands→ destruction of oligodendrocytes
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20
Q

Not Quite MS…

A
  • Clinically Isolated Syndrome (CIS)
    • looks like exacerbation but happens 1 time
  • Radiologically Isolated Syndrome (RIS)
    • Single time, has radiograph similar to MS, only one incident shown
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21
Q

Primary S/S MS:

A
  • Presents in # of ways→ depends on loc. of demyelination
  • Need useful SC vs. Cerebral (where plaques are)
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22
Q

Primary S/S MS:

Fatigue

A
  • Single most common complaint in MS*
  • Out of proportion to task causing it
  • Present even if strength normal
  • Fatigue→ Sx’s, HOW pt feels
  • Fatigability→ Sign, change in motor perform
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23
Q

PRIMARY Fatigue

A

Caused by actual MS

  • Lassitude→ sx of severe fatigue
  • DEC conductivity→ reduced impulse propagation
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24
Q

SECONDARY Fatigue

A

Consequence

  • infx
  • spasticity
  • ataxia
  • weakness
  • depression
  • sleep deprivation
  • polypharmacy (lots diff meds)
  • decond.
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25
Fatigue in PWMS and PT Implications
* **Ex. Type** * Diminished ability to tolerate lg amts of ex * DO: **Intermittent tx** * **Ex. Scheduling** * Schedule ex @ times of INC energy if they are willing to use that time to Ex.
26
**PRIMARY s/s MS:** **Sensory Changes**
* Parasthesias→ partial sensation loss * Dysesthesias→ abnorm sensation (burning) MORE FREQ.
27
PRIMARY s/s MS: Optic Neuritis
Optic neuritis \*NOTE: **some have abrupt loss of vision 2-3d** **COMMON**
28
PRIMARY S/S MS: ## Footnote **Weakness**
* **PRIMARY→** from _plaques_ (demyelination) * **SECONDARY→** disuse, deconditioning, disuse atrophy
29
PRIMARY S/S MS: Weakness **A note about Flexibility**
* MS does NOT directly cause prob w/ flex, but weakness and other sx cause probs * W/out adequate flex→ person loses norm biomechanics for **gait & balance**
30
PRIMARY S/S MS: ## Footnote **Spasticity** **\*know the Mod Ashworth Scale!!**
* UMN Syndrome **common in PWMS** * **worsens over time** * **IF spinal origin→** Intrathecal Baclofen pump * NOT USEFUL IF CORTICAL LVL MS
31
PRIMARY S/S MS: ## Footnote **Heat Sensitivity**
* Common * Worse fatigue and weakness w/ elevation in body temp * transitory→ NOT permanent * **Some benefit from cooling BEFORE ex.**
32
Primary S/S MS: ## Footnote **Ataxia**
* Due to plaques in **cerebellum and DCML** * **B/L** * Dysmetria, dysdiadochokinesia, tremor, vertigo * CNS vs. PNS vertigo
33
Primary S/S MS: ## Footnote **Pain**
* Spasms from **hypERtonia** * Burning dysesthesias from plaques in **thalamus or spinothalamic tract** * **MSK pain** from inapp. mvmt patterns → weakness, disuse atrophy
34
**Primary S/S MS:** **Psychiatric**
* Euphoria→ late stages * Depression * **Most common Cog. changes→** memory loss, impaired safety awareness\*\*\*
35
Secondary S/S MS: **Weakness and Fatigue** that occur due to MS causes what?
Series of 2\* probs → VERY IMPORTANT TO PT's!!!
36
2\* S/S MS: MSK issues
* Inapp mvmt patterns due to: * **Weakness** * **Fatigue** * **Spasticity** * Overuse syndromes/tendonitis 2\* to spasticity
37
2\* S/S MS: ## Footnote **Weakness**
PRIMARY weakness cannot be affected by ex, 2\* CAN
38
2\* S/S MS: Posture
* due to prolonged sitting * Can benefit from pos'ing out of shortened pos. * Poor posture leads to skin breakdown, contracture, resp. comps
39
2\* S/S MS: **Balance Loss**
* Combo of 1\* and 2\* effects * **1\*** * weakness, spasticity, ataxia, sensory loss, diminished motor control, visual loss, depression, fatigue * **2\*** * 2\* weakness, contractures
40
Other 2\* S/S MS:
* Osteoporosis * Infections
41
Medical Mgmt MS: ## Footnote **One you should know**
Ocrevus→ **only FDA approved med to tx progressive types→** _Slows progression_ * **Steroids** * Tx of choice for **acute exacerbation** * **suppresses immune function**
42
MS and Spasticity Keep in mind..
**Spasticity** can be **Useful!** * Eradication of spasticity can _diminish underlying strength_
43
MS and 2\* Fatigue
* Improve fitness thru ex. * **Energy Conservation tech's** combined w/ **meds** * → Tx of choice for fatigue
44
Psychosocial Factors MS
Demanding dis. for both pt and caregiver→ **unpredictable and hard to see**
