Osteoporosis Drugs Flashcards

1
Q

what are the drug classes for osteoporosis (7)

A

calcium salts- to combat hypocalcemia

vitamin D

calcitonin

parathyroid hormone

bisphosphonates

selective estrogen receptor modulator

RANKL inhibitor

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2
Q

what are the drug classes for Gout

A

NSAIDS

Glucocorticoids

Microtubule formation disrupter

Xanthine Oxidase inhibitor

Recombinant Uricase

Uricosurics

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3
Q

two types of vitamin D

A

ergocalciferol D2- in plants

cholecalciferol- D3 from out skin upon exposure to sunlight (prescription)

**high in salmon and tuna- fortified foods

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4
Q

calcitonin-salmon MOA , effects, Clinical applications

A

same as normal calcitonin in the body, to stop osteoclastic resobrtion of bone

used for treatment of established osteoporosis not the prevention of it

can be given intranasally

(works but not as well as other agents)

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5
Q

what is the suffix most bisphophonates have?

A

-dronate

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6
Q

what is the MOA of bisphophonates? effects, CA, toxcitiy

which bisphophonate has the highest risk of toxicity and is give IV

A

they are analogs of pyrophosphate (normal consitute of bone)

they are incorporated into the bone and they stop bone resorption by decreasing osteoclastic function/number

first drug of choice in osteoporosis and pagers disease

toxicity: esophagitis, osteonecrosis of the jaw, atypical femur fractures (break in thick cortical bone)

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7
Q

taking bisphosphonates stops the healing of ?

A

micro fractures

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8
Q

what is raloxifene

side effects

A

this is a selective estrogen receptor modulator that blocks estrogen in the breast and uterus and is an agonist at bone to make the bone tough and not crack

it is used to treat and present postmenopasusal osteoporosis

can cause DVT. PE. and stroke, DO NOT USE IN PREGNANCY, and can cause hot flashes

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9
Q

what is teriparatide (PTH 1-34)

A

this is a shortened version of PTH that acts just like it

normally has osteoclastic and osteoblastic actvity

when given in pulses its osteoblastic activity predominants and is the only drug known to increase bone formation!!!!

given as pre filled injections

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10
Q

what is denosumab

what does rank L stand for

how often do we give denosumab in osteoporsos

side effects

A

this is a monoclonal antibody that is a rank L inhibitor used to decrease osteoclastic function

receptor activator of nuclear factor kappa B and ligand

injected every 6 months subcutaneously

delayed fracture healing, osteonecrosis of the jaw

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11
Q

MCCs of osteoporosis in men

A

hypogonadism - low T

glucorticoids

androgen deprivation

***van give T replacement
bisphoponates are the first line
denosumab is 2nd line

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12
Q

what drug is approved to treat hypercalcemia of malignancy

A

bisphophonates

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13
Q

what drug can chelate calcium

A

edetate disodium

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14
Q

what is cinacalet

A

this is a calcimimetic drug that binds to CaSR in the parathyroid gland it increases their sensitivity to extracellular calcium which decreases pTH being released

used in primary hyperparathyroidism or secondary hyperparathyroidism due to CKD

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15
Q

treatment for osteoarthritis

A

NOTHING can stop or prevent!!!- just to treat pain

NSAIDS!
TOPICAL NSAIDS, CAPSACIN
duloxetine
opioid anaglesics
intraarticular (platelet rich plasma)

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16
Q

treatment of osteomyelitis

A

clindamycin, rifampin, TMX-SMP, fluoroquinolone

to treat the bone wound that won’t heal - for 4-6 week course

17
Q

acute gout can be treatment with _ to reduce inflammation

A

anti-inflammatory drugs

18
Q

recurrences of gout can be treated with

A

increasing uric acid excretion (uricosuric drugs)

and

reduce uric acid production with xanthin oxidase inhibitors, recominante uricase

or diet

19
Q

general principles for acute gout

A

NSAIDS

if contraindicated

colchicine

if contrainticated

glucocorticoid

20
Q

NSAIDS for gout

A

naproxen- non selective

indomethacin -COX1

celecoxib- COX 2

21
Q

colchicine MOA and clinical applications

A

binds tubulin and blocks microtubule formation which leads to the inhibition and migration of phagocytosis

**used if NSAID contraindication or intolerance in gout

22
Q

xanthine oxidase inhibitors

A

allopurinol, feboxustat

23
Q

allopurinol MOA

effects

clinical applications

toxicity

A

competitive inhibitor of xanthine oxidase

blocks conversion to urate- hypoxanthine builds up instead

used in recurrent gout and cancer induces hyperurecemia from tumor lysis syndrome

stevens johnson syndrome with HLA b*5801

-acute gout attack

24
Q

febuxustate

MOA

clinical applications

toxicities (BBW)

A

non competitive inhibitor of xanthine oxidase leading to hypoxanthine excretion

used in recurrent gout for people who cannot tolerate allopurinol or chemo induced hyperurecemia

BBW: can cause cardiovascular death in those with cardiovascular disease

(EXPENSIVE)

25
Q

what is pegloticase

A

uricase that is attached to methods polyethylene glycol that converts uric acid to allotoin

used in refractory gout

can cause infusion reactions

26
Q

what is rasburicase

A

a uricase that is cont conjugated to polyethylene that converts uric acid to allantoin

used to prevent uric acid neuropathy in lymphoma and tumor lysis syndrome

27
Q

what are the probenecid and sulfinpyrazone

A

organic acids that act in the renal tubule to block urate reabsorption (URAT1) than urate secretion

increases the fractional excretion of urate (pee out more)

only used in underexcreters of uric acid and the GFR must be greater than 60 with no stones

can cause stones and contains sulfur

low dose aspirin( increased reabsorption)