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PHAR 190 exam 3

flashcards for exam 3

Max lipid lowering effect of bile acid sequestrants decrease LDL 15-30%, increase HDL 3-5%, no change or increase in TG
Max lipid lowering effect of cholesterol absorption inhibitor decrease LDL 18%, increase HDL 1%, decrease TG 8%
Max lipid lowering effect of statins decrease LDL 18-55%, increase HDL 5-15%, decrease TG 7-30%
Max lipid lowering effect of Niacin decrease LDL 5-25%, increase HDL 15-35%, decrease TG 20-50%
Max lipid lowering effect of fibric acid derivatives decrease LDL 5-20%, increase HDL 10-20%, decrease TG 20-50%
Max lipid lowering effect of omega-3 fatty acids may increase LDL, decrease TG up to 45%
Starting age and interval for testing cholesterol >20 years of age, screen at least every 5 years
Goals for TC, HDL, and TG <200mg/dL, >40mg/dL, <150mg/dL
Primary diagnostic for lipids LDL<100mg/dL
Equation for calculating LDL (and when the equation does not work) LDL = TC - (HDL + TRG/5) Equation does not work when TG>400mg/dL
C-reactive protein Marker of low-level inflammation, helps in predicting CHD risk beyond LDL and major CHD risk factors
5-risk factors for CHD involved in LDL modification 1. Age (men≥45, women≥55) 2. Family hx of premature CHD events (men <55, women <65) 3. HTN (≥140/90mmHg) or on any anti-HTN medication 4. HDL <40mg/dL (≥60mg/dL is -1 RF) 5. Cigarette smoking within past month
Determine patient's LDL goals CHD or CHD risk equivalent: <100mg/dL 2+ risk factors: <130mg/dL 0-1 risk factors: <160mg/dL
When to calculate Framingham score Calculate if patient has 2+ risk factors in order to determine CHD risk category
What Framingham result tells you % risk of developing CHD over a 10 year period –serves as basis for deciding how intensively to treat hypercholesterolemia and other risk factors
CHD risk equivalents (conditions that put a patient at >20% risk of developing CHD over a 10-year period) CHD= MI, unstable/chronic angina, coronary bypass, angioplasty, stents CHD risk equivalent= multiple risk factors with 10-year risk for CHD>20%, diabetes, PAD, AAA, symptomatic CAD (stroke, TIA)
Non-HDL Non-HDL goal = LDL target + 30mg/dL Estimates cholesterol carried by all Apo-B-containing lipoprotein particles—represents sum of LDL, VLDL, and other TRG-rich particles
When to initiate TLC or drug therapy; how much of LDL reduction possible through TLC? Adequate trial of TLC in all patients (3 months) Consider drug therapy when LDL >30+ above goal. TLC can reduce LDL by 10%
TLC Saturated fats to <7% of total calories (↓ trans fats) Dietary cholesterol <200mg/day Plant stanols/sterols 2g/day Soluble fiber 10-25 g/day Weight reduction Increase physical activity (expend >200calories/day) Consider: alcohol and smoking
Calculating recommended saturated fat intake/day (Desired daily calorie intake x 0.07) / 9 7% of total calories; 9 kcal=1g fat
Definition of liver toxicity LFTs greater than 3x the upper limit
Definition of myopathy CK greater than 10x the upper limit
MOA of statins HMG-CoA reductase inhibitors
Common AE of statins Constipation, abdominal pain, diarrhea, dyspepsia, nausea
Statins not metabolized by cyp3a4, therefore have no interaction with grapefruit juice Pravastatin, rosuvastatin, fluvastatin (minimal)
When to focus on TG lowering over LDL When TG>500, trumps focus over LDL
Interaction with grapefruit juice and statins GPJ inhibits CYP3A4 metabolism in the gut, allowing more drug to be absorbed and reach higher levels, increasing chance of adverse effects. GPJ>1 quart to have significant impact on inhibiting PGP efflux.
