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;
132 Cards in this Set
- Front
- Back
Intermittent asthma
|
Symptoms <2 days/week, brief exacerbations, nighttime symptoms <2 nights/month
Tx: Only when symptoms occur, quick reliever med=SABA (albuterol), systemic oral steroids if needed during exacerbation |
|
Mild persistent asthma
|
Symptoms >2x/wk but <1x day, exacerbations affect activity, nighttime symptoms >2x/month
Tx: low dose inhaled steroid daily (Flovent), alt: cromolyn, singulair, theophylline, + SABA (albuterol) for acute exacerbations |
|
Moderate persistent asthma
|
Daily symptoms, exacerbations are long and severely affect activity level, symptoms >1x wk at night
Tx: medium dose inhaled steroid and long acting B2 agonist, alt=singulair or theophylline + SABA (albuterol) for acute symptoms, +systemic steroids if needed |
|
Severe persistent asthma
|
continuous symptoms, uses SABA multiple times per day, frequent exacerbations, limited physical activity
Tx: high dose ICS + long acting B2 agonist systemic steroids if needed, SABA for acute symptoms |
|
Dyskinetic cilia syndrome
|
Causes bronchiecstasis and chronic sinusitis, a/w male infertility, if seen with situs inversus look for Kartagener’s syndrome (situs inversus, chronic sinusitis, bronchiecstasis)
|
|
Steroids
|
Reverses regulation of B receptors, prevents migration of inflammatory cells, prevents cytokine and histamine production
S/E: cough, thrush, growth suppression |
|
Inhaled steroids
|
Fluticasone, used for long term prevention of symptoms
|
|
Systemic
|
Prednisone, use in short bursts or to prevent symptoms in severe asthmatics
|
|
B2 Agonist
|
Stimulates B2 receptors causing bronchodilation, stabilize mast cells
S/E: tachycardia, palpitations, tremors, dizziness, HA, nausea, decreased potassium, increased glucose |
|
Short acting B2 Agonist
|
Albuterol, epinephrine used to stop symptoms of asthma
|
|
Long acting B2 Agonist
|
Formoterol/salmeterol, used to prevent symptoms, long-term
|
|
Mast cell stabilizers
|
Inhibits degranulation of mast cells and mediator release from eosinophils, neutrophils, macrophages, monocytes, do not dilate bronchioles Cromolyn/nedocromil, can be used before exercise to prevent EIA or as an additional
Tx for asthma S/E: bad taste, dry mouth, pharyngitis, cough, N, HA |
|
Leukotriene modifiers
|
Block leukotriene synthesis to prevent allergy response, broncho constriction and mucous production Montelukast/zafirlukast/zileuton (Singulair) Used to prevent allergic rhinitis/persistent asthma
S/E: HA, nausea, abdominal pain, infection, dyspepsia, Increased ALT |
|
Bronchiolitis
|
Bronchiole inflammation caused by viral infection, RSV, common in children <2 years, increased risk for preemies, neonates, underlying disease
|
|
Bronchiolitis (S/S)
|
Rhinitis, cough, development of respiratory distress (tachypnea, use of accessory muscles, noisy/rasp breathing, wheezes, fever), hyperinflation seen on chest X-ray
|
|
Bronchiolitis (Tx)
|
Supportive care and hospitalize if needed, Synagis to prevent RSV in high risk infants,
|
|
Bronchitis
|
Inflammation of the lower airways, can be acute or chronic
|
|
Bronchitis (Causes)
|
Viral: rhinovirus, RSV, parainfluenza
Bacterial: mycoplasma, pneumo, chlamydiophilia pneumo, pseudomonas (in kids with CF) |
|
Bronchitis (S/S)
|
Dry cough, substernal discomfort, SOB, possible productive cough, low or no fever, URI symptoms, fine/moist rales, rhonchi
|
|
Bronchitis (Tx)
|
Supportive, antibiotics
|
|
Croup
|
Acute upper airway inflammation and obstruction, 6-36 months (peak incidence at age 2)
|
|
Croup (S/S)
|
Barking cough, URI symptoms, fever, stridor, symptoms worse at night, possible dyspnea, STEEPLE SIGN (radiologic sign)
|
|
Croup (Tx)
|
Symptomatic relief: cold, steam, humidity, corticosteroids: dexamethasone 2 mg/kg/day, bronchodilator, hospitalize if severe
|
|
Pneumonia (Viral)
|
