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Aurothioglucose drug class
Gold compounds
Aurothioglucose formulation
IM injection
Auranofin drug class
Gold compounds
Auranofin formulation
PO
Gold sodium Thiomalate drug class
Gold compounds
Gold sodium Thiomalate drug formulation
IM injection
Side effects of gold compounds
dermatitis, mouth lesions, pulmonary disorders, nephritis
antidote for gold compound for severe toxicity
chelating agents (dimercaprol and penicillamine)
Gold compound DDI
concurrent administration of drugs that also produce blood dyscrasias
- phenylbutazone
- Antimalarial
- immunosuppressive
Chloroquine drug class
antimalarials
hydroxychloroquine drug class
antimalarials
antimalarials main SE
retinal damage
antimalarial monitoring
baseline, then Q6M
Leflunomide drug class
immunosuppressant
Azathioprine drug class
immunosuppressants
Sulfasalazine drug class
immunosuppressants
Cyclophosphamide drug class
Immunosuppressant
Cyclophosphamide place in therapy
for life threatening RA
Methotrexate drug class
immunosuppressant
Methotrexate DDIs
- NSAIDS
- Penicillin
- Probenecid
Methotrexate Monitoring
liver enzymes
What condition can be worsened in use with the drug Infliximab
CHF
Etanercept (enbrel) drug class
TNF
Infliximab (Remicade) drug class
TNF
adalimumab (Humira) drug class
TNF
rituximab drug class
TNF
Anakinra drug class
IL-1 receptor antagonist
Tocilizumab drug class
IL-6 receptor antagonist
Colchicine place in treatment
Relieve the pain of acute gout and is the drug of choice for acute gouty attack
Colchicine MOA
Retard the inflammation process initiated by the deposition of urate crystal
- does not lower the serum levels of uric acid
Colchicine main side effect
GI disturbance (development of diarrhea)
Probenecid and sulfinpyrazone MOA
Promote the excretion of uric acid by inhibiting the urate anion exchange transporter (URAT1), decreasing the reabsorption of uric acid, decrease plasma uric acid concentration
Probenecid and sulfinpyrazone DDIs
uricosuric effects are antagonized by salicylates
Allopurinol MOA
decrease uric acid formation by inhibiting xanthine oxidase. Prevent or reduce the formation of urate deposits and the incidence of attacks.
Febuxostat MOA
1st nonpurine selective xanthine oxidase inhibitor. Results in fewer side effects relative to allopurinol
Pegloticase MOA
enhancing the degradation of uric acid
- enhances the excretion of uric acid by converting it into a more excretable metabolite
Infliximab dosing route and schedule
I.V
Etanercept dosing route and schedule
SubQ once or twice weekly
Adalimumab and Certolizumab dosing route and schedule
SubQ every other week
Golimumab dosing route and schedule
SubQ monthly
TNF alpha serious side effect
Malignancy (Hodgkins or non-Hodgkins)
Anifrolumab MOA
Treat SLE. Binds to IFNAR1/2 blocking the effects of IFN alpha and IFN beta to stimulate the inflammatory response
Anifrolumab most common SE
Upper respiratory tract infections
Prolia place in therapy
First in class FDA approved fully human MAb to treat OA
Prolia MOA
binds to RANKL blocking maturation of pre-osteoclasts into osteoclasts, protecting bone from degradation, and helps counter the progression of osteoporosis
Romosozumab MOA
inhibits sclerostin, a regulatory factor in bone metabolism that inhibits Wnt/beta catenin signaling pathway regulating bone growth
Romosozumab warning
potential increase risk of Myocardial infraction, stroke, and CV death
RA description
systemic chronic autoimmune inflammation disease characteristics by small joint swelling, pain, and stiffness
Characteristics of joint swelling, pain, and stiffness
- Joint pain is typically symmetrical and polyarticular (more than 1 joint)
- joint swelling with morning stiffness lasting longer than an hour that improves with use throughout day
RA incidence
50-75 years of age where women are three times more likely to have RA as compared to men however the sex differential becomes less with age
What is the goal for treatment of RA
remission or low disease activity
RA pathophysiology
synovium lines the joint capsule and early in the disease, there is microvascular injury and an increase in the number of synovial lining cells
This process then begins to protrude into the joint cavity
- Leads to joint destruction and loss of cartilage
RA extra-articular involvement
Rheumatoid nodules, vasculitis, pulmonary complications, ocular manifestations, and cardiac involvement,
Rheumatoid nodules in RA
Most commonly develop on pressure areas including the elbows and finger joints
Vasculitis in RA