Order of statin's potency Rosuvastatin>atorvastatin>simvasatatin> lovastatin=pravastatin>fluvastatin
Monitoring for statins Baseline LFT, then 6-12 weeks after starting therapy or increase dose, then annually. Check CK if muscle pain and/or brown urine, discontinue therapy if >10x normal upper limit
Contraindications of statins Active liver disease, elevated serum transaminases, concomitant use of strong CYP3A4 inhibitors, concomitant use of gemfibrozil, pregnancy, breast-feeding
Precautions of statins Hepatic impairment/alcohol use, renal impairment
MOA of bile acid-binding resins/sequestrants Bind to bile acids in gut, forming complex that is excreted in the feces. Loss of bile causes compensatory conversion of hepatic cholesterol to bile, causing an upregulation of LDL receptors
Adverse effects of BAS's Limited to GI tract: nausea, constipation, bloating, flatulence
Precautions of BAS's Renal impairment, separate dose 1 hr before or 4 hrs after other medications
MOA of Zetia Blocks biliary and dietary cholesterol absorption via NPC1L1 transporter in brush border of small intestine-causes decrease delivery of cholesterol to liver, reduction of hepatic cholesterol stores, induce upregulation of LDL receptors
Contraindications of Zetia Active liver disease, unexplained persistent elevations in LFTs, pregnancy, breastfeeding
Precautions of Zetia hepatic impairment, renal impairment
Adverse effects of Zetia diarrhea, fatigue, arthralgia, URTI, sinusitis, influenza, elevated transaminases
MOA of Niacin inhibit fatty acid release from adipose tissue, inhibits fatty acid and TG production in liver cells. Result: increase degradation of Apo B and decrease LDL. Reduces uptake of HDL particles.
Ways to minimize flushing with niacin take with food, avoid hot liquids, take NSAID or aspirin 30 mn prior, start at lowest dose and gradually titrate up
Adverse effects of niacin flushing, pruritis, gastric distress, HA, HA, hepatotoxicity, hyperglycemia, hyperuricemia
Precautions of niacin can raise uric acid levels (caution with gout), can raise blood glucose levels in diabetic patients. Renal impairment, hepatic impairment
MOA of fibric acid derivatives decrease APOs B, C-III, and E; increase Apos A=I and A-II thru activation of PPAR-alpha. Result: decrease TG-rich VLDL and IDL, and increase HDL
Adverse effects of fibric acid derivatives Nausea, diarrhea, abdominal pain, rash, dyspepsia, flatulence, muscle pain, fatigue, increased risk of rhabdomyolysis when taken with a statin. Associated with gallstones, myositis, hepatitis
Contraindications of fibric acid derivatives Gall bladder disease, liver dysfunction, severe kidney dysfunction, breastfeeding
Fibric acid derivatives with statins Increased risk of rhabdomyolysis. Prefer fenofibrate over gemfibrozil due to potential less inhibition of glucuronidation/clearance of statins.
Contraindications of niacin Active liver disease, unexplained persistent elevation in LFTs, active peptic ulcer, arterial hemorrhage
MOA of O3FAs modulation thru PPAR-alpha and decrease Apo B-100 secretion
Adverse effects of O3FAs Diarrhea, excess bleeding, may increase glucose levels
Counseling points for O3FAs Take with meals. Need dose 4g/day for effect on TGs
When should a repeat lipid panel be drawn? TC>200mg/dL or LDL>100mg/dL
Which cholesterol medications require LFT monitoring? Statins,eztimibe, niacin, fibric acid derivatives
Which cholesterol medications require creatinine monitoring? All of them (all have caution or contraindication of renal impairment except O3FAs)
Components used in assessment of overweight or obese patient BMI, waist circumference, comorbidities, readiness to lose weight
BMI classification for weight Underweight <18.5kg/m2 Normal weight 18.5-24.9 kg/m2 Overweight 25-29.9 kg/m2 Obese (1) 30-34.9 kg/m2 Obese (2) 35-39.9 kg/m2 Extreme obesity (3) >40 kg/m2
High-risk waist circumference for men and women Men > 40in (102cm) Women > 35in (88cm)
Comorbidities that heighten need for treatment of overweight or obese patient HTN (>140/90) or on bp med, LDL >160, LDL >130 + 2 RF, HDL <40, impaired FPG (100-125 mg/dL), CHD, atherosclerosis, T2DM, sleep apnea
