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132 Cards in this Set

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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