Peds Flashcards

1
Q

12 Month Milestones

A

MOTOR: walks, throws objects

LANGUAGE: 1-3 words, follows 1-step command

SOCIAL: stranger and separation anxiety

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2
Q

4 Year Milestones

A

MOTOR: draw a cross, identify body parts, hops on one foot, throws overhand, copies a square (4.5)

LANGUAGE: language understood by strangers, uses past tense

SOCIAL: plays with other kids, social interaction

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3
Q

Imaging in hypertrophic pyloric stenosis

A

Thickened pyloric muscles via US

Upper GI w/Contrast may show elongated pyloric canal and a “double track” sign (two thin tracts of barium created by compressed pyloric mucosa)

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4
Q

Peritonsillar abscess

A

Infection of the superior pole of tonsils, most common in young teenagers. Presents with fever, sore throat, muffled voice, drooling, trismus, and neck pain.

May have deviation of uvula

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5
Q

1 Month Milestones

A

MOTOR: Reacts to pain

LANGUAGE: Responds to noise

SOCIAL: Regards human face, eye contact

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6
Q

Hypertrophic Pyloric Stenosis

A

Usually presents @ 3-6wk as “hungry baby” with projectile vomiting that is non bilious and occurs immediately after meals.

Physical exam will reveal olive shaped mass at RUQ and peristaltic waves across upper abdomen moments before emesis.

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7
Q

3-Year Milestones

A

MOTOR: copies a circle, pedals a tricycle, builds 3-block tower, repeats 3 numbers

LANGUAGE: speaks in sentences, 3/4 speech understood

SOCIAL: group play, plays games, knows gender, knows first and last name

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8
Q

2 Year Milestones

A

MOTOR: runs, walks up and down stairs, kicks a ball, copies a line

LANGUAGE: 2-3 word phrases, half of speech understood by strangers

SOCIAL: parallel play

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9
Q

Child lead screening?

A

All kids not previously enrolled in Medicaid should be screened @ 36-72mo

All children @ risk for exposure should be screened @ 1 yr

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10
Q

Intussusception

A

Telescoping of intestine → intermittent severe abdominal pain, associated vomiting that becomes bilous as obstruction occurs.

May get currant jelly stools and elongated mass palpable in right abdomen

Most common in ileocecal junction

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11
Q

4 Month Milestones

A

MOTOR: Eyes move past midline, rolls over

LANGUAGE: laughs and squeals

SOCIAL: regards hand

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12
Q

5 Year Milestones

A

MOTOR: copies a triangle, catches a ball, partially dresses self

LANGUAGE: writes name, counts 10 objects

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13
Q

2 Month Milestones

A

MOTOR: eyes follow object to midline, head up prone

LANGUAGE: Vocalizes

SOCIAL: social smile, recognizes parent

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14
Q

6 Year Milestones

A

MOTOR: skips with alternating legs, ties shoes, draws a person with 6 parts

LANGUAGE: identifies right from left leg

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15
Q

6 Month Milestones

A

MOTOR: sits unsupported, transfers object from hand to hand, and rolls prone to supine

LANGUAGE: babbles

SOCIAL: recognizes strangers

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16
Q

Retropharyngeal Abscess

A

Most common in kids 2-4 y/o via extension of pharyngeal infection, prenetrating trauma, iatrogenic instrumentation, or foreign body.

Will get fever, drooling, dysphagia, stridor, etc… May have tender enlarged cervical lymp nodes.

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17
Q

Young patient with 3-days of low grade fever and runny nose followed by erythematous rash on cheeks…cause?

A

Parvovirus → erythema infectiosum or “fifths disease”

18
Q

Retropharyngeal abscess treatment

A

Cephalosporin

Antistaph penicillin

19
Q

Conjunctivitis Treatment

A

Self limited in 10-14 days, can decrease to 2-3 days with sulfonamide given locally TID

20
Q

What adolescents needs to see a cardiologist before getting cleared for their sports physical?