Risk factors that heighten need for treatment of overweight or obese patient Cigarette smoking, family history of premature CHD (male <55, female <65), males >45, females >55
Recommended initial weight loss goal and time frame 10% weight loss with 1-2 lbs (0.45-0.9kg) per week, meeting goal in 6 months
Who is weight loss indicated for? Patients with BMI 25-29.9kg/m2 or elevated waist circumference + 2 or more comorbidities. Any patient with BMI >30kg/m2 (After 6 months of lifestyle changes)
How many calories reduces equals one pound of weight loss? 3500kcal (500kcal/day for 1 week)
When should pharmacotherapy be initiated in addition to lifestyle modifications? BMI>30kg/m2 or BMI>27kg/m2 with other obesity-related risk factors
Qsymia components Phentermine/topiramate
MOA of Qsymia P: sympathomimetic, result in CNS stimulation and appetite suppression T: appetite suppression and satiety enhancement, block VG-Na channels, enhance GABA, antagonize AMPA, weakly inhibit carbonic anhydrase
Duration of Qsymia treatment Titrating up, may take for up to 7 months
Dosing of Qsymia Titrate up dose to maximum of 15mg/92mg ER once daily. Do not D/C abruptly due to risk of seizure
Adverse effects of Qsymia HA, insomnia, xerostomia, constipation, palpitations, chest discomfort, DZ, anxiety, depression, fatigue, irritability, abnormal taste, nausea, blurred vision, kidney stones
CI of Qsymia Hyperthyroidism, glaucoma, concomitant MAOI use, pregnancy, (kidney stones)
Monitoring patients on Qsymia Periodic blood chemistry profile, HR, signs of depression, BP
MOA of phentermine increase NE and dopamine release in CNS--CNS stimulation, appetite suppression
Duration of phentermine treatment Up to 6 months
Adverse effects of phentermine Palpitations, tachycardia, increase BP, stimulation, restlessness, DZ, insomnia, euphoria, dysphoria, tremor, HA, dry mouth, constipation, diarrhea, abuse potential
CI of phentermine Unstable cardiac status, HTN, hyperthyroidism, agitated states, glaucoma, concomitant MAOI, alcohol use, hx of substance abuse, patients <16 y/o
MOA of diethylpropion Sympathomimetic amine-CNS stimulation and appetite suppression
Duration of diethylpropion treatment Up to 12 months
AE of diethylpropion overstimulation, restlenssness, DZ, insomnia, euphoria, tremor, HA, jittery, anxiety, nervousness, depression, DQ, malaise, mydriasis, blurred vision, decrease seizure threshold, tachycardia, increase BP, palpitation, dry mouth, constipation
CI of diethylpropion Pulmonary HTN, advanced arteriosclerosis, severe HTN, hyperthyroidism, agitated states, glaucoma, hx of substance abuse, MAOI use, anorectic agents, pt <16 y/o
MOA of lorcaserin (Belviq) Activate 5-HT2c receptors, stimulating POMC neurons resulting in satiety and decreased food intake
Duration of lorcaserin (Belviq) treatment Evaluate at week 12, maximum 2 years
Adverse effects of lorcaserin (Belviq) Abuse potential (euphoria, hallucinations), HA, hypoglycemia in DM patients, back pain, URTI, HTN, DZ, fatigue, anxiety, insomnia, nausea, diarrhea
CI of lorcaserin (Belviq) Pregnancy
MOA of orlistat act locally in GI tract-inhibit pancreatic and gastric lipases and TG hydrolysis-undigested TGs not absorbed, result in caloric deficit and weight loss
Duration of orlistat treatment Maximum of 4 years
Dosing of orlistat Take during or up to 1 hour after meal. Omit dose if meal missed or contains little fat. May need multivitamin with fat-soluble ADEK
Adverse effects of orlistat Local: fatty/oily stools, oily spotting/evacuation, abdominal pain, flatulence, soft stools, N/V/D, increased defecation, fecal incontinence, bloating Dypepsia, HA
CI of orlistat Pregnancy, breastfeeding, chronic malabsorption syndrome, cholestasis (kidney stones)
Location, severity, duration, and frequency of migraines Unilateral, moderate to severe, 4-72 hours (w/o aura) 4-60 mns (w/ aura); 5+ attacks (w/o aura), 2+ attacks (w/ aura)
Location, severity, duration, and frequency of TTH bilateral, mild to moderate, 30mn-7 days, 10+ attacks on avg less than 1day
Chronic tension headache Avg headache frequency >15 days/month (180 days/yr) for >6 months
Symptoms of migraine Pulsating/throbbing pain that interrupts or worsens with physical activity, N/V, photophobia, phonophobia, osmophobia, seek quiet and solitude. Possible aura.
