MS pathologies pt. 3 ( infection/trauma) Flashcards

(57 cards)

1
Q

Osteomyelitis pahto ?

A

Bacterial or fungal infection in bone

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2
Q

Osteomyelitis routes ?

A

hematogenous

exogenous ( surgery or trauma)

contiguous ( soft tissue infection nearby )

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3
Q

Osteomyelitis – 
ACUTE hematogenous patho ?

A

Bacteria lodge in end artery of metaphysis and multiply below periosteum

**rarely goes into the joint and cause septic arthritis cause the epiphyseal is a barrier ** - can see its not in the joint cause the epiphyseal plate

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4
Q

Osteomyelitis – 
ACUTE hematogenous Hx ?

A

Have history of infection, e.g. strep throat, skin, UTI

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5
Q

Osteomyelitis – 
ACUTE hematogenous sxs ?

A

pain, malaise, anorexia, vomiting, fever ( vague)

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6
Q

Osteomyelitis – 
ACUTE hematogenous dx ?

A

blood culture (+/-)

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7
Q

Osteomyelitis – 
ACUTE hematogenous pathologic organisms ?

A

S. aureus, Hemolytic strep, H. flu

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8
Q

Osteomyelitis – 
ACUTE hematogenous Tx ?

A

IV antibiotics, possibly surgical drainage

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9
Q

Osteomyelitis – CHRONIC patho ?

A

Occurs when acute infection is untreated or tx fails

Fragment of necrotic bone gets walled off – sequestrum

May lie quiet for months-years

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10
Q

Osteomyelitis - Chronic facts ?

A

More sequestra form, bone gets deformed

Diabetics more prone cause they do not heal well cause circulation

Multiple organisms common

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11
Q

Osteomyelitis - Chronic tx ?

A

surgical debridement, bone reconstruction

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12
Q

Sprains – ligamentous injury 1st degree ?

A

minimal pain, no joint instability

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13
Q

Sprains – ligamentous injury 2nd degree ?

A

moderate pain, min. joint instability, partial ligament rupture

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14
Q

Sprains – ligamentous injury 3rd degree ?

A

severe pain, completely unstable joint, complete ligament tear

**later angle injuries are more common more inversion injuries **

**tuning fork on it - hurts? then yes fracture but it does not hurt if the ligament is tore etc **

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15
Q

Strains – muscle injury 1st degree ?

A

– mildly or slightly pulled muscle, pain, spasm, swelling, ecchymosis

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16
Q

Strains – muscle injury 2nd degree ?

A

– moderately pulled, pain, spasm, swelling, torn muscle fibers

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17
Q

Strains – muscle injury 3rd degree ?

A

– severely pulled, loss of muscle function, palpable defect, ruptured muscle or tendon. Possibly avulsion fx at tendinous attachment ( ecchymosis, spasms, and prolongs liability)

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18
Q

Compartment syndrome causes and patho ?

A

Fx, crush injury, hemorrhage, burn, edema –

increased pressure in fascial compartment on arteriole walls

Compromises circulation in that space

**not diffusely the whole limb just a compartment and the blood is taking up space and it causes pressure o the arterial wall ( distal pulses are okay)

no risk of whole limb ischemia just the compartment ischemia **

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19
Q

Compartment syndrome Red Flags ?

A

Pain is out of proportion to injury

Pain is persistent & progressive

Weakness or paralysis of muscle

Tense compartment on palpation

Distal pulses remain intact

**casting should make them feel better but if in a cast and still pain then this is a problem and it is probably this

distal pulses are still okay

pain that is unrelieved with rest **

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20
Q

Compartment syndrome dx ?

A

check compartment pressure with monitor

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21
Q

Compartment syndrome tx ?

A

fasciotomy ASAP, with partial closure ( slices through the tissue and let compartment breath again)

**which compartment has a higher pressure **

they will do a partial closure and wait for swelling to go down ( and maybe need to go back to the OR to get all the other stuff out of there)

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22
Q

Fibromyalgia Syndrome etiology ?

A

Etiology unknown

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23
Q

Fibromyalgia Syndrome sxs and PE ?

A

Widespread muscle pain, worst in AM

No limitation of movement but stiffness

Trigger points – symmetric, often neck, shoulders, hands, back, knees

24
Q

Fibromyalgia Syndrome own notes ?

