Neonatal Hyperbilirubinemia
Conditions
Brief summary
Jaundice occurs in most newborn infants. Most jaundice is benign, but because of the potential toxicity of bilirubin, newborn infants must be monitored to identify those who might develop severe hyperbilirubinemia an, in rare cases, acute bilirubin encephalopathy or kernicterus. Jaundice is a commonly observed, usually harmless condition in newborn infants during the first week after birth. However, in some babies the amount of bilirubin pigment can increase to dangerous levels and require treatment. Treatment of jaundice in newborn infants is done by placing them under phototherapy, a process of exposing their skin to light of a specific wavelength band. Fluorescent tubes or halogen lamps have been used as light sources for phototherapy for many years. A light-emitting diode (LED) is a newer type of light source which is power efficient, has a longer life and is portable with low heat production. Several technologies and devices are developed around this LED and specially a compact system. The purpose of this study is to evaluate efficacity of LED phototherapy by comparing with conventional phototherapy (non-LED) and satisfaction of the parents and the professional staff about comfort of this new technology. The newborn infant is placed in a sleeper with the device B' bloo ® which maintains him in position (lap or dorsal) allowing to pass the blue light. This one is generated by the module LED and transmitted in the braid of optical fibers which takes place directly on the mattress of the cradle in which is placed the patient usually. The device is endowed with an hour counter to schedule the time of treatment. The energy illumination varies between 3 and 4 mW / cm ² for an average 3,6 mW / cm ².
Interventions
DEVICEtwo sessions of 4 hours Phototherapy treatment
two sessions of 4 hours Phototherapy treatment
Sponsors
Hopital Antoine Beclere
Bicetre Hospital
Association Pédiatrique des Groupes d'Acuueil et de Recherche
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
35 Weeks to 42 Weeks
Healthy volunteers
No
Inclusion criteria
* Newborn infants ≥ 38 gestation weeks without or with risk factors of severe icterus (G6PD or pyruvate-kinase deficiency, red blood cells membrane defects, hemoglobinopathies, cephalohematoma or significant bruising, decreased breastfeeding) * newborn at 35 and 38 gestation weeks without risk factor of severe icterus (qs) * hyperbilirubinemia to deal according to the curves of indication of phototherapy of the APP on 2004 * no opposition of parents
Exclusion criteria
* opposition of parents * newborn infants less than 33 weeks * newborn infants at 35 or more weeks of gestation with risk factors of severe icterus * Jaundice in first 12 hours * Hyperbilirubinemia \> 340 µmol/L whatever is the age
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| EDIN Scale | base line, 60minutes, 240minutes | EDIN scale will be measured 3 times during phototherapy treatment (base line, at 1 hour and at 4 Hour) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Evaluation of Blood Bilirubin level | base line, at 12 hour and at 24 hour | blood bilirubin concentration will be measured 3 times during phototherapy treatment (base line, at 12 hour and at 24 Hour) |
Countries
France
Contacts
Primary Contactemmanuelle letamendia, MD
Backup Contactclaire boithias, MD
Outcome results
None listed