|
Iowa Neonatology Handbook: Pulmonary
Treatment of the Respiratory Distress Syndrome
Jonathan M. Klein, MD
Peer Review Status: Internally Peer Reviewed
The treatment of the Respiratory Distress Syndrome (RDS) is
directed at correction of the pathophysiological conditions that
exist in this disease process: A) surfactant deficiency, B) hypoxia,
C) acidosis, D) pulmonary vasoconstriction, E) atelectasis, and F)
shock.
I. SURFACTANT REPLACEMENT THERAPY (page 64)
II. Correction of hypoxia with oxygen. Infants requiring increased
ambient oxygen concentration, and who are breathing spontaneously,
can be placed on NPCPAP. The concentration of inspired oxygen should
maintain the infant's arterial oxygen tension at 50-70 mm Hg. If
oxygen required is greater than 50%, consider endotracheal intubation
with surfactant replacement (see relevant section). Always confirm
diagnosis with a chest radiograph.
III. Nasal pharyngeal CPAP for RDS should start at 6 cm H2O. If
the infant is having recurrent apnea, persistent respiratory acidosis
(pH less than 7.20) or if the PaO2 is inadequate in 50% or more
oxygen with usage of nasal CPAP, the infant should be intubated and
treated with surfactant.
IV. Once intubated, the neonate with RDS should be ventilated by a
pressure respirator according to the protocol found on page 36. To
minimize both barotrauma and BPD, peak inspiratory pressures should
be decreased as tolerated to keep the pCO2 between 40 and 60 mm Hg as
long as the pH > 7.25. If pCO2 remains above 60 mm Hg, consider
increasing the respiratory rate first, then, if necessary, increase
PIP.
V. If barotrauma occurs (PIE or pneumothorax), consider high
frequency ventilation (see separate section on HFV).
VI. To maintain body temperature, the infant is placed in an
incubator or on a radiant heater bed. The skin probe is placed on the
mid-epigastrium and covered with heat reflecting tape. The
servocontroller is set at 36.5°C.
VII. Intravenous fluids (D10W or D5W) are given at an initial rate
of 60-80 ml/kg body weight per 24 hours with fluid therapy reassessed
every 8-12 hours. Infants with birth weights less than 750g should be
given fluids at an initial rate of 80-150 ml/kg per day due to their
increased insensible losses and fluid therapy should be reassessed
every 6-8 hours. Sodium received as sodium bicarbonate will also have
to be taken into consideration when calculating the daily sodium
requirement. IT IS IMPERATIVE THAT FLUID THERAPY BE READJUSTED EVERY
8 TO 12 HOURS, BASED ON INTAKE AND OUTPUT, CHANGE IN BODY WEIGHT,
SERUM ELECTROLYTE CONCENTRATIONS AND SERUM AND URINE OSMOLALITY
DETERMINATIONS. See section on fluid therapy for additional
details.
VIII. Metabolic acidosis (pH< 7.20) is corrected by a slow
infusion of sodium bicarbonate (0.5 mEq/ml.; 4% solution) through a
peripheral IV at the rate of 1 mEq/kg body weight per hour. The
formula for calculation of the base deficit is: mEq of NaHCO3 = base
excess x 0.6 x body weight in kg. Give one-half of the calculated
dose and then recheck pH and pCO2 within one-half hour.
IX. Shock is corrected by use of normal saline or Plasmanate R;
the dose is 10 cc/kg infused over 15 to 30 minutes. Normal values for
systolic and mean aortic pressures are found on pages 1 and 2. Please
note the values for infants <1000 grams. Carefully evaluate the
need for correction of low BP based on numbers alone in a premature
infant who is otherwise well oxygenated, since acute changes in blood
pressure may be an etiologic factor in intracranial hemorrhage.
X. Oral feedings may be initiated even if the infant is
mechanically ventilated, or on nasal-pharyngeal CPAP, however,
feedings should not be initiated until the infant's condition is
stable. Ultimately, the oral intake should provide 100-120
calories/kg/day (see feeding protocol).
XI. When the infant is on CPAP or mechanical ventilation, a chest
film should be obtained immediately after initiating therapy and
subsequently at least once every 24 hours until the infant's
condition is stable.
References:
Kraybill EN, et al. Risk factors for Chronic lung disease in
infants with birth weights of 751 to 1000 grams. J Pediatr
1989;115:115-120.
Van Marter LJ, et al. Hydration during the first days of life and
the risk of bronchopulmonary dysplasia in low birth weight infants. J
Pediatr 1990;116:942-949.
Avery ME, et al. Is chronic lung disease in low birth weight
infants preventable? A survey of eight centers. Pediatrics
1987;79:26-30.
Carlo WA, Martin RJ. Principles of neonatal assisted ventilation.
Pediatr Clin North Am, 1986;33:221-237.
Stark AR, Frantz ID. Respiratory distress syndrome. Pediatr Clin
North Am, 1986;33:533-544.
Section Top | Title Page
|