RSV, CMV, influenza, rhinovirus (ALL AGES)
|
|
Pneumonia (Bacterial)
|
Group B strep gram (-)
Neonates: listeria 1-3 months: staph, chlamydia, strep. pneumo 4mos-5yrs: strep. pneumo, HIB, M. pneumo >5yrs: Mycoplasma pneumo, chlamydiophilia pneumo, strep. pneumo Mycoplasma is usually mild |
|
Pneumonia (S/S)
|
Cough, wheeze, URI symptoms, chest pain, high fever (bacterial), GI symptoms, tachypnea, crackles, pleural effusion, dullness, retractions, nasal flaring
|
|
Cystic fibrosis
|
Autosomal recessive, dysregulation of chloride channels –dehydrated viscous secretions in the airways, bile ducts, pancreas, intestines, vas deferens, sweat glands Leads to chronic pulmonary disease, nasal polyps, malnutrition, steatorrhea, biliary cirrhosis, male infertility, increased sweat production, pancreatitis, poor growth, diabetes, rectal prolapse
|
|
Cystic fibrosis (Dx)
|
Sweat test (could be from newborn screen), family history, and mutation detection
|
|
Cystic fibrosis (Tx)
|
Refer to CF center, abx to cover pseudomonas (Cipro + aercolized tobra) chest PT, pancreatic enzymes, nut support
|
|
Hyaline membrane disease/respiratory distress syndrome
|
Deficiency of surfactant=poor lung compliancy, tachypnea, grunting, nasal flaring, chest retractions, cyanosis, ground glass appearance, most common respiratory illness of the newborn
Tx: oxygen, CPAP, surfactant |
|
Transient tachypnea of the newborn
|
Results from incomplete evacuation of fetal lung fluid in FT infants, common in C sections (no big squeeze), tachypnea, grunting, retractions, rare cyanosis
Tx: oxygen, will resolve 24-48 hours |
|
Bronchopulmonary dysplasia
|
Infant requires oxygen at 36 weeks or greater with radiographic changes=chronic lung disease Increased incidence in LBW infants, caused by multifactorial (lung immaturity, barotrauma) Respiratory distress (cough/wheeze), poor growth/feeding, cyanotic episodes, fluid overloading
Tx: supplemental oxygen, supplemental nutrition/fluids, bronchodilators, diuretics, immunize, Synagis, decrease risk factors in environment |
|
Meconium aspiration syndrome
|
Meconium is aspirated in utero of with first breath
Term or PT at highest risk due to placental insufficiency, tachypnea, retractions, grunting, cyanosis, Supportive care and management of respiratory distress |
|
Foreign body aspiration
|
Rapid onset of gagging, coughing, choking w/ subsequent stridor, wheezing, cyanosis, can be asymptomatic if object is small and non-obstructive but will cause secondary infections/symptoms
Chronic recurrent pneumonia if retained in the lung |
|
Intussusception
|
Invagination of the bowel, sausage mass in RUQ, with emptiness in the RLQ (DANCE SIGN)
|
|
Intussusception (S/S)
|
Intermittent colicky abdominal pain, vomiting, bloody mucous stool, currant jelly stool, screaming and drawing up the legs with episodes of calm in between
|
|
Intusussception (Tx)
|
Air/barium enema to reduce DANCE SIGN—RLQ concavity due to missing bowel
|
|
Physiologic GER
|
Normal in infancy, infrequent, episodic vomiting after feeds, caused by over-feeding or lack of burping, painless, effortless with no growth abnormalities
|
|
Pathologic GERD
|
Frequent vomiting that causes FTT, esophagitis, aspiration pneumonia, Sandifer syndrome (turning head/arching back), related to other neurological disease
Dx: esophageal pH monitoring pH<4= reflux |
|
Treatment for GER/GERD
|
Empiric therapy should be tried based on symptoms Most physiologic GER will resolve, Thicken formula, prone position after feeding, small/frequent feedings, probiotics, acid suppression therapy (antacid, H2 blockers, PROTON PUMP INHIBITORS RECOMMENDED FOR CHILDREN AS 1ST LINE AGENT) Nissen fundoplication if severe
|
|
Clinical characteristics of lactose intolerance
|
Abdominal pain, diarrhea, nausea, flatulence, and bloating occur after ingesting lactose, can be due to primary or secondary lactase deficiency
|
|
