CLIPP case 7. Newborn (respiratory distress, hypoglycemia, discharge) Flashcards

1
Q

Risk factors for respiratory distress of newborn

A

-Maternal GDM, drug exposure
-Infection, GBS
-Prematurity
-PROM >/= 18 hours before delivery
(neonatal sepsis)
-C-section
-Meconium in amniotic fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

APGAR score

A

-appearance, pulse, grimace, activity, respiration
-significance is fetal-to-neonatal transition
-correlates poorly with the future neurological
outcome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Classification of birthweight

A
  • LGA: >90%ile
    • DM mothers
    • Cx: traumatic delivery with C-section/ forceps/ vacuum, injury of clavicle/brachial plexus/facial nerve, hypoglycemia
  • Appropriate: 10-90%ile
  • SGA: <2500g
    • Cx: Hypothermia, hypoglycemia (inadequate glycogen stores), polycythemia
    • (IUGR: Diagnosis of fetus)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Ballard assessment

A

-Assessment of gestational age
-Should be performed on every infant within 24hr life
+/- 2 weeks accuracy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Fetal circulation

A

In utero, oxygenated blood from the placenta is transported to the fetus by the umbilical vein. A portion of this blood perfuses the liver. The remainder bypasses the liver through the ductus venosus and enters the IVC.

One-third of this vena caval blood crosses the PFO to the left atrium and is pumped to the coronary, cerebral and upper body circulations. The remaining two-thirds combines with venous blood from the upper body in the right atrium, and is directed to the right ventricle and out the pulmonary artery.

Vasoconstricted pulmonary arterioles produces high PVR, allowing only 8-10% of the blood from the RV to flow through the pulmonary vasculature. The remaining 90-92%, is shunted through the PDA to the descending aorta.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Transition to extrauterine respiration

A
  • Vaginal delivery uterine contractions squeezes fluid out of lungs, and lymphatics absorb it. *Delayed absorption causes TTN.
  • Cutting the umbilical cord removes the low-resistance placental circulation
  • Breathing replaces lung fluid with air
  • Pulmonary arterial resistance drops
  • PFO and PDA close
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Signs of respiratory distress

A

Tachypnea, retractions, and grunting

  • Intercostal and subcostal retractions reflect the increased work of breathing due to decreased lung compliance, either due to primary lung pathology or edema.
  • Grunting occurs at the end of expiration, and is the audible sound of air being expelled through a partially closed glottis as the infant attempts to increase transpulmonary pressures, increase lung volumes, and improve gas exchange.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Differential of the cyanotic newborn

A
  • Pulmonologic: TTN, RDS, less commonly pneumothorax, diaphragmatic hernia, choanal atresia, pulmonary hypoplasia
  • CHD: Tetralogy of Fallot, Transposition, less commonly truncus arteriosus, tricuspid atresia, total anomalous pulmonary venous return, pulmonary atresia
  • CNS: Hypoxemic-ischemic encephalopathy, intraventricular hemorrhage, sepsis/meningitis
  • Other: Septic shock or meningitis, depression from maternal meds, hypothermia, polycythemia/hyperviscosity syndrome
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Oxygen challenge test

A
  • Hyperoxia test
  • In cyanotic infants, helps differentiate pulmonary and cardiac etiology based on PaO2 increase (less increase if cardiac)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Maternal hyperglycemia

A

Maternal hyperglycemia causes fetal hyperglycemia (fetal BG = about 2/3 maternal BG), but insulin does not cross the placenta. Fetal pancreatic beta cell stimulation and hyperinsulinemia results.

First trimester A1c >12% increases malformation risk 12x.

Third trimester insulin is the primary anabolic hormone for fetal growth. Causes growth of fat, heart, liver, muscle. LGA results. Brain and kidneys normal.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Advantages of breastfeeding

A
  • Lower renal solute load than formula
  • Ant-infective and anti-allergic
  • Bonding
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

TTN on CXR

A

-Perihilar streaking (interstitial fluid and engorged lymphatics), pleural fluid, coarse fluffy densities (fluid filled alveoli)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

RDS on CXR

A

-Air bronchograms, diffuse reticulogranular appearance of lung fields (“ground-glass
appearance”)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Hip dysplasia tests

A
  • Barlow (in adduction, push down to test for dislocation)
  • Ortolani (in abduction, push up to test for relocation)
  • Examine regularly up to 18 months old
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Hip dysplasia risk factors

A
  • Breech birth
  • Female 9:1
  • Family history
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Newborn hospital discharge considerations

A
  • Exam without major defects
  • Minimal/no jaundice
  • No blood group incompatibility
  • Breast feeding every 2-4 hours
  • Transition from meconium to seedy soft tan/yellow stools
  • Wt loss < 10%
  • 6 wet diapers per day
  • Vitamin D rX, review co-bedding and Back to Sleep program, car seat and adequate home support, PCP follow-up at 48hr and within week 1
17
Q

34-week-gestation premature infant is delivered via Caesarean section with no meconium and no premature rupture of
membrane (PROM) from a diabetic mother with fair glucose control and unknown
GBS status. He presents with respiratory distress. APGAR scores were 8 at 1 minute and 9 at 5 minutes. On exam, he is LGA, tachypneic, with no heart murmur, good
perfusion, and equal breath sounds. CXR shows “wet”-looking lungs, no consolidation, and no air bronchograms. Labs show he is hypoglycemic.

