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hypothyroidism
underactivity of the thyroid gland
intolerance to cold, bradycardia, lethargy
hyperthyroidism
overactivity of the thyroid gland; intolerance to the heat, tachycardia, increased blood pressure
thyroid function tests
hypothyroid: increased tsh, decreased t3/t4
hyperthyroid: decreased TSH, increased t3/t4
levothyroxine
treats hypothyroidism
synthetic preparation of t4
should be taken in the morning 30-60 min before breakfast
thyrotoxicosis: tachycardia, angina, tremor, nervousness, insomnia, hyperthermia, heat intolerance, sweating
methimazole
treats hyperthyroidism
adjunct to radiation therapy until effects of radiation become manifest
suppresses thyroid hormone synthesis in preparation for thyroid gland surgery
causes agranulocytosis (infection); not recommended in pregnancy/breastfeeding
Propylthiouracil
treats hyperthyroidism, adjunct to radiation therapy, preparation for thyroid gland surgery; short half life; causes severe liver injury
propranolol
beta blocker
suppresses symptoms of grave's disease like tachycardia
type 1 diabetes mellitus
pancreatic beta cells are destroyed; body makes no insulin at all
type 2 diabetes mellitus
insulin resistant or their pancreas does not secrete enough insulin
pre diabetes
patients at risk for developing type 2 diabetes mellitus
gestational diabetes
placenta produces hormones that antagonize the actions of insulin
short term complications of diabetes
hypoglycemia (fatgie, sweating, pallor)
hyperglycemia (polyuria, polydipsia)
ketoacidosis (persistent severe hyperglycemia with production of ketoacids, rotten smelling urine/fruity breath; can cause hemoconcentration, acidosis, and coma)
long term complications of diabetes
macrovascular damage (heart disease, htn, stroke)
microvascular damage (retinopathy, nephropathy, neuropathy, gastroparesis, amputations secondary to infection, ED)
goals of treatment
prevent long term complications, tighten blood glucose control, control blood pressure and blood lipids
monitoring treatment
Self-monitoring of blood glucose (SMBG) (weekly for patients on oral medications for T2DM)
Hemoglobin A1C (goal is below 7, or below 8 for severe hypoglycemia history/decreased life expectancy)
blood glucose target
80-130 before meals, <180 1-2 hrs after meals, 100-140 at bedtime
hypoglycemia
blood glucose <70, rapid treatment with glucose/glucagon is mandatory
other complications with insulin
lipohypertrophy, allergic reactions, hypokalemia
types of insulin
short duration rapid acting (lispro/aspart)
short duration slower acting (regular insulin) intermediate duration (NPH)
long duration (insulin glargine)
insulin storage
- Do not heat/freeze
- In use vials may be left at room temp up to 4 weeks
- Extra insulin should be refrigerated
- Avoid exposure to direct sunlight
insulin lispro
short duration rapid acting (15-30 min onset) peaks 1/2-2 1/2 hours; duration 3-6 hours; administered immediately before eating or after eating
insulin aspart
short duration rapid acting; 10-20 min onset; 1-3 hr peak, 3-6 hr duration; should be injected 5-15 minutes before meals (aspart as part of your appetizer)
regular insulin
short duration slower acting; 30-60 min onset, 1-5 hr peak, 10 hr duration, can be given IV
NPH insulin
intermediate duration, 60-120 min onset, 6-14 hr peak, 16-24 hr duration, only suitable insulin to mix with short acting ones, allergic reactions are possible
insulin glargine
long duration, 360 min onset, no peak, lasts more than 24 hours, usually given once a day at bedtime
insulin detemir
long duration, 60-120 min onset, no peak, lasts longer than 24 hours, onset is faster than glargine but is otherwise similar
metformin
biguanide
gi effects, weight neutral, severe renal failure with IV radiocontrast media that contain iodine
glipizide
sulfonylurea,treats type 2 diabetes causes weight gain (glizzies cause weight gain)
repaglinide and nateglinide
weight gain, taken with each meal, treats t2d
pioglitazone
thiazolidinedione; usually combined with additional therapy, can cause unintended pregnancy due to ovulation, treats t2d
acarbose
alpha glucosidase inhibitor;treats t2d causes increased flatulence and liver dysfunction (carbs make me gassy)
sitagliptin
DPP-4 inhibitor, usually combined with other therapies, causes URI/UTI (usually does not sit alone); treats t2d
canagliflozin
SGLT-2 inhibitors, improves cv/renal outcomes in pts with history of CV disease, causes weight loss, treats t2d
exenatide
GLP-1 receptor antagonist, weekly injections, reduces appetite and causes weight loss
pharmacological birth control methods
oral, etonogestrel implants, injectable medroxyprogesterone acetate, IUD, vaginal ring
non pharmacological birth control methods
surgical sterilization, mechanical devices, avoiding intercourse
oral contraceptives
inhibition of ovulation (combination OC or progestin only OC)
ethinyl estradiol/norethindrone
