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Published on: October 19, 2013
Advances in paediatric pulmonary vascular disease associated with bronchopulmonary dysplasia
Thomas Rossor1, Anne Greenough
1Division of Asthma, Allergy and Lung Biology, MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London, England, UK.
Insights
Recent advances in diagnosing and treating pulmonary hypertension (PH) in infants with bronchopulmonary dysplasia (BPD) show promise, but more research is needed to confirm long-term benefits.
Area of Science:
- Pediatrics
- Neonatology
- Cardiology
Background:
- Pulmonary hypertension (PH) is a frequent complication in infants with bronchopulmonary dysplasia (BPD).
- Effective management strategies for BPD-related PH are crucial for improving patient outcomes.
Purpose of the Study:
- To review recent advancements in the diagnosis and treatment of PH.
- To evaluate the potential benefits of these advances for infants and children with BPD-related PH.
Main Methods:
- Literature review of recent studies on PH diagnosis and treatment in BPD.
- Analysis of current diagnostic tools, including echocardiography, and emerging biomarkers.
- Assessment of various therapeutic options, such as inhaled nitric oxide, sildenafil, prostacyclin, PDE3 inhibitors, and endothelin receptor blockers.
Main Results:
- Echocardiography is the primary diagnostic tool but has limitations; improved diagnostic techniques and biomarkers are needed.
- Inhaled nitric oxide offers short-term benefits only.
- Sildenafil demonstrated significant mortality reduction in resource-limited settings.
- Evidence for other therapies (prostacyclin, PDE3 inhibitors, endothelin receptor blockers) is limited to case reports/series.
Conclusions:
- Further randomized controlled trials with long-term follow-up are essential to establish the efficacy of PH therapies in children with BPD.
- Developing novel diagnostic methods and biomarkers is critical for accurate PH assessment in this population.
Abstract:
Pulmonary hypertension (PH) is a common finding in infants with bronchopulmonary dysplasia (BPD). The aim of this review is to describe recent advances in the diagnosis and treatment of PH and discuss whether they will benefit infants and children with BPD related PH. Echocardiography remains the mainstay of diagnosis but has limitations, further developments in diagnostic techniques and identification of biomarkers are required. There are many potential therapies for PH associated with BPD. Inhaled nitric oxide has been shown to improve short term outcomes only. Sidenafil in resource limited settings was shown in three randomized trials to significantly reduce mortality. The efficacy of other therapies including prostacyclin, PDE3 inhibitors and endothelin receptor blockers has only been reported in case reports or case series. Randomized controlled trials with long term follow up are required to appropriately assess the efficacy of therapies aimed at improving the outcome of children with PH.
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