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Published on: January 27, 2023
Different interventions for the treatment of patent ductus arteriosus in children: a protocol for a network
Xin Zhang1,2, Xiao-Dong Hou2,3, Wen-Xin Wang1,2
1The First School of Clinical Medicine of Gansu University of Chinese Medicine, Lanzhou, China.
Insights
This study compares the effectiveness and safety of various treatments for patent ductus arteriosus (PDA), a common congenital heart defect. A Bayesian network meta-analysis will determine the best intervention sequence for PDA children.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Medical Interventions
Background:
- Patent ductus arteriosus (PDA) is a prevalent congenital heart disease requiring timely intervention.
- Current treatment options for PDA include pharmacological therapy, surgical closure, and interventional closure.
- The comparative effectiveness and safety of these interventions remain a subject of debate.
Purpose of the Study:
- To conduct a Bayesian network meta-analysis to assess the efficacy and safety of different interventions for PDA.
- To estimate the optimal sequence of therapies for PDA management in children.
- To provide a comprehensive comparison of various PDA treatment modalities.
Main Methods:
- A systematic search of multiple databases (PubMed, Embase, Cochrane Library, Web of Science, etc.) will be performed.
- Data extraction and reporting will adhere to PRISMA-P guidelines for Bayesian network meta-analysis.
- Outcomes include PDA closure rates, success rates, mortality, procedure times, and complication rates. Study quality will be assessed using ROB and GRADE.
Main Results:
- This section is not applicable as the study is a protocol and results are yet to be determined.
- The study protocol outlines the planned analysis of primary and overall PDA closure, technical and surgical success rates.
- Planned analysis includes assessment of mortality, operation time, ICU stay, radiation exposure, and complication rates.
Conclusions:
- This Bayesian network meta-analysis aims to clarify the optimal treatment strategy for PDA.
- The findings will inform clinical decision-making regarding the management of PDA in pediatric patients.
- This research will contribute to evidence-based guidelines for PDA treatment.
Introduction:
Patent ductus arteriosus (PDA) is one of the most common congenital heart diseases. Once the PDA is diagnosed, it needs to be dealt with in time. At present, main methods include pharmacological treatment, surgical closure, and interventional closure for treatment of PDA. However, the effect of different interventions in PDA management is still controversial. Thus, our study aims to assess the effectiveness of different interventions together and estimate the sequence of these therapies for PDA children. Meanwhile, it is necessary to conduct a Bayesian network meta-analysis to compare the safety of different interventions comprehensively.
Methods And Analysis:
To the best of our knowledge, this is the first Bayesian network meta-analysis comparing the efficacy and safety of different interventions for the treatment of PDA. PubMed, Embase, Cochrane Library, Web of Science, gray literature, and trial registry databases were searched from inception to December 2022. We will extract and report data according to methodological guidelines for Bayesian network meta-analysis by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P). Primary PDA closure, overall PDA closure, technical success, surgical success rate, mortality during hospital stay, operation time, intensive care unit stay, intraoperative radiation dose, radiation exposure time, total postoperative complication rate, and postoperative major complication rate will be defined as the outcomes. The quality of all random studies will be assessed using ROB, and quality of evidence for all outcomes will be judged by using the Grading of Recommendations Assessment, Development and Evaluation (GRADE).
Ethics And Dissemination:
The results will be disseminated through peer-reviewed publication. Since no private and confidential patient data will be contained in the reporting, there are no ethical considerations associated with this protocol.
Systematic Review Registration:
INPLASY2020110067.
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