Effects of Prefeeding Oral Stimulation on Feeding Performance in Preterm Infants
Preterm Infant, Oral Feeding Performance

About this trial
This is an interventional prevention trial for Preterm Infant focused on measuring preterm infant, feeding difficulties, prefeeding oral stimulation
Eligibility Criteria
Inclusion Criteria:
- preterm infants from 26 to 33+6 weeks' gestational age, as determined by date of last menstruation and first-trimester ultrasound, hospitalized in our neonatal unit.
Exclusion Criteria:
- Congenital malformations (chromosomal disorders, malformations of head and face, neurological, cardiac, digestive or pulmonary malformations)
- Severe asphyxia (hypoxic-ischemic encephalopathy)
- Presence of third or fourth degree intracranial haemorrhage
- Severe periventricular leukomalacia
- Severe chronic lung disease
- Severe hospital infection during the study period
- Necrotising enterocolitis during the study period
- Feeding interruption for more than 10 days during the study period
- Death during the study period
- Transfer to another hospital before discharge.
Sites / Locations
- Service de néonatologie, Centre Hospitalier de Luxembourg
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control group
Oral stimulation, interventional group
No prefeeding oral stimulation Infants in the control group received neither oral stimulation nor a pacifier before or during gavage feeding.
Infants in the interventional group received pre-feeding oral stimulation. The intervention started on infants born within 32 gestational weeks when the patients were stable and tube-fed, receiving more than 100 ml/kg/day of milk. On infants born after 32 weeks, the intervention started immediately after clinical stability was achieved. The pre-feeding oral stimulation program consisted of a 15-minute stimulation program delivered by one of the eight trained nurses or one trained member from the medical staff in accordance with the stimulation program proposed by Fucile, Gisel and Lau. The stimulation program was administered 15 to 30 minutes prior to tube feeding, once daily for at least 10 days. The program was stopped when the infants attained more than three oral feedings per day. The program was interrupted if the infants were medically unstable and/or had episodes of desaturation, apnoea and/or bradycardia during the intervention