45
Rehab/PT Mgmt MS:
* No cure * Tx focused on medically controlling **current exacerbation** * Prevent 2\* deficits * **EDUCATION→** teach pt and family as much as poss. about disease esp **self mgmt of comps**
46
MS and Evidence for Exercise
* Aerobic, MSK strength, Resp endurance * Good therapeutic response to Ex. * PTs should be **confident** in prescribing ex. in PWMS
47
NOTE: Great Quote
“PWMS respond to exercise the **same way** as those w/out MS: **they become _More Fit!!!”_**
48
MS more commonly dx'd b/w ___ and \_\_\_\_
30 and 35yo
49
Pathological features of MS: Radiographs “Plaques”
see pics
50
Primary s/s MS: Where? Clinical Presentation?
* MS can affect **white matter anywhere t/o CNS** * Clinical presentation depends on **loc of demyelination** * may not correlate w/ imaging findings * Wide variety s/s
51
Common s/s in PWMS
See pics
52
2 Ways to Classify MS:
1. Disease **subtype→ Phenotype** 2. Disease **severity**
53
Sub-Types of MS: 4
1. Relapsing-Remitting→ **most common** 2. Progressive-Relapsing 3. Primary (Chronic)-Progressive 4. 2\* Progressive
54
Subtypes MS: ## Footnote **Relapsing-Remitting** **\*most common**
* Rapid, abrupt deterioration w/ variable degs of recovery over time * **aka exacerbating-remitting**
55
Subtypes MS: ## Footnote **Progressive-Relapsing** **aka Exacerbating-Progressive**
* Relapses w/ lg deg of residual impairment
56
Subtypes MS: ## Footnote **Chronic-Progressive** **aka Primary-Progressive**
* Steady progressive deterioration * PACE of deterioration may be **steady or varied**
57
Subtypes MS: ## Footnote **2\* Progressive**
* BEGINS as **relapsing-remitting** THEN becomes **chronic-progressive**
58
MS Education for pt. ## Footnote **Exacerbation vs. Pseudo-Exacerbation** **Talk about pseudo-exacerbation**
* Transient (temporary) worsening of sx's that can occur due to **stress, infection, overheating, overexertion**→ Full recovery occurs * EX. Person w/ pseudo-exacerbation * Temp. change in sensory sx's due to exercise but will **recover completely** w/in short pd of time
59
Remember…**for definitive dx for MS you NEED:**
* 2 clinical or para-clinical spatial and temporal distinct lesions @ 2 diff times * **2 clinical findings OR** * **2 radiological findings @ 2 diff times**
60
Not Quite MS:
* **CIS→** Exacerbation happens ONCE * **RIS→** Radiographic evidence ONCE w/ both→ **more likely to dev. MS in future**
61
MOST COMMON DISABILITY SCALE FOR MS
EDSS Extended Disability Status Scale \*Low reliability \*see pics
62
WHERE DO WE SEE MOST PWMS? Following EDSS
SEE PICS
63
MS: ## Footnote **Disease Severity**
* Other measures * Disease Steps (previous picture) * Pt-Determined Disease Steps * **NOTE:** plastic changes/compensations BEFORE sx's reach clinical threshold **aka become noticeable** * **Relapse→** could be old recurring sx's OR new sx's
64
Med. Interventions for PWMS: 3:
1. **Mgmt of Acute Exacerbations** 2. **Long-term dis. mgmt** 3. **Sx mgmt**
65
Med. Interventions for PWMS: ## Footnote **Mgmt of Acute Exacerbation**
* Goal: Halt inflamm process * Tx: * **high dose methylprednisolone: IV** * **high dose prednisone: oral** * **acthar (ACTH): subq/intramuscular** **ALL= immunosuppress/anti-inflamm**
66
Disease Modifying Agents for MS: ## Footnote **know this one**
\***Ocrevus→** only drug FDA approved to tx **progressive MS** **\***Botoxin for **hypertonia**
67
MS: ## Footnote **Med. Sx Mgmt**
* B&B dysf * depression * dizzy/vertigo * emotional changes * **Fatigue** * itching * pain * sex. dysf * spasticity * tremors * walking diff.
68
The Examination for MS pt.
* Some **MS-specific considerations** * **Hx-taking** * **Tests & Measures**
69
Examination for MS: **MS-Specific Considerations**
* Systems review **should consider** BOTH **observed and occult** (not seen, pt not complaining about it) * CV/Pulm * autonomic→ monitor resp to ex. * Integumentary * Neuro/MSK * PT Exam MUST ID Pt. problems that are **primary (**due to MS) **AND secondary (**consequence of another impair, act. limit., or participation restrict), or **combination** ***NOTE:** 2*\* problem IF **quick response** to intervention
70
MS Examination: ## Footnote **Taking the Hx**
* verbal/non-verbal comm. * **What do you see w/ simple observation?** * facial express * posture * equip * spont. mvmts * **Things to Consider:** * PMH * Social Hx * Current LOF * Overall lvl of phys act. * Any prev/current rehab/ex program
