Rheumatoid Arthritis Flashcards

1
Q

Who is affected by most by rheumatoid arthritis, risk factors

A

Women between 50 and 75/ smoking, genetics, presence of autoantibodies

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2
Q

What is Rheumatoid arthritis

A

autoimmune disease that causes inflammation that can lead to bone surface erosions

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3
Q

Clinical presentation of rheumatoid arthritis

A

symmeterical joint swelling (synovitis). morning stiffness lasting more than one hour

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4
Q

What should be monitored when giving therapy for Rheumatoid arthritis

A

acute phase reactants ( C-reactive protien and erythrocyte sedimentation rate)

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5
Q

What are goals of treatment for rheumatoid arthritis

A

control disease activity, alleviate pain, maximize quality of rate, induce complete remission

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6
Q

What is the best way evaluate the disease activity of rheumatoid arthritis

A

DAS/DAS28 (ESR or CRP, patient global assessment)

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7
Q

What non-pharmacologic therapy for rheumatoid arthritis

A

rest, physical therapy, achieve ideal body weight, stop smoking

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8
Q

What is an important Non-Disease-Modifying therapy for Rheumatoid arthritis, benefits

A

Corticosteroids, controls symptoms quickly, used in flares, can be used intraarticularly

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9
Q

What is the biggest complication with using corticosteroids

A

Long term adverse affects

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10
Q

T/F: All vaccines should be avoided when patients are on DMARDs

A

False: Live attenuated vaccines should be avoided while on biologic DMARDs

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11
Q

What are the non-biologic DMARDs

A

Methotrexate, Sulfasalazine, Hydroxychloroquine, Leflunomide

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12
Q

What drug is the cornerstone of rheumatoid arthritis therapy, what is the MOA

A

methotrexate, dihydrofolate reductase inhibitor while also inhibiting production of IL-1

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13
Q

What is the biggest adverse effect of methotrexate

A

hepatotoxicity

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14
Q

What is the dosing for methotrexate

A

10-25 mg per week (as 2.5 mg tablets)

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15
Q

What is the drug that can be used as an alternative to methotrexate, MOA

A

Leflunomide, inhibits dihydroorotate dehydrogenase

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16
Q

What non-biologic DMARD is often used in combination, what is a possible drug interaction

A

Sulfasalzine, warfarin

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17
Q

What are common adverse effects, what side effect could lead to a larger problem

A

Nausea, vomitting and diarrhea/ Rash

18
Q

Which of the non biological DMARDs is an antimalarial, MOA

A

Hydroxychloroquine, interferes with antigen processing in APCs

19
Q

What drug is a severe adverse effects of hydroxchloroquine

A

Ocular toxicity and retinopathy

20
Q

T/F: Ocular toxicity caused by hydroxychloroquine is reversible through reducing use of medication while the retinopathy is irreversible

21
Q

What are the risk factors of hydroxychloroquine causing retinopathy

A

Daily dose greater than 5mg/kg, duration of use after 5 years

22
Q

How should retinopathy be monitored when using hydroxychloroquine

A

Eye exam within the first year and every year

23
Q

When should DMARD therapy be modified

A

repetitive flares, unacceptable disease activity, progressive joint damage

24
Q

What are biologic DMARDs

A

Etanercept, Infliximab, Adalimumab, Certolizumab, Golimumab

25
What are the basics of biologic DMARDs
administered parenterally, work quickly, potential for serious side effects
26
Which biological DMARDS work on the T-cell receptor resulting in down regulation of T cells, which work on CD20 of B cells, which are IL-6 receptor inhibitors
Abtacept, Rituximab, Tocilizumab and Sarilumab
27
When would biologic DMARDS used
used for moderate to severe rheumatoid arthritis , often used in patients who fail MTX, can be added as a steroid sparing agent
28
T/F: It is fine to combine more than one Biologic DMARD
False: Do not combine more than one biologic DMARDS due to overlapping side effects
29
What is the first line biologic DMARD for rheumatiod arthritis
Anti-TNF agents
30
T/F: If one biological DMARD from its class is not working it is reasonable to use a 2nd biological DMARD from the same class as long as it's not at the same time
True
31
What must be monitored when using Anti-TNF agents
TB skin or blood test, Hep B reactivation, histoplasmosis, malignancy
32
What is the MOA of abatacept, what patients should avoid this medication
binds B7 using the extracellular domain of CTLA-4 therefore down regulating T cells, patients with COPD and/or smoke
33
T/F: There is no evidence of increased incidence of TB in patients and no evidence of increased incidence of cancer when taking rituximab
True
34
What are the ADRs for rituximab
infusion reaction, reaction of Hep B, Stevens-Johnson, PML caused by JC virus
35
What must be monitored before using Tocilizumab and Sarilumab
Do not start if ANC is less than 2000, PLT is less than 100,000 (tocilizumab) or 150,000 (Sarilumab)
36
What are adverse efffects of Tocilizumab and Sarilumab
GI perforation and dyslipidemia
37
What are the JAK Kinase inhibitors, how are they taken
Tofacitinib and baricitinib, by mouth
38
T/F: Janus Kinase inhibitors can be combined with a biologic and potent immunosuppresive drugs for peak efficacy
False: Do not combine Jak/Stat inhibitors with biologics and avoid in patients who are taking tacrolimus, cyclosporine, and azathioprine
39
Which Jak/Stat inhibitor goes through extensive liver metabolism and may be effected by CYP induces or inhibitors
Toacitinib
40
Which Jak/Stat inhibitor is not recommended due to the CrCl less than 60
Baricitinib
41
What are the ADRs of Janus Kinase inhibitors
Thrombosis (baricitinib), GI perforation, lipid changes