• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/117

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

117 Cards in this Set

  • Front
  • Back
Osteoporosis
1. low bone mass and structural deterioration of bone tissue
2. leads to bone fragility
3. leads to increased fractures ( spine, hip, wrist)
Function of the Skeleton (Bone Physio)
1. structural support
2. protect organs
3. contains calcium and phosphorus stores
Types of Bone (Bone Physio)
1. Trabecular/cancellous (metabolic) - supplies minerals when deficient
2. Cortical (structural) - outer part of bone
Osteoblasts
responsible of bone formation
Osteoclasts
responsible for bone resorption
Types of Osteoporosis
1. Postmenopausal - decline in estrogen production
2. Age-Related(senile) - hormone, calcium and Vit D deficiencies
3. Secondary (drugs, diseases, other)
Clinical Presentation of Osteoporosis
SIGNS: shortened stature, fracture, humpback (kyphosis) or hollow back/saddle back (lordosis)

SYMPTOMS: pain, immobility
Non-modifiable Risk Factors for Osteoporosis
1. Family history of disease in 1st degree relative
2. Family history of fracture in 1st degree relative
3. age at menarch and menopause
Lifestyle Risk Factors for Osteoporosis
1. low calcium intake
2. inadequate physical activity
3. thinness
4. vitamin D deficiency
5. smoking
6. high caffeine intake
7. alcohol (>3 drinks/day)
8. falling
9. high salt intake
Diseases that are Risk Factors for Osteoporosis
1. rheumatoid arthritis
2. prior fracture
3. hyperparathyroidism
4. hypogonadism
5. inflammatory bowel disease
6. epilepsy
7. alcoholism
8. diabetes
Medications that are Risk Factors for Osteoporosis
1. glucocorticoids (>5mg/d of prednisone for >3 months)
2. cyclosporine
3. chemo
4. anticonvulsants
5. depo-medroxy
6. drugs that alter calcium absorption or elimination
Bone Mineral Density Test (BMD)
The LOWER the BMD, the HIGHER the fracture risk
Gold standard for measuring BMD for diagnosis and monitoring
Central Dual X-Ray Absorptiometry (DXA)
Bone Density Value is measured as
g/cm^2
T-score
value that represents the patient's BMD compared to the peak/optimal bone density for a young adult of the same sex
Normal T-score
at -1 or above
T-score for osteopenia (low bone mass)
-2.5 to -1
T-score for osteoporosis
-2.5 or below
Severe or established osteoporosis
<-2.5 and a history of fracture
Z-Score
value that represents the patients BMD compared to what is expected for someone with the same age and sex
Deficient in Vitamin D
<20 ng/ml
Insufficient in Vitamin D
21-29 ng/ml
Normal Vitamin D
>30 ng/ml
if you are given multiple T-scores (1 from spine, L & R hip, L & R femoral neck), which one do you take
take the worst score (the most negative)
Goals of Treatment for Osteoporosis
1. Birth - 30yrs = obtain highest bone bass possible and optimize bone quality
2. >30 yrs - maintain BMD, minimize bone loss, prevent falls/fractures
3. with fractures = control pain, restore independence and quality of life, prevent further fractures
Non-Pharm Treatment for Osteoporosis
1. Adequate Calcium and Vitamine D Intake
2. Exercise - weight bearing and muscle strengthening
3. Fall prevention (exercise, cane, walker, meds)
4. Good Habits - smoking cessation, limit alcohol, reduce caffeine/soda intake
Daily requirements for adults over 50 years old
CALCIUM: 1200mg

VITAMIN D: 800-1000 IU
Foods that contain calcium
1. milk (x300)
2. yogurt (x300)
3. cheese (x200)
4. collard greens (178)
5. broccoli (100-180)
6. soy beans (88-130)
7. tofu (253)
Pharmacological Treatment Options for Osteoporosis
1. Calcium/Vitamin D
2. Bisphosphonates
3. Estrogen agonists/antagonists
4. Calcitonin
5. Denosumab
6. Hormone Therapy
7. Parathyroid Hormone
Calcium Carbonate
MOA: increase/maintain BMD

