# Parenteral treprostinil in paediatric pulmonary arterial hypertension: a systematic review and meta-analysis

**Authors:** Julie Wacker, Raphael Joye, Maurice Beghetti

PMC · DOI: 10.1183/16000617.0033-2025 · 2026-03-25

## TL;DR

This study reviews and analyzes the effectiveness and safety of using treprostinil to treat pulmonary arterial hypertension in children.

## Contribution

The paper provides a systematic review and meta-analysis of parenteral treprostinil's efficacy in pediatric PAH, despite limited randomized trials.

## Key findings

- Parenteral treprostinil shows treatment benefits for pediatric PAH based on available data.
- Meta-analysis results indicate statistically significant improvements in PAH-related outcomes.
- Treprostinil is deemed effective and safe for treating pediatric PAH according to current evidence.

## Abstract

Paediatric pulmonary arterial hypertension (PAH) shares commonalities with adult disease but is essentially different regarding complexity and is usually more challenging to treat. Current treatment recommendations are based on expert opinion, small-scale paediatric studies and knowledge and consolidated guidelines for adults. Parenteral prostacyclins are recommended for high-risk patients but evidence is limited to cohort studies and retrospective data evaluations. The aim of this article was to summarise the available evidence on the efficacy and safety of parenteral treprostinil for paediatric PAH through a systematic review and to evaluate selected efficacy end-points through meta-analysis.

A systematic literature search (January 2000–April 2024) was conducted in PubMed, Google Scholar and clinical trial registries. Eligible studies included those reporting long-term outcomes of parenteral treprostinil in children with PAH. Moreover, a meta-analysis of selected efficacy end-points was performed based on published results from studies meeting predefined criteria.

32 studies encompassing 766 paediatric PAH patients treated with parenteral prostacyclins were identified; 649 patients received treprostinil. The meta-analysis was based on five publications including a total of 143 treprostinil-naïve patients. Despite the lack of randomised controlled trials, available data clearly indicate a treatment benefit of parenteral treprostinil in paediatric PAH. Literature data are supported by statistically significant results in the meta-analysis for PAH-relevant efficacy end-points.

Based on currently available published data, parenteral treprostinil is effective and safe in the treatment of paediatric PAH.

Despite a long history of use of parenteral treprostinil in treatment of paediatric PAH, evidence is limited. This work summarises available efficacy and safety data, including a meta-analysis of efficacy end-points.
https://bit.ly/48EEBq8

## Linked entities

- **Chemicals:** treprostinil (PubChem CID 54786)
- **Diseases:** pulmonary arterial hypertension (MONDO:0015924), PAH (MONDO:0015924)

## Full-text entities

- **Genes:** PAH (phenylalanine hydroxylase) [NCBI Gene 5053] {aka PH, PKU, PKU1}, PVR (PVR cell adhesion molecule) [NCBI Gene 5817] {aka CD155, HVED, NECL5, Necl-5, PVS, TAGE4}, ERAL1 (Era like 12S mitochondrial rRNA chaperone 1) [NCBI Gene 26284] {aka CEGA, ERA, ERA-W, ERAL1A, ERAL1B, H-ERA}
- **Diseases:** connective tissue disease (MESH:D003240), newborn (MESH:D006475), dislocation (MESH:D004204), disorders (MESH:D009358), pulmonary hypoplasia (MESH:C562992), tissue (MESH:D017695), Infusion (MESH:D000075662), DLD (MESH:C573012), IPAH (MESH:D065627), BSIs (MESH:D018805), insomnia (MESH:D007319), PAH (MESH:D000081029), joint, muscle, jaw pain (MESH:D063806), pulmonary veno-occlusive disease (MESH:D011668), chronic thromboembolic pulmonary hypertension (MESH:D011655), bronchopulmonary dysplasia (MESH:D001997), Group 1 PH (MESH:D006976), right heart failure (MESH:D006333), flushing (MESH:D005483), diarrhoea (MESH:D003967), skin (MESH:D012871), vomiting (MESH:D014839), HPAH (MESH:C563358), swelling (MESH:D004487), congenital heart disease (MESH:D006330), nausea (MESH:D009325), mPAP (MESH:D000071079), CLIs (MESH:D007239), congenital malformations (OMIM:163000), dizziness (MESH:D004244), oedema (MESH:C536897), WU (MESH:C567479), itching (MESH:D011537), CTEPH (OMIM:612862), vascular (MESH:D057772), cardiac defects (MESH:D006331), cardiac shunt defect (MESH:C562451), rash (MESH:D005076), system (MESH:D015619), Pain (MESH:D010146), developmental lung disease (MESH:D008171), gastrointestinal (MESH:D005767), congenital diaphragmatic hernia (MESH:D065630), headache (MESH:D006261)
- **Chemicals:** Treprostinil (MESH:C427248), iloprost (MESH:D016285), nitric oxide (MESH:D009569), prostacyclin receptor agonists (-), prostaglandins (MESH:D011453), prostacyclins (MESH:D044062), Epoprostenol (MESH:D011464)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13014287/full.md

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Source: https://tomesphere.com/paper/PMC13014287