71
MS Examination: ## Footnote **Other questions to consider** **\*have gen. idea**
see pics
72
MS Pt. Exam: ## Footnote **Fatigue**
* Special consideration for PWMS * **_Participation-level_ measures→ “Trait”** * what they exp **most of the time** * MFIS- canvas * FSS- canvas * FSMC- canvas * **_Immediate_ measures→** “**State”** * how you feel **right now** * VAS of Fatigue
73
MS Pt. Exam: ## Footnote **Integumentary**
check skin ask questions about skin safety-- esp lot of time in bed, w/c, sitting chair
74
What should be measured during the MS pt. Examination?
* **Vital signs→** vitals are vital!!! * A/PROM * Strength/motor control * UMN signs * Sensation * Pain * Posture * Balance+Fall hx * **Cerebellar function** * tremor * \*coordination * nystagmus * Bed mobility-**functional mobility** * Transfers-**functional mobility** * Walking + Gait-**functional mobility** * Stair climbing-**functional mobility**
75
Vital Signs and PWMS
* IMPORTANT!!! * CV **autonomic dysf** common in PWMS * orthostatic dysreg, cardiac arrhythmias, blunted ex responses
76
A/PROM in PWMS
56.4% have contracture in @ least one major UE or LE jt * Ankle=43.9% * Shoulders=13.1% * Hips=28.8% * Knees=17%
77
Flexibility in PWMS
* w/ out adequate flex→ person loses norm biomechs necessary for walking, gait, balance * **HIGHER prevalence in those w/ _progressive_ types of MS**
78
Strength and Motor Control in PWMS
70% have weakness (MMT = 3/5) in one mm group * LE= ankle, knee, hips (50-53%) * UE= shoulder, elbow, wrist (61-62%) \***NOTE:** differentiate whether person has **normal motor control**, then test strength accordingly
79
\*Changes in flex and strength are **often present very EARLY in disease, even in absence of limits in function!**
see pics
80
Testing UMN Signs
* Spasticity * **Mod Ashworth** * DTRs * biceps, tris, brachioradialis, quad, gastroc * Clonus * wrist, ankle * Babinski
81
Examining Pain in PWMS:
* **Consider:** * location(s) * description * intensity when **worst** * worsened by.. * improved by.. * activities impaired * **NOTE:** important to diff whether pain is **primary (neurogenic), secondary (jt pain due to compensatory mvmt patterns), or unrelated to MS (MSK source of pain)**
82
Bed Mobility and Transfers in PWMS
* GEN measured w/ **_observational analysis_** * Consider **objective tests:** * 5STS * timed mobility tests * **Observe carefully** to assist in **eval'ing critical contributors to limits.**
83
Posture in PWMS Exam
Sitting AND standing \*if bed/chair bound→ **posture in these environments must be considered**
84
Balance in PWMS: Taking a Fall Hx
* Ask SPECIFIC QUESTIONS about falls * people have poor recall of falls **unless catastrophic/injurious** * dig deep! * how/when/why falls happening? * how many? frequent? * SPLATT (another slide)
85
**SPLATT** Questions: **Related to Falls** **SPLATT:**
* **S:** Symptoms @ time of fall * **P:** Previous falls you've had * **L:** Location of falls * **A:** Activity you were doing * **T:** Time of day * **T:** Trauma→ injured @ all?
86
Balance Exam in PWMS:
REVIEW BALANCE!!! * Consider test(s) to use * Standing: * Berg * DGI * MiniBEST * 4-Square Step Test * Functional Reach * Sitting: * Function in Sitting Test * Trunk Impairment Scale USE CLINICAL DECISION MAKING SKILLS!
87
Walking and Gait in PWMS
* 40-50% PWMS exp. **walking diff.**→ 70% report **one of their most _limiting problems_** * 30-40% of care partners report walking limits causes **sig caregiver burden** and **neg. impacts their QOL**
88
Contributors to **Walking and Gait Dysf in Pts w/ MS**
see pics
89
Examining Walking and Gait in **PWMS**
* **Observational Analysis\*→** W/ and W/out AD * Distance? Device? Assist needed? * **_Repeatable_ measures of walking:** * Timed 25'-Walk Test * 2, 3, 6-Min Walk Test * 12-item MS Walking Scale- **canvas**
90
Other Considerations for Examination of PWMS:
* **Vision** * acuity * oculomotor function * **Vestib Function** * Substantially HIGHER incidence of **peripheral vestib dysf** in PWMS vs age/sex matched peers * **Mentation/cognition** * **Resp strength/cough/breath support** * use PFTs! * common early in disease
91
3 places where **Fatigue** MUST be Considered:
1. Examination 2. Evaluation 3. Intervention
92
Fatigue…
