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Anemia of Prematurity - Portal Neonatal

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MEDICATION Section 7 <strong>of</strong> 11<br />

Drug Category: Immunomodulators -- Normalize the antibody level in patients with primary<br />

defective antibody synthesis. Prevent and treat certain bacterial and viral infections. Reduce the<br />

immune-mediated hemolysis and phagocytosis.<br />

Intravenous immunoglobulin (Gamimune, Gammagard,<br />

Sandoglobulin, Gammar-P) -- Several studies have reported success<br />

in minimizing the need for exchange transfusion in severe HDN with<br />

IVIG. It is an effective adjunct to phototherapy. The mechanism <strong>of</strong><br />

action appears to be related to blockage <strong>of</strong> Fc receptors in the<br />

neonatal reticuloendothelial system. Studies have also documented<br />

Drug Name decreased hemolysis after administration <strong>of</strong> IVIG using<br />

carboxyhemoglobin levels. Administration <strong>of</strong> IVIG in doses <strong>of</strong> 500-<br />

1000 mg/kg in the first few hours <strong>of</strong> life to a newborn with severe<br />

hemolysis should be considered. Its efficacy, however, depends on<br />

timing <strong>of</strong> administration, duration <strong>of</strong> treatment, and severity <strong>of</strong><br />

hemolysis.<br />

Adult Dose 1 g/kg IV qwk for maternal alloimmunization<br />

0.5-1 g/kg IV in first few h following birth for severe hemolysis in<br />

newborn; start infusion at rate <strong>of</strong> 0.01 mL/kg/min for 30 min, then<br />

Pediatric Dose<br />

increase q15-30min; not to exceed rate <strong>of</strong> 0.06 mL/kg/min; if adverse<br />

reactions occur, reduce rate to a previously well-tolerated rate<br />

Contraindications Documented hypersensitivity; IgA deficiency; anti-IgE/IgG antibodies<br />

Globulin preparation may interfere with immune response to live virus<br />

Interactions vaccine (MMR) and reduce efficacy (do not administer within 3 mo <strong>of</strong><br />

vaccine)<br />

Pregnancy C - Safety for use during pregnancy has not been established.<br />

Ensure that patient is not volume depleted before initiation <strong>of</strong> therapy;<br />

periodic monitoring <strong>of</strong> renal function and urine output should be<br />

undertaken in those at increased risk for developing acute renal<br />

failure (eg, preexisting renal insufficiency, diabetes mellitus, age >65<br />

y, hypovolemia, sepsis, paraproteinemia, those on nephrotoxic drugs);<br />

in such patients, reduce rate <strong>of</strong> infusion and discontinue if renal<br />

Precautions<br />

function deteriorates; patients with agammaglobulinemia or extreme<br />

hypogammaglobulinemia who have never received IVIG before or<br />

have not received IVIG within preceding 8 wk are at increased risk <strong>of</strong><br />

developing inflammatory reaction after IVIG infusion (these reactions<br />

are manifested by fever, chills, nausea, and vomiting and appear to<br />

be related to rate <strong>of</strong> infusion)<br />

FOLLOW-UP Section 8 <strong>of</strong> 11<br />

Further Inpatient Care:<br />

• The stabilization <strong>of</strong> a hydropic newborn requires a high level <strong>of</strong> intensive coordinated<br />

management by a neonatal team well prepared for the possibly affected infant. In general,<br />

immediate intubation followed by draining <strong>of</strong> pleural effusions and ascites results in immediate<br />

improvement in respiratory gas exchange. A cautious correction <strong>of</strong> anemia with packed RBCs<br />

or by exchange transfusion is necessary to prevent circulatory overload. These neonates have<br />

normal blood volume but elevated central venous pressure. A close monitoring <strong>of</strong> metabolic

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