# Caffeine Treatment for Prostaglandin E1–Induced Apnea Prevention in Congenital Heart Disease Neonates: A Randomized Clinical Trial

**Authors:** Ladan Salamati, Bahar Dehghan, Mohammad Reza Sabri, Alireza Ahmadi, Mehdi Ghaderian, Chehreh Mahdavi, Davood Ramezani Nezhad, Atefeh Karbasi, Mohsen Sedighi

PMC · DOI: 10.1155/ccrp/4923280 · Critical Care Research and Practice · 2025-05-11

## TL;DR

This study tested if caffeine can prevent apnea caused by a heart treatment in newborns with heart defects but found no significant benefit.

## Contribution

The study is the first randomized clinical trial to evaluate caffeine's effect on prostaglandin E1-induced apnea in congenital heart disease neonates.

## Key findings

- Caffeine therapy did not significantly reduce the prevalence of apnea compared to PGE1 alone.
- Neonates in the caffeine group received a higher mean dose of PGE1.
- Age had a significant effect on time to apnea in patients receiving caffeine.

## Abstract

Background: Congenital heart diseases (CHDs) are structural abnormalities of the heart or great vessels. Prostaglandin E1 (PGE1) is used to maintain the ductus arteriosus open in neonates with ductal-dependent heart lesions but is associated with apnea. We aimed to investigate the effects of caffeine therapy on the occurrence of apnea in neonates with CHD.

Methods: This single-blinded randomized clinical trial was performed on 51 CHD neonates who were treated with PGE1 or PGE1 + caffeine. PGE1 dose ranged from 0.01 to 0.1 mcg/kg/min, and caffeine was administered initially at 20 mg/kg, followed by a daily bolus dose of 10 mg/kg. Demographic and clinical data, prevalence of apnea, and PGE1 side effects were recorded and analyzed.

Results: A total of 51 CHD neonates receiving PGE1 + caffeine (n = 25) and PGE1 (n = 26) were included. The median age of total neonates was 2 (1–7) days, and 57% were female. There was no statistically significant difference between the baseline characteristics of participants, but neonates in the caffeine group received a higher mean dose of PGE1 (0.03 ± 0.17 vs. 0.02 ± 0.02, p=0.049) over the course of the treatment. The prevalence of apnea was 20% in the PGE1 + caffeine group and 42% in the PGE1 group (p=0.086). In the Cox regression model, the age of neonates had a significant effect on time to apnea in patients receiving caffeine (HR = 0.87, p=0.04).

Conclusion: Our findings fail to demonstrate that caffeine therapy reduces PGE1-induced apnea. A larger randomized controlled trial is required to confirm or refute the efficacy of caffeine in reducing the incidence of apnea associated with PGE1 infusion.

Trial Registration: Iranian Registry of Clinical Trials: IRCT20220503054729N1

## Linked entities

- **Chemicals:** caffeine (PubChem CID 2519), prostaglandin E1 (PubChem CID 5280723)
- **Diseases:** congenital heart disease (MONDO:0005453), apnea (MONDO:0000106)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** dependent (MESH:D019966), Apnea (MESH:D001049), vessels (MESH:C536223), heart lesions (MESH:D006331), CHDs (MESH:D006330)
- **Chemicals:** Caffeine (MESH:D002110), PGE1 (MESH:D000527)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12086028/full.md

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Source: https://tomesphere.com/paper/PMC12086028