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Neonatal Resuscitation
Neonatal Resuscitation
Chapter 121
Neonatal Resuscitation
and Delivery Room
Emergencies
Jennifer M. Brady and
Beena D. Kamath-Rayne
NEONATAL RESUSCITATION
See also Chapter 81.
Guidelines for the Neonatal Resuscitation Program (NRP) are based
on recommendations from the International Liaison Committee on
926 Part XI ◆ The Fetus and the Neonatal Infant
136 million
babies born All babies require immediate assessment at birth
and simple newborn care
(assess breathing, dry, and put the baby skin-to-skin with mother)
Fig. 121.4 EXIT procedure. Baby with teratoma and critical high airway obstruction syndrome. Trachea is displaced to the lateral neck. (Courtesy
of Dr. Mark Wulkan, Pediatric Surgery, Emory University.)
Studies are investigating whether the onset of respirations before delayed Airway Obstruction
cord clamping is beneficial for both hemodynamic stability and decreased Hypoplasia of the mandible with posterior displacement of the tongue
neonatal mortality. may result in upper airway obstruction (Pierre Robin, Stickler, DiGeorge,
and other syndromes; see Chapter 337). Symptoms may sometimes be
SPECIAL CIRCUMSTANCES IN temporarily relieved by pulling the tongue or mandible forward or
THE DELIVERY ROOM placing the infant in the prone position. Other rare causes of upper
Meconium airway obstruction at birth include laryngeal atresia or stenosis, teratomas,
Meconium staining of the amniotic fluid may be an indication of fetal hygromas, and oral tumors. Critical fetal and then neonatal airway
stress. Previously, the presence of meconium-stained amniotic fluid in obstruction represents an emergency in the delivery room. High-risk
a nonvigorous infant required tracheal intubation to attempt to aspirate perinatal care has led to the more frequent prenatal diagnosis of these
meconium below the cords; NRP recommendations (7th edition) no disorders. When diagnosed prenatally, planning can identify the location
longer support this practice. If an infant is born through meconium- of delivery and interventions available at delivery. The ex utero intra-
stained amniotic fluid, it does not matter whether they are vigorous or partum treatment (EXIT) procedure allows time to secure the airway
nonvigorous; the infant should receive the same initial steps of basic in an infant known prenatally to have critical airway obstruction, before
resuscitation and should be assessed as any other infant. Tracheal the infant is separated from the placenta (Fig. 121.4). Uteroplacental
intubation may delay the initiation of effective PPV, which will help gas exchange is maintained throughout the procedure.
the baby to breathe and achieve effective gas exchange.
Respiratory Distress
Placental Abruption Both congenital abnormalities and iatrogenic causes secondary to
Placental abruption (abruptio placentae) at birth can lead to massive required resuscitation can contribute to respiratory distress in the
fetal blood loss and a hypovolemic, anemic infant at delivery. Infants neonate. A scaphoid abdomen suggests a diaphragmatic hernia, as
can present pale and apneic with poor tone, decreased perfusion, and does asymmetry in contour or movement of the chest. An infant with
bradycardia. In addition to performing routine neonatal resuscitation, a known diaphragmatic hernia should be immediately intubated in the
when an infant is suspected to be symptomatic from a placental abruption, delivery room and an orogastric tube placed to avoid gaseous distention
an emergency low-lying umbilical venous catheter (UVC) should be of the bowel from crying or PPV. The infant should then be transferred
placed and emergent type O Rh-negative blood should be obtained. In to a tertiary referral center for surgical evaluation and treatment
acute blood loss, the blood should be administered as quickly as possible (see Chapter 122.1).
in 10 mL/kg aliquots in the delivery room. Adequate communication In infants with a prenatal diagnosis of hydrops, pleural effusions
between obstetrics and pediatrics regarding suspected abruption is may be present at delivery, preventing adequate lung expansion and gas
crucial to early recognition and treatment of the infant. exchange. Similarly, infants requiring PPV in the delivery room are at
risk for developing a pneumothorax. Infants with pulmonary hypoplasia
Neonatal Encephalopathy or meconium-stained fluid are at increased risk of this complication.
