OA Flashcards

1
Q

joints primarily affected

A

hands, hips, knees

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2
Q

primary OA

A

idiopathic

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3
Q

secondary OA

A

due to somethign

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4
Q

protective features of the joint

A

synovial fluid reduces friction
ligaments and tendons allows for the right tension
bone - shock absorbing
cartilage - thin coating at two opposing ends of bones

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5
Q

general pathophys

A

complex interaction of may extra and intracellular molecules
bone turnover favors cartilage destruction

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6
Q

risk factors for osteo

A
ethnicity 
age
gender (men at first then women)
bone density 
nutritional 
joint injury 
obesity 
occupation 
joint biomechanics
muscle weakness
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7
Q

clinical diagnosis

A

> 45
activity related joint pain
morning stiffness <30min
lab tests only to rule out other causes

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8
Q

symptoms **

A

stiffnes in morning or after periods of inactivity <30min
localized to affected joint
pain worse with activity or prolonged use

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9
Q

signs ***

A

often unilateral
joints not tender or inflamed
joint instability
no systemic symptoms

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10
Q

cause of pain

A

not due to destruction of catilage
from activation of nociceptive nerve endings within the joint by mechanical and chemical irritants
may be due to distension of the synovial capsule

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11
Q

what do we see in xrays

A

narrowing of joint space
osteophytes
bone cysts

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12
Q

when do we do xrays

A

not needed for intial usual presentation of OA or follow up

symptoms dont correlate with image abnormalities

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13
Q

nodes in OA

A

heberden

bouchard

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14
Q

reasons for further evaluation in patient complaining of new onset joint pain

A
duration > 1week 
recent significant trauma 
fever, infection, rash
injury 
muscle weakness
burning, numbness, tingling
inflammation or stiffness >1hr
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15
Q

goals of therapy***

A

relieve or eliminate pain
improve/restore joint function adn mobility
improve muscel strength to protect the structures
prevent and reduce damage to the joint structures
max quality of life
educate the patient to promote adherence

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16
Q

algorithm for treatment

A
  1. non pharm, topical analgesics
  2. acetaminophen
  3. asses GI and CV risks and choose a nsaid
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17
Q

low GI and CV risk

A

low dose non selective nsaid

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18
Q

low GI and high CV

A

naproxen + gastroprotection

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19
Q

high GI high CV

A

naproxen + gastroprotection +
low dose celecoxib ?
avoid

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20
Q

high GI low CV

A

low dose NSAID + gsatroprotection or low dose celecoxib

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21
Q

high GI and CV factors, previous ulcers, use of oral corticosteroids or anticoagulants (including low dose ASA)

A

low dose celecoxib + gastroprotection

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22
Q

options for hand OA

A

topical capsaicin or nsaids

oral nsaids

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23
Q

options for knee OA

A

acetaminophen
topical and oral nsaids
intraarticular corticosteroids injections
not topical capsaicin

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24
Q

options for hip OA

A

acetaminophen first line
intrarticular corticosteroid injections
oral nsaid
not topical capsaicin

25
non pharms
``` strength training and aerobic exercise weight loss joint protection supportive footwear assistive devices social support heat and cold therapy massage surgery ```
26
acetaminophen dosing
325-100mg every 4-6 hrs for 2 weeks | max 4g/day
27
acetaminophen role
first line
28
acetaminophen efficacy
same as nsaids in mild non inflammatory | less effective in advanced
29
safety of acetaminophen
max 3.2g/day in elderly avoid in >3 drinks per day warfarin hepatotoxicity
30
capsaicin dosin
apply tid-qid for 3-4 weeks
31
capsaicin role
first line in hand
32
capsaicin onset
2 weeks to take effect
33
safety of capsaicin
tingling, burning, redness
34
topical diclofenac role
first line in hand or knee
35
safety of topical diclofenac
minimal systemci safety concerns
36
NSAID role
alternative for hand if cant toleracte skin reactions or inadequate relief in knee and hip if fail or contraindication to acetaminophen
37
safety of nsaids
nausea, abd pain, diarrhea | ulcer, GI bleed, kidney disease, hepatitis
38
what is considered high CV risk
on lose dose ASA | high 10yr CV risk
39
methylprednisone dosing
10mg per joint, 20-80 for large | max 3 injection/joint/year
40
IA steroids role
alternative first line for knee and hip when pain control with acteaminophen or nsaids suboptimal
41
efficacy of IA
superior to placebo in alleviating pain but relatively short duration (4-6 weeks)
42
safety og IA steroids
inexpensive, safe, effective | hyperglycemia, edema, increase BP, flushing
43
sodium hyaluronate dosing
injection once or weekly for 3-5week
44
role of IA hyluronic aicds
not recommended | limited efficacy and serious events
45
IA hyluronic acid safety
increased pain, joint swelling, stiffness | pseudogout
46
duloxetine dose
60mg daily
47
duloxetine role
adjunctive in partial response to first line analgesics | second line in patients with neuropathic pain as well
48
duloxetine efficacy
as an add on shown effiacy | reduction of pain occurs in 4 weeks
49
safety of duloxetine
nausea, vomit, constipation | CI in liver disease and severe renal impairment
50
tramadol dose
25mg AM titrate 25mg to reach 100tid
51
tramadol role
alternative first line in knee/hip who failed everything else can add on to acet or nsaid
52
tramadol efficacy
mod improvement as add on | reduction in pain occurs in 4 weeks
53
tramadol safety
nausea, vomiting, dizzy, constipation, headache | taper
54
cox 2 inhibitors gastroprotective effects are negated by
ASA
55
glucosamine chondroitin efficacy
not shown to improve pain control and function | studies that showed any benefit were short duration
56
risk factors for UGI event
``` >65yo use of anticoagulants use of steroids history of PUD high dose NSAID presence of hpylori ```
57
bottom line for corticosteroids shots
reduce pain at 6 weeks but then less and less | long term pain relief uncertain but serious events are very rare
58
adequate trial of duloxetine
if min response at 6 weeks probably wont get a beter one
59
monitoring
``` decrease in pain daily pain relief daily hepatotoxicity baseline and annual blood in vomit or stool BP iwithin 1 week of nsaid therapy renal function - edema, scr ```