Summary
Vitamin K deficiency bleeding (VKDB) is a condition characterized by spontaneous bleeding in infants due to low levels of vitamin K-dependent coagulation factors. Because vitamin K has poor placental transfer, is present in low concentrations in breast milk, and the neonatal gut is initially sterile, all newborns have low vitamin K stores at birth. VKDB is rare in industrialized countries due to the standard prophylactic vitamin K injection given at birth. The condition is categorized as early-onset (within 24 hours after birth), classic (within 1 week), or late-onset (1 week to 6 months). Common bleeding sites include the gastrointestinal tract, umbilical stump, or nose, though life-threatening intracranial or subgaleal hemorrhages can occur. Treatment focuses on managing active bleeding with vitamin K administration and, in severe cases, blood products like four-factor prothrombin complex concentrate to restore homeostasis.
Epidemiology
- Without prophylaxis: affects 0.25–1.7% of newborns [1]
Epidemiological data refers to the US, unless otherwise specified.
Etiology
The underlying cause is always a deficiency of vitamin K, which can be due to various factors:
-
Vitamin K deficiency in the mother
- Because of therapy with anticonvulsants, antibiotics, antituberculosis agents, or warfarin: most important in early-onset VKDB
- Maternal malnutrition
- Poor placental passage of vitamin K
- Underdeveloped intestinal flora (which produces vitamin K), e.g., due to premature birth
- Exclusive breastfeeding: low vitamin K levels in breast milk (most important in late-onset VKDB)
- Chronic diarrhea of the newborn
- Cholestatic diseases (e.g., biliary atresia)
- Long-term antibiotic treatment in newborns
References:[2]
Classification
- Early onset: within 24 hours after birth
- Classic: : within 1 week after birth
- Late onset: between 1 week and 6 months after birth; highest risk of intracranial bleeding
Clinical features
-
Common bleeding sites
- Cutaneous: generalized ecchymoses and easy bruising (notably the face and neck)
- Gastrointestinal: hematochezia, melena, or hematemesis
- Umbilical: persistent oozing or frank bleeding from the umbilical cord stump
- Mucosal: epistaxis and bleeding from the gums
- Urogenital: hematuria
- Deep tissue: large intramuscular hemorrhages
-
Life-threatening manifestations
- Intracranial hemorrhage (ICH): the most serious complication, often presenting with a bulging fontanelle, irritability, seizures, or altered consciousness
- Signs of hypovolemia: pale skin, tachycardia, and poor perfusion due to acute blood loss
Diagnosis
- ↑ Prothrombin time (PT)
- Normal or ↑ activated partial thromboplastin time (PTT)
- Normal bleeding time
- ↓ Factors II, VII, IX, and X
Treatment
- Nonmajor bleeding: PO or IM vitamin K
-
Major bleeding (with hemodynamic instability)
- IV vitamin K (slow infusion)
- Four-factor prothrombin complex concentrate (4F PCC) for rapid factor replacement
- If 4F PCC is unavailable, fresh frozen plasma (FFP)