ArticleChest2026
Treatment Patterns in Patients With Incident Pulmonary Hypertension: Real-World Data From the Pulmonary Hypertension Association Registry.
Article in Chest, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Glutathione Redox Changes in Pulmonary Arterial Blood After Remote Ischemic Conditioning in Pulmonary Hypertension: A Single-Arm Pilot Study.Antioxidants (Basel, Switzerland) · 2026Article
- Comorbidities and Events of Clinical Interest in Patients with Pulmonary Arterial Hypertension (PAH): Analysis of Real-World Data.Pulmonary circulation · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
backgroundCurrent evidence supports risk-based treatment for pulmonary arterial hypertension (PAH) with an endothelin receptor antagonist and phosphodiesterase type 5 inhibitor as initial therapy for patients with low- and intermediate-risk PAH, and triple therapy with the addition of a parenteral prostacyclin for patients with high-risk PAH. RESEARCH QUESTION: What are the current treatment patterns for patients with newly diagnosed PAH in the Pulmonary Hypertension Association Registry (PHAR)? STUDY DESIGN AND
methodsThis analysis was performed in a prospectively collected cohort of patients with incident PAH diagnosed by right heart catheterization and enrolled in the PHAR between September 30, 2015, and February 14, 2024. The primary objective was to assess the guideline-recommended risk-based treatment approaches and their impact in the real world. All-cause mortality was compared across risk groups and between patients receiving monotherapy, dual therapy, and triple therapy for PAH across risk strata.
resultsThere were 1,019 patients with incident PAH in the PHAR who received either initial monotherapy (n = 344, 33.8%), dual therapy (n = 557, 54.7%), or triple therapy (n = 118, 11.6%). Of 323 patients with complete data for risk classification who received initial monotherapy, 25.1% were low risk, 31.3% were intermediate risk, and 43.7% were high risk by Registry to Evaluate Early and Long-term PAH Disease Management Lite 2 risk score. For the 540 patients treated with initial dual therapy, 35.7% were low risk, 26.5% were intermediate risk, and 37.8% were high risk. Finally, among the 113 patients who received initial triple therapy, 31.9% were low risk, 28.3% were intermediate risk, and 39.8% were high risk. All-cause mortality was lowest for patients with low-risk PAH at baseline and highest for those with high-risk PAH at baseline across the entire cohort and for patients treated with initial monotherapy, dual therapy, or triple therapy.
interpretationThis analysis highlights the underutilization of PAH therapies for patients with newly diagnosed PAH in this real-world patient population.
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