Diseases and disorders of muscoskeletal system Flashcards

1
Q

What is the purpose of the skeletal system?

A

sturdy framework and protect internal organs and the central nervous system.

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2
Q

how does muscoskeletal system work?

A

Bones are held together at joints, some of which
permit movement of the skeletal framework.

Skeletal muscles attach to the bones via tendons.

When muscle tissues contract, they shorten and move the skeleton at joints.

Thus, the muscles that span a joint bring about action at that joint.

Groups of muscles may have opposite or antagonistic actions on a joint (one group
of muscles extends (straightens) the knee, while
another group flexes (bends) the knee

other muscles stabilize joints, preventing undesired movement

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3
Q

What is bone made of?

A

calcium and phospate (minerals) (hardness and rigidity) embedded in collagen (protein) (flexibility)

osteocytes (mature bone cells)
ocsteoblasts (bone-forming cells)
osteoclasts (bone-resorbing) receive nutrients by an organized system of bv

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4
Q

types of bone?

A

either long, flat or irregularly shapped

most r covered with a layer of bone tissue called compat bone (cells, minerals, proteins and bc r arranged in regular, organized fashion)

spongy bone (cintains many bone marrow-filled speace, found at ends of long bones and is the site of blood cell formation )

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5
Q

parts of the bone?

A

long bones found in arms and legs have hollow cavity (medullary cavity) filled with yellow bone marrow primarily consisting of fat
- growth plate ( = growth of long bones) (area of cartilage near end of bone where new bone is formed, pushing ends apart from each other until full growth is achieved which is when cartilage turns into bone, called ossification)
periosteum ( highly vascular layer of fibrous connective tissue covering surface of bones and contains cells capapble of forming new bone tissue + site of attachment for tendons)

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6
Q

What are joints?

A
  • articulating site btwn bones
  • degree of movement + ROM depends on type of joint + bone shape and connective tussie
  • shoulder is most freely movable joint but is most easily dislocated
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7
Q

Tissue comprising a joint?

A
  • ligaments: for hoints that freely move, strong bc strangs of collagen (joint capsule consisting of ligaments and connective tissue surrounds the bone ends)
  • synovial membrane: secretes synovial fluid, inner surface of capsule, lubricates joints
  • bursae: sacs of synovial fluid r situated near some joints like shoulder and knee, where the reduce friction during movement
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8
Q

What is skeletal muscle?

A

aka voluntary muscle
firmly attached to bones by tendon
- some voluntary muscles (like those responsible for facial expression) r attached to soft tissue
- consists bundles of muscle fibers (muscle cells) held together by connective tissue
- when stimulate by nerves at myoneural junction, muscle fibers contract and bc muscles r attached to bones, shortening of muscles moves bone

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9
Q

What is smooth and cardiac muscle?

A

smooth - found in walls of internal organs and walls of blood vessels

cardiac - involuntary striated muscle and is only in heart

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10
Q

diagnostic tests and procedures of muscoskeletal system?

A
  • x-ray & CT for fractures, joint dislocations, bone deformities, calcification
  • MRI to visualize joints, bones and shoft tissue
  • arthroscopy to visualize inside of a joint cavity
  • aspiration of joint fluid for microscopic and chemical analusis
  • electromyography to measure electrical activity of muscles and reveals some abnormalities of muscle function
  • biopsy
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11
Q

What is osteomyelitis?

A
  • uncommon bacterial infection of bone, mostly after bone trauma or in diabetics
  • most common in upper ends of humerus and tibia, lower end of femur and occasionally vertebrae
  • caused by staphylococcus aureus (90%) and next is streptococcal bacteria (rarely viruses and fungi), bloodborne pathogens r deposited in metaphyseal area of bone
  • in children and infants osteomyelitis can develop as a secondary infection to streptococcal pharyngitis (strep throat0
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12
Q

s/s of osteomyelitis?

A
  • purulent mateiral called subperiodsteal abscess may develop, causing pressure and eventualfracturign of small pieces of bone
  • inflammation
  • swelling
  • pain
  • redness
  • localized heat
  • chills
  • fever
  • leukocytosis
  • sweating
  • malaise
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13
Q

how to diagnose and treat osteomyelitis?

A

diagsnoe - history and physical exam, bone biopsy, WBC count, MRI and CT (xray wont reveal early infection), and blood culture, ESR

treatment - antibiotics, maybe surgery to remove nectroci bone tissue, increase intake of proteins and vitamin A, B, and C

prevention - treat infections and compound fractures

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14
Q

What is tuberculosis of bone?

A

rare and assoicated with pulmonary tuberculosis

occurs when bacteria spread from lungs to bones

affects bones include ends of long bones and ertebra

can be treated with antibiotics although straisn of Mycobacterium tuberculosis have devloped multiple drug resistance, surgery may be able to correct bone deformities

prevention: treat pulmonary tuberculosis

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15
Q

What is required for proper bone formation and maintenece

A

calcium and phospourous (calcium can only be absorbed if digestive tract has vitamin D so no vitamin D - soft, malformed or fragile bones)

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16
Q

What is osteoporosis?

A
  • porous bone that is abnormally fragile and susceptible to fracture
  • 80% of thiose affected by osteoporosis r women
  • etiology is idiopathic but associated with aging
  • most common metabolic bone disease (imbalance between breakdown of old bone tissue and production of new bone), hormonal or dietary factors or disue, trauma, radiaiton treatments, malabsorption, smoking, alcohol abuse, calcium-wasting nephropathy, immobility, chroni disease (RA), lack of estrogen andtestosterone, use of certain meds
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17
Q

risk factors for osteoporosis?

A
  • Low bone mass
  • Low calcium intake
  • Female
  • Vitamin D deficiency
  • Small frame
  • Sedentary lifestyle
  • Family history
  • Cigarette smoking
  • Postmenopausal
  • Excessive alcohol use
  • Hysterectomy
  • Caucasian or Asian
  • Amenorrhea
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18
Q

Osteoporosis affects ___% of all Caucasian women over age ___, and more than __ of Caucasian women over age __ have low bone density, which elevates their risk for developing osteoporosis.

