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Published on: January 27, 2019
Erythromycin treatment for gastrointestinal dysmotility in preterm infants
1Department of Paediatrics, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong.
Insights
Oral erythromycin effectively treated severe gastrointestinal dysmotility in preterm infants, enabling full enteral feeding within two weeks. This approach offers a potential alternative to prolonged parenteral nutrition in select cases.
Area of Science:
- Neonatal Medicine
- Gastroenterology
- Pharmacology
Background:
- Severe gastrointestinal dysmotility is a significant challenge in preterm infants.
- Prolonged total parenteral nutrition (TPN) is associated with serious complications.
- Establishing enteral feeding is crucial for preterm infant development.
Purpose of the Study:
- To evaluate the clinical efficacy of oral erythromycin for severe gastrointestinal dysmotility in preterm infants.
- To assess the safety and tolerance of erythromycin in this population.
Main Methods:
- A case series of seven preterm infants with severe intestinal dysmotility.
- Infants were treated with oral erythromycin in a tertiary neonatal center.
- Six of the seven infants were of very low birthweight.
Main Results:
- All seven infants responded positively to oral erythromycin treatment.
- No adverse effects were observed during the treatment period.
- Full enteral feeding was achieved within 1-2 weeks of initiating erythromycin therapy.
Conclusions:
- Oral erythromycin may be a viable therapeutic option for preterm infants with severe gastrointestinal dysmotility who fail to establish enteral feeding.
- This treatment could reduce the need for prolonged TPN and its associated risks.
- Further randomized controlled trials are necessary to establish the definitive role of erythromycin in treating intestinal dysmotility in preterm infants.
Objective:
To report our clinical experience on the use of oral erythromycin for the treatment of severe gastrointestinal dysmotility in preterm infants.
Methodology:
A case series study of seven preterm infants (six were very low birthweight) with severe intestinal dysmotility in a tertiary neonatal centre.
Results:
All responded favourably without adverse effects and tolerated full enteral feeding within 1-2 weeks of the commencement of the drug.
Conclusions:
As prolonged total parenteral nutrition carries significant risk of complications, this therapy could be considered in selected preterm infants who fail to establish enteral feeding after an extended period, and in whom an anatomically obstructive lesion of the gastrointestinal tract has been excluded. Meanwhile, we would caution against the widespread implementation of this therapeutic approach until formal evaluation by randomized controlled trials have established the exact role of erythromycin, or its analogues, in the treatment of intestinal dysmotility in preterm infants.
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