Chapter 59: Rheumatoid Arthritis Flashcards

1
Q

goal of treatment for RA

A

1) relieving symptoms
2) maintaining joint function and range of motion
3) minimizing systemic involvement
4) delaying disease progression

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2
Q

RA symptoms

A

joint stiffness and pain- most intense in the morning and abate as the day advances…swollen tender warm joints

can also be systemic with fever, multiple joints, etc

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3
Q

nondrug treatment for RA

A

PT

exercise

surgery

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4
Q

classes of antiarthritic drugs

A

NSAIDS
Glucocorticoids
DMARDs (Disease- modifying antirheumatic drugs)

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5
Q

NSAIDS and glucocorticoids provide ______ in RA treatment

A

rapid relief

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6
Q

Differences in NSAIDS vs. glucocorticods in treating RA

A

NSAIDS provide rapid relief of symptoms but do not prevent joint damage and do not slow disease progression

Glucosteroids can slow disease progression as well as provide rapid relief of symptoms

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7
Q

DMARDS MOA

A

reduce joint destruction and slow disease progression

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8
Q

Major Drugs of focus Conventional DMARDs

A

Methotrexate
Leflunomide (arava)
Hydroxychloroquine (Plaquenil)

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9
Q

Targeted DMARDs- Janus Kinase Inhibitor

A

Tofacitinib (Xeljanz, Xeljanz XR)

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10
Q

DMARDS are contraindicated in

A

pregnancy and breastfeeding

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11
Q

when should DMARD therapy be started

A

ASAP, close to diagnosis the better but deff within three months

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12
Q

While waiting for DMARDs to start to work what is usually given?

A

NSAIDS

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13
Q

What is given for short term flare ups related to RA

A

Glucocorticoids

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14
Q

GI effects from NSAIDS occur due to inhibition of what?

A

COX-1 (causes GI ulceration etc)

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15
Q

what must be supplemented when giving methotrexate

A

Folate at least 5mg/week

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16
Q

MTX MOA for RA

A

B and T lymphocytes

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17
Q

AE effects of MTX

A

hepatic fibrosis, bone marrow suppression, GI ulceration and pneumonitis

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18
Q

what labs should be followed when a patient is taking mtx

A

liver, kidney function, and cbc

19
Q

caution use of mtx in patients with hx of

A

renal/ liver impairment

20
Q

if taking mtx what kind of vaccine do you have to have?

A

inactivated

21
Q

second line use if mtx is not effective is

A

leflunnomide (Arava) - but is usually more hazardous and more expensive

22
Q

Leflunnomide (arava) can cause fetal effects due to

A

liver injury- avoid in patients with hx of liver impairment

23
Q

Leflunnomide (arava) AE:

A

diarrhea, infection, alopecia, and rash. Pancytopenia, Stevens- Johnson Syndrome, peripheral neuropathy, interstitial lung disease and severe hypertension, immunosuppression

24
Q

Before starting Leflunnomide patients should be screened for

A

TB

25
Q

Before getting pregnant a patient must stop Leflunnomide (Arava) and do what?

A

take cholestyrammine 8g tid for 11 days (without this it may take two years for it to clear)

verify drug levels are less than 20ug/L

men who wish to father a child should do the same thing.

26
Q

Leflunomide can inhibit the metabolism of what drugs?

A

NSAIDS -causing their levels to rise

27
Q

Leflunomide can cause liver damage when used in combination to other hepatic toxic drugs

A

like mtx

28
Q

rifampin can raise leflunomide levels by

A

40%- causing risk for toxicity

29
Q

Hydroxychloroquine (Plaquenil) usually used in combination with what drug for RA?

A

MTX

30
Q

onset of symptom management for Hydroxychloroquine include

A

a 3-6 month time period while NSAIDS and steroids are being used to manage symptoms until effects begin to work

31
Q

most common risk with hydroxychloroquine (plaquenil)

A

Retinal damage, patient should receive eye exam prior to start and annually after. should d/c if any issues, not common with low doses but more common with higher doses

32
Q

Hydroxychloroquine AE

A

cardiac arrthythmias including prolonged QT interval

hypoglycemia, proximal myopathy and neuropathy, and worsening psoriasis

may cause GI distress take with milk or food

33
Q

Hydroxychloroquine half life

A

is extremely long, about 40 days

34
Q

Tofacitinib (Xeljanz, Xeljanz XR) MOA

A

prevents activation of the STAT pathway by preventing JAK enzyme signaling

35
Q

When is Tofacitinib used?

A

after methotrexate is tried and other trials of DMARDS are complete but not working, this is because the medication is newer and long-term safety has not been established

36
Q

Tofacitinib AE

A

infections developing due to immunosuppression, bradycardia, prolonged PR interval, intersitial lung disease, GI perforations, drug induced liver injury, hyperlipidiemia, and increase occurence of malignancies

37
Q

Tofacitinib drug interactions

A

CYP enzymes can increase/decrease levels

DMARDS have additive toxic effect do NOT combine DMARDs with tofacitinib

38
Q

Tofacitinib black box warning

A

potential for developing fatel infections including TB

39
Q

when should you get vaccines when starting DMARDs

A

2 weeks prior to start of medication, once started live viruses must be avoided.

40
Q

Baseline data for drugs:

MTX:

Hydroxychloroquine:

Leflunomide:

A

M: CXR, pulmonary and GI

H: opthalamologic exam, cardiac and exam with ECG if indicated

L: Consider CXR, emphasis on BP and pulmonary status. s/s of peripheral neuropathy

41
Q

non pharmacological RA interventions

A

heat or cold applied to the joint

pt

combine with meds for best outcomes

42
Q

If the patient is having multiple joints involved/ pain your going to want to treat with what?

A

systemic corticosteroids

43
Q

If only one joint is involved you could possibly just give what kind of steroid?

A

intra articular steroid to local area