OA, RA Flashcards

1
Q

Most common form of arthritis is

A

OA

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2
Q

leading cause of disability in ages over 65

A

OA

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3
Q

OA a/w

A

age, obesity, previous trauma, and abnormal joint mechanics

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4
Q

how is ROM affected in OA

A

decreased

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5
Q

types of nodes in OA

A

heberden’s- DIP, bouchards- PIP

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6
Q

labs ordered in OA

A

CBC with diff, CMP, ESR, CRP, ANA/RA

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7
Q

XRAY finding in OA

A

joint narrowing d/t loss of articular cartilage, subchondral bone thickening and hardening, sclerosis, subchondral cysts, osteophytes

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8
Q

joint aspiration in OA vs. RA

A

OA is non-inflammatory so cell count less than 500, mostly mononuclear. RA is inflammatory- cell count more than 2,000, predominantly NEUTROPHILS

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9
Q

calcium pyrophosphate dihydrate crystals seen in joint aspiration- suspect…

A

pseudogout

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10
Q

If bone pain at night, think-

A

metastatic bone cancer

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11
Q

ddx of OA that is characterized by fracture, subluxation, and/or dislocation of a joint that goes unnoticed d/t neurologic damage

A

charcot’s joint

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12
Q

charcot’s joint most commonly affected joint-

A

ankle- highly stressed

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13
Q

tx of OA focused on..

A

weight loss (reduces pressure of joints), regular exercise (low impact- water aerobics, yoga), and treating joints with respect- avoid repetitive or improper use. keep stretching!

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14
Q

injections FDA approved for knee and shoulder in OA

A

viscosupplement. steroids can also be used for larger joints

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15
Q

surgery types in OA

A

arthroscopy, osteotomy, partial/total

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16
Q

nsaid contraindication and SE

A

contraindicated in pregnancy. SE- GI bleed, kidney disease, CAD

17
Q

4 risk factors a/w RA

A

HLA-DR4 and HLS-DR4 surface antigen, family history, native american ethnicity, female 20-50

18
Q

target population for testing RA

A

1 or more joints with definite clinical synovitis, synovitis cannot be explained by other diseases (r/o overuse, virus, lyme disease)

19
Q

classification criteria for RA

A

6 or more points out of 10- can include joint involvement (more joints involved- more points), serology (RF), abnormal ESR or CRP, and duration of symptoms (6 or more weeks is a point)

20
Q

atypical RA

A

palindomic rheumatism, presting with systemic symptoms or generalized fatigue first then joint pain follows

21
Q

characteristics of palindromic rheumatism

A

episodic RA, 1- several joint areas affected, symptoms last for hours to days, can involve symptom free episodes, often progresses to CLASSIC RA

22
Q

describe CLASSIC RA

A

AM stiffness more than 1 hour, symmetrical joint pain, stiffness, swelling esp of PIP, MCP, MTP, wrist. can be a/w polymyalgia rheumatica

23
Q

RA polyarthroapy or monoarthropathy?

24
Q

predominate sign in RA

A

synovial thicking- boggy joint (wet, not firm) and heat generally present, redness rarely

25
worst case of RA=
felty's syndrome
26
what is triad of felty's?
neutropenia, splenomegaly, deforming RA
27
Xray in RA
loss of joint space (joint narrowing), periarticular thinning, ulnar deviation, MCP swelling joint destruction and disassociation
28
four characteristics of RA
inflammatory, polyarticular, periarticular, and symmetric
29
RA vs. fifth's disease
fifths disease is common in children and is self limited. RA- will not go away
30
RA vs. polymyalgia rheumatica
blood test. tenderness on palpation of temporal a.
31
RA vs. rheumatic fever
strep test, ASL
32
Tx in RA focuses on:
treating pain, and preventing deformity and disability
33
OT and PT tx options for RA
joint protection and adaptive quipment, ultrasound, low level laser therapy (helps with AM stiffness)
34
meds for RA
NSAIDS- for pain, corticosteroids, synthetic or biologic DMARDS, combinations
35
synthetic DMARDS- first and second line
first line- methotrexate oral or sc. 2nd line- sulfasalazine
36
Biologic DMARDS site of action
TNF inhibitors- Adalimumab, influximab. Non- TNF DMARDS- Abatacept (blocks t cell stimulation), Rituximab (anti CD20), tocilizumab- blocks IL-6
37
describe hand deformities in RA
ulnar deviation, boutonniere deformity (flexion of PIP, hyperextension of DIP), and swan-neck deformity (extension of PIP, flexion of DIP)
38
associated condiitons with RA
felty's and sjogrens
39
felty's syndrome initital and later descriptions
initially- neutropenia, splenomegaly, leg ulcers, RA positive. Later- lymphadenopathy, thrombocytopenia, HLA-DR4