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Updated: Sep 30, 2026

Closure of a Patent Foramen Ovale (PFO): An Intervention Sequence
Published on: December 23, 2022
Indomethacin for closure of patent ductus arteriosous in preterm neonates
P Arun Kumar Nair1, Sheila Karan1
1Department of Neonatology, Institute of Child Health, Niloufer Hospital, Hyderabad.
Insights
Oral indomethacin effectively closes patent ductus arteriosus (PDA) in premature infants. This treatment significantly improves survival rates compared to fluid restriction and decongestive therapy.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Pharmacology
Background:
- Patent ductus arteriosus (PDA) is a common condition in premature infants.
- Effective treatment for PDA is crucial to improve infant outcomes.
Purpose of the Study:
- To evaluate the efficacy and safety of oral indomethacin for PDA closure in low birth weight premature infants.
- To compare oral indomethacin treatment with conventional management.
Main Methods:
- A study involving 15 low birth weight premature infants diagnosed with PDA who received oral indomethacin (0.2 mg/kg, 3 doses at 12-hour intervals).
- A control group of 18 premature infants managed with fluid restriction (80-100 ml/kg/day) and decongestive therapy.
- Comparison of PDA closure rates and survival between the two groups.
Main Results:
- Nine out of 15 infants (60%) treated with indomethacin showed PDA closure, compared to only 2 out of 18 (11.1%) in the control group (P<0.01).
- Survival rates were significantly higher in the indomethacin group (11/15, 73.3%) versus the control group (6/18, 33.3%) (P<0.01).
- Overall mortality attributed to PDA alone was 58.9%.
Conclusions:
- Oral indomethacin is a safe and effective treatment for closing PDA in premature infants when administered early.
- This treatment modality is feasible within the Indian healthcare system.
- Early intervention with oral indomethacin can significantly reduce mortality in premature infants with PDA.
Abstract:
Fifteen low birth weight premature infants with a diagnosis of PDA were administered 0·2 mg/kg of indomethacin orally, 3 doses at 12 hourly intervals. The results were compared with 18 prematures who were managed by fluid restriction (80-100 ml/kg/day) and decongestive therapy. Nine out of the 15 cases who received indomethacin met with the criteria of response, compared with only 2 out of 18 in whom there was spontaneous closure (P<0·01). Eleven of 15 cases who received indomethacin survived compared to only 6 of 18 in the control group (P<0·01). Overall mortality due to PDA alone was 58·9 per cent. Indomethacin when administered orally and sufficiently early, is safe and effective in closing PDA in premature infants. This modality of treatment is feasible in the Indian set up.
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