A

20% over 50

more than 1/2 over 50

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19
Q

s/s of osteoporosis?

A

no ss until bone veaken enough to fracture
- weightbearing bones of vertebrae and pelvis r susceptible to fracutre
- accumulate compression fracture in thes ebones = decrease in height and bending of spine and compressed vertebrae can press on spinal nerves = great pain

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20
Q

how to diagnose and treat osteoporosis?

A

diagnose - pt history and bone density tests, hormone imbalances, kidney disease, diet inadequeacy, intestinal malabsorption, blood serum studies, radiography, urinalysis, CT, bone scanning, dual energy x-ray absorptiomentry (DEXA), bone biopsy

treat - no cure so prevention by lifelong diet rich in calcium and vitamin D along with weightbearing exercise = development of dnse and strong bone and slows progression of disease, avoid smoking and alc and caffeine consuupmtion should be minimized. may need meds to promote calcium uptake in bones, estrogen replacement

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21
Q

What is rickets?

A

rare disease of infancy or early childhood i nwhich bones do not properly ossify = bones that r soft, bend easily and become deformed

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22
Q

how to prevent rickets?

A
  • vitamin D- fortified milk and exposure to sunlight (sunglight converts dehydrocholesterol in skin to vitamin D)

treatment is sunlight exposure
and treatment with vitamin D concentrate

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23
Q

What is osteomalacia + etiology, diagnose and treat?

A
  • softening or decalcification of bones in adults
  • rare in US, most prevalent in Asia among women who have had multiple births, eat cereal- based diet, little exposure to sunlight
  • caused by inadequate dietary vitamin D and dietary deficiency of calcium or phosphourous (or could be from inadequate exposure to sunlight, with prevents body from synthesizing its own vitazmin D, intestinal malapsorption of vitamin D)
  • diagnose with blood test (serum calcium serum alkaline phosphatase, vitamin D levels, and ESR), radiographic studies, bone scanning and possibly bone biopsy
  • treated with vitamin D supplements and adding adequate caclim ad phosphrous to diet
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24
Q

s/s of osteomalacia?

A
  • bowing of legs
  • chest deformity
  • muscle weakness
  • wt loss
  • bone pain
  • bones of vertebral column, legs and leovis readily bend and fracture under mild stress
  • general fatigue
  • progressive stiffness
  • tender, painful bones
  • backaches
  • muscle twitches and cramps
  • difficulty standing up
  • fracture
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25
Q

What is Paget’s disease/

A

aka osteitis deformans
- overproduction of bone, particularly in skull, vertebrae and pevlis
- rare worldwide and affefcts approx 2.5 M ppl (mostly men ove 40) in US
- begins with bone softenining, then bone overgrowth (new bone is abnormal and tends to fracture easily) which causes skull to enlarge, pressing on cranial nerves and impairs vision and hearing,in spina colum = curvatures and in legs = deformities
- another complication is osteogenic sarcoma

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26
Q

how to diagnose and treat paget’s disease?

A

diagnose - examination, x-ray, bone scan and bone and possibly bone marrow biopsy, blood work (show elevated serum concentration of alkaline phosphatase), urinalysis reveals elevated hydroxyproline concentration

treat - analgeics, antiinflammatory drugs, cytotoxic agents, calcitonin and etidronate (reduce bone resorption) and mithramycin (decreases calcium)

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27
Q

What is scoilosis?

A
  • abn lateral curvature of spine usually first ientified during childhood
  • may be caused by fusion of vertebrae during development, neuromuscular abn, weak or asymmetric back muscle development or idiopathic
  • s/s r lower back pain and fatigue, SOB on exertion (in women first indicator is often unequal bra strap lengths)
  • cause is mostly idiopathic, could be caused by deformties of bertebrae, uneven leg lengths, muscle degeneration, paralysis from disase, poliomyelititis, cerebral palsy and uscular dystrophy
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28
Q

how to diagnose and treat scoliosis?

A

diagnose - history, physical exam and xray

treatment - if mild (less than 20 degrees (common)) than no treatment, more severe = braces or surgery (fuses vertebrae and itnernal fixation with rods, wires or plates and pedicle screws) (if neuromuscular scoliosis than usually related to other diseases like muscular dystrophy, spina bifida, or cerebral palsy), exercise to strengthen weak muscles, milwauee brace, boston brace, moded pastic clamshell kacket or WIlmington brace

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29
Q

What is kyphosis?

A
  • exaggerated posterior curve of thoracic spine, first occurring in adulthood and more noticable in older adults
  • most often caused by collapse of vertebrae affected by osteoporosis or by degerative changes associated with arthritis of vertebra
  • if in adolescent kyphosis is usually related to Scheurmann disease (degenerative defromity of thoracic vertebrae)
  • additional disease processes that contribute to occurence of kyphosis include tumors or tbueroculosis of ertebral bodiesand ankylosing spondylitits
  • atnerior wedging (wearing away f anterior portion of bertebrae in wedge shape) or deterioraton of vertebrae = excesive curvature with kyphosis
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30
Q

s/s of kyphosis?

A
  • insidious onset and is asymptomatic until hump becomes obvious
  • mild back pain
  • back fatigue
  • tenderness
  • difficulty breathing bc compression of throacic cage
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31
Q

how to diagnose and treat kyphosis?

A

diagnose - physical exam and x-rays, test for loss of bone density

treatment - few and no cure (if osteoporosis is underlying than treat like that, if underlying is arthritis than relieve pain and immobility to limited degree), exdrcises to streghten muscle and ligaments, back braces, spinal fusion, tomparory immoilization, vertebroplasty (bone cement is inserted with vertebra to maintain the reestablished vetebral height and reduce pain)

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32
Q

What is lordosis?

A
  • aka swayback or saddleback deformity
  • inward curvature of lumbar vertebrae
  • some degree of curvature is normal and most cases r benign
  • can be caused by added adominal girth from pregnancy, obesity, large abd tumor, no cause, s/s could be non or low back pain bc strains on muscle and ligaments
  • often notes in prepubescent girls (one possible cause is rapid skeletal growththat occurs without necessary natural strechign of posterior soft tissue) or osteoporosis
  • treat with wt loss, strengthened abd muscles, use of brace, spinal fusion and displacement osteostomy (surgical division of vertebrae)
  • if untreated can lead to degenerative lumbar disk disease or ruptured lumbar disks
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33
Q

What is bone cancer?

