ic18 osteoporosis Flashcards

1
Q

what is “osteoporosis”

A

a metabolic bone disease characterised by
i) low bone density
ii) microarchitecture disruption (impaired mineralisation)
iii) decr bone strength
iv) incr risk of fractures

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2
Q

what are possible causes of decreased bone mass (which are the most common)

A
  1. age *most common
  2. menopause *most common
  3. low serum Ca (malnutrition)
  4. alchol consumption (alcohol leads to incr RANKL which incr bone resorption and (ii) incr oxidative stress which results in osteoblast apoptosis
  5. smoking
  6. physical inactivity
  7. medication use (glucocorticoids, immunosuppressants like cyclosporin, ASM like PB and PHT, GnRH antagonists and agonists, heparin, cancer chemotx, aromatase inhibitors)
  8. secondary to other diseases (endocrine - hyperPTH, hyperT, DM; GI - celiac, alcohol related liver disease, chronic active hepatitis, IBD, vitD/Ca deficiency)
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3
Q

what are the clinical manifestations of osteoporosis

A

i) asymptomatic
ii) often undiagnosed until presented with fragility fracture
iii) fractures may then give rise to pain and disability

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4
Q

what are the types of fragility fractures

A
  1. spine (vertebral compression)
    i) result in height loss and kyphosis (exaggerated forward rounding of the upper back)
  2. hip
    i) neck of femur
    ii) intertrochenteric
  3. wrist
    i) colles
  4. humerus
  5. pelvis
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5
Q

what are the risk factors of osteoporosis

A

i) postmenopausal women
ii) men 65yo and above
iii) ageing
iv) family hx of osteoporosis or fragility frac
v) prev fragility frac
vi) hx of falls
vii) low Ca intake (<500mg/d)
viii) excessive alcohol consumption (>2u/d)
ix) low body weight
x) height loss (>2cm within 3yr)
xi) drugs
xii) medical conditions that can decr bone density or incr frac risk
xiii) prolonged immobility
xiv) smoking
xv) early menopause (,45yo)

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6
Q

what tool can be used to screen bone mineral density (elaborate on the scoring and whether any further investigations should be done)

A

osteoporosis self assessment tool for asians (OSTA) to detect a woman’s osteoporosis risk

high risk if >20 (consider DXA scan bc likelihood of finding osteoporosis is high)
medium risk if 0-20 (consider DXA scan if any other risk factors present)
low risk if <0 (defer DXA)

OSTA score = age in yrs - weight in kg

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7
Q

how is osteoporosis diagnosed

A
  1. through hx of fragility fracture
    i) at vertebral, hip, wrist, pelvic, humerus, rib
    ii) occur spontaneously or from a minor trauma
    iii) asymptomatic vertebral fracture can be visually identified as >20% decr in vertebral height
  2. BMD measurement
    i) done using dual-energy xray absorptiometry (DXA) of hip and/or spine
    ii) T score </= -2.5SD indicates osteoporosis; T score -1 to -2.5SD indicates osteopenia (conduct FRAX); T score >/=-1SD indicates normal bone density
  3. fracture risk assessment tool (FRAX)
    i) to be conducted for pts whose T score from BMD measurement reflects osteopenia
    ii) consider starting tx if 10yr probability is high for major osteoporotic fracture (>/=20%) or hip fracture (>/=3%)
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8
Q

differentiate between T score and D score (what D score to note of)

A

T score compares BMD against a young adult ref pop (20yo) while Z score compares BMD against the expected BMD for the pt’s age and sex

Z score of >/= -2SD suggests coexisting problems eg. glucocorticoid tx or alcoholism that can contribute to osteoporosis

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9
Q

differentiate between the two types of DXA

A

DXA scans generates scores for two locations (hip and spine), typically consider the worse number

hip BMD is q predictive for hip fracture vs spine BMD can be useful in assessing response to tx

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10
Q

how can we identify secondary causes of osteoporosis

A

look at clinical hx, physical exam and labs

most common labs incl:
i) Cr (determines baseline renal func which can influence agent selected and may also indicate any presence of CKD-MBD)
ii) FBC (show malignancies and malabsorption)
iii) corrected Ca (incr levels of corrected Ca indicate primary hyperPTH or malignancy, decr levels can indicate malabsorption or vitD deficiency)
iv) vitD (determine baseline level, aim for >20mg/mL)

