Module 8: Unic C OSA Flashcards
Example Bisphosphonates
-NATE
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
Indications:
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
Prevention and treatment of osteoporosis in postmenopausal women
Treatment of osteoporosis in men
Prevention and treatment of glucocorticoid-induced osteoporosis (GIOP)
MOA:
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
They are absorbed and integrated into the bone, causing suppression of resorption of bone by inhibiting osteoclast activity (and ↓ # of osteoclasts). Recruits osteoblasts which in turn inhibit osteoclast formation.
Contraindications for Biophosophonates (-NATEs)
Hypersensitivity; hypocalcemia; abnormalities of the esophagus which slow or obstruct emptying; inability to stand or sit upright for at least 30 minutes; ↑ risk of aspiration
Adverse effects:
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
Esophagitis, atypical femoral fractures, small risk of esophageal CA, MSK pain, ↑ increased risk (slight and rare) of ocular problems, osteonecrosis of jaw, afib
Pt teaching with:
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
Take oral bisphosphonates in the morning with water and wait at least 30 minutes after dosing to eat (60 m w/ibandronate). Remain upright (seated or standing) at least 30 minutes after taking.
(Atelvia, a delayed-release form of risedronate, is the exception as it SHOULD be taken with food)
Do not take any products with Ca, Fe, or Mg within two hours of oral bisphosphonates (antacids, mineral supplements, MVI)
Monitoring with
alendronate (Fosamax)
ibandronate (Boniva)
risedronate (Actonel)
zoledronic acid (Reclast)
Obtain baseline DXA, accurate height (actually measured with a stadiometer), calcium, BMP or CMP (creatinine), and 25(OH)D.
Repeat DXA every 1-2 years. Monitor labs
Examples Selective estrogen receptor modulators (SERMs)
raloxifene (Evista)
Indication raloxifene (Evista)
Prevention and treatment of osteoporosis in postmenopausal women
Protection against estrogen receptor-positive breast CA
MOA raloxifene (Evista)
Exerts agonist/antagonist estrogenic effects, acting as an estrogen agonist in the bone to prevent bone loss and antagonist activity to ↓ estrogen effects in the breast and uterine tissues.
↓ bone resorption, ↑ bone mineral density, and ↓ fracture incidence.
Contraindications and SE/AE: raloxifene (Evista
Contraindications: Pregnancy, ↑ risk of fetal harm
↑ risk of thromboembolic events (DVT, PE, stroke)
weight gain
hot flashes
BBW raloxifene (Evista
Increased risk of VTE:
Increased risk of DVT and PE have been reported with raloxifene. Women with an active or past history of VTE should not take raloxifene.
Cardiovascular disease:
Increased risk of death due to stroke occurred in a trial in postmenopausal women with documented coronary heart disease or increased risk for major coronary events. Consider the risk-benefit balance in women at risk for stroke.
Special considerations raloxifene (Evista
D/c for at least 72 h before long periods of immobilization (surgery, bed rest, long-distance traveling)
Monoclonal antibody/Rank ligand inhibitors
Parathyroid hormone analogs examples
Teriparatide (Forteo)