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Efficacy of prophylactic oral erythromycin to improve enteral feeding tolerance in preterm infants: a randomised
M Mohammadizadeh1, M Ghazinour, R Iranpour
1Department of Paediatrics, Al-Zahra Hospital, Isfahan University of Medical Sciences, Sofe Bolvar, Isfahan 8174675731, Iran. m_mohammadizadeh@med.mui.ac.ir
Insights
Prophylactic low-dose oral erythromycin (a motilin agonist) significantly reduced the time to full enteral feeding in preterm infants. This intervention also decreased feeding interruptions and intolerance symptoms, showing promising results for improving infant nutrition.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Gastroenterology
Background:
- Enteral feeding intolerance is a significant challenge in the care of preterm infants.
- Erythromycin, a motilin agonist, is explored as a prokinetic agent to mitigate feeding intolerance.
Purpose of the Study:
- To evaluate the safety and efficacy of prophylactic low-dose oral erythromycin in preterm infants.
- To determine if erythromycin reduces the incidence of enteral feeding intolerance.
Main Methods:
- A prospective randomized controlled trial involving 70 preterm infants (28-34 weeks gestation, 1000-1500g).
- Infants received either low-dose oral erythromycin (6 mg/kg/day for 10 days) or a placebo.
- Primary outcomes measured were time to full enteral feeding and duration of feeding interruptions.
Main Results:
- Erythromycin group reached full enteral feeding significantly faster (10.11 vs. 12.71 days, p=0.01).
- The control group experienced longer feeding interruptions (84.00 vs. 32.57 hours, p=0.005) and more abdominal distention.
- No cardiac arrhythmias or pyloric stenosis were observed in the erythromycin group.
Conclusions:
- Prophylactic low-dose oral erythromycin appears safe and effective in improving enteral feeding tolerance in preterm infants.
- Further studies are recommended to confirm the efficacy and safety profile of erythromycin in this population.
Introduction:
Enteral feeding intolerance is a major problem in preterm infants. This study evaluated the safety and efficacy of prophylactic low-dose oral erythromycin, a motilin agonist, as a prokinetic agent in reducing the incidence of this problem.
Methods:
From February to May 2008, a prospective randomised controlled trial was conducted at the Isfahan University of Medical Sciences, Isfahan, Iran. 70 uncomplicated preterm infants (28-34 weeks' gestation) weighing 1,000-1,500 g were randomly assigned to either a case group receiving low-dose oral erythromycin (6 mg/kg/day, in four doses over ten days) or a control group (n is 35 in each group) until they were fully fed enterally (150 ml/kg/day). Gavage feeding of the mother's milk was started within the first three days of life, and erythromycin was given simultaneously. The time taken to reach full enteral feeding and the total duration of feeding interruption due to intolerance were compared.
Results:
The time taken to reach full enteral feeding was significantly shorter in the erythromycin group than the control group (10.11 +/- 2.51 versus 12.71 +/- 5.76 days, p is 0.01). In the control group, the mean duration of feeding interruption was significantly longer (84.00 +/- 62.58 versus 32.57 +/- 11.93 hours, p is 0.005) and more episodes of abdominal distention and significant gastric residue were also noted (p less than 0.05). No infant in the erythromycin group developed cardiac arrhythmias or pyloric stenosis.
Conclusion:
The prophylactic use of erythromycin may be warranted in very low birth weight infants, provided the efficacy and safety of the drug can be confirmed in further studies.
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