A
  • malignant bone tumors
  • priamry is uncommon (1% of malignancies)
  • primary is mostly in males, esp children and adolescents
  • chondrogenic (from cartilage), osteogenic (from bone) and fibrogenic (fibrous tissue)
  • main s/s is pain, esp at night or with exercise, limping, painful soft tissue swelling
  • if metastasized it’s from breast, lung, prostate, thyroid and kidney cancer
  • bones most affected are pelvis, vertebrrae, ribs, hip, femur and humerus
  • diagnose with radiographym radionuclide bone scanning, PET, CT, MRI (for ewing sarcoma bone marrow aspiration), elevated serum alkaline phospatase level for ostesarcomas and elevated lactate dehydrogenase in Ewing sarcoma
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34
Q

What is osteogenic sarcoma?

A
  • in bony tissue
  • frequeitnyl affects ends of long bones, esp knee and distal femur, follwoed by proximal tibua and humerus
  • cause is unknown
  • s/s: dull localized pain that intensifies at night, bone masses and fractures near sarcona
  • metastasize to lungs
  • diagnose: biopsy, x-ray and CT (appears to have sunburst appearance on radiograph)
    treatment - chemo, surgical removal
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35
Q

What r s/s of fracture?

A
  • Visibly out-of-place limb or joint
  • Swelling, bruising, or bleeding
  • Intense pain
  • Numbness and tingling
  • Broken skin with bone protruding
  • Limited mobility or inability to move a limb
  • edema
  • tenderness
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36
Q

how to diagnose and treat fracutres?

A

diagnose - based on s/s, MRI, bone scanning, physical exam, bone biopsy

treat - closed: immobilization with splint or cast or open: others need surgery, pins and plates, external or interal fixation (surgically implanted pins, wires, rods, plates, screws, etc.)

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37
Q

Types of fractures?

A

closed - bone breaks clean but no penetration (simple fracture)

open - broken bits protrude through skin (make = oesteomyelitis) (compound fracture)

communicated - bone fragments into many pieces (common in conditions causign brittle bones)

compression - bone is crushed (common in osteoporosis))

impacted = broken ends r forced into each other (common frm fall and hip fracture)

depressed - broken bone presses inward (skull fracure)

spiral - jagged break due to twisting force applied to bone (common in sport injuries)

greenstick - bone breaks incompletely (common in children whose bones r more flexible)

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38
Q

What is arthritis?

A
  • inflammation of hoin
  • ss r persistent joint pain and stiffness
  • hoints may swell, lose mobility, and become deformed and noonfunctional
  • commonly in lower vertebrae, hips, figners and knees
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39
Q

What is rheumatoid arthritis?

A
  • chronic, debitiliating, autoimmune, systemic, inflammatory disease that affects several hoints, surrounding muscles, tnedons and ligaments
  • affects mrore than 1 M americans
  • one of the most sever e forms of arthritis, commonly causing deformity and disability
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40
Q

risk factors for rheumatoid arthritis?-

A
  • family history
  • gender (3x more in women)
  • age (30-60)
  • smoking
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41
Q

What is pathogenesis of RA

A
  • rheumatoid factors that form antibody complexes in synovial fluid which attracts neutrophils to joints = inflammation and destruction of synovial joint tissue
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42
Q

s/s of RA

A
  • as RA progresses joint tissue is repalced iwth thichkend granulatio called pannus
  • joint pain and stiffness (particularly on waking)
  • joints r swollen, red and worm
  • joints r affected on both sides of body
  • fatigue
  • weakness
  • wt loss
  • further destruction = joint eriosion, scarring and fusion (called ankylosis)
  • inflammation and edema of synovial membranes surrounding a joint
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43
Q

How to diagnose and treat RA?

A

diagnose - physical exam, xray for joint changes, rheuamtoid factor test, synovial fluid analysis, radiographic studies, blood tests that show elevated levels of rheumatoid factor, CBC, serum protein electrophoresis, ESR, citrulline antidoy and antinuclear antibody titer

treatment - as early as possible, disease-modifying anti-rheumatic drugs (DMARDS), anti-inflammatory (aspririn or NSAIDs) and immune-suppressants, new DMARD drug approved in 2018 for treatment of RA (baricitinib), special splints, surgery to correct deformity, relieve e pain and improve ROM

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44
Q

What is osteoarthritis?

A
  • most common form of arthritis
  • aka degenerative joint disease or degenerative arthritis
  • breakdown and eventual loss of cartilage of one or more joints
  • 27 M americans (men and women equally)
  • primary occurs with normal aging
  • secondary assoicated with joint injury, trauma, diabetes, or obesity
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45
Q

s/s of osteoarthritis?

A
  • pain
  • stiffness in joints
  • muscle tension and fatigue
  • lose of ROM
  • edema
  • pain in morning
  • stiffness
  • crepitation with joint movement
  • assoicated muscles weaken
  • mainly in large weight-bearing joints (esp knees and hips)
  • tendenct for smallest joints at ends of fingers to be affeced by spur formation which leads to Heberden node
  • lesser degree = involvement of joints of fingers at proximal interphalangsal (PIP) joints (Bouchard nodes), wrists, elbows, and ankles
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46
Q

How does degerantion occur in osteoarthritis?

A
  • articular carilage that caps bone surface (where bones meet) starts to degenerate, meaning underlying bone is exposed and damaged so new bone is deposited in and around joints, causing them to thicken and develop sharp irregular bone surface structures called spicules and spurs

(small joints like knucles enlargen and become knobby)

47
Q

how to diagnose and treat osteoarthritis?

A

diagnose - physical exam, history, x-ray, CT, MRI

treatment - no cure, just relieve pain w/ combo of rest, mild exercise, heat application to maintian ROM (if medical than anti-inflammatory meds, steroids like corisone r injected to relieveinflammation and pain as well analgesics, muscle relaxants, and NSAIDs), surgically repair severely damaged knee or hip

48
Q

What is gout?