Examples of aura symptoms May be positive or negative symptoms. + visual perception of flickering lights, spots, or wavy lines. - partial loss of vision, scotoma. dysphasic speech, change in smell, feeling of euphoria/dysphoria, something out of the norm.
Symptoms of TTH band-like tightness or pressure around head, nonpulsating pain, possible anorexia, either photophobia or phonophobia (not both)
Symptoms of cluster headache Intermittent, explosive, excruciating, short, stabbing pain. conjunctival injecting, lacrimation, nasal congestion, rhinorrhea, sweating, eyelid edema, miosis, ptosis. excited, restless during attacks
Location, severity, duration, and frequency of cluster headaches unilateral (orbital, supraorbital, temporal), severe, lasts 2 seconds-10 minutes (15-180mn). 1 qod to 8/day. 5+ attacks.
Theories for pathophysiology for migraine 1. Tissue pain generated by vascular reactivity (not supported). 2. Pain induced by neuronal imbalances accompanies by trigeminovascular system overactivity (supported)
Current accepted theory for pathophysiology for migraine Depressed neuronal activity spread across brain, activate trigeminal sensory nerves, release vasoactive peptides to produce inflammation around vascular structures
"Red Flags" for headaches New onset sudden and/or severe pain Onset >40 y/o Stereotyped pattern worsens Systemic signs Focal neurologic symptoms (other than aura) Papilledema Cough, exertion, or valsalva-triggered HA Pregnancy or postpartum Pt with cancer, HIV, etc Seizur
Information for headache diary Date, day of week, onset time, duration, intensity/severity, location, nausea, light/sound sensitive, triggers, meds taken
Behavioral triggers of HA fatigue menstruation menopause sleep excess or deficit stress vigorous physical activity
Environmental triggers of HA flickering lights high altitude loud noises strong smells tobacco smoke weather changes
Food triggers of HA MSG (Asian food, seasoned salts) Nitrates (processed meats) Saccharin/aspartame (diet soda, diet food) sulfites (shrimp) tyramine (cheese, wine, meats) yeast
Medication triggers of HA cimetidine estrogen OCs indomethacin nifedipine nitrates reserpine theophylline withdrawal due to overuse of analgesics/BZDs/decongestants/ergotamines
Why start pharmacologic treatment early for acute headache? Abort intensification of pain, improve response to therapy Initial severity of headache correlates with symptomatic response Delay may lead to decreased analgesia thru dvpt of refractory central pain sensitization
Nonpharmacologic management of HA disorders Limit exposure to triggers Rest in dark, quiet area Relaxation, stress management Limit alcohol use, stop tobacco use Psychological interventions
Triptan with long half-life Frovatriptan (Frova)
Triptan with dosage repetition after 4 hours Naratriptan (Amerge)
Triptan with dosage repetition after 1 hour Sumatriptan injection (Imitrex)
Triptans with ODT dosage form Rizatriptan (Maxalt) Zolmitriptan (Zomig)
Triptans with nasal dosage form Sumatriptan (Imitrex) Zolmitriptan (Zomig)
Triptan with injection dosage form Sumatriptan (Imitrex)
Triptans with potential CYP3A4 interaction Almotriptan (Axert) Eletriptan (Relpex)
Rebound headache Acute withdrawal as result of overuse of APAP causing tolerance or dependence--result of poor attention to prevention therapies leading to chronic use of daily analgesics
Headache recurrence Return of headache pain, usually within 24 hrs, after an initially good response to medication (triptans, ergots)
Drug of choice for mild to moderate headache attacks APAP (not recommended alone), aspirin, NSAIDs
Drugs of choice for moderate headache attacks APAP, aspirin, NSAIDs, Ergots, Triptans, combination
Drug of choice for severe headache attacks IM or IV DHE; SQ or oral triptan; IM or IV ketorolac; IM, IV, intranasal or oral opioids
Dosage forms best for treatment of cluster headache? Intranasal, SQ, IM, IV (Need rapid onset of action due to rapid onset/short duration of cluster headache)
Primary novel therapy for treatment of cluster headaches High-flow-rate oxygen: 100% at 5-10 L/min for 15 minutes