1. limit single dose to 600mg elemental Ca
2.Take with food
3. preferred form of calcium - least expensive, fewest number of tablets
Calcium Citrate
MOA: increase/maintain BMD

1. take with or without food
Drug Interactions with Calcium Supplements
1. Iron
2. Quinolone
3. Tetracycline
4. Levothyroxine
Side Effects of Calcium Supplements
constipation, gas, stomach upset
Vitamin D Supplement
MOA: maximizes Ca absorption

1. Cholecalciferol (D3) - preferred - OTC
2. Ergocalciferol (D2) - OTC and RX
MOA of Bisphosphonates
1. decrease osteoclast activity
2. increase/maintain BMD
3. reduce fracture risks
Bisphosphonates
1. Alendronate (Fosamax)
2. Risedronate (Actonel)
3. Ibandronate (Boniva)
4. Zoledronic Acid (Reclast)
Gold Standard for treating Osteoporosis
Bisphosphonates
Which bisphos doesn't decrease his fractures
ibandronate (boniva)
Administration of Alendronate and Risedronate
1. take 1st thing in morning, at least 30 minutes prior to food, drink, or other meds
2. take tablet with at least 8oz of plain water
3. remain sitting or standing for at least 30 minutes
Common ADRs of Bisphosphonates
1. abdominal pain, dyspepsia, nausea (ORAL)
2. fever, flu-like symptoms, injection site reactions (IV)
Alendronate (Fosamax)
1. 10mg PO daily
2. 70mg PO weekly
Risedronate (Actonel)
1. 5mg PO daily
2. 35mg PO weekly
3. 35mg PO weekly EC
4. 75mg PO x2 consecutive days per month
5. 150mg PO monthly
Ibandronate (Boniva)
1. 150mg PO monthly
2. 2.5mg PO daily
3. 3mg IV push q3months

**must check before each dose: serum Ca, SCr, Vit D
Administration of Oral Ibandronate
1. separate from food, drink, other meds by at least 60 minutes
2. remain sitting or standing for at least 60 minutes
Missed a dose of oral bisphosphonates
DAILY: take next thing, 1st thing in morning

WEEKLY: take next day - >1day elapsed, skip week

MONTHLY: same date each month
Zoledronic Acid (Reclast)
1. 5mg IV once a year
2. check creatinine before each dose
3. SIDE EFFECTS: fever, headache, muscle/joint pain, flu-like symptoms, fatigue
*pretreat with APAP*
Advantages of IV bisphos treatment
1. less risk of GI ADRs
2. improved bioavailability
3. increased adherence
4. good if patient cant stay sitting or standing for 30-60 minutes
Reasons to not use Bisphosphonates
1. hypocalcemia
2. CrCl < 35
3. upcoming dental work
4. risk of atypical fractures
5. severe GERD
Mixed Estrogen Agonists/Antagonists
1. Raloxifene (Evista)
2. Calcitonin (Fortical, Miacalcin)
Raloxifene (Evista)
MOA: estrogen agonist on bone, but antagonist on breast/uterus, decreases vertebral fractures, increases spine/hip BMD

DOSE: 60mg PO daily

ADRs: hot flashes, flu-like symptoms, peripheral edema, leg cramps
Major ADR for Raloxifene
Increased risk of Thromboembolic Disease (3-fold)
*do not take if immobilized
Clinical Pearls of Raloxifene (Evista)
1. less potent than bisphosphonates
2. decreases LDL and total cholesterol levels
3. no increased risk of breast or endometrial cancer
Calcitonin (Fortical, Miacalcin)
MOA: decreases vertebral fractures (intranasal form)