Lactose intolerance (Dx)
|
Lactose/sucrose, breath hydrogen ion testing, lactose free trial resolves symptoms
|
|
Cow’s milk protein intolerance
|
Non-IgE mediated, CMP not broken down
|
|
Cow’s mile protein allergy
|
IgE mediated, causes antibody production, can have GI symptoms (bloody stool, diarrhea, vomiting, food refusal) skin symptoms (atopy, hives) resp (cough/wheeze) or anaphylaxis
|
|
Cow’s milk protein intolerance/allergy (Dx)
|
Food challenge, clinical improvement on CMP free diet, CMPI resolves by 1-3 years, CMA will continue for life
|
|
Toddler’s diarrhea
|
Chronic diarrhea with no definite cause in a child 6-24 months, with normal growth, usually caused by increased carbs, decreased fat & protein—causing osmotic diarrhea
Tx: Normalize diet, eliminate sorbitol containing fluids, remove offending foods/fluids |
|
Appendicitis
|
Pain preceded vomiting—usually only one or two times, vague periumbilical pain that moves to the RLQ, Can be complicated by variable bowel changes, anorexia, and fever, if perforates pain will improve but fever will develop and abdomen will be tense Guarding/rebound tenderness over McBurney’s (RLQ) point (+) Rovsing, obdurator, markle jar heel test, heel strike, and psoas signs
|
|
Appendicitis (Dx)
|
Ultrasound, CT is gold standard, may have increased WBC
|
|
Rovsing sign
|
Pressure on LLQ causes pain in RLQ
|
|
Psoas sign
|
Patient on left side, extend/flex right leg/hip causes pain = (+)
|
|
Obdurator sign
|
Internally rotate right leg/hip causes pain = (+)
|
|
Markle jar heel test
|
Stand on toes, drop to heels=pain
|
|
Celiac disease
|
Most common malabsorption syndrome, inflammatory reaction caused by gluten=intestinal damage Impaired growth, diarrhea, steatorrhea, abdominal distention, wasting, fatigue, delayed puberty, anemia, dermatitis herpeticum, enamel hypoplasia
|
|
Celiac disease (Dx)
|
Endoscopy/biopsy=definitive diagnosis Lab testing: preferred test: Anti-tissue transglutaminase antibodies (tTG)-IgA, total IgA level
|
|
Celiac disease (Tx)
|
Restrict gluten from diet
|
|
Infantile colic
|
Persistent crying in an infant <3 months of age, cries 3 hours/day 3 days/week, is inconsolable and keeps legs stiff and fists clenched
Tx: is supportive, colic will resolve over time Diet alterations, limit overstimulation, use crib vibrators, infant massage as needed, provide support to parents, swaddle |
|
Ulcerative colitis
|
Inflammation of the colon
|
|
UC (S/S)
|
Bloody diarrhea, weight loss, delayed growth, anorexia, arthritis, abdominal pain, oral ulcers, skin lesions
|
|
UC (Dx)
|
ESR, CRP, CBC, colonoscopy, endoscopy=definitive dx
|
|
UC (Tx)
|
Elemental diet, aminosalicylates, steroids, immune modulators, surgery, monitor nutrition/growth, refer to ophthalmology, stool for fecocalprotectin
|
|
Meckel diverticula
|
Ectopic gastric mucosa within the diverticulum, common source of significant lower GI bleeding—usually painless but can cause large blood loss
|
|
Giardia
|
Flagellate protozoan, found in contaminated water and food, fecal-oral spread, seen in childcare and deviation disability settings, incubation 1-4 weeks, may be asymptomatic
|
|
Giardia (S/S)
|
Cramps, flatulence, bloating, anorexia, weight loss, diarrhea is watery/greasy. foul can be debilitating and long term
|
|
Giardia (Tx)
|
Metronidazole 15 mg/kg/day for 5 days alt: nitazoxanide, tinidazole
|
|
Peptic ulcer disease
|
Mucosal defects in the stomach/duodenum; can be idiopathic PRIMARY (DUODENUM) SECONDARY (STOMACH), H.pylori and CMV can also be a cause
|
|
Peptic ulcer disease Major Criteria
|
Abdominal pain and recurrent vomiting
|
|
Peptic ulcer disease Minor criteria
|
Hematemesis, heartburn, anorexia, nausea, increased belching/hiccups, anemia, guaiac +
|
|
Peptic ulcer disease (Dx)
|
Endoscopy=standard + biopsy (stool antigen test can be used in primary care)
|
|
Peptic ulcer disease (Tx)
|
Antacids (1st line), Amoxicillin, clarithromycin, omeprazole