Options available for adjunctive therapy for patient experiencing nausea? Metoclopramide, chlorpromazine, prochlorperazine Begin at first sign of HA Best given 15-30 mn before abortive med
When is prophylactic (TTH) headache treatment warranted? If headache is severe and frequent, or if TTH use of NSAIDs more than 2 days/week
Main option for TTH prophylaxis TCAs (amitriptyline) Also, propranolol
Main option for cluster HA prophylaxis CCB verapamil Also, lithium, ergotamine, corticosteroids
Common side effects of triptans Dizziness, sensation of warmth, chest tightness, nausea, fatigue, tingling, weakness, somnolence. May precipitate ischemic vascular events
CI of triptans associated with neurologic focality, hx of previous stroke, uncontrolled HTN, unstable angina, pregnancy, concurrent ergotamine administration (w/in 24h), liver/kidney disease
CI for specific triptans Severe renal impairment (nara) Severe hepatic impairment (ele, nara, zolmi NS) MAOI w/in 14 days (suma, riza, zolmi) Potent CYP3A4 inh w/in 72hr (ele) Propranolol (riza)
Common side effects of ergots N/V/D, itching, vertigo, muscle pain, weakness, increase BP, numbness or tingling in fingers or toes DHE nasal: rhinitis, DZ, somnolence, N/V/D, taste disturbances, pharyngitis
Extreme side effect of ergots Ergotism-severe peripheral ischemia and development of gangrene
CI of ergots CAD, uncontrolled HTN, peripheral vascular disease, liver/kidney disease, pregnancy, w/in 24 hrs of taking triptan, breastfeeding
Indication for prophylactic tx of migraines Frequent, prolonged, or severe/disruptive migraine attacks More than 2-4 times/month, last more than 48 hrs, or cause dysfunction Symptomatic therapies have failed or serious SE Pt unable to cope with HA attacks HA occur in a predictable pattern
General guidelines for migraine prophylaxis Monotherapy preferred Consider comorbid conditions Gradual dose increase Minimum trial of 2 months Re-evaluate after 6-8 months
Difference between cortical bone and trabecular bone Cortical: dense, compact, responsible for bone strength. 80% of skeleton. on surface of long and flat bone Trabecular: sponge-like, along inner surfaces of long bones, more susceptible to bone remodeling due in part to larger SA
Osteoclasts versus osteoblasts -clasts: resportion/breakdown of bone, continuously create miscroscopic cavities in bone tissue -blasts: bone formation, continuously mineralize new bone in cavities created by osteoclasts
What age do patients attain peak bone mass? 25-35 years old
Difference between t-score and z-score T: # of SD from mean bone mineral density in normal young adult, sex adjusted Z: # of SD from mean bone mineral density of age- and sex- matched controls
WHO definitions of normal, osteopenia, or osteoporosis Normal: >-1 Osteopenia: -2.5 to -1 Osteoporosis: <-2.5
Recommended standardized approach to bone mineral density measurement Measuring bone mineral density at the lumbar spine and femoral neck (hip)
Indications for BMD testing All women 65+ and men 70+ Postmenopausal women, men 50-69 with clinical RFs Fracture after age 50 Medical conditions or medications Assessment for osteoporosis treatment initiation/monitoring D/C of estrogen therapy
Calcium intake recommendations (RDA) 1000mg: men 25-65, women 25-50, women 51-65 on estrogens 1500mg: women 51-65 not on estrogens, people >65
Vitamin D recommendations <50: 200 IU 50+: 800-1000 IU
Max amount of calcium that can be taken at one time 500-600 mg/dose
Amount of calcium that can lead to toxicity 2500 mg/day
What patients are recommended for osteoporosis treatment? >50 with: hx of hip or vertebral fracture; t-score <2.5 at femoral neck/spine; or osteopenia & 3%+ 10-year probability of hip fracture or 20%+ 10-year probability of major osteoporosis related fracture
What does FRAX tell you? Evaluates an individual's 10-year risk for hip and major osteoporotic fracture
MOA of bisphosphonates decrease bone resorption by binding to bone matrix and inhibiting osteoclast activity
