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Osteoporosis
An Inpatient Topic?
July 2006
Background
 The problem
 Osteoporosis is common
 Over 50% of women and 30-45% of men over age 50
have osteopenia/osteoporosis
 White woman over age 50: 50 % lifetime risk of
osteoporotic fracture, 25% risk vertebral fracture, 15%
risk of hip fracture
 Man over age 60 has 25% risk osteoporotic fracture
 70% over age 80 have osteoporosis
Background
 Hip fractures are bad
 20% patients with hip fracture die within the year
 25-30% need placement in skilled nursing facility
Why is this an inpatient topic?
 Older patients have frequent admissions and increased length
of stay, increasing possible points of contact
 Patients from nursing facilities, those at greatest risk, may
have little continuity
 Discharge medications for patients going to skilled nursing
facilities can have LARGE impact
 Study: Only 6% of patients admitted with hip fracture to a
tertiary care hospital were adequately treated for osteoporosis
at discharge, only 12% at 5 years!
 Another study: only 21% medicare beneficiaries with hip
fracture had any prescription treatment; patients older than 74
and those with other comorbidities were least likely to receive
treatment
What is Osteoporosis?
 Loss in total mineralized bone
 Disruption of normal balance of bone breakdown
and build up
 Osteoclasts: bone resorption, stimulated by PTH
 Calcitonin: inhibits osteoclastic bone resorption
 Major mechanisms:
 Slow down of bone build up: osteoporosis seen in older
women and men (men after age 70)
 Accelerated bone breakdown: postmenopausal
 Normal loss .5% per year after peak in 20s
 Up to 5% loss/year during first 5 years after menopause
Defining Osteoporosis
 “systemic skeletal disease characterized by
low bone mass and microarchitectural
deterioration of bone tissue, leading to
enhanced bone fragility and a consequent
increase in fracture risk”
 True Definition: bone with lower density and
higher fracture risk
 WHO: utilizes Bone Mineral Density as
definition (T score <-2.5); surrogate marker
Who Gets Osteoporosis?
 Age
 Estrogen deficiency
 Testosterone deficiency
 Family history/genetics
 Female sex
 Low calcium/vitamin D intake
 Poor exercise
 Smoking
 Alcohol
 Low body weight/anorexia
 Hyperthyroidism
 Hyperparathyroidism
 Prednisone use
 Liver and renal disease (think about vit d synthesis)
 Low sun exposure
 Medications (antiepileptics, heparin)
 Malignancies (metastatic disease; multiple myeloma can present as osteopenia!)
 Hemiplegia s/p CVA/ immobility
Diagnosing Osteoporosis
 Outcome of interest: Fracture Risk!
 Outcome measured (surrogate): BMD
 Key: Older women at higher risk of fracture than younger
women with SAME BMD!
 Other factors: risk of falling, bone fragility not all related
to BMD
 Osteoporosis: disease of bone that increases risk of
fracture; more than BMD goes into causing a fracture;
BMD is important, but in reducing fractures must also
consider falls risk, age and other factors!!!
Diagnosing Osteoporosis
 Laboratory Data
 Limited value in diagnosis
 Markers of bone turnover (telopeptide) more useful in
monitoring effects of treatment than in diagnosis
 Helpful to exclude secondary causes
 Hyperthyroidism
 Hyperparathyroidism
 Estrogen or testosterone deficiency
 Malignancy
 Multiple myeloma
 Calcium/Vitamin D deficiency
Methods to evaluate for osteoporosis
 Quantitative Ultrasonography
 Quantitative computed tomography
 Dual Energy X-ray Absorptiometry (DEXA)
 ?”gold standard”
 Measurements vary by site
 Heel and forearm: easy but less reliable (outcome of
interest is fracture of vertebra or hip!)
 Hip site: best correlation with future risk hip fracture
 Vertebral spine: predict vertebral fractures; risk of falsely
HIGH scores if underlying OA/osteophytes
How to interpret the BMD
 T score: standard deviation of the BMD from the average sex
matched 35-year-old
 Z score: less used; standard deviation score compared to age
matched controls
 WHO: Osteoporosis: T score <-2.5
 Osteopenia: T score -1 - -2.5
 For every 1 decrease in T score, double risk of fracture
 1 SD decrease in BMD = 14 year increase in age for
predicting hip fracture risk
 Regardless of BMD, patients with prior osteoporotic fracture
have up to 5 times risk of future fracture!
