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adult ms disorders pt 2
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soft tissues: myofacial compartment syndrome
compromised function of nerves, mm and vessels within a closed myofacial compartment 2 degrees increased interstitial pressure
facia doesnt stretch so increase in pressure :(
soft tissues: 2 types of myofacial compartment syndrome
acute: fracture
chronic: running 1 mile and pain, then when they’re resting it go away (shin splints dont go away w rest)
soft tissues: myofacial compartment syndrome common areas?
lower leg, forearm, thigh, and foot
soft tissues: myofacial compartment syndrome clinical predisposition?
-fractures
-severe contusions
-crash injuries
-trauma (dropping weight)
soft tissues: myofacial compartment syndrome risk factors?
burns
circumferential wraps/ dressings (too much compression)
casting/immobilization
soft tissues: myofacial compartment syndrome s+s?
-pain (excrusiating, fx pain will go away w meds…this will not)
-paresthesia distal to area of involvement
-passive stretching increases pain
soft tissues: myofacial compartment syndrome tx?
surgery to relieve pressure
untreated= ischemia, irreversible mm loss, functional disability (amputation, foot drop)
soft tissues injuries: subluxation is?
-partial disruption (not fully dislocated but moved)
mobile joints most affected (bc they have room)
GHJ most common
acromial clavicular joint
sacroiliac
elbows in peds
soft tissues injuries: dislocation is?
complete disruption (out of socket)
mobile joints most affected
GHJ is most common
(can be late manifestation of chronic condition)
soft tissues pathologies: what is heterotopic ossification?
bone formation in non osseous tissue (soft tissue = mm or tendons)
soft tissues pathologies: when does heterotopic ossification happen?
-after trauma, mm are injured, fx, spinal cord injury
-surgery- commonly seen in total hip
-hereditary for exists although rare
soft tissues pathologies: what is myositis ossification?
bone formation in soft tissues after in mm after trauma
soft tissues pathologies: what is neurogenic heterotopic ossification?
bone formation in soft tissues after a neurologic injury
soft tissues pathologies: what is heterotopic ossification risk factors?
patient hx
gender (males higher risk)
soft tissues pathologies: what is heterotopic ossification pathology?
-Pluripotent mesenchymal stem cells differentiate into osteoblasts (Differentiation begins early after trauma/ surgery, peaks at 32 hours)
-Histologically similar to reformation of bone in fractures
–Histologically different structure
soft tissues pathologies: what is heterotopic ossification clinical manifestations?
depends
pain and loss of motion
progressive loss of joint function
soft tissues pathologies: what is heterotopic ossification classification grades?
class 1
class 2
class 3 and 4
soft tissues pathologies: what is heterotopic ossification class 1?
slight ossification, no ROM limitation
soft tissues pathologies: what is heterotopic ossification class 2?
presence of HO, mild ROM limitations
soft tissues pathologies: what is heterotopic ossification class 3 and 4?
presence of HO w/ anklyosis preventing motion
soft tissues pathologies: what is heterotopic ossification prevention, diagnosis, tx:
prevention: radiation tx, meds, traumatic injury avoidance, no rough passive stretching!!
diagnosis: pt hx and x ray
tx: preventative measures, surgical resection, rehab
soft tissues pathologies: what is mixed connective tissue disease (MCTD)
overlap connective tissue disease
overlapping syndrome of more than one rheumatic disease can include CREST
CREST = ?
C
R
E
S
T
soft tissues pathologies: mixed connective tissue disease (MCTD) risk factors:
autoimmune disease (Hypergammaglobulinemia, + rheumatoid factor, High titer ANA’s))
gender= females higher risk
soft tissues pathologies: mixed connective tissue disease (MCTD) etiology and pathogenesis:
normal cells modify itself to fight infection and immune system thinks it not self
soft tissues pathologies: mixed connective tissue disease (MCTD) diagnosis and tx:
diagnosis: high titers of ANAs in blood work
tx: drug therapy (corticosteroids)
prognosis= good
soft tissues pathologies: what is polymyalgia rheumatica (PMR)
an inflammatory disorder that causes muscle pain and stiffness, especially in the shoulders, neck, and hips, and primarily affects older adults (usually over age 50)
bed mobility and sit to stand transfers are most notable affected
soft tissues pathologies: what is polymyalgia rheumatica (PMR) risk facotrs?
-age >70 yrs
-caucasian
-gender= female more likely
-common (1 in 200)
soft tissues pathologies: what is polymyalgia rheumatica (PMR) etiology?
