Ped Flashcards

1
Q

Differenciate : Gastroschisis and Omphalocele

A
  • Gastroschisis is the right of midline and without a membrane. It’s typically not associated with chromosomal abnormalities but is more susceptible to twisting and infection. Think “angry sounding” and “angry looking” disease.
  • Omphalocele is in the midline and covered with a membrane. It’s more commonly associated with chromosomal abnormalities (such as Beckwith-Wiedemann syndrome).
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2
Q

Describe : Neural Tube Defects

A
  • Neural tube disorders are a product of genetic syndromes and folate deficiency in mom during pregnancy.
  • Spina bifida stems from difficulties with fusion of the caudal neural tube. That means the front of the spine forms normally, but back of it doesn’t.
  • This is a spectrum of disease, from an incomplete spine but with skin intact (Spina Bifida Occulta) to a complete open sac of neural tissue and CSF (meningomyeloscele).
  • Spina Bifida is treated (Folate supplementation) and screened for during pregnancy.
  • A **Positive AFP screen will prompt an Ultrasound **of baby revealing the defect.
  • If prenatal care was absent, the physical exam of the neonate could show something as subtle as a tuft of hair or a dimple up to something as obvious as a large sac-like structure.
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3
Q

Differenciate : Spina Occulta, Meningocele and Myelomeningocele

A
  • Occulta = bony defect without protrusion of meninges or spina cord; may have overlying hair
  • Meningocele = extrusion of meninges (no spinal cord) in sac outside spine
  • Myelomeningocele = extrusion of meninges and spinal cord in sac outside spine
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4
Q

When is clef lips and palates repaired?

A
  • Cleft lips : by 10-12 weeks
  • Palates : by 10-12 months
    to preserve speech function.
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5
Q

Describe : Choanal Atresia (8)

A
  • This is an atretic or anatomically stenosed connection between the nose and mouth.
  • Unilateral or bilateral (which is an emergency).
  • In severe cases the baby will be blue at rest as they are obligate nose breathers (think breathing and breastfeeding simultaneously).
  • They will pink up with crying (as he/she uses his/her mouth).
  • If there’s a partial obstruction there might be a childhood snore. Kids shouldn’t snore.
  • If there’s complete atresia a catheter will fail to pass.
  • If it’s incomplete a fiber-optic scope will identify the lesion.
  • Surgery is required to open the atretic passage.
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6
Q

Describe : Necrotizing Enterocolitis (NEC) (4)

A
  • If it’s a **premature baby **and bloody diarrhea the diagnosis can essentially be assumed.
  • An** x-ray / babygram** will show pneumatosis intestinalis (air in the wall of the bowel) to confirm the diagnosis.
  • The baby needs to go NPO immediately and get started on TPN and IV antibiotics.
  • Hold off from surgery unless there’s no improvement or conditions worsen.

EN RÉSUMÉ : Premature infant + bloody stool = NEC Make NPO and start antibiotics

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7
Q

Describe : Meckel’s Diverticulum

A
  • remnant of the omphalomesenteric (Vitelline) duct which can contain gastric tissue. That can cause acid secretion and contribute to bleeding by forming ulcers.
  • It presents with either Fecal Ocult Blood Test + , iron deficiency anemia, or hematochezia
  • The bleeding is painless and may be intermittent.
  • The classic rule of 2s is often pimped, but rarely tested: <2 years old, 2:1 ♂:♀, 2 inches in length, 2 feet from the ileocecal valve, 2% of the population.
  • To diagnose, do a** Meckel’s scan (technicium-99 radionucleotide scan)**.
  • Treat it surgically.
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8
Q

Describe : Swallowed blood in neonates (5)

A
  • A baby presenting with blood emesis or stool can cause some excitement.
  • During the peripartum process, babies can swallow maternal blood which can cause bloody GI outs.
  • The** Apt test **(alkali denaturation test) in neonates can determine if the blood is of maternal or fetal origin.
  • Fetal blood is resistant to denaturation, yield a positive test and require further investigation.
  • Maternal blood will yield a negative test; it just requires reassurance that no further testing is needed.
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9
Q

How are acute asthma exacerbations streated? (3)

A
  • ** albuterol/ipratropium (Duonebs®) **and IV steroids that get transitioned to orals.
  • Treatment may require escalating therapy (magnesium, subQ epi) up to intubation.
  • Hospital admission is determined based on the need for supplemental oxygen, as well as the Peak Flow prior to and after bronchodilator therapy in the ED.
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10
Q

Describe difference unconjugated and conjugated bili

A

Conjugated = ALWAYS pathalogical

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11
Q

Describe difference between physiologic and pathalogic bilirubin

A
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12
Q

Describe workup for jaundice

A
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13
Q

Describe : Breast feeding jaundice (4)

A
  • quantity issue in newborns** ≤ 7 days** old.
  • Without sufficient volume, the bowels don’t move fast enough; the **body reabsorbs bilirubin and bilirubin builds up. **
  • By increasing the number of feeds the problem fixes itself.
  • In order to be reabsorbed from the gut the bilirubin must be unconjugated so there will be an elevation in indirect bilirubinemia.
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14
Q

Describe : Breast milk jaundice (aka “human milk jaundice”) (4)

A
  • a “quality” issue that occurs at 6-14 days.
  • The thought is that **breast milk inhibits glucuronyl transferase **(the conjugation enzyme).
  • This typically does not cause kernicterus.
  • Formula can be temporarily substituted for breast feeding (preferred) or used to supplement breast feeding.
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15
Q

What’s the difference between breast feeding jaudice and breast milk jaundice?