A

aka gouty arthritis
- chronic disorder of uric acid metabolism that manifests as an acute, episodic form of arthritis, chronic deposits of uric acid forming hard nodule in tissue and/or kidney impairemnt or stones
- affects joints of ft, particularly metatarsophalangeal joint of great toe
- 3 M americans
- risk facotrs: men over 40 and for postmenopausal women, minor injury, excessive eating r drinking or heredity
- more in men then women, more in women aftter menopause

49
Q

What is the pathogenesis of gout?

A

gout attacks r rleated to excess uric acid in blood from defect in metabolism of purines (component of nucleioc acid) or abn retention of uric acid which leads to depositing or uric acid crystal in joints and kidneys (= kidney stones)

50
Q

s/s of gout?

A
  • gout attacts r sudden
  • affects joints r inflammed (pain, heat, swelling and redness)
  • last from days to many weeks
  • slight fever, chills, headache, or nausea, renal dysfunction, hyperuricemia and renal calculi
  • resolution of acute attack is 6 months to 2 yrs w/o symptomslight
51
Q

how to diagnose and treat gout?

A

diagnose - microscopic exam of aspirated joint fluid (reveals needlelike urate crystals), serum of uric acid test shows hyperuricemia, x-ray of affected joints appear normal until chronic gout damages bone and cartilage

treatment - if acute than rest, application of hot or cold compresses, analgesics, colchicine and corticosteroids, if chronic than colchinine (prevents acute attacks), agents that promote excretion of uric acid, NSAID, low-upurine diet and adequate fluid intake, antihyperuricemic meds, gradual wt reduction

52
Q

What is septic arthritis?

A
  • medical emergency
  • result of bacterial infection of hoint
  • cartilage and bone destruction may lead to ankylosis and life threatenign septicemia (bloodborne bacteiral infection)
  • caused by streptococci and staphylcocci (after suyrgery) and neisseria gonorrhoeae (spread to joints via blood from priamry infeciton site)
  • treat with antibiotics
53
Q

What is bursitis?

A

inflammation of bursae (small, synovial fluid-filled sacs located near joints that cushion and reduce friction during movement), particularly in shoulder joint, elbow, knee, hip and tibia
- pain = less joint mobility
- s/s r tenderness, pain when moving affected part, flexion and extension limitation, edema, point tenderness, calcification, adhesions
- causes includes repetitie motion, irritation or injury of a bursa, can be caused by systemic disease and infection
- diagnose with history and phusical, MRI, radiographis, aspiration of fluid
- treatment is rest, anti-inflammatories, moist heat applications, steroids may be injected into joint to reduce inflammation, corticosteroids, NSAIDs, antibiotics, surical excision

54
Q

What are herniated discs?

A
  • ruptures of cartilaginous pads btwn bony bodies of adjacent vertebrae that oresses in nearby tissue and nerves
  • main cause of lower back pain, one of most common orthopedic problems in US
  • risk factors include age, obesity, trauma and genetics
  • primarly in lumbar region
  • treated with antiinflammatories, analguesics and surgery
55
Q

What is a dislocation/

A
  • displacement of bones from normal spot in joint
  • most common in shoulder and finger joint
  • usually cause is severe injury tht exerts force, could be congenital weakness or complication of arthritis
  • causes pain and reduced mobility
  • bone msy be reset and immobilized to allow healing of torn ligaments and tendons
  • congential disolcation of hop results from improperly formed joint and r treated in infancy with cast or surgery
56
Q

What are sprains?

A
  • wrenching or twisting of a joint like ankle that injuries ligaments
  • bv, surrounding tissues, muscles, tendons and nerves may also be damaged
  • swelling and discoloration due to hemorrhaging from ruptured bv occyrs
  • v painful, joint shouldnt be used while severely inflammed
  • immobilized with splint or cast for more severe ‘
  • cold compresses reduce swelling immediately after injury wherease later, heat applicatio nrelieve discomfoort and speed healing
57
Q

hat is a whiplash?

A
  • sprain in which cervical (neck) ligaments and tissue are injuryed
  • most often result of rear-end motor vehicle accidents
58
Q

What are strains?

A
  • pulled muscles result from tearing of muscle and/or its tendon from excessive use or stretching
  • prevent by conditioning and warm-up
    = treat with rest, ice intiially, later iwth warm compresses to encourage blood flow
  • severe strains may need many months
59
Q

What is RICE?

A
  • for joint trauma like sprains and strains
  • rest: immobilize joint to prevent further damage
  • Ice: reduce inflammation and pain (10 min several times per day)
  • compression: with badange, immboliuzes joint and reduces inflammation
  • elevation: above heart level, reduce blood flow to joint (also reduces inflammation and pain)
60
Q

What is carpal tunnel sundrome?

A
  • painful condition of hand
    affects 10% of working popilation in US
  • repetitive motion injury (when tendons within tunnel become inflamed from repetitive overuse of the hand, wrist, or fingers causing entrapment and pinching of median nerve)
  • wome r 3x more likely
  • many women attribute s/s during prgancy which is attributed to accumulation of fluid within tissue
  • negins as numbness or tinggling in hand byt progresses to pain radating up arm to shoulder (most severe at night)
  • simple tasks requiring finge rmovement become difficult
61
Q

what r risk factros of carpal tunnel syndrome?

A
  • performancy of repetitive manual tasks like knitting, driving, typing, computing and piano playing
62
Q

How to diagnose and treat carpal tunnel syndrome?

A

diagnose - physical exam, history, tingingling in area of the thumb, index, middle, part of 4th, electromyogram, nerve conduction study to measure velocity of nerve conduction (if electrical impulses r slow than compression) and Phalen wrist flexor test

treatment - avoid repetitive action, immbolizing hand and wrist with a light-weight, molded plastic splint, injection of steroidal anti-inflammatory drug into carpa tunnel, oral corticosteroids, surgery odivide wrist’s transevere ligament ot relieve compression of meidan nerve

63
Q

What is muscular Dystrophy (MD?

