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Published on: May 11, 2015
Advances in targeted therapy for pulmonary arterial hypertension in children
Li Li1, Xinyu Zhu1, Xiaojie Chen1
1Department of Scientific Research, Gansu Provincial Hospital, 204 West Donggang R.D., Lanzhou, 730000, China.
Insights
Pediatric pulmonary arterial hypertension (PAH) treatments are evolving with targeted drugs like endothelin receptor antagonists and PDE5 inhibitors. This review summarizes recent advances in PAH-targeted therapy for children, informing future treatment strategies.
Area of Science:
- Pediatric cardiology and pulmonology
- Vascular medicine
- Pharmacology
Background:
- Pulmonary arterial hypertension (PAH) in children is a rare, severe condition with high mortality.
- Current treatments rely on adult data and clinical experience, with limited pediatric-specific trials.
- The etiology of pediatric PAH is complex, making targeted drug selection challenging.
Purpose of the Study:
- To review research advances in targeted therapy for pediatric pulmonary arterial hypertension (PAH) over the last decade.
- To provide a theoretical basis for future studies and guideline development in pediatric PAH treatment.
- To summarize drug mechanisms, dosages, and adverse reactions of available targeted therapies.
Main Methods:
- Literature review of studies on targeted PAH therapies in children published in the last 10 years.
- Analysis of existing clinical trial data and expert clinical experience.
- Synthesis of information on drug classes, efficacy, safety, and mechanisms of action.
Main Results:
- Targeted drugs, including endothelin receptor antagonists, PDE5 inhibitors, and prostacyclins, have shown promise in improving hemodynamics and functional class in children with PAH.
- New agents like riociguat are under investigation.
- Further randomized controlled studies are needed to optimize drug combinations, treatment strategies, and clinical endpoints.
Conclusions:
- Pediatric pulmonary arterial hypertension (PAH) is a serious condition requiring specialized treatment approaches.
- Advances in targeted therapies offer improved outcomes for children with PAH.
- Continued research, particularly randomized controlled trials, is crucial for refining pediatric PAH treatment guidelines.
Abstract:
Pulmonary arterial hypertension (PAH) is a rare and devastating disease of the pulmonary vasculature with a high morbidity and mortality rate in infants and children. Currently, treatment approaches are mostly based on adult guidelines and pediatrician clinical experience, focusing on specific pulmonary antihypertensive therapy and conventional supportive care. The advent of targeted drugs has led to significant advances in the treatment of PAH in children, including endothelin receptor antagonists, phosphodiesterase type 5 inhibitors, and prostacyclins, which have been studied and proven to improve hemodynamics and functional class in children PAH. A new targeted drug, riociguat, is assessing its safety and efficacy in clinical trials. However, more randomized controlled studies are needed to evaluate the combination of drugs, treatment strategies, and clinical endpoints of targeted therapy in children PAH. In this review, we summarize the research advances of PAH-targeted therapy in children over the last decade in order to provide a theoretical basis for future studies.
Conclusion:
Pulmonary arterial hypertension (PAH) is a rare and devastating pulmonary vascular disease that is associated with a variety of diseases of any age in childhood onset.
What Is Known:
• Therapeutic strategies for targeted drugs for PAH in children are based almost exclusively on data from adult studies and clinical experience of pediatric specialists. • Due to the complex etiology of PAH in children and the relative lack of clinical trial data, the selection of appropriate targeted drug therapy remains difficult.
What Is New:
• We redefine the definition of pulmonary arterial hypertension in children and summarize the progress of targeted therapy of pulmonary arterial hypertension in children in the past ten years. • The dosage and adverse reactions were summarized, and the mechanism of action was drawn according to the available targeted drugs. It can provide theoretical support for the development of guidelines and treatment strategies for the diagnosis and treatment of pulmonary arterial hypertension in children.
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