Predictors of Rebound Hyperbilirubinemia Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2-28
SponsorHaseki Training and Research Hospital

About this trial

\## Brief Summary

Neonatal hyperbilirubinemia is one of the most common causes of neonatal hospitalization and phototherapy treatment. Although phototherapy is highly effective, rebound hyperbilirubinemia following discontinuation of phototherapy may occur in some infants and may require repeat treatment. Early identification of neonates at risk for clinically significant rebound hyperbilirubinemia could help optimize discharge timing and reduce unnecessary hospital stay and repeat bilirubin testing.

This prospective observational study aims to evaluate the predictors of rebound hyperbilirubinemia after phototherapy discontinuation in neonates admitted to the NICU. Particular focus will be placed on the role of delta total serum bilirubin (ΔTSB), defined as the difference between the phototherapy threshold and the measured bilirubin level at the time of phototherapy discontinuation. Clinical, demographic, laboratory, hemolytic, feeding-related, and phototherapy-related variables will also be analyzed.

The primary outcome will be clinically significant rebound hyperbilirubinemia requiring repeat phototherapy within 24-48 hours after discontinuation of the initial phototherapy treatment. Secondary outcomes include rebound bilirubin levels, duration of hospitalization, and factors associated with repeat phototherapy.

Eligibility criteria

Qualifiers

Neonates admitted to the NICU with neonatal hyperbilirubinemia

Gestational age ≥35 weeks

Requirement for phototherapy according to institutional protocol and current guideline-based phototherapy thresholds

Receipt of standard and/or intensive phototherapy

Disqualifiers

Major congenital anomalies

Conjugated hyperbilirubinemia

Neonates requiring exchange transfusion before completion of initial phototherapy

Severe perinatal asphyxia

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

300 Participants
are grouped into 1 trial group