A
  • several forms, all r heredity
  • most common and serious is Duchenne’s MD (sex-linked, affects 2 in 10,000 ppl, appears in 3-5 y/o)
  • occurs bc cytoskeletal protein called dystrophin is missing = death of muscle fibers which r replaced by fat and connective tissue, weakening skeletal muscle fast
  • in most severe from heart muscles r affected, calf muscles enlarge from fat deposition, child becomes weak and thin so child doesn’t live to adulthood
  • only affects males and generally is inherited through female carriers
  • in 1/3 to 1/2 of cases no family history of MD so newly acquired mutation
64
Q

how to diagnose and treat MD?

A

diagnose - electromyogprhay (weak muscle contraction), bopsy off muscle (abn muscle fibers, varaiton in fiber sizes, fat deposits and absence of dystrophens), immunologic and moelcualr biology techniques

treatment - physical and occupational therapy, exercise, use of orthopedic appliances (no cure or preventio)

65
Q

What is mysasthenia gravis (MG)?

A
  • disorder of myonerual junction in which nerves fail to transmit impulse for contraction to muscle, = muslce atropy
  • mainly affects women btwn 20 and 40 + men over 60
  • autoimmune bc resarch shows antibodies attach near myoneural juntion and destroy acetylcholine or its receptors
  • thought to be caused by autoimmune mechanism in which faulty transmission of nerve impulses to and from CNS occurs
66
Q

s/s of MG?

A
  • fatigue
  • extreme muscular weakness w/o atrophy (first in face w/ drooping eyelids, diplopia, difficulty chewing, talking, swallowing)
  • inabilty to use voluntary muscles including muscles of facial expression, and eyelids
  • difficulty chewing and talking
  • respiratory failre bc respiratory ventilation r unable to contract
67
Q

diagnosis and treatment for MG?

A

diagnose - physical exam, tensilon test (intravenous administration of short-acting acetylcholinesterase inhibitor to see if administration improve muscle strength), test for antibodies against acetylcholine, EMG

treatment: restricted actiivty, completely bed rest, soft or liquid diet, anticholinestrase drugs r effective initially, pyyridostigmine bromide (Mestinon) is drug of choice, if thymoma is present then thymectomy, corticosteroids, immunisuppression, drigs that increase acetylcholine levels at myoneural junction

68
Q

What r tumors of muscle?

A
  • rare but r usually malignant
  • most common in buttocks, groin, extremities, head and neck region, trunk and retroperitoneum
  • rare bc muscle do not continuoisly divide like blood or epithelial cells
  • malignant tumor of skeletal muscles r called rhabdomyosarcoma
  • appear as painless lump of a few weeks or months often with erythema, sometimes painand tenderness (if smooth muscle then pain in and.or bleeding)
  • grow by local extension and infiltration along tissue planes
  • diagnose iwth MRI, radiography, CT, core-needly bopsy, bone marrow aspiration
  • requires surgical removal, radiation, chemo
  • prognosis is poor bc rhabdomyosarcoma metastasizes early and is ually advanced when diagnosed
69
Q

age-related diseeases of bone?

A
  • amt, desnity and strenght of bone decline with age bc osteoblast activty decline with age
  • at menopause bone loss accelerates, making women more suscpetible to osteoporosis and its effects
  • 80% of those with osteoporiss r women and majory of women over 60 have low bone density or osteoporosis
70
Q

age-related disease of joints?

A

joint mobilty decrease with age bc cartilage becomes stiff, ligaents lose flexiblity and elasticity and synovial membranes become fibrous stiff and produce less synovial fluid
- changes begin at 20, signficatn by 30 esp if not regula exercise and strentching
- arthritis increases with age
- fewer than 20% of young adults
have arthritis, 60% of adults over age 60 have
some form of arthritis

71
Q

age-related disease of muscles?

A

= with age number of muscle fibers decrease and become shorter and thinner, reducing muscle strenght and ROM
- muscles become less sensitive to stimulation with age meaning they take longer th conrtact
- recovery following conrtactio becomes slowly, diminishign the abilty to sustain repreated conrtactions and reducing enduarnce
- Exercise reduces the rate of these changes and helps maintain muscle mass, strength, and flexibility

72
Q

s/s of MD?

A
  • affects muscles of shoulders, hips, thighs and calves = waddling gait and toe walking
  • affected muscles sometimes look larger than normal bc fat replaces atrophied muslce
  • lordosis or other spinal deformites
  • diffiulcty climbing stairs and running
  • tends to fall easily
  • difficulty getting up
  • contractures
  • inreased susceptible to serious pulmonary infections like penuomiia
  • often impaired mentally
73
Q

What is juvenile idiopathic/rheumatoid arthritis (JRA)?

A
  • most common childhood arthritis and a form of RA that affects children (age < 16 yrs) and begins most commonly btwn age 2 and 5 yrs
74
Q

types of JRA

A
  • 3 subtypes r pauciarticular, polyarticular, and system (aka Still isease)
  • pauciarticular affects no more than 4 joints and affects girls 6:1 (has best prognosis and abt 40% of cases)
  • polyarticular JRA affects more than 5 joints and affects girls 2:1 (40%, better prognosis then systemic but potenital to cause delayed growth)
  • systemic onset begin at any age and affects boy and girls equally (20%)
  • usually large joints, attack lasts for several for several weeks and tend to lessen in severity w/ time usually disappearign completely by puberty
75
Q

systemic onset of JRA s/s

A
  • temp flucuating from normal to below in morning, rising to around 103F in evening
  • poor appetite w/ resulting wt loss
  • blotchy, salmon-colored rash over limbs and trunk of body
  • anemia
  • swollen, stiff, and painful joints, most commonly involving neck, elbows, knees and ankles
  • red, painful eyes
  • swollen cervical or axillary lymph glands
  • irritabilty
  • acute pericarditis
  • damage to epiphyseal plates of long bones = impaired skeletal developpment
76
Q

how to diagnose and treat JRA?

A

diagnose - history and physical exam, results of blood tests for rheumatoid factor, exam may show lack of growth or delayed physical growth that would be appropriate fro age of child, other forms of arthritis such as spondylitis, arthritis of inflammatory bowel disease, psoriatic arthritis, and sarcoidosis

treat - same treatment as adult w/ RA + participation in school and social acitvies, well-balanced diet w/ plenty of protein, physical therapy, braces or splints

77
Q

What is ankylosing spondylitis?

