Evidence map›Paper›PMID 41371490›Full record

ArticleChest2026

Treatment Patterns in Patients With Incident Pulmonary Hypertension: Real-World Data From the Pulmonary Hypertension Association Registry.

Sarah L Khan, Carly J Paoli, Noah Kime, Kayleen Williams, Gabriela Gomez Rendon, Adriano R Tonelli, Hector Cajigas, Stephen C Mathai, Sandeep Sahay

Abstract readMulticenter Study
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Sarah L KhanDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Carly J PaoliJohnson & Johnson, Titusville, NJ.
Noah KimeUniversity of Washington Department of Biostatistics, Seattle, WA.
Kayleen WilliamsUniversity of Washington Department of Biostatistics, Seattle, WA.
Gabriela Gomez RendonJohnson & Johnson, Titusville, NJ.
Adriano R TonelliDepartment of Pulmonary and Critical Care Medicine, Integrated Hospital Care Institute, Cleveland Clinic, Cleveland, OH.
Hector CajigasMayo Clinic Rochester Division of Pulmonary and Critical Care Medicine, Rochester, MN.
Stephen C MathaiDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Sandeep SahayDivision of Pulmonary, Critical Care & Sleep Medicine, Houston Methodist Hospital, Houston, TX. Electronic address: ssahay@houstonmethodist.org.

Funding

Distinguishing Phenotypes of Pulmonary Hypertension in Patients with Connective Tissue Disease-related Interstitial Lung DiseaseF32HL170482 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KHAN, SARAH · 2023 to 2024
$185k
NHLBI NIH HHS F32 HL170482
6 · The paper itself

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.

Indexed as

Antihypertensive AgentsEndothelin Receptor AntagonistsEpoprostenolHypertension, PulmonaryPhosphodiesterase 5 InhibitorsPulmonary Arterial HypertensionAgedCardiac CatheterizationDrug Therapy, CombinationFemaleHumansIncidenceMaleMiddle AgedProspective StudiesRegistriesAntihypertensive AgentsEndothelin Receptor AntagonistsEpoprostenolPhosphodiesterase 5 Inhibitorsmortalitypulmonary hypertensionREVEAL risk scorerisk stratificationsurvivaltreatment

Identifiers

PMID41371490
PMCPMC13176901

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.