A
  • Transient tachypnea of the newborn
  • DDx:
    • Respiratory distress syndrome
    • Sepsis/pneumonia
    • Pneumothorax
    • Congestive heart failure
    • Hypothermia
  • Hypoglycemia: too tachypneic to breastfeed, so given breastmilk and formula via feeding tube
18
Q

Acrocyanosis

A

If not resolved within 8 hours or with warming, may be sign of cyanotic congenital heart disease

19
Q

RDS of newborn

A
  • Deficiency in lung surfactant
  • Most common cause of respiratory distress in premature infants
  • Risk factors:
    • Prematurity up to 37 weeks
    • GDM due to delayed lung maturation
    • Sibling with history of RDS
    • Male
    • C-section delivery without labor
    • Perinatal asphyxia
  • CXR can help distinguish between TTN and RDS
20
Q

TTN of newborn

A
  • Delayed clearance of lung fluid after birth causing early onset mild respiratory distress. *Benign, self-limited disease related to newborn transition. No long-term dysfunction. *Disorder of term infants, but can occur in premature infants
  • Risk factors:
    • C-section delivery
    • Male
    • Macrosomic
    • GDM
  • CXR can help distinguish between TTN and RDS
  • If respiratory symptoms do not improve, suspect pneumonia -> repeat CXR and abx
21
Q

CHF

A
  • Important cause of tachypnea
  • Most often caused by a congenital heart defect
  • Increased risk of heart defect if GDM, and therefore increased risk of CHF
  • Usually presents with heart murmur
22
Q

Sepsis/pneumonia

A

*Early signs of neonatal sepsis are subtle and
nonspecific - poor feeding, lethargy, irritability *May also present initially with tachypnea and progress to more severe illness rapidly *Risk factors:
- PROM
- GBS

23
Q

Hypoglycemia in infants

A

*GDM due to the chronic hyperinsulinemic
state that occurred during gestation
*Tachypnea is non-specific response

  • Send serum BG (glucometer is 10-15% lower)
  • Breastfeed > bottle if can -> NG tube feeds -> IV dextrose if BG remains <45. Maintain BG 41-50 mg/dL
24
Q

Congenital diaphragmatic hernia

A
  • Rare. Bochdalek hernia (posterolateral hernia) accounts for majority (> 95%) of cases:
    • Allows passage of abdominal organs into chest cavity and severely impairs lung development
    • Most defects occur on the left side
  • Absent breath sounds or presence of bowel sounds on one side
  • CXR: Air-filled loops of bowel in left side of chest, displacement of heart to contralateral side
25
Q

Pneumothorax

A
  • Caused by a collection of gas in the pleural space with resultant collapse of lung tissue. *Risk factors:
    • Mechanical ventilation
    • Meconium aspiration or severe RDS
  • Absent breath sounds on one side of the chest in combination with respiratory distress
26
Q

Meconium aspiration syndrome

A
  • Passage of meconium in utero may indicate fetal stress and hypoxia. Aspiration of meconium may occur in utero with fetal gasping, or at first breath at delivery.
  • Often presents with symptoms of respiratory distress, including tachypnea
27
Q

Transposition of the great arteries

A
  • Congenital heart defect in which the aorta and pulmonary arteries are transposed, resulting in respiratory distress and severe cyanosis shortly after birth as PDA closes.
  • Risk factor: IDM. Often associated with other congenital heart defects such as a VSD. *Murmur may be heard
28
Q

Hypothermia of newborn

A
  • Should be considered in the differential of a tachypneic newborn
  • May be associated with neonatal sepsis
  • Risk factors:
    • SGA and premature infants because of small body size and relatively large surface area
29
Q

Severe coarctation of the aorta

A
  • May cause respiratory distress if there is severe LVOT obstruction
  • Classically, diminished pulses in the lower extremities or asymmetric blood pressure readings suggest the diagnosis
  • In severely ill neonates, there may be no differences in the pulses because cardiac output is so poor.
30
Q

Echo in newborn

A
  • Gold standard in diagnosis of congenital cardiac lesions and persistent pulmonary hypertension of the newborn
  • Indicated when there is persistent cyanosis and no indication of lung disease, or when there are other signs suggesting a heart defect, such as a murmur, abnormal electrocardiogram (ECG), or chest X-ray showing abnormal cardiac contour