A
  • systemic, progressive, inflammatory disease affecting primarily spinal column
  • etiology isn’t exactly known but studes support genetic basis and association w/ several genses including human leukocyte antigen (HLA)-B27 which predispose a person to development of immune response
78
Q

s/s of ankylosing spondylitis + most common gender

A
  • commonly affects young men (several times more common)
  • first affects sacroiliac area of spine and adjacent soft tisse structures
  • pt may have recurring morning low back pain and stiffness that improves with activity
  • fatigue
  • wt loss
  • fever
  • diarrhea
  • eye pain
  • photophobia caused by uveitis
  • pain and tenderness over site of inflammation
  • heel pain
  • inflammatory bowel disease
  • family incidence of arthritic condition
  • cervical or thoracic axial pain and stiffness w/ paraspinal muscular spasm
79
Q

how to diagnose and treat AS?

A

diagnose - clinical eval includign back pain, stiffness, joint pain with limitation of motion, positive family history, lab results reveal a negative rheumatoid factor and confirm the inflammatory nature of disease w/ mildly elevated ESR or cross-reactive (CRP), HLA-B27 is found in 95% of Caucasian individuals

treatment - no cure, relieve pain and swelling w/ antiinflammaotry meds, analgeiscs, phhhyiscal therapy, moderate exercise

80
Q

What is polymyositis?

A
  • disease of muscle that features inflammation of muscle fibers, mostly those closest to trunk or torso
  • chronic illness w/ flare-ups or relapses and decreased symptoms known as remissions
  • occurs when WBCs spontaneously invade and injure muscles
81
Q

s/s of polymyositis

A
  • muscle weakness involving muscles closest to trunk of body (gradual or rapid)
  • loss of strength can be noted as difficulty getting up from charis, climbing stairs or lifting above shoulder
  • trouble with swallowing and weakness in lifting head from pillow
  • occasionally muscles ache and r tender to touch
  • may have skin inflammation called dermatomyositis (appear and spread over face, shoulders, arms and bony prominences)
  • nearly 2/3 of pt w/ disease r women
82
Q

how to diagnose and treat polymyositis

A

diagnose - phyiscal exam w/ throuough search for muscle conditions, thyroid disorder, sarcoidosis, infection, cancer, med + phyiscal exam documenting weakness, blood analysis to detect elevated levels of muscle enzymes (CPK, aldolase, serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT) and lactate dehydrogenase (LDH)) + EMG and muscle biopsy

treat - stopping inflammation w/ high dose of steroids and inhibiting overactive immune system w/ immunosuppressive agents such as cyclophosphamide and methotrexate

83
Q

What is fibromyalgia?

A
  • chronic pain condition associated with stiffness and tenderness that affects muscles, tendons and joints
  • characterized by restless sleep, depression, fatigue, anxiety and bowel dysfunction
  • cause is unknown (pt experiences pain in response to stimuli that are not perceived as painful) but appears to be linked to changes in how brain and spinal cord process pain signals (elevated levels of nerve growth factor and chemical signal called substance P in spinal fluid, low serotonin, impaired REM)
84
Q

s/s of fibromyalgia?

A
  • fatigue
  • diffuse aching or burning in muscles
  • stiffness
  • disturbed sleep patterns
  • poor concentation
  • irritablity
  • depression
  • extreme tenderness of varoius areas of body
  • headhacnes
  • jaw pain
  • sensitivity to odors, bright lights and loud noises
  • symptoms of irritable bowel syndrome of “spastic colon” including nausea, diarrhea, constipation, or abd pain with gas and distention
  • urinary urgency or frequency brought on by bladder spasms and irritbilty
  • wake up feelign tired, een if they have slept all through the night (others sleep lightly ad wake up during the night)
85
Q

diagnose and treat fibromyaliga?

A

diagnose - many medical conditions mimick fibromyalgia, blood testing and physical exam to exclude conditios such as hypothyroidism, hypoparathyroidism, other muscle diseases, bone disease, iral ifectiosn and cancer (completely based on clinical grounds and on through history and phyiscal exam) grounds of exam r widespread pain lasting at least 3 months,presences of other symptoms such as fatuge, waking up tired and trouble thinking, no other underlying condition

treat - pt ed, stress reduction, physical activity, meds to reduce pain and improve quality of sleep (antidepressant amitriptyline (Elavil), NSAIDS, muscle relaxants,

86
Q

What is lyme disease?

A
  • aka lyme arthritis
  • infectious disease caused by Borrelia burgdorferi (spirochete bacterium) in US and in europe it’s Borrelia afzelii and is transmitted to humans while they are camping or hiking in areas tick inhabit
  • ticks that bite the skin spread Lyme disease by injecting bacterium from their gut into human body whend drinking blood
  • first detected in 1975 in Lyme Connecticute (more prevalent in NE US which has large areas of forests and fileds as habitats for ticks)
87
Q

s/s of lyme disease?

A
  • characteristic red, itchy rash with a red circle center resembling the bull’s eye on a target
  • similar to arthritis and causes influenza-like symptoms such as headahce, fever, fatigue, joint pain and gerneal malaise
  • late complications of muscle weakness, paralysis, and neurological conditions (learning difficulties, excessive fatigue, muscle corrdination problems), encephalitis, gastritis or carditis
88
Q

diagnose and treat Lyme disease?

A

diagnose - complete history, physical, lab tests for infecitous diease, forms of arthritis, immune disease, muscle disease and even cancer

treatment - removal of tick, doxycycline, amoxicillin or cefurixime, IV antibiotics, antipyretics, bed rest, physical therapy, antiinflammatory

89
Q

s/s of paget disease?