Fracture Reduction
 Goal: prevent fracture, not just treat BMD
 Osteoporosis treatment options
 Calcium and vitamin D
 Calcitonin
 Bisphosphonates
 Estrogen replacement
 Selective Estrogen Receptor Modulators
 Parathyroid Hormone
Osteoporosis Treatment: Calcium and
Vitamin D
 Fewer than half adults take recommended amounts
 Higher risk: malabsorption, renal disease, liver
disease
 Calcium and vit D supplementation shown to
decrease risk of hip fracture in older adults
 1000 mg/day standard; 1500 mg/day in
postmenopausal women/osteoporosis
 Vitamin D (25 and 1,25): 400 IU day at least;
 Frail older patients with limited sun exposure may need
up to 800 IU/day
Osteoporosis Treatment: Calcitonin
 Likely not as effective as bisphosphonates
 200 IU nasally/day (alternating nares)
 Decrease pain with acute vertebral
compression fracture
Osteoporosis Treatment:
Bisphosphonates
 Decrease bone resorption
 Multiple studies demonstrate decrease in hip and
vertebral fractures
 Alendronate, risodronate
 IV: pamidronate, zolendronate (usually used for
hypercalcemia of malignancy, malignancy related
fractures, and multiple myeloma related osteopenia)
 Ibandronate (boniva): once/month
 Those at highest risk of fracture (pre-existing
vertebral fractures) had greatest benefit with
treatment
Bisphosphonate Associated
Osteonecrosis (BON)
 Jaw osteonecrosis
 Underlying significant dental disease
 Usually associated with IV formulations
 Case reports associated with oral formulations
Bisphosphonates: Contraindications
 Renal failure
 Esophageal erosions
 GERD, benign strictures, most benign GI
problems are NOT a contraindication
 Concern for esophageal irritation/erosions from
direct irritation, recommendations to drink water
after and not lie down at least 30 minutes
 Reality: no increased GI side effects compared to
placebo group in multiple studies
Osteoporosis Treatment: Estrogen
Replacement
 Reduction in bone resorption
 Proven benefits in treatment
 FDA approval, now limited because of recent
concerns from HERS trial and other data
suggesting possible increased total risks with
HRT (?increased cardiac risk, increased risk
VTE, increased risk cancer)
Osteoporosis Treatment: Selective
Estrogen Receptor Modulators
 Raloxifene
 FDA recommended
 Decrease bone resorption like estrogen
 No increased risk cancer (decrease risk breast
cancer)
 Increase in vasomotor symptoms associated
with menopause
Osteoporosis Treatment: PTH
 Teriparatide
 Why PTH when well known association with
hyperparathyroidism and osteoporosis???
 INTERMITTENT PTH: overall improvement in
bone density
 Optimal bone strength relies upon balance between bone
breakdown and bone build up; studies with increased
density but increased fracture risk/fragility with flouride
show that just building up bone is not enough!!!
Intermittent PTH: Teriparatide
 Studies suggest improved BMD and decreased
fractures
 ?risk osteosarcoma with prolonged use (over 2
years): studies with rats
 SQ, expensive
 Option for severe osteoporosis, those on
bisphophonates for 7-10 years, those who can not
tolerate oral bisphosphonate
 Optimal effect requires bone uptake
 Not for use in combination with Bisphosphonate!
 May need to stop bisphosphonate up to 1 year prior
Reducing Fractures
 1. Decrease osteoporosis/improve BMD
 2. Decrease risk of break: hip protectors
 3. Decrease risk of fall
Hip Protectors
 Padding that fits under clothing
 Multiple studies demonstrate effectiveness at
preventing hip fractures
 Likely cost effective
 Problem: adherence!
Falls Reduction
 Falls are a marker of frailty
 Hip fracture is a marker of frailty
 Mortality after hip fracture:?due to hip fracture or hip fracture as
marker for those who are declining?
 Increased risk of falls:
 Prior fall (fear of falling)
 Cognitive decline
 Loss of vision
 Peripheral neuropathy
 Weakness
 Stroke
 Medications: anticholinergics, tcas, benzos…
 ETOH
Current Guidelines
 US Preventive Task Force
 Test Bone Mineral Density in all women over age
65, younger postmenopausal women with at least
one risk factor, and postmenopausal women with
a history of fracture
 Treat patients with T score <-2 and no risk
factors, T score <1.5 if any risk factors, and
anyone with prior vertebral/hip fracture
Who is left out?
