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 |