A
  • affected aras produce more bone tissue then it breaks down
  • 2 stages: 1) vascular (bone tissue is broken down and spaces r filled with blood vessels and fibrous tissue) 2) scleroitc stage (highly vascualr fibrous tissue hardens andbecomes similar to bone but is fragile instead of being strong)
  • can occur in prt of 1 bone, all of one bone or multiple (most common r pelvis and tibia, next common r femur, spine, skull and clavicle)
  • most in indiv older than 40
  • no symptoms, mostly just local boe pain (disabing, continous aching, worse at night, edema or deformity, hearing loss or deafness, frequent fractures, spinal cord injuries, hypercalcemia, renal calculi)
90
Q

What is Marfan syndrome?

A
  • group of inherited conditions featuring abnormal connective tissue with weakenss of blood vessels and excessive length and flexivility of extremities
  • is autsomal dominiant genetic disorder caused by affected gene in long arm of chormosome 15
  • s/s r abnormally long extremities and digits (hyperextensible) , dvisual difficulties (subluxation of lens of eyes) and heart and vascular anomalies (cause mitral valve prolapse, thickening of heart valves, aoritc aneurysm) , tall and slender, asymmetry of skull
91
Q

how to diagnose and treat Marfean syndrome?

A

diagnose - sometimes confused with homocystinuria (amino acid disorder) but diagnosis is made based on family history, physical exam, lens dissociation, mitral valve prolapse, ECG reveal potential aortic dissection

treatment - hormoens before puberty, preventing glaucoma, controlling bp, and preventing aortic dissection, ophthalmic exam, surgical replacement of diseased portion and aoritc and mitral valves)

92
Q

What is ewing sarcoma

A
  • mostly involves pelvis and lower extremitiey
  • looks onion-like in radiograph
  • metastasize to lungs
93
Q

ewhat is chondrosarcoma?

A
  • most often arises in the pelvis and proximal femur
  • lobular pattern
  • primarily in indv between 30 and 60
  • gorw more slowly and r locally invasive
94
Q

What is a bunion?

A
  • hallux valgus
  • localized area of enlargement of inner portion of first metatarsophalangeal (MTP) joint at base of big tose
  • local inflammation, pain, inflamed bursa, great toe may override or undercut the second toe
  • often caused by foot disorder known as hallux valgus (great toe is positioned toward midlin of body) and is assocaited with RA, flatfoot, improperly fitting or high-heeled shoes
95
Q

diagnose and treat bunion>

A

diagnose - physical exam, history of symptoms, radiographic studies, degenerative arthritic joint changes

treat - wearing shoes with roomy “toe box”, low heel, using padding btwn toes or around bunion, applying ice to bunion to reduce inflammatio nand lessen pain, analgesic meds for pain, itraarticular injections of corticosteroids, bunionectomy, osteotomy, artrhoplasty

96
Q

What is hallux rigidus?

A
  • stiff big toe that develops as a result of degeneration of cartilage of first MTP joint
  • cause pain and loss of motion in joint, painful, stiff, and swollen
  • caused by result of injury or underlying arthritis, constant war and tear on joint or repetititive minor trauma causes the articular cartilage of the joint to degenerate, resulting in raw bone surface rubbing against raw bone surface
  • diagnose with history of pain (continuous or when walking), restricted ROM, straight hallux with an enlarged tneder joint with limited dorsiflexion
  • treat with drug therapy with antiinflammatory meds, wearing show with tihck, hard soles and low heels, cheilectomy (remove bone spurs and degernative changes), arthroplasty
97
Q

What is hammer toe?

A
  • condition in which toe bends upward like a claw bc of abnromal flexion of PIP joint (can occur in any one of four lesser toes)
  • most offten in second 2, can be painful and often causes abrasion and inflammaiton where flexied toe rubs agaisnt footwear, = corn and callus
  • congenital tendency of a long second, short shoes with pointed toes or high heels, insult to nerves of toe muscles, underlying arthritis
  • diagnose with history of pain, visual inspection, imaging studies
  • treat iwth proper shoesm splitning toe, arthroplasty and possible fusion of PIP joint
98
Q

What is a colles fracture?

A
  • fracture of distal head of radius, with possible involvement of ulnar styloid
  • result from fall in which person attempts to break fall with extended arm and open hand
  • pain and swelling r expeireiences
  • ## treat with closed reduction of fracture and immobilization of arm, including elbow with a ast
99
Q

what is basilar skull fracture, leFort fracutre and Pott fracture?

A
  • fracture of floor of cranial vault
  • usually result of massive trauma to head caused by motor vehicle accident
  • leFort fracture (bilateral horizontal frature of maxilla) often from face force agaisnt teering wheel
  • Pott fracutre (lower part of fibula)
100
Q

What is adhesive capsulitis?

A
  • aka frozen shoulder
  • condition in which shoulder is signficantly limited in its ROM as a result of inflammation, scarring, thickening, and shrinage of capsule
  • shouder is stiff and apinful (localized or spread out, often sever enough to disrupt sleep)
  • usually caused by inflammation fo capsule of joint with secondary scarring, usually begins after a slight injury or minor porlbem, suhc as bursitis or tenditis which prevent normal use of joints
  • diagnose with symptoms alone, may use radiographic test for underlying problems
  • treatment is keep in motion with physical or occupation therapist, analgesics, antiinflammatory agents, inejction of steroids meds, shoudler manipulation under general anesthesia
101
Q

What is a severed tendon + diagnose and treat?

A
  • torn tendom completely into 2 sections so muscle cant move body part
  • immediate, severe pina, infallmation and immboility
  • caused by injury or laceration
  • involves forearm, hand, calf of leg or foot
  • diagnose with physical exam of injured site and pt inabilty to move affected area, radiographic study
  • treat with tenorrhaphy (suture 2 ends of tendn together), or they can isnert a piece oftendom from elsewhere in the body
102
Q

What is shin splints?

A
  • painful condition involving inflammatio nfo periosteum, extensor muscle in lower leg and surrounding tissues
  • s/s r inflammation, edema, pain, tenderness along inner apsect of tibia which worsens with exercise andthen disappears with rest
  • cause is overuse and overponation which places abnoral stress on calf muscle
  • diagnose with physical exam and history of pain
  • treat with rest, application of ice or heat, aspirin or NSAIDS, physical therapy, specially designed shoes to correct overpronation
103
Q

What is plantar fasciitis?

