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Anemia of Prematurity - Portal Neonatal

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life. Recently, meta-analyses <strong>of</strong> these trials was presented at the Society for Pediatric<br />

Research.<br />

� Neurodevelopmental follow-up studies <strong>of</strong> infants treated with dexamethasone suggest<br />

that although this therapy improves short-term pulmonary outcome, long-term<br />

outcome appears significantly worse.<br />

� The routine use <strong>of</strong> dexamethasone in infants with BPD is not currently recommended<br />

unless severe pulmonary disease exists. A rapid tapering course starting at 0.25<br />

mg/kg/d and lasting for 5-7 days appears to be adequate. If no response is observed<br />

after 3 days, then discontinue dexamethasone. Inhaled glucocorticoid therapy has<br />

been studied in neonates to prevent BPD. In 1999, Cole and colleagues found that<br />

early therapy with beclomethasone did not prevent BPD, but it did decrease the need<br />

for systemic steroids. Further studies and the development <strong>of</strong> more efficient aerosol<br />

delivery systems are definitely needed.<br />

o Vasodilators: NO is a short-acting inhaled gas that relaxes the pulmonary vasculature. NO<br />

is metabolized rapidly by RBCs, thereby minimizing systemic hypotension. NO in vitro<br />

may have direct effects on the tracheobronchial tree. In 1999, Banks and colleagues<br />

studied the effect <strong>of</strong> inhaled NO in 16 preterm infants with severe BPD. Eleven <strong>of</strong> 16<br />

infants had improved oxygenation after 1 hour <strong>of</strong> inhalation, an effect that persisted in<br />

some infants. Further controlled studies are necessary to define the use <strong>of</strong> NO in the<br />

prevention and treatment <strong>of</strong> BPD.<br />

• Because the routine use <strong>of</strong> surfactant replacement has begun, survival <strong>of</strong> the most immature<br />

infants has improved. Along with other advances in technology and improved understanding <strong>of</strong><br />

neonatal physiology, infants with BPD now appear to have less severe disease. Infants with<br />

severe BPD remain at high risk for pulmonary morbidity and mortality during the first 2 years<br />

<strong>of</strong> life.<br />

• Fortunately, pulmonary function slowly improves in most survivors with BPD, likely secondary<br />

to continued lung and airway growth and healing. Northway followed the cases <strong>of</strong> patients with<br />

BPD to adulthood. In 1992, Northway reported that these patients had airway hyperreactivity,<br />

abnormal pulmonary function, and hyperinflation noted on chest radiography.<br />

Rehospitalization for impaired pulmonary function is most common during the first 2 years <strong>of</strong><br />

life. In 1990, Hakulinen et al found a gradual decrease in symptom frequency in children aged<br />

6-9 years as compared to the first 2 years <strong>of</strong> life. Bader in 1987 and Blayney et al in 1991<br />

found persistence <strong>of</strong> respiratory symptoms and abnormal PFT results in children aged 7 and<br />

10 years. High-resolution chest CT scanning or MRI studies in children and adults with a<br />

history <strong>of</strong> BPD reveal lung abnormalities that correlate directly with the degree <strong>of</strong> pulmonary<br />

function abnormality.<br />

Consultations: Infants with BPD have multisystem involvement. Therefore, consultations should be<br />

obtained from various pediatric subspecialists. They include a cardiologist, pulmonologist,<br />

gastroenterologist, developmental pediatrician, ophthalmologist, neurologist, physical therapist, and<br />

nutritionist. They may also assist the pediatrician with the ongoing care <strong>of</strong> these infants after patients<br />

are discharged from the hospital.<br />

Diet: Infants with BPD have increased energy requirements.<br />

• Early parenteral nutrition is <strong>of</strong>ten used to minimize the catabolic state <strong>of</strong> the preterm infant.<br />

The most immature and unstable preterm infant <strong>of</strong>ten has a difficult transition to complete<br />

enteral nutrition. Frequent interruption <strong>of</strong> feedings secondary to intolerance or patient<br />

instability complicates the management <strong>of</strong> these patients. Enteral feeding <strong>of</strong> breast milk may<br />

provide the best nutrition, while possibly preventing feeding complications (eg, sepsis,<br />

necrotizing enterocolitis).<br />

• The energy content <strong>of</strong> expressed breast milk and formulas can be enhanced to provide<br />

increased energy intake, while minimizing fluid intake. Infants may require 120-150 kcal/kg <strong>of</strong><br />

body weight per day to adequately gain weight.<br />

• Diuretics may <strong>of</strong>ten be used to prevent or treat fluid overload.<br />

• Early insertion <strong>of</strong> percutaneous central venous lines may help to improve energy density <strong>of</strong><br />

parenteral nutrition. Accomplish progressive increases in protein and fat supplementation to<br />

provide approximately 3-3.5 g/kg <strong>of</strong> body weight per day and 3 g/kg <strong>of</strong> body weight per day.<br />

• Rapid and early administration <strong>of</strong> high concentrations <strong>of</strong> lipids may worsen hyperbilirubinemia<br />

and BPD through pulmonary vascular lipid deposition and bilirubin displacement from albumin.

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