*corrected Ca is an estimate of total Ca conc had albumin func been normal (bc serum albumin level decr w age)
(corrected calcium = serum calcium + 0.8 (4 - serum albumin))

other labs incl:
i) TSH (decr levels of TSH may indicate hyperT or over replacement w thyroxine)
ii) ESR (very high ESR might indicate rheumatological diseases)
iii) alkaline phosphate (incr levels may indicate liver disease, paget’s disease, recent frac or other bone pathology)
iv) serum phosphate (abnormal levels may indicate vitD deficiency or renal phosphate wasting)
v) spot urine Ca/ creatinine ratio (if elevated can indicate idiopathic hyperCa)
vi) serum total testosterone (decr levels can indicate hypogonadism)

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11
Q

what are the clinical risk factors in FRAX

A

i) age
ii) sex
iii) weight in kg
iv) height in cm
v) prev frac
vi) parent frac
vii) current smoking
viii) glucocorticoids
ix) rheumatoid arthritis
x) secondary osteoporosis (T1DM, osteogenesis imperfecta in adults, long standing untreated hyperT, hypogonadism or premature menopause (<45yo), chronic malnutrition, malabsorption, chronic liver disease)
xi) alcohol >3u/d
xii) BMD

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12
Q

what are the tx for osteoporosis

A
  1. lifestyle and diet
    i) exercise (weight bearing for 30mins daily, muscle strengthening and balance 2-3x/w eg. walking, elastic band exercises, taichi)
    ii) Ca
    iii) vitD
    iv) smoking cessation and appropriate alcohol intake (<2u/d)
    v) educate on fall risk, home safety through fall prevention strategies, types of footwear to reduce risks of falls
    (pt specific interventions like for impaired vision/ cataract, footwear, home modifications, medication review)
  2. antiresorptive agents
    i) bisphosphonates (alendronate, risedronate, zoledronic acid)
    ii) RANKL inhibitors (denosumab)
    iii) estrogen (raloxifene)
    iv) calcitonin (calcitonin)
  3. anabolic agents
    i) PTH analogue (teriparatide)
    ii) sclerostin inhibitor (romosozumab)
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13
Q

what is the target of Ca intake and when should supplementation be considered, also consider types of food with high Ca level and ddi of Ca

A

Ca target: 1000mg/d for healthy adults 51yo and above, 800mg/d for 19-50yo

benefit: slight incr in BMD

ddi:
i) PPI
ii) fiber
iii) bisphosphonates
iv) Fe
v) FQ, tetracyclines
vi) thyroid suppl
(i and ii decr Ca absorption; Ca decr acsorption of iii to vi)

supplementation given: when dietary Ca intake <700mg/d

DIETARY Ca INTAKE
i) milk (diary or non diary) 240mL = 300mg
ii) orange juice 240ml = 300mg
iii) yogurt 138g = 250mg
iv) tofu 0.5cup = 435mg
v) ice cream/ frozen yogurt 0.5cup = 100mg
vi) beans 0.5cup = 60-80mg
vii) green leafy vege cooked 0.5cup = 50-135mg
viii) orange = 60mg
ix) almonds 24pcs = 70mg
x) cottage cheese 0.5cup = 130mg
xi) cheese 28g = 195-335 (hard cheese = higher Ca)

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14
Q

what is the target of vitD intake and when should supplementation be considered, also consider ddi of vitD

A

target vitD: 600IU/d for 51-70yo, 800IU/d for >70

benefit: reduces falls and confers small reduction in fracture when combined with Ca suppl

ddi: rifampicin, ASM, cholestyramine, orlistat, Al containing product
(orlistat binds to fats and since vitD is fat soluble it will bind to vitD)

fdi: take after or w/o food (bc vitD is fat soluble)

supplementation: 800IU/d cholecalciferol to those at risk or has vitD insufficiency

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15
Q

what are the medications that can incr risk of falls and why

A

medications below are sedating/ has drowsiness s/e thus can incr risk of falls

i) benzodiazepines
ii) psychotropics
iii) some antidepressants
iv) first gen antihistamine
v) anarex
vi) codeine

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16
Q

list the agents that can be used for management of osteoporosis (drug, route, class, adminstration, c/i, s/e and any other considerations)

