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Anemia of Prematurity - Portal Neonatal

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Drug Name<br />

Pediatric Dose<br />

Phytonadione (Phytomenadione, AquaMEPHYTON) -- Vitamin K, a fatsoluble<br />

vitamin that is a c<strong>of</strong>actor in the synthesis <strong>of</strong> clotting factors. May<br />

be ineffective if liver disease is severe. Coagulation factors should<br />

increase in 6-12 h after PO dosing and in 1-2 h after parenteral<br />

administration. Monitor efficacy with PT.<br />

Aqueous (for injection): 2 mg/mL and 10 mg/mL diluted in 5-10 mL D5W<br />

or NS; maximum concentration 10 mg/mL; infuse over 15-30 min;<br />

maximum rate <strong>of</strong> infusion 1 mg/min<br />

Prophylaxis: 0.5-1 mg SC/IM<br />

Treatment: 1 mg SC or 1-10 mg IV<br />

Note: Use IM or IV administration routes only when SC is not feasible<br />

and condition justifies risk<br />

Contraindications Documented hypersensitivity<br />

Interactions<br />

Incompatible with phenytoin; antagonizes actions <strong>of</strong> warfarin; mineral oil<br />

decreases enteral absorption<br />

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

Precautions<br />

IV administration rate should not exceed 1 mg/min because <strong>of</strong> reported<br />

anaphylactoid reactions; IM administration can result in hematomas,<br />

particularly in infants with evidence <strong>of</strong> bleeding; hemolytic anemia and<br />

hyperbilirubinemia rarely occur with larger doses (10-20 mg)<br />

FOLLOW-UP Section 8 <strong>of</strong> 10<br />

Further Outpatient Care: Follow-up interval after discharge depends on the nature and severity <strong>of</strong><br />

bleeding, hematocrit at discharge, and any neurologic complications. Mild VKDB that has been treated<br />

successfully can be monitored at routine newborn visits.<br />

Transfer: Infants with evidence <strong>of</strong> intracranial bleeding may require transfer to a level III nursery after<br />

stabilization with SC or IV vitamin K.<br />

Deterrence/Prevention:<br />

• IM vitamin K prophylaxis at birth is the standard <strong>of</strong> care in the United States.<br />

• Commercial infant formulas in the United States contain supplemental vitamin K.<br />

• These measures have served to make VKDB a rarity. However, parental refusal <strong>of</strong><br />

prophylaxis and an increasing frequency <strong>of</strong> breastfeeding may cause a resurgence <strong>of</strong> VKDB in<br />

developed countries.<br />

Complications:<br />

• ICH is the primary serious complication <strong>of</strong> VKDB.<br />

• Complications <strong>of</strong> treatment include anaphylactoid reactions to IV vitamin K, hyperbilirubinemia<br />

or hemolytic anemia after high-dose vitamin K, and hematomas at the site <strong>of</strong> injection if<br />

administered IM.<br />

Prognosis: In the absence <strong>of</strong> ICH, the prognosis for VKDB in an otherwise healthy infant is excellent.<br />

Prognosis after ICH depends on the extent and location <strong>of</strong> the hemorrhage. Long-term sequelae <strong>of</strong><br />

ICH may include motor and intellectual deficits.

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