Infants with neonatal encephalopathy are born with abnormal neurologic Clinically, infants with a pleural effusion or pneumothorax present with
function, including level of consciousness, muscle tone, and reflexes. respiratory distress and hypoxia, with diminished breath sounds on the
Although there are many possible etiologies, when symptoms are affected side. Transillumination may be helpful to confirm the diagnosis.
accompanied by a defined perinatal event such as cord prolapse or Emergency evacuation of a pneumothorax or pleural effusion without
placental abruption, hypoxic-ischemic brain injury is the presumed radiographic confirmation is indicated in an infant who is unresponsive
cause. These infants are often born with impaired respiratory drive. In to resuscitation efforts and has asymmetric breath sounds, bradycardia,
addition to routine neonatal resuscitation, term infants with concern and cyanosis. An angiocatheter attached to a stopcock and syringe should
for neonatal encephalopathy should be passively cooled in the delivery be used for evacuation. For a pneumothorax, an angiocatheter should
room by not turning on the warmer bed. After initial resuscitation be inserted perpendicular to the chest wall above the rib in the 2nd
and stabilization, a more thorough neurologic examination can be intercostal space in the midclavicular line and air evacuated. For a pleural
performed to assess if the infant meets formal criteria for moderate to effusion, with the infant in the supine position, the angiocatheter should
severe encephalopathy in order to proceed with whole body cooling be inserted in the 4th or 5th intercostal space in the anterior axillary
(see Chapter 120.4). line and directed posteriorly to evacuate the fluid (see Chapter 122).
Abdominal Wall and Neural Tube Defects hypotension, tachycardia, or poor urine output. Regardless of the severity
Appropriate management of patients with abdominal wall defects of neonatal encephalopathy or the response to resuscitation, asphyxiated
(omphalocele, gastroschisis) in the delivery room prevents excessive infants should be monitored closely for signs of multiorgan hypoxic-
fluid loss and minimizes the risk for injury to the exposed viscera. ischemic tissue injury (see Chapter 120.4).
Gastroschisis is the more common defect, and typically the intestines
are not covered by a membrane. The exposed intestines should be gently Bibliography is available at Expert Consult.
placed in a sterile clear plastic bag after delivery. A membrane often
covers an omphalocele, and care should be taken to prevent its rupture.
A nasogastric tube should be placed and the infant transferred to a
tertiary referral center for surgical consultation and evaluation for
associated anomalies (see Chapter 125).
Similarly, infants born with neural tube defects such as a myelome-
ningocele need special care at delivery to protect the exposed neural
tube tissue from trauma and infection; infants should be placed on
their side or abdomen for resuscitation. The site of the neural tube
defect should be covered with a moist sterile dressing to prevent drying
and infection. The infant should then be transferred to a tertiary referral
center for surgical evaluation and treatment.
Fractures
The clavicle is the most frequently fractured bone during labor and
delivery. It is particularly vulnerable to injury with difficult delivery of
the shoulder in the setting of shoulder dystocia, as well as with extended
arms in breech deliveries. In the treatment of shoulder dystocia, the
obstetrician may intentionally fracture the clavicle so that delivery can
proceed. Symptoms of a clavicular fracture include an infant not moving
the arm freely on the affected side, palpable crepitus or bony irregularity,
and asymmetric or absent Moro reflex on the affected side. The prognosis
for this fracture is excellent. Often, no specific treatment is needed,
although in some cases the arm and shoulder on the affected side are
immobilized for comfort.
Fractures of the long bones are fairly rare. Injuries often present with
absent spontaneous movement of the extremity. Associated nerve
involvement may also occur. Treatment involves immobilization of the
affected extremity with a splint and orthopedic follow-up.