MOA of raloxifene SERM, estrogen-like activity on bones and cholesterol metabolism and estrogen antagonist activity in breast and endometrium-reduce bone resorption and decrease overall bone turnover
MOA of calcitonin inhibits bone resorption by binding to osteoclast receptors
MOA of teraparatide recombinant human parathyroid hormone-stimulates osteoblastic activity to form new bone when administered once daily
MOA of denusumab human monoclonal antibody that inhibits receptor activator of nuclear factor-kappa B ligand (RANKL) action (antiresorption)
BBW warning of Forteo and maximum duration of use In animal studies, associated with an increase in osteosarcoma. Do not use for longer than 2 years
Osteonecrosis of the jaw case reports--drug, dosage form, patient type? IV bisphosphonates in cancer patients
HRT use in osteoporosis Prevention only. Puts pts at higher risk for breast cancer and venous thromboembolism
Raloxifene (Evista) use in osteoporosis: use, benefits, risks SERM. Treatment and prevention in postmenopausal women. Reduces the risk of breast cancer. Risks-thromboembolic events, CHD.
Boniva (ibandronate) use in osteoporosis IV is treatment only, given every 3 months
Reclast (zoledronic acid) use in osteoporosis: use, risks Infusion given once a year. Risk-higher rate of afib, increase SCr, infusion-related SE
Which osteoporosis agents can be used in men and women? Alendronate, risedronate, teriparatide
Calcitonin salmon use in osteoporosis Available nasal or parenteral route, good for patients with or at risk for vertebral fractures
Forteo (teriparatide) use in osteoporosis Only agent that actually helps rebuild bones, can improve t-score. SC, needs to be refrigerated.
Recommendation for patients starting glucocorticoid treatment longer than 3 months? Bisphosphonate therapy and adequate calcium and vitamin D intake
How many months of amenorrhea should pt have experienced to be diagnosed as in menopause? 12 months
Which hormone is elevated with loss of ovarian follicular activity? FSH (10-15 fold increase)
What is perimenopause/climacteric? Transitional period prior to menopause when hormonal/biologic changes begin. Can occur 2-8 years prior, lead to irregular menstrual cycles, increase interval, decrease length. Also, may have hot flashes, night sweats
Common symptoms of menopause Vasomotor symptoms (hot flashes, night sweats) Irregular menses, episodic amenorrhea Sleep disturbances Vaginal dryness Depression, mood swings
Less common symptoms of menopause Fatigue Irritability Migraine Arthralgia Myalgia
Criteria for diagnosis of menopause Amenorrhea for 1 year FSH greater than 40 mIU/mL 5-fold increase in LH
Why is HRT only recommended for treatment of vasomotor and vaginal symptoms? HRT is not protective against the development of CHD
What contraindications exist for HRT? Hx of or active thromboembolic disease, breast cancer, or estrogen-dependent neoplasm, pregnancy, liver disease, undiagnosed vaginal bleeding
Is HRT approved for prevention and treatment of osteoporosis? No! HRT is only approved for prevention of osteoporosis, and should only be used short-term
Risks of HRT identified in WHI study? Could increase risk in of CHD in women with underlying risk factors, increase risk of breast cancer after 3 years of therapy
When is use of a progestin required for HRT? Women who have an intact uterus
Disadvantage of cyclic HRT administration? Return of menses in 90% of women 1-2 days following last progestin dose
Disadvantage of continuous HRT administration? Unanticipated breakthrough bleeding or spotting during the month
First-line dosage form for vulvovaginal atrophy? Topical preparations
Is a progestin needed with topical HRT? No, normal doses should have minimal systemic absorption
Can estradiol be used in treatment of vulvovaginal atrophy in patient with CI to estrogen therapy? Yes, topical creams, tablets, or rings
Estring vs. Femring Femring has systemic absorption, releases more estradiol per day Estring does not have significant systemic absorption and is considered topical