A
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16
Q

Name respiratory disorders in neonates (2)

A
  • Transient Tachypnea of the Newborn (TTN)
  • Respiratory Distress Syndrome (RDS)
17
Q

Describe : Transient Tachypnea of the Newborn (TTN) (5)

A
  • Delayed clearance of fetal lung fluid (mainly seen in Cesarean deliveries).
  • This is the (near) term infant that has grunting and tachypnea
  • Hyperexpanded and “wet” appearing CXR.
  • This can simply be a delayed transition (resolving under 6 hours after birth) but TTN can be present for 24-48 hours.
  • Treat with supplemental oxygen or CPAP/intubation if needed.
18
Q

Describe : Syndrome de détresse respiratoire (4)

A
  • Has multiple factors but usually from surfactant deficiency causing atelectasis.
  • This infant is usually premature and has a history of perinatal distress but will also present with grunting.
  • CXR will show low lung volumes and a uniform granular pattern.
  • If severe, will require surfactant administration and mechanical ventilation.
19
Q

Differenciate conjunctivitis in newborns (3)

A
20
Q

Name hip pathologies in peds (5)

A
  • Developmental Dysplasia of the hip
  • Legg-Calve-Perthe Disease
  • Slipped Capital Femoral Epiphysis
  • Septic Hip
  • Transient Synovitis
21
Q

Describe : Legg-Calve-Perthe Disease (3)

A
  • When a child is around six years old they can suffer from avascular necrosis of the hip.
  • There’ll be an insidious onset knee pain and an antalgic gait (spend less time on painful leg).
  • Diagnose by x-ray and then cast.
22
Q

Describe : Transient Synovitis (5)

A
  • On the differential for septic hip.
  • It’s synovial inflammation up to 4 weeks after URI or GI viral illness.
  • Differentiate by lack of fever, no leukocytosis, and decreased inflammatory markers (Kocher criteria - the more you have, the higher risk of septic joint).
  • The X- ray is normal.
  • Treat supportively.
23
Q

Describe : Erythema Infectiosum (8)

A
  • parvovirus B19
  • usually a nonspecific prodrome that gives rise to an erythematous rash.
  • It’s isolated to the face bilaterally (slapped-cheek).
  • You may see some spread to the trunk/limbs, which will be lacy or reticular in appearance.
  • This disease is benign on its own in a normal healthy baby and** resolves spontaneously**.
  • If there’s increased cell turnover with increased baseline reticulocyte production (sickle cell) or decreased production (anemia, heavy metals) this infection may precipitate an aplastic crisis.
  • If baby gets sick and is near mom while she’s pregnant it can cause hydrops fetalis in the new baby. Separate any gravid mom.
  • Can see arthritis in adults.
24
Q

Describe : Rougeole (4)

A
  • paramyxovirus
  • obvious prodrome of low grade fever and the “four hard Cs” – **cough, coryza (runny nose), conjunctivitis, and Coplik Spots (Koplik Spots) **
  • The rash starts on the face, after the prodrome. As it spreads to the body, fever starts with the rash.
  • Later in life a potentially lethal complication (subacute sclerosing panencephalitis) can occur.
25
Q

Décrire : Rubéole

A
  • Caused by the togavirus named Rubella
  • The rash itself looks just like rougeole. It starts on the face, spreads down to the toes, and is likewise macular.
  • However, during the rash these patients don’t look as sick as rougeole.
  • The rash tends to be fainter and spreads quicker.
  • The prodrome of tender generalized (periorbital, postauricular) lymphadenopathy precedes the rash.
  • Forchheimer spots on the palate (red enanthem) can be seen.
  • Since measles and rubella look the same they’re in the same vaccine.
26
Q

Describe : Roseole

A
  • Caused by HHV-6
  • there’s a prodrome of a high-fever (>40 C) that breaks as the rash starts.
  • The rash is a macular rash that begins on trunk and spreads to the face.
  • Febrile seizures may result from extreme fever during the prodrome.
27
Q

Describe : Varicelle (Chickenpox) (7)

A
  • varicella zoster virus.
  • A vague, nonspecific viral prodrome indicates contagion.
  • What follows is a rash that starts on the trunk and head followed by outward spread to extremities.
  • The vesicles are on an erythematous base and are in different stages (eruption, ulceration, crusting).
  • Contagion ends with a final crust.
  • Scarring and secondary infections (Staph and GAS) are two complications.
  • Shingles (reactivation) can be prevented with immunization.
28
Q

Differenciate epidural and subdural hematoma

A

The epidural hematoma
* caused by trauma to the side of the head
* a loss of consciousness followed by a lucid interval, then coma.
* The CT shows a **lens-shaped hematoma. **

The subdural hematoma
* caused by major trauma (peds struck, high speed MVA - teens) or by abuse (shaken baby – infants).
* There’s a coma and the child stays in it.
* Look for a concave or crescent shaped hematoma.

29
Q

Describe : West Syndrome (Infantile Spasm)

A
  • If that young (<1-year-old) child has symmetric jerking of the head, trunk, or extremities but without fever, consider infantile spasms.
  • This syndrome is confirmed by interictal EEG showing hypsarrhythmia.
  • The treatment is ACTH which can help with spasms, normalizing EEG.
  • Almost all kids with IS will have some sort of intellectual disability; 50% are severe.