Born at 37 weeks of gestation or less.
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Pathophysiology-anatomical and physiological immaturity of body systems compromises ability to adapt to extrauterine environment and independent life.
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Interference with protective functions
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Temperature regulation-unstable, due to:
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Lack of subcutaneous fat.
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Large body surface area in proportion to body weight.
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Small muscle mass.
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Absent sweat or shiver responses.
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Poor capillary response to changes in environmental temperature.
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Resistance to infection-low, due to:
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Lack of immune bodies from mother (these cross placenta late in pregnancy).
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Inability to produce own immune bodies (immature liver).
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Poor WBC response to infection.
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Immature liver
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Inability to conjugate bilirubin liberated by normal breakdown of RBCs-increased susceptibility to hyperbilirubinemia and kernicterus.
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Immature production of clotting factors and immune globulins.
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Inadequate glucose stores increased susceptibility to hypoglycemia.
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Interference with elimination: immature renal function-unable to concentrate urine-precarious fluid/electrolyte balance.
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Interference with sensory-perceptual functions: CNS-immature-weak or absent reflexes and fluctuating primitive control of vital functions.
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Etiology: often unknown; preterm labor.
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Iatrogenic-EDB miscalculated for repeat cesarean birth (rare).
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Placental factors
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Placenta previa.
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Abruptio placentae.
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Placental insufficiency.
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Uterine factors
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Incompetent cervix.
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Overdistention (multifetal gestation, polyhydramnios).
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Anomalies (myomas).
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Fetal factors
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Malformations.
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Infections (rubella, toxoplasmosis, HIVpositive status, AIDS, cytomegalic inclusion disease).
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Multifetal gestations (twins, triplets).
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Maternal factors
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Severe physical or emotional trauma.
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Coexisting disorders (PIH, hypertension, heart disease, diabetes, malnutrition).
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Infections (streptococcus, syphilis, bacterial vaginosis, pyelonephritis, pneumonia, influenza, leukemia, UTI).
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Miscellaneous factors
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Close frequency of pregnancies.
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Advanced maternal age.
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Heavy smoking.
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High-altitude environment.
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Cocaine use.
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Factors influencing survival:
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Gestational age.
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Lung maturity.
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Anomalies.
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Size.
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Causes of mortality (in order of frequency):
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Abnormal pulmonary ventilation.
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Infection.
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Pneumonia.
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Septicemia.
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Diarrhea.
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Meningitis.
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Intracranial hemorrhage.
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Congenital defects.
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Disorders affecting fluid-gas transport: RDS
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Pathophysiology-insufficient pulmonary surfactant (lecithin) and insufficient number/ maturity of alveoli predispose to atelectasis; alveolar ducts and terminal bronchi become lined with fibrous, glossy membrane.
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Etiology:
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Primarily associated with prematurity.
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Other predisposing factors:
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Fetal hypoxia-due to decreased placental perfusion secondary to maternal bleeding (abruptio) or hypotension.
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Birth asphyxia.
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Postnatal hypothermia, metabolic acidosis, or hypotension.
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Factors protecting neonate from RDS:
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Chronic fetal stress-due to maternal hypertension, PIH, or heroin addiction.
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PROM.
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Maternal steroid ingestion (betamethasone).
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Low-grade chorioamnionitis.
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Assessment:
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Usually appears during first or second day after birth.
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Signs of respiratory distress:
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Nasal flaring.
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Sternal retractions.
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Tachypnea (60 beats/min or more).
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Cyanosis-central.
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Expiratory grunt.
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Increasing number and length of apneic episodes.
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Increasing exhaustion.
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Respiratory acidosis-due to hypercapnea and rising CO2 level.
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Metabolic acidosis-due to increased lactic acid levels and falling pH.
- Analysis/nursing diagnosis:
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Impaired gas exchange related to lack of pulmonary surfactant secondary to preterm birth, intrapartal stress and hypoxia, infection, postnatal hypothermia, metabolic acidosis, or hypotension.
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Altered nutrition, less than body requirements, related to poor feeding secondary to respiratory distress, caloric demand.
- Nursing care plan/implementation:
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Goal: reduce metabolic acidosis, increase oxygenation, support respiratory efforts.
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Ensure warmth (isolette at 97.6°F).
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Warmed, humidified O2 at lowest concentration required to relieve cyanosis, through hood, nasal prongs, or endotracheal tube.
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Monitor continuous positive airway pressure (CPAP)-oxygen-air mixture administered under pressure during inhalation and exhalation to maintain alveolar patency.
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Position: side-lying or supine with neck slightly extended (“sniffing” position); arms at sides.
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Suction pm with bulb syringe-for excessive mucus.
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Goal: modify care for infant with endotracheal tube.
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Disconnect tubing at adapter.
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Inject 0.5 mL sterile normal saline.
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Insert sterile suction tube, start suction, rotate tube, withdraw.
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Suction up to 5 seconds.
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Ventilate with bag and mask during procedure.
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Reconnect tubing securely to adapter.
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Auscultate for breath sounds and pulse.
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Goal: maintain nutrition/hydration.
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Administer fluids, electrolytes, calories, vitamins, minerals PO or IV, as ordered.
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I&O.
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Goal: prevent secondary infections.
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Strict aseptic technique.
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Handwashing.
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Goal: emotional support of infant.
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Gentle touching.
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Soft voices.
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Eye contact.
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Rocking.
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Goal: emotional support of parents.
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Keep informed of status and progess.
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Encourage contact with infant-to promote bonding, understanding of treatment.
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Goal: minimize possibility of iatrogenic disorders associated with oxygen therapy.
- Evaluation/outcome criteria:
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Respiratory distress treated successfully; infant breathes without assistance.
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Infant completes successful transition to extrauterine life.
- Iatrogenic (oxygen toxicity) disorders: retinopathy of prematurity
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Pathophysiology-intraretinal hemorrhage-fibrosis-retinal detachment-loss of vision.
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Etiology-prolonged exposure to high concentrations of oxygen.
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Assessment-only perceptible retinal change is vasoconstriction. Note: Arterial blood (PaO2) gas readings less than 50 or more than 80 mm Hg.
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Nursing care plan/implementation: Goal: prevent disorder. Maintain PaO2 of
50-70 mm Hg.
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Evaluation/outcome criteria:
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Successful recovery from respiratory distress.
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No evidence of retinopathy.
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Iatrogenic (oxygen toxicity) disorders: bronchopulmonary dysplasia (BPD)
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Pathophysiology-damage to alveolar cells result in focal emphysema.
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Etiology-positive pressure ventilation (CPAP and PEEP) and prolonged administration of high concentrations of oxygen.
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Assessment-monitor for signs of:
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Tachypnea.
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Increased respiratory effort.
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Respiratory distress.
- Intraventricular hemorrhage
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Pathophysiology-rupture of thin, fragile capillary walls within ventricles of the brain (more common in preterm).
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Etiology:
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Hypoxia.
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Respiratory distress.
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Birth trauma.
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Birth asphyxia.
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Hypercapnia.
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Assessment:
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Hypotonia.
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Lethargy.
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Hypothermia.
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Bradycardia.
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Bulging fontanels.
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Respiratory distress or apnea.
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Seizures.
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Cry: high-pitched whining.
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Nursing care plan/implementation: Goal: supportive care-to promote healing.
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Monitor vital signs.
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Maintain thermal stability.
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Ensure adequate oxygenation (may be placed on CPAP).
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Evaluation/outcome criteria:
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Condition stable, all assessment findings within normal limits.
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No evidence of residual damage.