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

25
Before getting pregnant a patient must stop Leflunnomide (Arava) and do what?
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
Leflunomide can inhibit the metabolism of what drugs?
NSAIDS -causing their levels to rise
27
Leflunomide can cause liver damage when used in combination to other hepatic toxic drugs
like mtx
28
rifampin can raise leflunomide levels by
40%- causing risk for toxicity
29
Hydroxychloroquine (Plaquenil) usually used in combination with what drug for RA?
MTX
30
onset of symptom management for Hydroxychloroquine include
a 3-6 month time period while NSAIDS and steroids are being used to manage symptoms until effects begin to work
31
most common risk with hydroxychloroquine (plaquenil)
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
Hydroxychloroquine AE
cardiac arrthythmias including prolonged QT interval hypoglycemia, proximal myopathy and neuropathy, and worsening psoriasis may cause GI distress take with milk or food
33
Hydroxychloroquine half life
is extremely long, about 40 days
34
Tofacitinib (Xeljanz, Xeljanz XR) MOA
prevents activation of the STAT pathway by preventing JAK enzyme signaling
35
When is Tofacitinib used?
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
Tofacitinib AE
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
Tofacitinib drug interactions
CYP enzymes can increase/decrease levels DMARDS have additive toxic effect do NOT combine DMARDs with tofacitinib
38
Tofacitinib black box warning
potential for developing fatel infections including TB
39
when should you get vaccines when starting DMARDs
2 weeks prior to start of medication, once started live viruses must be avoided.
40
Baseline data for drugs: MTX: Hydroxychloroquine: Leflunomide:
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
non pharmacological RA interventions
heat or cold applied to the joint pt combine with meds for best outcomes
42
If the patient is having multiple joints involved/ pain your going to want to treat with what?
systemic corticosteroids
43
If only one joint is involved you could possibly just give what kind of steroid?
intra articular steroid to local area