|
|
Pinworms (enterobious vermicularis)
|
Pinworms (nematodes), roundworms (white, threadlike 1 cm) Preschool most common, often occurs in families, causes perianal/vaginal itching, urthritis, vaginitis, salpingitis rare complications
Tx: Mebendazole 100 mg/dose, repeat in 2 weeks, pyrantel pamoate 11 mg/kg, repeat in 2 weeks Wash hands/sheets/bedding |
|
Pyloric stenosis
|
Thickening of the pylorus muscle leading obstruction—PYLORIC OLIVE—RUQ hard mobile mass Presents between 3 weeks and 4 months of age, vigorous, projectile vomiting after eating with weight loss, constipation, dehydration—Surgically corrected
|
|
Pyloric stenosis
|
STRING SIGN, elongated pyloric channel and delayed emptying seen on upper GI
|
|
Crohn’s disease
|
Chronic IBD, causes skip areas, can affect entire GI tract
Hx: Weight loss, delayed growth, large joint pain, abdominal pain, bloating after meals, diarrhea, jaundice, mouth sores, extraintestinal signs can be seen—eye involvement, +family history |
|
Crohn’s Dx
|
ESR and CRP, nutrition labs, CBC, LFT, stool culture, bone age, upper GI, CT with contrast, endoscopy= definitive dx
|
|
Crohns Tx
|
Anti-diarrheals, corticosteroids, aminosalicylates, immune modulators, probiotics, antibiotics, surgery PRN, refer to optho
|
|
Hirschsprungs disease
|
Aganglionic megacolon, no stool in first 48 hours of life, severe constipation, FTT, abdominal distention, abnormal rectal anatomy, ant scrotal placement, vomiting, abnormal stool quality, empty ampulla upon exam with exposure evacuation upon removal—less common today, consider with intractable constipation
|
|
Mild dehydration
|
3-5% weight loss, thirst, cap refill >2 sec, slight decrease in urine production
|
|
Moderate dehydration
|
5-10% weight loss, slight increase in HR, >10 mmHg change in BP, irritable/thirsty, dry membranes/tears, norm-sunken fontanel, decreased cap refill (2-4 sec), decreased urine output >8-12 hours, SG >1.02
|
|
Severe dehydration
|
10-15% weight loss, increased HR, orthostatic BP (shock), irritability-lethargic, intense thirst, dry MM, sunken eyes/fontanel, cap refill >4 sec, oliguria/anuria
|
|
Shock
|
15% weight loss, increased HR, weak, unresponsive, dizzy cap refill >4 sec, anuria, acrocyanotic
|
|
UTI
|
Most common organism is E.Coli
|
|
UTI Infants/Neonates
|
Jaundice, hypothermia, FTT, sepsis, V/D, abdominal distension, lethargy, malaise, poor feeding, fever, malodor urine, dribbling
|
|
UTI Toddlers/Young children
|
Malodor urine, change in voiding, abdominal or flakn pain, enuresis, V/D (think pyelo), fever, diaper rash
|
|
UTI School age/adolescent
|
Dysuria with frequency, malodor, enuresis, abdominal or flank pain, fever, V/D (think pyelo), malaise
|
|
UTI Dx
|
Sterile cath in young children (+) nitrites, (+) leukocytes= suspicious, culture must conform diagnosis
|
|
UTI Tx
|
Afebrile UTI: Bactrim, alt Amoxil x 10 days, other alt= Augmentin, nitrofurantoin, Follow up culture: 48-72 hours after tx is started, pyridium can be given for >6 years for dysuria, pyelonephritis: hospitalize for IV abx
|
|
Hypospadias
|
Congenital abnormality of the urethral meatus, can be located anywhere along the penis or perineum Tx: surgical repair and circumcision
|
|
Hydrocele
|
Painless collection of serous fluid in the scrotal sac, can be communicating (fluid moves from abdomen to scrotum) or non-communicating (fluid only in scrotum)
|
|
Hydrocele (S/S)
|
Asymmetry of the scrotum, unilateral swelling, translucent on transillumination, can be tense, blue, and non-reducible if non-communicating
|
|
Hydrocele (Tx)
|
Non-communicating (no Tx, fluid will reabsorb, refer if fluid persists) communicating (refer for surgical repair due to HERNIA risk)
|
|
Cryptorchidism
|
Testicle that does not reside/manipulate into the scrotum, can be gliding/ectopic/or ascended, #1 GU d/o in males, empty scrotum, testicle that moves in and out of scrotum