 Older men
 Not included in recommendations
 Screening not recommended or paid for
 Significant problem, risk of osteoporosis, risk of
fracture, especially after age 70, even more so
after age 80
 Significant evidence that men with osteoporosis
benefit from treatment

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Osteoporosis Nutriforce Training HIMAGIKA

  • 2. Background  The problem  Osteoporosis is common  Over 50% of women and 30-45% of men over age 50 have osteopenia/osteoporosis  White woman over age 50: 50 % lifetime risk of osteoporotic fracture, 25% risk vertebral fracture, 15% risk of hip fracture  Man over age 60 has 25% risk osteoporotic fracture  70% over age 80 have osteoporosis
  • 3. Background  Hip fractures are bad  20% patients with hip fracture die within the year  25-30% need placement in skilled nursing facility
  • 4. Why is this an inpatient topic?  Older patients have frequent admissions and increased length of stay, increasing possible points of contact  Patients from nursing facilities, those at greatest risk, may have little continuity  Discharge medications for patients going to skilled nursing facilities can have LARGE impact  Study: Only 6% of patients admitted with hip fracture to a tertiary care hospital were adequately treated for osteoporosis at discharge, only 12% at 5 years!  Another study: only 21% medicare beneficiaries with hip fracture had any prescription treatment; patients older than 74 and those with other comorbidities were least likely to receive treatment
  • 5. What is Osteoporosis?  Loss in total mineralized bone  Disruption of normal balance of bone breakdown and build up  Osteoclasts: bone resorption, stimulated by PTH  Calcitonin: inhibits osteoclastic bone resorption  Major mechanisms:  Slow down of bone build up: osteoporosis seen in older women and men (men after age 70)  Accelerated bone breakdown: postmenopausal  Normal loss .5% per year after peak in 20s  Up to 5% loss/year during first 5 years after menopause
  • 6. Defining Osteoporosis  “systemic skeletal disease characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to enhanced bone fragility and a consequent increase in fracture risk”  True Definition: bone with lower density and higher fracture risk  WHO: utilizes Bone Mineral Density as definition (T score <-2.5); surrogate marker
  • 7. Who Gets Osteoporosis?  Age  Estrogen deficiency  Testosterone deficiency  Family history/genetics  Female sex  Low calcium/vitamin D intake  Poor exercise  Smoking  Alcohol  Low body weight/anorexia  Hyperthyroidism  Hyperparathyroidism  Prednisone use  Liver and renal disease (think about vit d synthesis)  Low sun exposure  Medications (antiepileptics, heparin)  Malignancies (metastatic disease; multiple myeloma can present as osteopenia!)  Hemiplegia s/p CVA/ immobility
  • 8. Diagnosing Osteoporosis  Outcome of interest: Fracture Risk!  Outcome measured (surrogate): BMD  Key: Older women at higher risk of fracture than younger women with SAME BMD!  Other factors: risk of falling, bone fragility not all related to BMD  Osteoporosis: disease of bone that increases risk of fracture; more than BMD goes into causing a fracture; BMD is important, but in reducing fractures must also consider falls risk, age and other factors!!!
  • 9. Diagnosing Osteoporosis  Laboratory Data  Limited value in diagnosis  Markers of bone turnover (telopeptide) more useful in monitoring effects of treatment than in diagnosis  Helpful to exclude secondary causes  Hyperthyroidism  Hyperparathyroidism  Estrogen or testosterone deficiency  Malignancy  Multiple myeloma  Calcium/Vitamin D deficiency
  • 10. Methods to evaluate for osteoporosis  Quantitative Ultrasonography  Quantitative computed tomography  Dual Energy X-ray Absorptiometry (DEXA)  ?”gold standard”  Measurements vary by site  Heel and forearm: easy but less reliable (outcome of interest is fracture of vertebra or hip!)  Hip site: best correlation with future risk hip fracture  Vertebral spine: predict vertebral fractures; risk of falsely HIGH scores if underlying OA/osteophytes
  • 11. How to interpret the BMD  T score: standard deviation of the BMD from the average sex matched 35-year-old  Z score: less used; standard deviation score compared to age matched controls  WHO: Osteoporosis: T score <-2.5  Osteopenia: T score -1 - -2.5  For every 1 decrease in T score, double risk of fracture  1 SD decrease in BMD = 14 year increase in age for predicting hip fracture risk  Regardless of BMD, patients with prior osteoporotic fracture have up to 5 times risk of future fracture!