-unknown
genetic factor (HLA-DR4)
infection
autoimmune malfunction
-no histological abnormalities
characteristice aching and stiffness = jt inflammation
soft tissues pathologies: what is polymyalgia rheumatica (PMR) clinical manifestation:
-gradual onset
-becomes evident suddenly
-symptoms often bilateral
-commonly misdiagnosed (osteoarthritis)
-possible dev to giant cell arteritits (send to emergency)
what does a long term high dose use of predisone cause?
osteoporosis, mm and bone weakness, high glucose
slide 17
do
soft tissues pathologies: what is rhabdomyolysis?
rapid breakdown of skeletal mm tissue 2 degrees mechanical, physical or chemical traumatic injury, resulting in creatine phosphokinase enzyme release
soft tissues pathologies rhabdomyolysis affects what?
kidneys
soft tissues pathologies: what is rhabdomyolysis causes?
physical: prolonged high fever, electric current, excessive physical exertion (cant make enough atp)
mechanical: crash injury, burns, compression, compartment syndrome
chemical; meds, excessive alcohol, electrolyte imbalance
soft tissues pathologies: what is rhabdomyolysis risk factors and etiology?
-high dose of statins
-performance athletes taking herbal supplements
-strenuous exercise
soft tissues pathologies: what are clinical manifestation of rhabdomyolysis ?
-statin induced
-strenuous exercise induced
hot and humid weather, analgesics, viral/bacterial infection, alcohol consumption/dehydration
-change in urine color to brown
-massive skeletal mm necrosis
soft tissues pathologies: rhabdomyolysis diagnosis tx and prognosis?
diagnosis: abnormal kidney function, elevated creatine phosphate kinase, urine dipstick, pos for blood
tx: rehydration, restoration of electrolyte balance, dialysis may be nexessary
prognosis can be good if fixed quickly
soft tissues pathologies: what is myofacial pain syndrome?
overuse or mm stress syndrome marked by the presence of trigger points within mm bands; characteristics pattern of trigger point and referred pain
ex. traps sore when pushed but gives headache
soft tissues pathologies: myofacial pain syndrome etiology and risk factors:
sudden overloading/overstretching of mm
direct impact trauma
postural faults (rounded shoulders)
sitting for a long time (glutes)
soft tissues pathologies: what is myofacial pain syndrome pathogenesis?
dysfunction of motor end plates
motor end plate dysfunction attributed to an excessive release of acetulcholine (ACh) from presynaptic motor nerve terminal
-ach triggers mm contraction, excessive ach causes contraction and no relaxation, nociceptors are now active and there is crosstalk btwn sensory and nociceptors.
soft tissues pathologies: what happenes in a mm w myofacial pain syndrome?
shortening of affected mm causes nodule
nodule in the center = CTrP: central trigger point
ATrP= attachment trigger points
soft tissues pathologies: what are myofacial pain syndrome clinical manifestation?
palpation myofacial bands= causes pain, you can feel nodule
may cause reduced ROM of joints, weakness of involved mm
soft tissues pathologies: diagnosis of myofacial pain syndrome?
clinical exam and palpation, no actual imagining or anything
soft tissues pathologies: tx for myofacial pain syndrome:
desensitize TrPs
injections
ice
laser
manual pressure
change posture
soft tissues pathologies: prognosis of myofacial pain syndrome?
responds well to local intervention
active TrPs may revert
joint pathologies: what is osteoarthritis?
slow degenerative jt disease origination in the cartilage and affecting the underlying bone, soft tissue, and synovial fluid
really common jt disease under age of 50 in men
joint pathologies: what are the 2 classifications of osteoarthritis?
primary OA: unknown cause
secondary OA: known cause
joint pathologies: classifications of osteoarthritis…what is primary OA?
unknown cause, happens over time due to aging and wear and tear
joint pathologies: classifications of osteoarthritis…what is secondary OA?
has known cause: results from another underlying condition, injury or mechanical factor
joint pathologies: risk factors of osteoarthritis?
-serious injury
-high intensity, contact sports
-generalized lig laxity
-mm weakness of any kind can lead to OA
-age
joint pathologies: pathogenesis of osteoarthritis?
too much load, bone thickens to help
cracking + not smooth
In OA, chondrocytes fail → collagen breaks down → proteoglycans decrease → cartilage loses shock absorption → bone takes more load → bone thickens and forms osteophytes.
joint pathologies: clinical manifestations of osteoarthritis?
-bony enlargement
-limited ROM
-crepitus in motion
-tenderness on pressure
-joint effusion
-gel phenomenon (stiffness and difficulty moving after a period of rest, goes away in less than 30 mins)****
in OA, what is heberdens nodes?
happens at DIP
in OA, what is bouchards nodes?
happens at PIP
joint pathologies: prevention and diagnosis, of osteoarthritis?
prevention: healthy lifestyle, moderate exercise, education
diagnosis: hx, physical exam, xrays (there is a grading scale) and lab testing
what is a predictor of OA of knee?
weak quads
joint pathologies: OA treatment:
-depends on pt, cause and extent
-begins w conservative care
-meds- traditional analgelsics and NSAIDS
-viscosupplementation- shot w hyaluronic acid, doesnt last long
-surgery
joint pathologies: what is rheumatoid arthritis?