|
|
Cryptorchidism (Tx)
|
Refer for surgical repair, esp. if age >6 mos, after 1 year requires immediate referral
|
|
Phimosis
|
Foreskin too tight to be retracted, tight pinpoint opening to foreskin, thickened rolled foreskin
|
|
Paraphimosis
|
Retracted foreskin that cannot be reduced, edema/blue color of the glans
|
|
Phimosis/paraphimosis (Tx)
|
Cleanse foreskin, betamethasone cream for phimosis, ice, surgical release for paraphimosis
|
|
Varicocele
|
Benign enlargement/dilation of testicular veins, “bag of worms,” painless scrotal mass S/S painless swelling, bag of worms texture,
Dx: US to r/o malignancy Tx: monitor, refer if large or painful |
|
Testicular torsion
|
Twisting of the testis leads to ischemic injury S/S: unilateral pain that starts acutely and gradually worsens, ill-appearing, anxious, testis can be swollen/erythematous, absent cremastearic reflex on affected side
tx: surgical emergency |
|
Epididymitis
|
Painful/acute inflammation of the epididymis often cause by n. gonorrhea, or chlamydia
S/S: scrotal edema/erythema, epididymis is hard, indurated and tender, PREHN’s sign (elevation of testis relieves pain), possible urethral discharge Tx: bed rest, scrotal support, site baths, NSAIDS, abx tx (ceftriaxone & doxy, alt=Levofloxacin) refer if does not resolve |
|
Labial fusion
|
Fusion of the tissue between labia minora, most common in girls 3 mo-6 years
S/S: think, flat membrane found of varying length, degree of opening varies Tx: Observation (can resolve with puberty) A&D ointment with pressure, estrogen cream 1%, only need to separate if impending vaginal/urine drainage, parental concern or prolonged |
|
Vulvovaginitis
|
Inflammation with discharge from infection or irritation caused by non-specific, bacterial, fungal, FB or pinworms
S/S: itching, irritation, discharge, urinary complaints Tx: Depend on cause, abx, anti-fungals, avoid exacerbating factors |
|
Bacterial vaginosis
|
Caused by gardnerella vaginosis/anaerobic bacteria, can be sexually transmitted, replaces normal vaginal fauna S/S foul odor, milky/white discharge, can be asymptomatic
Dx: pH >4.5, (+) whiff test= fish odor + clue cells Tx: metronidazole 500 mg BID PO x & days or metronidazole gel X 5 days or clindamycin cream X 7 days |
|
Primary amenorrhea
|
Absence of menarche by 16 years with normal puberty or by 14 years with no sexual secondary characteristics, caused by: delayed puberty, chronic illness, eating disorder, exercise, outflow obstruction, PCOS tumor, medications, drugs
|
|
Secondary amenorrhea
|
Absence of menses for 3 cycles or 6 months, caused by: pysch d/o, eating d/o, pituitary dz, pregnancy, exercise, PCOS, hypothyroid
|
|
Pregnancy
|
Amenorrhea, light short bleeding, N/V, urinary frequency, breast pain, abdominal fullness, weight gain/weight loss Dx: Serum HCG, post conception 48 hours, urine HCG 2-4 days post conception
|
|
Hegar sign
|
Cervical softening (2-3 months pregnant)
|
|
Goodell sign
|
softening of vaginal portion of the cervix
|
|
Chadwick sign
|
Blue cervix, vaginal, vulva
|
|
Turners Syndrome
|
XO karyotype with developmental cardiac, reproductive, genetic, and psyh issue; female with unexplained growth or pubertal delay, males can transmit gene (many affected embryos don’t live to term)
|
|
Turners (S/S)
|
Edema of hands/feet, nuchal folds (webbed neck), left sided cardiac anomalies, esp CO-ARC or HLH, low hairline, high palate, low ears, small mandible, short stature, Increased FSH, cubitus valgus, multiple pigmented nevi, short 4th metacarpal, no secondary sex characteristics
|
|
Turners (Tests and Tx)
|
Endocrine, psych, special ed if needed, cardio, ophtho, ENT, orthodontist, urology, screen for celiac
|
|
Short stature pathological causes
|
Chromosomal abnormalities, chronic disease, malnutrition, psychosocial deprivation, drugs, endocrine d/o’s (growth hormone deficiency, glucocorticoid excess, hypothyroidism)