  • 12. Fracture Reduction  Goal: prevent fracture, not just treat BMD  Osteoporosis treatment options  Calcium and vitamin D  Calcitonin  Bisphosphonates  Estrogen replacement  Selective Estrogen Receptor Modulators  Parathyroid Hormone
  • 13. Osteoporosis Treatment: Calcium and Vitamin D  Fewer than half adults take recommended amounts  Higher risk: malabsorption, renal disease, liver disease  Calcium and vit D supplementation shown to decrease risk of hip fracture in older adults  1000 mg/day standard; 1500 mg/day in postmenopausal women/osteoporosis  Vitamin D (25 and 1,25): 400 IU day at least;  Frail older patients with limited sun exposure may need up to 800 IU/day
  • 14. Osteoporosis Treatment: Calcitonin  Likely not as effective as bisphosphonates  200 IU nasally/day (alternating nares)  Decrease pain with acute vertebral compression fracture
  • 15. Osteoporosis Treatment: Bisphosphonates  Decrease bone resorption  Multiple studies demonstrate decrease in hip and vertebral fractures  Alendronate, risodronate  IV: pamidronate, zolendronate (usually used for hypercalcemia of malignancy, malignancy related fractures, and multiple myeloma related osteopenia)  Ibandronate (boniva): once/month  Those at highest risk of fracture (pre-existing vertebral fractures) had greatest benefit with treatment
  • 16. Bisphosphonate Associated Osteonecrosis (BON)  Jaw osteonecrosis  Underlying significant dental disease  Usually associated with IV formulations  Case reports associated with oral formulations
  • 17. Bisphosphonates: Contraindications  Renal failure  Esophageal erosions  GERD, benign strictures, most benign GI problems are NOT a contraindication  Concern for esophageal irritation/erosions from direct irritation, recommendations to drink water after and not lie down at least 30 minutes  Reality: no increased GI side effects compared to placebo group in multiple studies
  • 18. Osteoporosis Treatment: Estrogen Replacement  Reduction in bone resorption  Proven benefits in treatment  FDA approval, now limited because of recent concerns from HERS trial and other data suggesting possible increased total risks with HRT (?increased cardiac risk, increased risk VTE, increased risk cancer)
  • 19. Osteoporosis Treatment: Selective Estrogen Receptor Modulators  Raloxifene  FDA recommended  Decrease bone resorption like estrogen  No increased risk cancer (decrease risk breast cancer)  Increase in vasomotor symptoms associated with menopause
  • 20. Osteoporosis Treatment: PTH  Teriparatide  Why PTH when well known association with hyperparathyroidism and osteoporosis???  INTERMITTENT PTH: overall improvement in bone density  Optimal bone strength relies upon balance between bone breakdown and bone build up; studies with increased density but increased fracture risk/fragility with flouride show that just building up bone is not enough!!!
  • 21. Intermittent PTH: Teriparatide  Studies suggest improved BMD and decreased fractures  ?risk osteosarcoma with prolonged use (over 2 years): studies with rats  SQ, expensive  Option for severe osteoporosis, those on bisphophonates for 7-10 years, those who can not tolerate oral bisphosphonate  Optimal effect requires bone uptake  Not for use in combination with Bisphosphonate!  May need to stop bisphosphonate up to 1 year prior
  • 22. Reducing Fractures  1. Decrease osteoporosis/improve BMD  2. Decrease risk of break: hip protectors  3. Decrease risk of fall
  • 23. Hip Protectors  Padding that fits under clothing  Multiple studies demonstrate effectiveness at preventing hip fractures  Likely cost effective  Problem: adherence!
  • 24. Falls Reduction  Falls are a marker of frailty  Hip fracture is a marker of frailty  Mortality after hip fracture:?due to hip fracture or hip fracture as marker for those who are declining?  Increased risk of falls:  Prior fall (fear of falling)  Cognitive decline  Loss of vision  Peripheral neuropathy  Weakness  Stroke  Medications: anticholinergics, tcas, benzos…  ETOH
  • 25. Current Guidelines  US Preventive Task Force  Test Bone Mineral Density in all women over age 65, younger postmenopausal women with at least one risk factor, and postmenopausal women with a history of fracture  Treat patients with T score <-2 and no risk factors, T score <1.5 if any risk factors, and anyone with prior vertebral/hip fracture
  • 26. Who is left out?  Older men  Not included in recommendations  Screening not recommended or paid for  Significant problem, risk of osteoporosis, risk of fracture, especially after age 70, even more so after age 80  Significant evidence that men with osteoporosis benefit from treatment