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?

A

POLY

24
Q

predominate sign in RA

A

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

25
Q

worst case of RA=

A

felty’s syndrome

26
Q

what is triad of felty’s?

A

neutropenia, splenomegaly, deforming RA

27
Q

Xray in RA

A

loss of joint space (joint narrowing), periarticular thinning, ulnar deviation, MCP swelling joint destruction and disassociation

28
Q

four characteristics of RA

A

inflammatory, polyarticular, periarticular, and symmetric

29
Q

RA vs. fifth’s disease

A

fifths disease is common in children and is self limited. RA- will not go away

30
Q

RA vs. polymyalgia rheumatica

A

blood test. tenderness on palpation of temporal a.

31
Q

RA vs. rheumatic fever

A

strep test, ASL

32
Q

Tx in RA focuses on:

A

treating pain, and preventing deformity and disability

33
Q

OT and PT tx options for RA

A

joint protection and adaptive quipment, ultrasound, low level laser therapy (helps with AM stiffness)

34
Q

meds for RA

A

NSAIDS- for pain, corticosteroids, synthetic or biologic DMARDS, combinations

35
Q

synthetic DMARDS- first and second line

A

first line- methotrexate oral or sc. 2nd line- sulfasalazine

36
Q

Biologic DMARDS site of action

A

TNF inhibitors- Adalimumab, influximab. Non- TNF DMARDS- Abatacept (blocks t cell stimulation), Rituximab (anti CD20), tocilizumab- blocks IL-6

37
Q

describe hand deformities in RA

A

ulnar deviation, boutonniere deformity (flexion of PIP, hyperextension of DIP), and swan-neck deformity (extension of PIP, flexion of DIP)

38
Q

associated condiitons with RA

A

felty’s and sjogrens

39
Q

felty’s syndrome initital and later descriptions

A

initially- neutropenia, splenomegaly, leg ulcers, RA positive. Later- lymphadenopathy, thrombocytopenia, HLA-DR4