Inflammatory cells enter the vessels walls resulting in destruction of vessels and infarction of tissue distal to the area damage
- present in patients with long standing disease
Pulmonary complications
some rare, life-threatening complications
- 50% of patients with RA
Cardiac involvement in RA
pericarditis, myocarditis, pericardial effusion, and premature atherosclerosis
Comorbid Conditions of RA
- CVD
- Infections
- Malignancy
- Osteoporosis
Percent of deaths from CVD in patients with RA
40%
CV events occur about 10 years earlier than those without RA
What is considered a key clinical feature of RA
metacarpophalangeal (MCP) joints and proximal interphalangeal joints of the hands are often the first site
Average length of morning stiffness in an RA patient
lasts longer than one hour
What does the examination of the hands/wrist tell us about the RA patients
able to tell if the patient is having early, late, or progressive disease
what level of rheumatoid factor is more sensitive for RA
2 times the ULN
what is useful about rheumatoid factor in RA patients
patients with synovitis and high pre-test probability
- after 3 years 80% of patients with show a positive lab test
What lab valve is useful in diagnosis of RA
Anti-citrulline containing proteins (CCP) antibodies
- 3 times ULN
What lab valves are useful for acute phase reactants (inflammation)
- Erythrocyte sedimentation rate (ESR)
- C-reactive protein (CRP)
What lab value is associated with active severe RA
Antinuclear antibody (ANA)
What should taken after a diagnosis of RA
radiographic findings for baseline and periodically to check progression of disease
What will happen to the joint space after 2 years of an RA patient
estimation of 80% of patients with RA of less than 2 years will have joint narrowing on plain radiographs and 2/3 will have evidence of erosions
NSAIDs and corticosteroids place in therapy for RA
work quickly and reduce inflammation however they are not appropriate for long term use
Ideal duration of steroids for RA patient to reduce inflammation
< 3 months at the lowest effective dose
Recommended daily dose for prednisone
15 mg/day
DMARD drug class for Hydroxychloroquine
conventional synthetic disease-modifying antirheumatic drugs
Hydroxychloroquine place in therapy for RA
safest but least effective
When is hydroxychloroquine considered a therapeutic failure
After 6 months of use with not effect on RA
Can you use hydroxychloroquine in pregnant patients
yes
Monitoring that must occur for hydroxychloroquine
ophthalmologic exam at baseline and then annually within 5 years of therapy
DMARD drug class for MTX
conventional synthetic disease-modifying antirheumatic drugs
MTX initiation dose
7.5 mg QW
MTX target dose
15 mg QW
MTX max dose
25 mg QW
Main AE for MTX that limits dose
Gastrointestinal
What is a way to try and help with the GI related SEs for MTX
may split weekly dose and take two separate doses on the same day
- can even split into 3 doses
How often are you supposed to test liver, renal, and CBC function for MTX
Q4-8W
Contraindication for MTX usage
pregnancy, CKD, liver impairment, and heavy alcohol usage
MTX avoidance for men trying to conceive
avoid use at least 3 months before planned conception
MTX avoidance for women trying to conceive
avoid for 1 menstrual cycle before planned conception; avoid in breastfeeding
MTX DDIs
NSAIDs
MTX onset of action
4-6 weeks
Supplement of folic acid for MTX patients
5 mg of folic acid QW
DMARDs drug class of Leflunomide
conventional synthetic disease-modifying antirheumatic drugs
Leflunomide avoidance for men and women trying to conceive
Men or Women who wish to conceive a child need to D/C the leflunomide ad ingest cholestyramine 8 grams TID for 11 days
Is it appropriate to use biologics and MTX together
Yes, they should be used together
What should be screened prior to starting biologics DMARDs
- TB
- pre-existing conditions
- live vaccine will not be used (must receive all before starting these medications)
Should one DMARD biologics be used over another for RA patients
No, they all have similar efficacy
What is a primary response to TNF agents
lack of initial response to an TNF agent typically indicated and are unlikely to response to another TNF agent
What is a secondary response to TNF agents
initial response but loses efficacy over time. Able to switch to different agent in the same class
DMARDs drug class of Etanercept (Enbrel)
bDMARDs
DMARDs drug class of Infliximab (Remicade)
bDMARDs
Can Remicade be used in monotherapy for RA treatment
Only used in conjunction with MTX