A

BISPHOSPHONATES
1. PO alendronate
dose: 70mg q1w
administration: take 30mins to 1hr before breakfast, remain upright for at least 30mins after
c/i: CrCl <30, hypoCa, esophageal or gastric abnormalities, aspiration risk, inability to remain upright
s/e: ONJ, AFF
tx duration and other considerations: for low risk 5yrs, for high risk 10yrs, BMD repeated q2yr so consider restarting if decr >4-5%, ensure adequate Ca intake during tx
*first line

  1. PO risedronate
    dose: 35mg q1w
    administration, c/i, s/e and tx duration and other considerations same as PO alendronate
    *first line
  2. PO ibandronate
    dose: 150mg q1m
    administration, c/i, s/e and tx duration and other considerations same as PO alendronate
    *first line
  3. IV zoledronic acid
    dose: 5mg q1yr as a 30min infusion
    c/i: CrCl <35, hypoCa
    s/e: ONJ, AFF
    tx duration and other considerations: for low risk 3yr, for high risk 6yr, BMD repeated q2yr so consider restarting if decr >4-5%, ensure adequate Ca intake during tx
    *second line bc PO first line

RANKL INHIBITORS
1. SQ denosumab
dose: q6m
c/i: hypoCa
s/e: ONJ, AFF
other considerations: ensure adequate Ca intake during tx

SELECTIVE ESTROGEN RECEPTOR MODULATOR
1. PO raloxifene
dose: 60mg QD
c/i: hx or current VTE, CrCl <30, hepatic impairment
s/e: incr risk of VTE and stroke
other considerations: rarely used, mostly for women with no hot flushes but if have likely use HRT

PTH ANALOGUE
1. SQ teriparatide
dose: 20µg QD
c/i: CrCl <30, paget’s disease, hx of bone radiation, hyperCa
s/e: postural hypotension
tx duration: <2yr

SCLEROSTIN INHIBITOR
1. SQ romosozumab
dose: q1m
c/i: hx of CVS event (stroke, MI)
s/e: incr risk of MI, stroke and CVS death, ONJ, AFF
tx duration and other considerations: 1yr, $$$$$$$, ensure adequate Ca during tx

17
Q

what is the monitoring like for tx of osteoporosis

A
  1. tx review
    i) PO 5yrs
    ii) IV 3yrs
    iii) BMD repeated q2yr
  2. consider stopping tx at 5yr
    i) continue repeating BMD q2yr
  3. restart until 10yr
    i) if BMD found to have decr by >4-5%
18
Q

what should be checked before initiating tx

A
  1. serum Ca level
  2. serum vitD levels:
    >20-30ng/mL (50-75nmol/L) but <50-100ng/mL (125-250nmol/L)

if insufficient, give Ca and vidD supplementation bc bisphosphonates will cause Ca to decr so if low vitD then pt would not be able to adequately intake Ca

19
Q

what to monitor during tx

A
  1. SCr (bisphosphonates req renal adjustments thus measure SCr to calc CrCl to ensure not c/i)
  2. serum Ca (to ensure not hypoCa)
  3. serum vitD
20
Q

what are the two biggest safety concerns of bisphosphonates

A
  1. osteonecrosis of the jaw (ONJ)
    RISK FACTORS
    i) tooth extraction or other invasive dental procedures
    ii) hx of cancer or radiotherapy
    iii) poor oral hygiene
    iv) concom therapy w angiogenesis inhibitors, bisphosphonates, chemotx, corticosteroids, denosumab)
    v) comorbid disorders eg. anemia, coagulopathy, infection, preexisting dental or peridontal disease

ADVICE TO PT
i) smoking cessation
ii) avoid invasive dental procedures during bisphosphonate tx
iii) maintain good oral hygiene (brush teeth well, floss twice daily, avoid high carogenic foods)

  1. atypical femoral fracture (AFF)
    i) discontinue bisphosphonates bc if continue then there will be a risk of delaying fracture healing

CASE1: if pt presents w fragility fracture then should start tx w bisphosphonates but wait approx 2w after frac (when pt somewhat healed and able to sit) bc also cannot wait until fully healed bc what if too long

CASE2: if pt is on bisphosphonate then fragility frac occur, identify underlying reasons causing this fracture or cause the bisphosphonate to not be working