DOSE: 200mcg intranasally daily or 50-100mcg SC or IM daily

*Intranasal- last line
Denosumab (Prolia)
MOA: inhibits osteoclastogenesis and increases osteoclast apoptosis

IND: postmenopausal osteoporosis &osteoporosis in men with high risk of fractures

DOSE: 60mg SUBQ once every 6 months plus calcium and Vit D

ADRs: eczema and cellulitis
Clinical Pearls of Denosumab (Prolia)
1. correct hypocalcemia first
2. monitor Ca levels
3. no dosage adjustment in renal impairment
Teriparatide (Forteo)
*Recombinant Parathyroid Hormone*

MOA: increases bone formation and osteoblast activity

IND: treat osteoporosis for up to 2 years, reserved for patients with severe osteoporosis at highest risk of fractures who cant take bisphos

DOSE: 20mcg SC daily into thigh or abdomen
Contraindications for Teriparatide (Forteo)
1. hypercalcemia
2. history of bone cancer
3. history of cancer that has metastasized to the bone
4. Radiation to skeleton
Clinical Pearls for Teriparatide (Forteo)
1. most expensive
2. decreases vertebral fractures by up to 65%
3. caused osteosarcoma in rats when given high doses
4. don't know what happens after 2 years of therapy
Glucocorticoid-Induced Osteoporosis
1. drug class most commonly associated with secondary osteoporosis
2. greatest bone loss occurs in first 6-12 months of steroid therapy
MOA of Glucocorticoid-Induced Osteoporosis
decreased bone formation, increased bone resorption, decreased calcium absorption, increased calcium excretion, decreased estrogen and testosterone
Who is at risk for Glucocorticoid-Induced Osteoporosis
1. oral doses of prednisone >5mg (or equivalent)
2. Long term, high dose inhaled steroids
Management of Glucocorticoid-Induced Osteoporosis
1. Discontinue glucocorticoid
2. use lowest dose and shortest duration
3. check baseline BMD
4.ensure adequate daily Calcium and Vitamin D
5. Bisphosphonates are drug of choice!!!!
osteoarthritis
disease of localized joints associated with deterioration of cartilage and secondary changes in underlying bone
Pathophysiology for Osteoarthritis
1. cartilage water content increases
2. loss of proteoglycan
3. increase levels of protease enzymes
4. destruction of cartilage, structural changes in bone
CONSEQUENCES: pain, decreased functioning and mobility
Clinical Presentation of Osteoarthritis
1. PAIN - dull, aching
2. join stiffness (morning)
3. Inflammation
4. bony enlargements on fingers
5. loss of range of motion
6. joint tenderness
7. grating or crackling sound heard with joint movement
Risk factors for Osteoarthritis
1. obesity
2. repetitive joint stress, over use of joint
3. age (>50)
4. family history
5. Gender
Diagnosis of Osteoarthritis
1. Lab Findings (synovial fluid - clear/viscous, WBC and ESR - normal, RF negative)
Goals of Treatment for Osteoarthritis
1. relieve pain and joint stiffness
2. maintain &/or improve joint mobility
3. limit functional impairment
4. minimize ADRs
5. maintain or improve patient's QOL
6. educate
Non-Pharm Treatment of Osteoarthritis
1. Social Support services
2. weight loss
3. aerobic and muscle strengthening exercises
4. heat/cold therapy
5. PT or OT
6. surgery
7. assistive devices
Pharmalogical treatment of osteoarthritis
1. APAP
2. NSAIDS
3. COX-2 inhibitor
Tylenol for Osteoarthritis
1st line agent for mild-moderate pain due to safety profile and cost
Dosing for Tylenol
325-650mg q4-6h or 1000mg 3-4x/day

MAX: 4g/day
NSAIDS for Osteoporosis
used for moderate to severe pain

ADRs: GI effects

INTERACTIONS: anticoagulant, ASA, ACE-I, ARBs
Risk Factors for GI events
1. >65
2. lots of comorbidities
3. history of PUD
4. history of upper GI bleeding
5. on anticoagulants
6. high dose and long use of NSAIDS
Celecoxib (Celebrex)
for moderate to severe pain, possibly less GI toxicity
Capsaicin
*Topical Prep for Osteoarthritis*