A

bilateral above and below the waits

need 11/18 tender with no sxs. pressure points positive to dx or 6 with ass. sxs.

these patients are hypersensitive and have a lower pain threshd

paints dont sleep well and are very fatigued

25
Fibromyalgia patho ?
Unpredictable pattern of spread Maybe aberrant pain signaling and amplification
26
Fibromyalgia triggers ?
Triggers – immobility, overuse, cold temps. No edema, but TTP
27
Fibromyalgia dx ?
Dx of exclusion
28
Fibromyalgia tx ?
some what physically active but do not over due it
29
Polymyalgia Rheumatica (PMR) etiology ?
UKN
30
Polymyalgia Rheumatica (PMR) age and gender ?
+50 years, F>M ( middle age women)
31
Polymyalgia Rheumatica (PMR) locations ?
Hip, shoulders, neck, symmetric
32
Polymyalgia Rheumatica (PMR) sxs ?
Sudden or gradual onset Worst in AM Chronic, but ultimately self-limiting Associated malaise, depression, weight loss No true weakness * *muscle pain not the joints * *
33
Polymyalgia Rheumatica (PMR) dx ?
no dx test so we treat sxs.
34
Most common metabolic bone disease in US ( and preventable) ?
Osteoporosis
35
Osteoporosis gender ?
Females>Males ( cause estrogen loss after menopause)
36
Osteoporosis etiology ?
↓ estrogen, chronic us of steroids, hyperthyroidism not well controlled, immobilization, smoking, malignancy 50% of postmenopausal women sustain an osteoporosis-related fracture **alot of patient education here **
37
Osteoporosis risk factors ?
Postmenopausal +50 years Weight<154 lbs Low dietary calcium Vita D deficiency - no sunlight Tobacco and ETOH use Fx in a first degree relative Use of corticosteroids Medical conditions Medications Inflammatory disorders **thin petite people dietary supplemets are a much better source celiacs disease etc cause no absorptions ( this is alot of risk fcto5rs ) **
38
Osteoporosis: increased bone resorption ?
osteoclast
39
Osteoporosis: normal bone formation ?
osteoblasts
40
Osteoporosis have a high risk of ?
Fx **ridges are fragile and susceptible to breaking down ** **susceptible to compression fractures as they get older ( grandma getting shorter) loss of muscle bulk too **
41
Osteoporosis PE, signs?
Decreased height Usually asymptomatic until fx **susceptible to compression fractures as they get older ( grandma getting shorter) loss of muscle bulk too **
42
Osteoporosis dx ?
DEXA scan, check bone density
43
Osteoporosis: DEXA screening ?
Screen at 65, younger if at risk | unless they have been VD defficeicnt for a long time to on steroid for a long time you can check earlier
44
Osteoporosis sxs. ?
usually asxs, until fracture
45
Osteoporosis Tx ?
prevention! Dietary calcium (better than supplements) - 1200 mg a day ( but need VD for absorption) Vitamin D – sun, food, supplements ( havent seen a benefit of supplements after 5 years ( max out effectiveness) ) Weight-bearing exercise Bisphosphonates – Fosamax, Actonel, Boniva (decrease osteoclastic activity) Risk of osteonecrosis of the jaw - rare but dramatic when you see it ( side effect of bisphosphonates)
46
Bisphosphonates side effects ?
Risk of osteonecrosis of the jaw - rare but dramatic when you see it ( side effect of bisphosphonates)
47
Metastatic bone disease hx ?
Hx of a primary cancer in prostate, breast, lung, thyroid, kidney
48
Metastatic bone disease sxs. ?
nocturnal pain, unrelieved with rest, weight loss, hx of CA
49
Metastatic bone disease what may be the first sign ?
Pathologic fx may be first sign – from minor event, due to thin bones **first sing might be a fracture bone from a minor event like hitting it on the door or sneeze and break a rib **
50
Metastatic bone disease dx ?
bone scan, looking for “hot spots” of increased activity - ↑ serum alk phos **hot spot - increase uptake in dye ( no definitive - could just be more activity there but a good clue) **
51
Ehlers-Danlos Syndrome saying ?
“damn that girl is lose”
52
Ehlers-Danlos Syndrome patho ?
Hereditary connective tissue disorder (autosomal dominant or recessive trait)
53
Ehlers-Danlos Syndrome prevalence ?
1/10000 to 1/25000 20,000-50,000 EDS patients in the US
54
Ehlers-Danlos Syndrome signs and sxs. ?
joint hypermobility skin hyper extensibility tissue fragility pain recurvatum of the knees **runs in families and not common and they are in alot of pain no opioids they need to learn to cope with it **
55
Ehlers-Danlos Syndrome vascular types prevalence ?
5%
56
Ehlers-Danlos Syndrome vascular types ?
deficit of collagen TIII decreased /absent collagen synthesis or abnormalities in collagen secretion
57
Ehlers-Danlos Syndrome prognosis ?
poor prognosis most severe subtype ( vascular) life threatening vascular ruptures Anuerysm formation