What is bio-identical hormone therapy (BHRT) exogenous hormones identical to those produced in woman's body, commercially manufactured or chemically compounded
General approach to HRT Lowest dose for shortest duration possible (preferably <5 years)
Risk of BHRT? Custom HT formulation comopounded according to prescription: Not tested for efficacy, safety, batch standardization, or purity
Estrogen AE nausea HA Bloating Breast tenderness Bleeding
Progestin AE Nausea HA Weight gain Bleeding Irritability Depression
Benefits of HRT? relieve vasomotor symptoms and vulvovaginal atrophy osteoporosis prevention May reduce risk of colon cancer (inconsistent data)
Risks of HRT? cardiovascular disease breast cancer venous thromboembolism
Options for assisting with discontinuation of HRT Taper by dose decrease or day decrease
Nonpharmacologic interventions available for treatment of vasomotor symptoms Smoking cessation, limit alcohol/caffeine/hot beverages/spicy foods, keep cool, stress reduction, increase exercise, paced respiration
Nonpharmacologic interventions available for treatment of dyspareunia Water-based lubricants, moisturizers
Nonpharmacologic interventions available for treatment of stress incontinence Kegel exercises to strengthen pelvic floor muscles
Alternative treatment options for menopausal symptoms SSRIs (citalopram, paroxetine, venlafaxine, fluoxetine) Gabapentin Clonidine
"Natural" treatment options that have no benefit for hot flashes Red clover Dong Quia Vitamin E Evening Primrose oil
"Natural" treatment options that have some benefit for hot flashes *Black cohosh (remifemin): avoid if breast cancer, hepatotoxic-this is only one she'd recommend if forced Soy: may contribute to breast cancer Micronized progesterone creams
Normal VitD lab value >30 ng/mL
Calcium citrate vs clacium carbonate Calcium carbonate requires an acidic gastric environment. Patients on PPI or H2RAs should take calcium titrate.
4 functional phases of female menstrual cycle Follicular: FSH increase, estrogen increase, endometrium proliferate Ovulatory: surge of LH day 14 allows ovulation Luteal: luteal cells need LH and progesterone Menstrual: less progesterone/estrogen allow menses
Function of LH Promote androgen production, ovulation and oocyte maturation, convert cells to luteal cells that secrete progesterone after ovulation
Function of FSH promote growth of follicle in preparation for ovulation by causing granulosa clels to grow and produce estrogen
At what point during menstrual cycle are FSH and LH at peak levels? Just prior to ovulation
How to adjust OC if continued bleeding after menses (1st week) Higher estrogen content or have lower early progestin component in triphasic pills
How to adjust OC if have spotting or bleeding midcycle (2nd week) Difficult to determine cause, increase both estrogen and progestin component
How to adjust OC if have spotting or bleeding before finish active pills (week 3) Higher progestin content to increase endometrial support
Type of OC regimen recommended for patient diagnosed with dyslipidemia? Replace androgenic progestin with more estrogenic progestin. If TG >350mg/dL, EE 20-25mcg or progestin-only formulation
Formulation for patient having headaches during placebo week of OC Eliminate pill-free interval for 2-3 consecutive cycles
Which progestins believed to have less androgenic activity Synthetic "third generation" progestins: desogestrel and norgestimate
What OCs are FDA-approved for treatment of acne? Ortho Tri-Cyclen (EE/norgestimate) Estrostep Fe (EE/norethindrone)
Primary mechanism by which OCs prevent pregnancy? suppression of midcycle surge of both FSH and LH (mimics physiologic changes that occur during pregnancy)
Additional mechanisms by which OCs prevent pregnancy Induce changes in cervical mucus and endometrium that make sperm transport and implantation of embryo unlikely
Benefits of using combined OCs Reduction in risk of endometrial and ovarian cancer. Improve regulation of menstruation. Relief of benign breast disease. Prevent ovarian cysts. Reduce risk of symptomatic pelvic inflammatory disease. Improvement in acne control.
