NICU Flashcards

1
Q

Painless compressible mass with little involvement of underlying tissue. Transiluminate well. Often in posterior triangle of neck.

A

Cystic hygroma

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2
Q

Flattening of midfacial structures, maxillary hypoplasia, smooth philtrum, SGA. Can have septal cardiac defects

A

Fetal alcohol spectrum disorder

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3
Q

Colonic obstruction involving a sig. caliber reduction in sigmoid and descending colon associated with transient inability to pass meconium. Resolves spontaneously.

A

Small left colon syndrome

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4
Q

Maternal features most often present in infants with small left colon syndrome

A

Diabetic mother

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5
Q

Maternal medication expsoure leadign to ebstein anomaly

A

Lithium

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6
Q

IUGR, microcephaly, ventriculomegaly, echocenic foci in liver, circular scarring and deformities of the extremities.

A

Congenital varicella infection

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7
Q

Craniosynostosis and ocular proptosis

A

Crouzon syndrome

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8
Q

Craniosynostosis and syndactyly

A

Apert syndrome

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9
Q

Causes of asymmetric IUGR

A

uteroplacental insufficiency, chronic hypertension, multiple gestation, abnormal placental structure and high altitude

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10
Q

Causes of symmetric IUGR

A

genetic abnormalities, chronic alcohol abuse, congenital anomalies, early in utero infections, chronic maternal anemia, ciagrette use, maternal SLE

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11
Q

Respiratory distress shortly after birth, decreased breath sounds on right side, right hemidiaphragm elevation on CXR and brachial plexus palsy

A

Injury to 3-5th cervical roots on birth

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12
Q

Abnormal gas pattern with dilated loops of bowel and small air bubbled within bowel wall on abdominal film

A

NEC

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13
Q

Incomplete to absent develompent of the sacrum, and to a lesser extent lumbar vertebrae, varying degrees of decreased lower extremity and bowel neuro function, lower extremity growth impairment

A

Caudal regression syndrome

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14
Q

Respiratory depression, apnea, low tone, Gi hypomotility in an infant of a mother with gestational HTN

A

consider hyperMag in baby

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15
Q

Treatment for type II Crigler-Najar

A

phenobarbital

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16
Q

Failure to pass meconium, bilious emesis, granular material on plain film or abdominal xray

A

Meconium ileus

17
Q

When does ABO incompatibility occur

A

with type O mothers with infant with type A or B

18
Q

Translucent to blue nonblanching, fluctuant, pseudocyst lateral to midline in lower mouth

19
Q

Highest risk group for DDH

A

breech girls

20
Q

Most common location for CDH

A

posterolateral defect of diaphragm on the left

21
Q

medication exposure in utero that can lead to hypertelorism, short stubby digits, high arched eyebrows, short upturned nose, orofacial clefts, GU anomalies and VSDs

22
Q

medication exposure in utero that can lead to craniosynostosis and limb abnormalities

A

methotrexate

23
Q

medication exposure that can lead to microcephaly, external auditory canal anomalies, cardiac defects, thymic hypoplasia, facial nerve palsies and GU anomalies

A

retinoic acid

24
Q

Areola staging in pre-term infants

A

first raised at 34-35 weeks, palpable at 36-37 weeks

25
Pinna staging in pre-term infants
soft and folded between 24-31 weeks, pinna returns slowly from folding between 32-35 weeks, thin cartilage springs back 36-39 weeks, firm pinna after 39 weeks
26
Sole creases staging in pre-term infants
1-2 anterior creases on soles 32-33 weeks, 2-3 present 34-35 weeks, anterior 2/3s covered at 36-37 weeks, whole sole covered 38-40 weeks
27
Lanugo staging in preterm infants
covers entire body until 32 weeks, absent from face between 33-37 weeks, on shoulders only 38-41 weeks, afterwards absent
28
Penile length that warrants referral
< 2 cm
29
Management of asymptomatic <20% PTX
100% inspiried FiO2
30
Premature infant positioned on side and dependent side turns dark red, other side turns pale
Harlequin change - an exaagerated autonomic response, needs no further work up
31
post-term infant with nontender subQ nodules or plaques on trunks, buttocks, extremities typically after birth injury, hypoxia in birth, forceps delivery, or meconium aspiration
SubQ fat necrosis
32
Complication to watch for with subcutaneous fat necrosis
Hypercalcemia. Should monitor Ca every 1-2 weeks until lesions resolve