Summary on common pathologies/coniditions Flashcards
Osteoporosis Summary
- Increased bone resorption causes a decrease in bone density, brittle, weak bones
- More osteoclast activity than osteoblast
-Fractures in L and T spine. Distal arm, femoral neck - Do extension and core strengthening to improve postural stability
- AVOID flexion w/ resistance or deep flexion, heavy resistance, and ballistic movements. avoid rotation Too much stress in the spine due to flexion moment
- DO weight-bearing and resistance training as tolerated, aquatic therapy for conditioning but need WB/strengthening specifically (lunges, rows, leg press, etc.)
- Medications include calcium, Vit D. Raloxifene, Fosamax
- DEXA less than -2.5 is osteoporosis, -1 to -2.5 is osteopenia
Peripheral Arterial Disease
Narrowing of the lumen in blood vessels due to arteriosclerosis
- Intermittent claudication (cramping/pain, pallor w/ elevation and rubor in dependent position b/c blood flow is stuck due to occlusion), relieved with rest
- Other sx are Hair loss in the region, pain at rest, slow healing changes in skin color decreased temp, weakened pulse
- Higher risk for other circulatory issues
- Anticoagulants, anti platelets, thrombolytica to prevent clots
Exercise Program
4-6 weeks includes intermittent walking close point of max pain, then rest until fully relieved then repeat. Working up to 30 min straight. Include dynamics resistance and aerobics
=Leads to collateral circulation
For night sx, lift bed 4-6 inches for perfusion in legs
A type of PVD
Multiple Sclerosis
CNS disease with demyelination of neurons specifically in CNS. Impacts motor and sensory.
Sensitive to heat
Cognitive changes
Motor and sensory issues
Balance issues
Loss of coordination so closed chain exercise is better
Key sx - optic neurits (vision issues b/c optic nerve involved), UMN signs, weakness, coordination
Exercise 50-70% moderate intensity
Need breaks and days off
Alternate body parts within session
Type
- clinically isolated is first time and/or only time
- Relapsing remitting includes attacks followed by some level of recovery and no decline in between
- Secondary progressive is when it goes from relapsing remitting with recovery periods to constant decline aka disease progression-
- Primary progressive is when there is a constant decline throughout
Guillain-Barre Syndrome
-Often in response to infection
- RAPID onset with demyelination of peripheral nerves
- Distal to proximal weakness
- Decreased DTR, sensory disturbances
GBS typically involves rapid onset, bilateral ascending weakness or paralysis, as well as changes in sensation in a stocking-glove pattern (typically).
Myasthenia Gravis Summary
- Damage to neuromuscular junctions due to increase in anti-acetylcholine receptors
- Women ins 20s, 30s
- Cranial nerves impacted first= eye weakness, ptosis, chewing and facial weakness
- Proximal muscle like neck
- Severe fatiguing throughout day due to issues with nerve firing
- No UMN
ptosis that may fluctuate, and often, muscles involving speech, chewing, or swallowing are affected, as well.
Osteoarthritis
Always consider age in diff dx
Heberden’s nodes in fingers (more distal than bouch)
Stiffness less than 30 min morning
Cauda Equina syndrome
Anything L2 and below including sacral levels
Bowel and bladder changes
More radicular pain than lower back (makes sense because more distal nerve roots)
Saddle anesthesia
Absent reflexes
GRADUAL AND UNILATERAL
Severe pain Spinchther dysfunction is later
Conus Medullaris syndrome
L1-L2 level
Greater lower back pain than radicular (makes sense b/c more proximal in lumbar region)
Hyperreflexia (UMN)
SUDEEN AND BILATERAL
Early change in sphincter
Juvenile Rheumatoid Arthritis
Similar to RA
16 years or younger, girls more than boys
The most common type is pauciarticular which includes 4 joints or less and is seen is girls 8 or younger, Asymmetrical
vs
more severe polyarticular JRA is symmetrical and more than 4 joints
Expect contractures and periarticular damage and symptoms
Expect less ROM in functional activities like gait
Diabetes
Understand that if uncontrolled, then concerns are hyperglycemia b/c no insulin so no uptake into muscles
But if controlled and taking insulin, then concern is hypoglycemia, especially with exercise b/c increased uptake into other tissues. Important to have carbs before or during exercise.
Horners syndrome vs bells palsy
Horners is Loss of sympathetic nerve function to one side of face causeds loss of sweat (anhidrosis), ptsosis, miosis (pupil size smaller)
Bells palsy is facial nerve palsy on one side
Spinal stenosis
Prefers flexion, not extension
Supine positioning and encouragement of core training in order to increase muscular support for the lower back would be recommended for a patient with spinal stenosis.
In patients with spinal stenosis, exercises that encourage low back extension should be avoided; therefore long-distance ambulation on a flat surface would not be the most appropriate exercise for the PT to recommend.
Duchenne Muscular Dystrophy
Fat and CT begin to replace muscle due to the mutation of the dystrophin
Stretch Hip flexors and plantar flexors
2-5 yo
Gowers maneuver
Fatty deposit (pseudohypertrophy in calf)
Rapid progression cant walk by 10
Myelopathy
LMN at the level of lesion
UMN below the lesion
BL involvement (both motor and sensory)
Poly neuropathy
Motor, sensory, and autonomic changes BL in distal regioins