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Treatment for Post-hemorrhagic Ventricular Dilatation: A Multiple-Treatment Meta-Analysis.
Liam Mahoney1,2, Karen Luyt3, David Harding3
1Neonatal Unit, North Bristol NHS Trust, Bristol, United Kingdom.
Frontiers in Pediatrics
|July 14, 2020
Summary
Post-hemorrhagic ventricular dilatation (PHVD) in premature infants is a major cause of death and disability. A meta-analysis suggests Drainage Irrigation and Fibrinolytic Therapy (DRIFT) may be the most effective treatment to improve outcomes.
Area of Science:
- Neonatal neurology
- Pediatric neurosurgery
- Evidence-based medicine
Background:
- Post-hemorrhagic ventricular dilatation (PHVD) poses significant risks for premature infants, leading to death or long-term neurodevelopmental disability.
- Limited therapeutic options have been rigorously evaluated for managing PHVD in preterm neonates.
Purpose of the Study:
- To conduct a systematic review and multiple-treatment meta-analysis (NMA) evaluating interventions for PHVD in premature infants.
- To identify the most effective treatment strategy to prevent death or neurodevelopmental impairment.
Main Methods:
- Systematic literature search of PubMed, EMBASE, and Cochrane Library for intervention trials in preterm infants with PHVD.
- Bayesian random-effects network meta-analysis using Markov chain Monte Carlo methods.
- Calculation of Surface Under the Cumulative Ranking (SUCRA) curves to rank treatment probabilities.
Main Results:
- Ten trials involving 700 infants were analyzed, comparing seven intervention categories.
- No single intervention reached conventional statistical significance in pairwise comparisons.
- Drainage Irrigation and Fibrinolytic Therapy (DRIFT) demonstrated the highest probability (82.1%) of being the most effective treatment for the primary outcome.
Conclusions:
- PHVD remains a critical concern in neonatal care, necessitating further research into effective therapies.
- Current NMA findings indicate DRIFT as the most promising intervention for improving outcomes in infants with intraventricular hemorrhage-related PHVD.
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