|
|
History factors that are important to elicit
|
Signs of illness or malnutrition, chronic illness, timing of puberty, familial growth pattern, social stressor, use of medication
|
|
Physical exam: short stature
|
Signs of illness or malnutrition, stigma of Cushing’s syndrome, hypothyroidism, prader-willi, turner
|
|
Hypothyroidism S/S @ birth
|
No obvious signs during the first month of life; as infancy progresses: lethargy, growth deceleration, large fontanels, bradycardia, hypotonia, large tongue
|
|
Hypothyroidism (older children)
|
Weakness, muscle fatigue, poor growth, arthralgias, cramps, cold intolerance, constipation, weight gain, mental physical sluggishness, poor motor coordination, dry skin, thinning hair and brittle nails, puffy eyes, thick tongue, edema of hands and feet, alopecia, decreased DTR, hypoactive bowel sounds and diminished heart sounds
|
|
Work up for short stature
|
Bone age is helpful in making sure that the child does not have constitutional growth delay, Insulin growth factor (IGF-1), karyotype, thyroid functions, tissue transglutaminase for celiac disease, stool for O &P, sweat test, UA, head MRI
|
|
Workup for hypothyroidism
|
Elevated TSH, T4 and free T4 are both low or normal, increased liver enzymes, hyponatremia, hypoglycemia, anemia, T3 is not a good test for hypothyroidism
|
|
Signs of constitutional growth delay
|
While familial short stature looks like constitutional growth delay early on there is a difference in both bone age and pubertal staging.
Children with constitutional growth delay, there is a delay in bone age as well as puberty and they attain normal adult height Familial short stature: normal pubertal timing, bone age is the same as chronological age, final heigh is decreased from normal |
|
Signs of abnormal growth in children
|
If the growth falls off the curve by 2 SD, and is not between the mid parental height
|
|
Growth failure
|
Height falling from >2 SD below mean or from previously established growth, failure to grow more than 4 cm per year, being at 5th percentile or lower
|
|
Type 1 diabetes
|
Human leukocyte antigens, circulation islet cell antibodies can be found during the first few weeks
|
|
Triggers Type 1 DM
|
Infectious or toxic agents are thought to trigger the pancreatic B cells in predisposed people
|
|
S/S type 1 DM
|
Polydypsia, polyphagia, polyuria, nocturnal enuresis, weight loss and hunger, fatigue, weakness, and paresthesia, loss of subcutaneous fat and muscle wasting, peripheral neuropathy, skin & vaginal infection
|
|
Diagnostic testing type 1 DM
|
Serum fasting blood sugar >126 mg/dL on 2 separate occasions, random sugar of greater than 200 with polyuria, polydipsia, and weight loss, plasma ketones, BUN, creatinine may be elevated
|
|
Impaired glucose tolerance
|
Fasting blood glucose between 100 and 125
|
|
Conventional split dose insulin
|
2/3NPH and 1/3 regular insulin in AM, evening dose of ½ NPH and ½ regular.
|
|
Somogyi effect
|
Early AM hyperglycemia due to nocturnal hypoglycemia, hypoglycemia stimulates a surge of counter regulatory hormones that raise blood sugar, hypoglycemic at 3 AM and elevated BS at 7AM
Tx: reduce or eliminate the HS insulin |
|
Dawn phenomenon
|
Tissue is desensitized to insulin nocturnally, blood sugar is progressively higher through the night and is elevated at 7Am, due to presence of growth hormone at night.
Tx: Add or increase the dose of HS insulin |
|
Type 2 DM
|
90% of diabetes, not linked to HLA or islet cell antibodies, obesity & family history are factor
|
|
Type 2 DM tx
|
Metformin 500 mg TID or 850 BID
|
|
Hyperthyroidism or graves disease
|
Diffuse enlargement of the thyroid, can be from toxic adenoma, subacute thyroiditis, TSH secreting tumor, high dose amiodarone
|
|
Hyperthyroidism Tx
|
Propanalolol for symptoms, methimazole 30-60 mg per day, proplthiouracil 300 mg to 600 mg daily, radioactive iodine
|