MOA: inhibits release of Substance P in the peripheral nerves

ADRs: burning, stinging, erythema
Intra-articular Injections
1. glucocorticoids
2. hyaluronic acid
Glucocorticoid
1. effective knee for local inflammation
2. short term use
3. 4-6 month intervals (no more than 3-4 injections/year)
Hyaluronic Acid
1. for moderate to severe pain with ADR or contraindication to APAP, NSAIDs, or COX2
2. provides lubrication and shock absorbency
3. for knee only
4. pain relief occurs slowly, can last up to 6 months
Tramadol
for moderate to severe pain if no response or ADR or C/I to APAP, NSAIDs, COX-2

Dosing: 50-100mg q4-6h

ADRs: sedation, confusion, urinary incontinence, constipation
Narcotic and Analgesic Combos
for moderate to severe pain if no response or ADR or C/I to APAP, NSAIDs, COX-2 inhibits and tramadol

AVOID IN ELDERLY DUE TO FALL RISK
Glucosamine Sulfate
1. rebuild cartilage, decrease cartilage loss
2. ADRs - may increase INR, may cause GI upset and nausea
3. not FDA regulated
Rheumatoid Arthritis
chronic, systemic, inflammatory disease characterized by symmetrical joint involvement and a wide spectrum of other signs (rheumatoid nodules, vasculitis, ocular inflamation)
Risk Factors for RA
1. Genetics
2. increasing age (35-60yrs)
3. females
4. positive RF
5. maybe smoking?
Pathophysiology of RA
1. immune system cant distinguish between normal and foreign tissues - attacks normal synovial and connective tissues
2. Inflammation of synovial tissue - proliferation of synovial tissue (Pannus)
3. Pannus invades cartilage - erosion of bone
Signs and Symptoms of RA
PRODROME - weak, low fever, loss of appetite, join pain, fatigue

JOINT PAIN (hands, feet, wrists) - swelling(soft and spongy), read, warm, swan neck, grip problems,

1. fatigue, morning stiffness
2. Rheumatoid Nodules
3. Vasculitis
Lab and Radiology Tests for RA
1. CBC
2. Inflammatory markers
3. Radiologic Findings
Inflammatory Markers
1. Erythrocyte Sedimentation Rate - increased
2. C-Reactive protein - Elevated
3. Rheumatoid Factor - Positive
4. Anticyclic Citrullinated Peptide - present = aggressive
ACR/EULER 2010 classification criteria for RA
1. helps identify patients with undifferentiated inflammatory synovitis
2. uses a scoring system to help predict the severity
3. 4 categories
4. score of 6 out of 10 = definite RA
4 Categories of ACR/EULER classification criteria for RA
1. Joint Involvement
2. Serology
3. Acute-Phase reactants
4. Duration of Symptoms
Gols of Treatment for RA
1. improve QOL and improve/maintain functional status
2. control disease activity
3. decrease joint pain
4. improve ability to perform ADL
5. disease remission
Non-Pharm Treatments of RA
1. Rest - relieves stress
2. Physical Activity - range of motion and strengthening
3. OT/PT
4. Weight loss
5. Assistive devices - canes, walkers
6. Surgery
Immunizations all patients with RA should get
1. annual flu vaccine
2. Pneumococcal Vaccine
3. Hep B (with risk factors)
Symptomatic Relief for RA
1. Salicylates, NSAIDS, COX2 inhibitors
2. Corticosteroids - intra-articular or PO - must do DEXA scan
Initiation of Therapy with a DMARD
should not be delayed beyond 3 months for patient with established diagnosis of RA
Non-Biologic DMARDS
1. Methotrexate (Rheumatrex)
2. Leflunomide (Arava)
3. Hydroxychloroquine (Plaquenil)
4. Sulfasalazine (Azulfidine)
Methotrexate
*1st Line for mild-moderate-severe active disease

