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

A

Ranula

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

A

phenytoin

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
Q

Pinna staging in pre-term infants

A

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
Q

Sole creases staging in pre-term infants

A

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
Q

Lanugo staging in preterm infants

A

covers entire body until 32 weeks, absent from face between 33-37 weeks, on shoulders only 38-41 weeks, afterwards absent

28
Q

Penile length that warrants referral

A

< 2 cm

29
Q

Management of asymptomatic <20% PTX

A

100% inspiried FiO2

30
Q

Premature infant positioned on side and dependent side turns dark red, other side turns pale

A

Harlequin change - an exaagerated autonomic response, needs no further work up

31
Q

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

A

SubQ fat necrosis

32
Q

Complication to watch for with subcutaneous fat necrosis

A

Hypercalcemia. Should monitor Ca every 1-2 weeks until lesions resolve