A

Any adolescent with the stigmata of Marfan syndrome, a murmur suggestive of HCM (heard along left sternal border that gets worse with standing or valsalva and improves with squatting), a grade 3/6 systolic murmur, or any diastolic murmur

21
Q

9 Month Milestones

A

MOTOR: pincer grasp (10 mo), crawling, cruises (walks holding furniture)

LANGUAGE: “mama”, “dada”, “bye-bye”

SOCIAL: starts to explore

22
Q

Peritonsillar abscess treatment

A

Ampcillin-sulbactam

or

clindamycin

23
Q

Signs & Symptoms of Neonatal Sepsis

A

Temperature instability

Tachypnea, grunting, nasal flaring, retractions

Hypotension

Bradycardia

Overwhelming Shock → pallor & poor cap refill

24
Q

Factors that increase risk of Early Onset GBS

A
  1. Ruptured membranes > 18hr prior to delivery
  2. Chorioamnionitis
  3. Intrapartum fever
  4. Previous infant with GBS
  5. Mom < 20 y/o
  6. Low birth weight or prematurity
25
Q

Treatment for suspected neonatal GBS infection?

A

IV aminoglycosides (gentamicin, tobramycin) + Penicillin (ampicillin)

26
Q

Osgood Schlatter Disease

A

Microfractures in the area of the insertion of the patellar tendon into the tibial tubercle, most common in athletic adolescents.

Get swelling, tenderness, and increase in size in the tibial tuberosity.

27
Q

Orbital Cellulitis Treatment

A

Hospital admin w/CT or MRI to determine extent of infection

IV abx

28
Q

Complications of orbital cellulitis in children

A

Cavernous sinus thrombosis

Meningitis

Brain abscess

Vision loss from increased intraorbital pressure w/retinal artery occlusion

29
Q

Febrile, ill-appearing child with proptosis and restriction of eye movement

A

Orbital cellulitis

30
Q

5 year old boy with itchy rash that was on his face as an infant but as he got older moved to his flexural areas. Rash is worse during winter.

Rash is maculopapular, red, and weepy.

A

Eczema

Initial Presentation = papulovesicular, weeping eruption that progresses to a scaly, lichenified dermatitis

From 3 mo-2 yr typical on cheeks, wrists, scalp, arms, and legs.

From 2-12 yr moves to mostly extensor surfaces

31
Q

Presentation of head lice

A

Intensely itchy scalp that can be weepy, boggy, and red.

May also get swollen posterior auricular and suboccipital LN

32
Q

Head Lice Treatment

A

Children > 6 mo: Topical ivermectin

Rid & Nix (OTC) often have resistance

33
Q

Tuberculous Meningitis

A

Most common between 6 mo-4 yrs

Stage 1 = 1-2 wk of non-specific symptoms such as vomiting, irritability, listlessness, fever, regression of milestones, etc…

Stage 2 = begins abruptly with seizures, lethargy, hypertonicity, hydrocephalus, and focal neurologic signs

Stage 3 = coma, HTN, posturing, decompensation, & death

34
Q

Leukocyte Adhesion Deficiency Type 1 (LAD-1)

A

Intact umbilical cord after 1 month

Overwhelming bacterial infections

CBC will show leukocytosis; can make diagnosis by measuring CD11b using flow cytometry

35
Q

Screening for lead poisoning

A

Blood Lead Level, preferably venous

Toxicity can occur at levels as low as 10ug/dL and EPO may not be elevated in such low-level poisonings

36
Q

Fragile X Syndrome Characteristics

A

Macrocephaly w/long face, large ears, & prominent jaw

High arched palate

Evidence of mitral valve prolapse

Macroorchidism

Pectus excavatum

Repetitive speech, gaze avoidance, and hand flapping

37
Q

1-wk old infant with transient rash = splotchy areas of erythema with a central pustule whose fluids reveal eosinophils

A

Erythema toxicum

2-3cm erythematous macules, occasionally with central yellow-white pustule

38
Q

Adolescent boy with 3-5cm red rash at nape of neck that gets more significant with exertion or emotion

A

“Salmon patch”

Aka: nevus simplex or nevus flammeus

Vascular lesions that occur on face, nuchal, and occipital regions

39
Q

3-day old African-American boy with 3mm pustules filled with milky fluid that are easily wiped away to reveal an underlying small hyper-pigmented macule

A

Pustular Melanosis

More common if African-Americans

Usually found at birth and consistent of 1-2mm pustules → hyperpigmented lesion encircled by scale after they rupture.

40
Q

1-day old with a 0.5cm oval lesion on the righ occiput that is yellowish and slighly raised, hairless, and “orange-peel” in texture.

A

Sebaceous nevi = small sharply edged lesions on head and neck of infants.

Can get malignant degernation after adolescence