MOA: dihydrofolate reductase inhibitor

ONSET: 4-8 weeks

*should also take a folate supplement
Toxicities and Monitoring for Methotrexate
1. Pregnancy Category X
2. myelosuppression, hepatic fibrosis, cirrhosis

MONITOR: CBC, LFTs
Leflunomide (Arava)
*Used alone or in combo with MTX*

MOA: inhibits pyrimidine synthesis

ONSET: 4-12 weeks
Toxicities and Monitory for Leflunomide
1. Pregnancy Category X
2. diarrhea, rash, hepatotoxicity

MONITOR: CBCs and LFTs, may increase INR
Hydroxychloroquine (Paquenil)
*first line choice for early or mild disease*

MOA: antimalarial, inhibits T-cell and B-cells

ONSET: 8-24 weeks
Toxicities and Monitory for Hydroxychloroquine
1. nausea, diarrhea, macular damage
2. Retinal toxicity

MONITOR: eyes
Sulfasalazine (Azulfidine)
*1st line for mild-moderate disease*

MOA: suppression of pro-inflammatory cytokines

ONSET: 8-12 weeks

*alternative agent for pregnant patients (Cat B)
Toxicities and Monitoring for Sulfasalazine
1. n/v/d, rash, photosensitivity, yellow-orange urine
2. sulfa allergy
3. myelosuppression, leukopenia, LFT elevation

MONITOR: CBC, LFTs
Biologic DMARDS
*1st line Moderate - Severe RA*
1. genetically engineered protein molecules that target and block pro-inflammatory cytokines such as TNF-a and IL-1
2. No lab monitoring required
3. risk of serious infection
TNF Antagonist
**1st Line Biologic DMARD**

ONSET: 1-4 weeks
BLACK BOX: infection risk

MUST HAVE TB screening prior to starting treatment
TNF Antagonists
1. Etanercept (Enbrel)
2. Infliximab (Remicade)
3. Adalimumab (Humira)
4. Golimumab (Simponi)
5. Certolizumab (Cimzia)
Etanercept (Enbrel)
*TNF ANTAGONIST*

1. administered SUBQ at home
2. 25mg twice weekly or 50mg once weekly
Infliximab (Remicade)
*TNF Antagonist*

1. administered in doctor's office
2. IV infusion over 2hrs at 0,2,6 weeks then q8 weeks
3. usually given with MTX
Adalimumab (Humira)
*TNF Antagonist*

1. administered SUBQ at home
2. 40mg every other week
Golimumab (Simponi)
*TNF Antagonist*

1. administered SUBQ at home
2. once monthly in combo with MTX
Certolizumab pegol (Cimzia)
*TNF Antagonist*

1. administered at home
2. at weeks 2 & 4, then either every other week or every 4 weeks
Anakinra (Kineret)
*IL-1 Antagonist*

1. self-administered at home
2. daily SUBQ injection
**LAST LINE**
Rituximab
*Anti-CD20 monoclonal antibody*

1. Used in combo with MTX (moderate-severe RA)
2. administered IV, then a second dose 2 weeks later
Abatacept (Orencia)
*Selectie Co-Stimulation Modulator*

1. targets T lymphocytes
2. administered in doctor's office
3. IV infusion over 30 minutes
4. usually give steroid to pretreat
Tocilizumab (Actemra)
*Humanized monoclonal antibody to IL-6 Receptor*

1. used after failure of TNF antagonist and/or DMARD
2. used in combo with MTX
3. IV infusion every 4 weeks
Tofactinib (Xeljanz)
*Janus Kinase Inhibitor*

1. inhibits intracellular signaling mediated by JAK-STAT pathway
2. taken orally BID
3. newest agent for moderate to severe RA who have problems with MTX