A
  • aka calcaneal spur, calcaneal or heel spur sundrome
  • inflammatory response at botton of calcaneus (where fascia acts like bowstring for arch of foot to attack to bottom of heel)
  • common problem in ppl in sports (begins dull, intermittent pain on botton food and can progress to a sharp, persistent pain, worse on getting out of bed, 1st steps in morning ,sitting for time, after standing or walking, beginning exercise)
  • caused by when fascia is placed under tension which causes an inflammatory response which can lead to spike-like projectio nof new bone called calcaneal (heel) spurs
  • diagnose with physical exam and pt histroy, radiographs
  • treat with resting, ice, antiinflammaotry or analgesic meds, heel pads, local cortisone injection can reduce inflamted tissue, tape food
104
Q

What is ganglion?

A
  • benging, saclike swelling or cyst that is filled with colorless, jellylike fluid
  • ganglion is formed from tissue that lines joint or tendon
  • most common on back of wrist, can develop near joints such as ankle, behind knees and on fingers, soft or firm to touch, painless or somewhat bothersome, pain when moving wrist from wrist ganglion., most r size of pea, some make be 1 in or more in diameter
  • sometimes cuased by repetitive minor injureies, could be sign of arthritis
  • diagnose with palapation, obervation, needle aspiration
  • treat ONLY IF DISFIGUREMENT OR INTERFREE WITH WRIST FUNCTION BY RUPTURE GNAGLIONN, NEEDLE ASPIRATION, INSTILLATION OF STEROIDS, GANGLIONECTOMY
105
Q

wHAT IS A TORN MENISCUS?

A
  • crack or fissure resulting from wear or injury of meniscus (semilunar cartilage in knee joint, split into medial and lateral)
  • medial meniscus is larger and more resitrcted in movement and so is injured mor eoften (may accompay anteroir and posteroir cruciate ligament tears)
  • acute pai nwhen puittign full wt on affected leg and knees, lock or gives away, snapping or crepitus on flexion or extension, full flexion is difficult
  • mostly related to sport injuries (sudden twisting or external rotaito nof legs)
  • diagnose with phyiscal exam, radiographic studeis and MRI
  • treat with immobilization, ice, antiinflammaotry or analgesic, arthroscopically surgical repair, meniscectony
106
Q

What is the rotator cuff?

A
  • there are 4 tendons of the rotator cuff (formed by muscles of shoudler, partially surround the head of humerus and stabilize it in glenoid cavity or socket
  • infraspinatus muscle rotates humer externally and subscapularis muscle rotates humerus internally)
  • supraspinatus and teres minor
107
Q

s/s, diagnose, treatment and etiology of rotator cuff tears?

A
  • s/s r immediate snapping sound and acute pain, may be unable to abduct arm, ROm becomes limited
  • etiolgoy is from acute trauma or from degerativ echanges, calcium deposits in insertion sitres bc of degeratnvie changes and may predispose tendons to tears or ruptures, steroids inejction
  • diagnose is based on physical exam and pt history, limited and painful ROM, atrhogram or MRI, screen for bursitis and arthritis
  • treat with pain-relieving meds, acetaminophen for moderate, antiinflammaotry meds, rest n=and conservative therapy, surgical repair for signficant acute tendon tears, shoulder imobilizer or avudction splint
108
Q

What is cumulative trauma?

A
  • aka repetitive motion trauma and overuse syndrome
  • at risk for those who workin in industries w/ repetitve tasks: working on computers, cashiers, target practice, other sports
  • result from repeated motions that r unnatural such as overexertion, twisting or muscle fatiuge, improper pressure
  • pressure centered on the hand or the wrists
109
Q

What is De Quervain Disease?

A
  • inflammation fo the tendons of the thumb
  • caused by irritation of the long absductor and short extensor tendons
  • repetitive motion causes edema and tenderness in thumb and its base
110
Q

What is tennis elbow ?

A
  • aka lateral humeral epicondylitis
  • result of repeititive movement involving flexion of the wrist against resistance which = inflammaotry condition of the tissue at the distal portion of the humerus
  • s/s r pain in lateral aspect of the elbow and lower arm, weakness
  • diagnose w/ clincal findings and physical exam
  • treat by stopping repeptive task, resting arm, elastic brace, NSAIDs, ice paks, steroid injectiosn
111
Q

What is trigger finger?

A
  • aka stenosing tenosynovitis
  • index finger has a lump or knot that appears on the flexor tendon
  • flexion or extension of the finger may be interrupted and then begin again i nta jerking or snapping type of motion when is opened and closed
  • cause is excessive use of index finger resulting from difficulty repeptotive finger movement ortrauma to the tendon sheath
  • diagnose w/ clinical findings, histroy, physical exam
  • treat - cessation of repetitive activity, rest, ice packs, stretching exercise, NSAIDs, cortisone, surgical intervention
112
Q

What is thoracic outlet syndrome?

A
  • aka brachial plexus injury
  • compression of brachial plexus nerves
  • causes pt to experience pain in the arm of affected side, paresthesia of fingers, weakness and dimished grasp capability in the fingers and the thumb, small muscles of the hand may even begin to waste away
  • causes is continual hyperabduction of te arm, continual dropping of the shoulder girlde, cervical rib or a fibrous band that develops around the nerve plexus
113
Q

diagnose and treat thoracic outlet syndrome?

A

diagnose - clnical findings, history, physical exam, electromyography

treat - cessation of any continued hyperabduction of the arm, specific types of exercises or physical therapy, if cerbical rib is the cause than remove surgically, if entrapment of brachial plexusi nerve by anterior scalene muscle than surgical release of any fibrous band or entrapping tissue

114
Q

What is tendintis/ tendonitis?

A
  • inflammation of a tendon that is usually caused by insult or injury to the tendon (calcium deposits often r associated w/ tendinitis, bursa around tendon also may be involved)
  • nonspecific pain anywhere along the route of the tendon or its attachments (mot common symtpom is acute pain)
  • diagnose w/ history, if shoulder than 50-130 degree abduction = pain, hard to diagnose
  • treat with rest, oral antiinflammatory drugs, ice, steroid injhections, surgery if adhesions