combination oc; causes thromboembolic disorder, hypertension, cancer, stroke in patients with migraine, nausea, breakthrough bleeding; contraindicated in heavy smokers, women with history of thromboembolism, women with other risk factors for thrombosis; (decrease risk for ovarian/endometrial cancer, ovarian cysts, BPH, anemia, favorable effect on menstrual cycles, diminished cramps)
missed combination OC
more than one in first week: take 1 ASAP, use another method for 7 days
1-2 in second/3rd week: take 1 ASAP, skip placebo week and go straight to next pack
more than 3 second or third week: same instructions, use extra method for 7 days
progestin only OCs
do not cause thromboembolic disorders, slightly safer, decrease efficacy, increase irregular bleeding
transdermal contraceptive patch
1 per week for three weeks, followed by one week off; causes breast discomfort, headache, local irritation, nausea, menstrual cramps
vaginal contraceptive ring
1 per month, left in place for three weeks then removed for one week, replace after one week
causes vaginitis, headaches, URI, leukorrhea, sinusitis, weight gain, nausea (wash in warm water if it falls out, if it falls out for more than 3 hours use backup contraceptive for 7 days)
subdermal etonogestrel implants
nexplanon
daily release of etonogestrel
gradually declines over 3 years
replaced after 3 years
irregular bleeding, weight gain
depot medroxyprogesterone acetate
IM or subQ injection, protects against pregnancy for 3+ months, causes menstrual irregularities, bone loss, and weight gain
Intrauterine device
amongst most reliable form of reversible birth control, placed within seven days of onset of menses, replacement can be inserted during any phase of menstrual cycle, good for 5-10 years
testosterone male sex characteristics
pubertal transformation, spermatogenesis
testosterone female sex characteristics
clitoral growth, maintenance of normal libido, overproduction of androgens (virilization)
other testosterone effects
anabolic: skeletal muscle
erythropoietic effects: synthesis of erythropoietin, men have higher hematocrit than women
testosterone therapeutic uses
male hypogonadism, replacement therapy, delayed puberty, gender affirming treatment
testosterone adverse effects
virilization in women, girls, and boys
premature epiphyseal closure
hepatotoxicity
effects on cholesterol levels
use in pregnancy
prostate cancer
edema
hypogonadism preparations
oral androgens, intramuscular ester, transdermal patch/gel, implantable pellets
impotence (ED) treatments
lifestyle measures, drug regimens (remove drugs that cause ED) drug therapy (PDE5 inhibitors)
sildenafil
PDE5 inhibitor, plasma levels peak in one hour, high fat meals slow absorption, causes hypotension and priapism (painful erection lasting 6+ hours, immediate medical intervention is required at 4 hours); nitrates can cause life threatening hypotension, take 24 hours in between each other
tadalafil
PDE5 inhibitor, effects last up to 36 hours, causes headache, dyspepsia, back pain, myalgia, limb pain, flushing, and nasal congestion; do not take with nitrates
finasteride
5-alpha-reductase inhibitor
treats benign prostatic hyperplasia
decrease ejaculate volume and libido, causes gynecomastia, decrease levels of prostate specific antigen
alpha 1 adrenergic antagonists
treats dynamic obstruction (-zosin, tamsulosin, silodosin)
asthma
chronic inflammatory disorder of airway
SOB, chest tightening, wheezing, dyspnea, cough; caused by immune mediated airway inflammation
COPD
chronic progressive largely irreversible disorder characterized by airflow restrictions and inflammation
chronic cough, excessive sputum, wheezing, dyspnea, poor exercise tolerance; caused by smoking cigarettes
treatments for asthma/copd
anti inflammatory agents (glucocorticouds, leukotriene modifiers, cromolyn, omalizumab) bronchodilators (SABA/LABA, methylxanthines, anticholinergic drugs)
inhalation drug therapy benefits
therapeutic effects are enhanced, systemic effects are minimized, relief of acute attacks is rapid
MDIs
metered dose inhaler, separate puffs by one minute
spacers
increase MDI delivery to lungs, decrease risk for thrush
glucocorticoids
most effective drugs available for long term control of airway inflammation; used as prophylaxis to prevent exacerbations
Inhaled glucocorticoids
first line therapy, used daily if persistent, safer than systemic; adverse effects: oropharyngeal candidiasis/dysphonia, rinse mouth with water and gargle, use a spacer
oral glucocorticoids
should be used only when symptoms cannot be controlled with safer medication, brief as possible; adverse effects: adrenal suppression, osteoporosis, hyperglycemia, pud, growth suppression, d/c must be done slowly
leukotriene modifiers
reduce bronchoconstriction and inflammatory responses such as edema and mucous secretions
monteluksat
leukotriene modifier; prophylaxis of maintenance therapy of asthma, prevention of EIB, well tolerated, neg behavior changes in kids
cromolyn
prophylaxis of inflammation, not quick relief, in patients with mild to moderate asthma; safest of all