Risks of using combined OCs Increased risk of STDs Increase risk of MI or stroke w/ high dose EE and uncontrolled HTN Increase risk of venous thromboembolism Glucose intolerance, gallbladder disease w/ pre-existing gallstones. Hepatic tumors, cervical cancer.
Absolute CIs to using combined OCs Hx of: thromboembolic disease, stroke, CAD, breast carcinoma, estrogen-dependent neoplasm, hepatic tumor Undiagnosed abnormal uterine bleeding Pregnancy Heavy smokers (>15/day) who are >35y/o Active liver disease
Relative CIs to using combined OCs Smoking >15/day at any age Hx of migraine headache disorder HTN Fibroid tumors of uterus Breastfeeding DM
Lybrel and Amethyst Continuous cycle OC (non-cyclic), active pills taken every day of year. Advantage: no periods SE: spotting, breakthru bleeding in initial months
Seasonale and Seasonique Monophasic, 91-day cycle (84 active, 7 placebo). Allow 4 menses/yr. Higher rate of D/C due to unacceptable bleeding/spotting
Ortho Tri-Cyclen and Estrostep Fe Approved for moderate acne in females 15+
Yasmin anti-androgenic properties, anti-mineralcorticoid activity Risk for hyperkalemia
Mircette 21 active, 2 placebo, 5 low dose EE Minimize bleeding during menstrual cycle
Ovcon 35 CHEWABLE TABLET! spearmint flavoring
Ortho-Evra transdermal patch applied once weekly for 3 weeks, then 1 patch-free week
NuvaRing transvaginal delivery system, insert on or before day 5 of cycle, remove 3 weeks later, then 7 ring-free days If falls out for >3 hrs, use backup for 7 days
DepoProvera injectable depot of progestin-only, administer IM every 3 months. Return of fertility can be delayed 10-12 months
Depo-SubQ Provera injectable depot of progestin-only, adminstered SQ every 3 months. Lower dose of medroxyprogesterone compared to DepoProvera
Mirena or Skyla levonorgestrel-releasing IUD: up to 5 years
Paragard T 380A Copper IUD: up to 10 years
Implanon or Nexplanon Etonogestrel-releasing system surgically implanted under skin of upper arm: up to 3 years
Plan-B Levonorgestrel 0.75mg: take 1 tablet w/in 72 hrs of unprotected intercourse, second dose 12 hours later
Progestin-only pills MicroNor, Camilla, Errin, Heather, Jolivette, NorQD
How to handle 1 missed dose of combined OCs? Take ASAP, take next pill at regular time. No back up needed
How to handle missing 2 doses of combined OC? Take 1 extra pill per day for 2 days. Use backup for 7 days.
How to handle missing 3+ doses of combined OC? Discard pack and restart as previously instructed. Use backup for 7 days Sunday starter: may take 1qd until Sunday, then start new pack.
When to begin a progestin-only pill (POP)? Start on first day of menses and use backup for 7 days. Take pill at same time each day!
What to do if miss a dose of progestin-only pill? (POP) If missed by more than 3 hours, use backup method for 48 hours. Do not take missed doses if past 3 hour time-frame.
Candidates for POPs? Breastfeeding High risk for estrogen adverse effects Smoker >35 years (?) lower efficacy rate than COCs
Candidates for implantable contraceptives? Women >1 child (except Skyla) Monogamous relationship No hx of PID No hx or risk of ectopic pregnancy
Created by: steponmegrace