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Clarithromycin treatment in preterm infants: a pilot study for prevention of feeding intolerance
Tulin Gokmen1, Ramazan Ozdemir, Senol Bozdag
1Neonatal Intensive Care Unit, Zekai Tahir Burak Maternity Teaching Hospital , Ankara , Turkey.
Insights
Oral clarithromycin significantly reduced feeding intolerance in very low birth weight (VLBW) infants compared to placebo. However, it did not speed up achieving full enteral feeding in these preterm infants.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Clinical Trials
Background:
- Feeding intolerance is a common complication in very low birth weight (VLBW) infants, impacting growth and increasing healthcare costs.
- Early identification and management of feeding intolerance are crucial for improving outcomes in preterm neonates.
Purpose of the Study:
- To evaluate the efficacy of oral clarithromycin in preventing feeding intolerance in VLBW infants.
- To compare the time to achieve full enteral feeding between clarithromycin and placebo groups.
Main Methods:
- A prospective, randomized controlled trial involving 38 preterm infants (birth weight <1500 g).
- Infants were randomized to receive either oral clarithromycin (7.5 mg/kg/dose every 12 hours) or a placebo.
- Primary outcome measures included feeding intolerance and time to achieve full enteral feeding.
Main Results:
- Clarithromycin treatment resulted in a significantly lower incidence of feeding intolerance compared to placebo (p=0.031).
- There was no significant difference in the time to achieve full enteral feeding between the clarithromycin and placebo groups.
Conclusions:
- Oral clarithromycin demonstrates potential in improving feeding intolerance in VLBW infants.
- Further research is needed to optimize clarithromycin's prophylactic use and investigate its impact on enteral feeding progression.
- Recruiting only infants with established feeding intolerance might yield different results.
Objective:
To compare the effectiveness of oral clarithromycin versus placebo treatment in preventing feeding intolerance in very low birth weight (VLBW) infants.
Study Design:
A prospective, randomised controlled trial in which two groups of preterm infants (birth weight <1500 g) were randomised to clarithromycin (7.5 mg/kg/dose every 12 h) or placebo treatment. During the period, 38 infants, whose parents accepted participation, were enrolled in the study. Feeding intolerance and time to achieve full enteral feeding were considered as primary outcome measures.
Results:
Feeding intolerance was significantly longer in placebo than clarithromycin (p = 0.031). Time to achieve full feeding after beginning the treatment was equal among the groups.
Conclusion:
This is the first randomised controlled study of clarithromycin and placebo treatment that compares the improvement of feeding intolerance in VLBW infants. Our findings indicate a dramatic improvement in feeding intolerance after oral clarithromycin treatment. But according to our results, clarithromycin-treated infants were not able to attain full enteral feeding more quickly than placebo. This may be due to prophylactic usage of clarithromycin. Significant differences might have resulted if only infants who had feeding intolerance were recruited.
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