omalizumab
ages 12+, subQ, can cause life threatening anaphylaxis
bronchodilators
provide symptomatic relief but do not alter inflammation, should also be taking glucocorticoid for long term suppression of inflammation
B2 Adrenergic Agonists
activate b2 receptors in the smooth muscle of the lung, promote bronchodilation, relieve bronchospasm
SABA
short acting b2 agonist (albuterol), taken PRN, hospitalized patients undergoing severe attack should used nebulized form, delivery with MDI outpatient
LABA
long acting b2 agonist (salmeterol) long term control, taken on a fixed basis not PRN, treats stable COPD, must always be combined with glucocorticoid if treating asthma
theophylline
methylxanthine; used for maintenance therapy of chronic stable asthma, narrow therapeutic index (10-20), interacts with caffeine, tobacco, marijuana
theophylline toxicity
20-25: nausea, vomiting, diarrhea, insomnia, restlessness
above 30: severe dysrhythmias, convulsions
treatment: stop theophylline, activated charcoal and cathartic (dysrhythmias respond to lidocaine), IV diazepam may help with seizures
ipraproprium
anticholinergic; improves lung function by blocking muscarinic receptors in the bronchi, causes anticholinergic effects, therapeutic effects begin in 30 minutes, peak n 3 hours, persist for 24 hours (improves with subsequent truth, should see improvement within a week)
tiotropium
long acting inhaled anticholinergic approved for maintenance therapy of bronchospasm associated with COPD, not approved for asthma, therapeutic effects begin in 30 min, peak in 3 hours, persist about 24 hours
glucocorticoid LABA combos
fluticasone/salmeterol, budesonide/formoterol, mometasone/formoterol (indicated for long term maintenance in adults and children)
acute asthma exacerbation
requires immediate attention; give SABA, oxygen,ipratropium, glucocorticoid
COPD exacerbation
SABAs, systemic glucocorticoids, antibiotics, supplemental o2 (88-92%)
peptic ulcer disease
group of upper GI disorders, degrees of erosion to the gut wall that can cause hemorrhage and perforation; caused by H.pylori, NSAID use, smoking
PUD treatment goals
alleviate symptoms, promote healing, prevent complications, prevent recurrence
treatment for PUD
h pylori ulcer: antibiotics and antisecretory agents
NSAID induced ulcer: PPI for prophylaxis, histamine blockers (no antacids, sucralfate, and h1 blockers)
non drug treatment for PUD
smaller more frequent meals; avoid smoking, aspirin, nsaids, and alcohol; reduce stressors
h pylori treatment
tetracycline, amoxicillin, clarithromycin, metronidazole, bismuth (2-3 prescribed) (B-MATC)
histamine 2 receptor antagonists
treats gastric and duodenal ulcers, promote healing by suppressing secretion of gastric acd
famotidine
h2 receptor antagonist, causes confusion, hallucinations, CNS depression, and CNS excitation; elevation of gastric pH may increase risk of pneumonia
proton pump inhibitors
omeprazole, esomeprazole, pantoprazole; most effective drugs for suppressing secretion of gastric acid; can increase risk of serious adverse events, including fracture, pneumonia, acid rebound, intestinal infection with c.diff
sucralfate
mucosal protectant; creates a protective barrier for up to 6 hours; administering antacids at least 30 minutes apart from sucralfate; take 1 hour before meals and at bedtime
aluminum hydroxide/magnesium hydroxide
take other medications at least an hour before or 2 hours after; antacids
medications for allergic rhinitis
glucocorticoids (intranasal) antihistamines (oral/intranasal) sympathomimetics (oral/intranasal)
intranasal glucocorticoids
budesonide, fluticasone, triamcinolone; first choice- most effective for treatment and prevention of rhinitis; can cause drying of mucosa, sore throat, epistaxis, headache
oral antihistamines
diphenhydramine, fexofenadine; for allergic rhinitis, do not reduce nasal congestion, most effective if taken prophylactically and regularly throughout the season, 1st gen is more sedating
intranasal antihistamines
azelastine, olopatadine; indicated for allergic rhinitis in 12+ years, systemic absorption can be sufficient to cause somnolence
intranasal cromolyn sodium
prophylaxis, administer before symptoms start, response develops in 1-2 weeks
sympathomimetics
phenylephrine, pseudoephedrine; reduce nasal congestion (not rhinorrhea, sneezing, itching) causes rebound congestion, CNS stimulation, CV effects/stroke, abuse, do not use more than 5 days in a row
antitussives
suppress cough; opioid antitussives: codeine and hydrocodone; non opioid antitussives: dextromethorphan, benzonatate
expectorants
renders cough more productive by stimulating flow of respiratory tract secretions; guanifecin
functions of histamine
stimulates secretion of acid, acts as a neurotransmitter, dilates small blood vessels and increases capillary permeability, constricts smooth muscle
h1 antagonists MOA
block the actions of histamine at h1 receptors, do not block h2 receptors, some bind to muscarinic receptors