* **Essential part** of **neuro. disability** * Part of **mobility loss** in neuro patho may be due to **fatigue** * **MUST BE CONSIDERED IN:** * Exam * Eval * Intervents.
93
Fatigue vs. Fatigability vs. Pathologic fatigue/fatigability
* **Fatigue= Symptom** * _Subjective_ state of being tired * Feeling of not being able to perform a task or activity **effectively,** if at all * **Fatigability= Sign (change in ability)** * _Observational decline_ in performance during _sustained activity_ * Can be observed on ANY prolonged and/or intensive task **NOTE: Pathologic fatigue or fatigability→** happens faster or more severely than expected in a non-disabled person\*
94
Recognizing **Fatigue vs. Fatigability** **Fatigue (symptom):**
* NO ENERGY * pt c/o fatigue * pt avoids ex program or other activities * caregiver report * dec'd scores on self-report fatigue measures * can also present as depression, anxiety
95
Recognizing **Fatigue vs. Fatigability** ## Footnote **Fatigability (Sign):**
* **progressive** slowing of gait * **progressive** weakness of rep'd contracts * **worsening** of sensation/speech/vision during repetitive task * **DECd performance** on a functional measure following exertion * physio. measures→ temp, EMG, CV * Pt caregiver complaint/ID
96
Interaction of **Primary** and **Secondary Fatigue/Fatigability**
Less mvmt is performed→ Deconditioning results→ tasks become “unlearned” \**Where can we as clinicians intervene in this cycle?→***ALL LVLS!**
97
SPECIAL CONSIDERATION: **FATIGABILITY**
* **Decline in performance** w/ repetition OR during a prolonged work bout * Need frequent breaks/rest!!!
98
Ex. Fatigability
6MWT see pics…
99
Crux about **Fatigability**
* Evidence that there is a **declination in performance** after rep'd attempts and/or other fatiguing activity in PWMS * Found in: * Rxn time testing * Postural control * Functional balance tests * Gait and walking * Speech and communication function
100
Fatigue vs. Fatigability \*Key thing to remember
**Always differentiate _symptom_ from _sign_!**
101
Fatigue is a \_\_\_\_\_\_
Symptom
102
Fatigability is a \_\_\_\_\_
Sign
103
Evaluation aka…
Putting it all together!!!
104
What is the **Evaluation?**
* Time to consider **all of the findings** and develop **hypotheses** that may be confirmed or refuted by these findings * **Add. testing/measuring/questioning** may be needed to confirm/refute equivocal findings * **End Result→** Includes overall assessment of the pts condition, along w/ **specific prob list of what _needs to be addressed_**
105
Developing Intervention Plan
* HOW are you developing plan? * What are “General” probs you might ID→ ones that may be amenable to trad. interventions? * What are **MS-specific probs** that will req more individualized plan?
106
Remember in PWMS….
“Persons w/ MS respond to exercise the same way as those w/out MS: **they become more fit!”** -Karpatkin, 2005
107
Developing Intervention Plan What should it **focus on?**
* Focus on **maximizing function!** * Consider components of the **motor relearning program** * **task analysis** * **practice whole task** * **practice missing components** * **transference of training** * Address impairs of body structure/function as needed
108
**Considering Fatigue**
* MUST BE CONSIDERED when working w/ PWMS * **One of the _main limiters_ of the effectiveness of PT interventions for PWMS** * Must be balanced w/ the need to maximize therapy dosing
109
What can be done to combat fatigue during PT Interventions? 2 Leads:
1. **Intermittent Training** 1. work up until fatigability then break 2. **Maximal Strength Training** 1. Ex. 4 sets of 4 reps @ 90% 1RM
110
Intermittent Training
Work up until fatigability then break
111
Maximal Strength Training \*\*\*
Ex. 4 sets of 4 reps @ 90% 1RM
112
What about interventions for those who are **more disabled?**
* Maintain **max. flex and strength** * Protect skin * Address **person-specific goals** * other ideas: * mech. lifts * chest PT * incentive spirometer * etc.. * **In the late to end stage:** * you may fill role of hospice PT * help do things THEY WANT TO DO * participate where they want to participate
113
Bottom Line for PWMS:
* DON'T hesitate to work w/ PWMS * Conduct **comprehensive exam** bc _no pre-defined clinical picture_**\*** * Treat as aggressively **as tolerated**→ **DO NOT UNDERDOSE!** * Refer to other pro's as approp. * Be in touch w/ more knowledgeable mentors to help when you're not sure what to do!