Evidence map›Paper›PMID 41410826›Full record

ArticlePulmonary therapy2026

Real-World Treatment Patterns and Burden of Chronic Thromboembolic Pulmonary Hypertension Patients across Consultation Settings in the USA.

Belinda Rivera-Lebron, Alison Witkin, Carly J Paoli, Mark Small, Mia Harvey, Daniel Graham, Sumeet Panjabi, Gabriela Gomez Rendon, Josanna Rodriguez-Lopez

Abstract read
In one paragraph

Article in Pulmonary therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Belinda Rivera-LebronUniversity of Pittsburgh Medical Center, 200 Lothrop Street, Pittsburgh, PA, 15213, USA. riveralebronbn@upmc.edu.
Alison WitkinMassachusetts General Hospital, Boston, MA, USA.
Carly J PaoliActelion Pharmaceuticals US Inc, San Francisco, CA, USA.
Mark SmallAdelphi Real World, Bollington, UK.
Mia HarveyAdelphi Real World, Bollington, UK.
Daniel GrahamAdelphi Real World, Bollington, UK.
Sumeet PanjabiActelion Pharmaceuticals US Inc, San Francisco, CA, USA.
Gabriela Gomez RendonActelion Pharmaceuticals US Inc, San Francisco, CA, USA.
Josanna Rodriguez-LopezMassachusetts General Hospital, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChronic thromboembolic pulmonary hypertension (CTEPH) is a rare, progressive pulmonary hypertension characterized by chronic fibrotic thrombi. Treatment includes surgical, endovascular, and pharmaceutical options. With varied treatments, it is essential to understand how they are deployed across real-world settings. We aimed to describe clinical characteristics, treatment patterns, and quality of life across real-world settings in the USA.

methodsData were drawn from the Adelphi Real World CTEPH Disease Specific Program™, a cross-sectional survey of US physicians and patients, conducted September 2023-May 2024. Physicians recruited by local fieldwork agents using a short screening questionnaire provided demographics, clinical characteristics, and treatment patterns for 1-6 consecutively consulting patients with right heart catheterization confirmed CTEPH. These patients self-completed a form containing the EQ-5D-5L, visual analog scale (EQ-VAS), workplace and activity impairment scale (WPAI), pulmonary arterial hypertension symptom and impact scale. Data were stratified by treatment setting (accredited or nonaccredited pulmonary hypertension center). Analyses were descriptive.

resultsIn total, 98 physicians provided data on 153 patients, of whom 53 completed the patient self-complete form. Mean (standard deviation) patient age was 59.2 years, 59.5% female, and 73.2% considered operable. Of those who had undergone a surgery/procedure (n = 68), 82.1% had undergone pulmonary thromboendarterectomy (PTE), and 19.1% balloon pulmonary angioplasty (BPA). Overall, 82.4% were prescribed any pharmaceutical medication for their CTEPH; of those treated, 81.0% were prescribed anticoagulants. Monotherapy (45.7%) was the most reported regimen in nonaccredited settings; for accredited settings, this was dual therapy (45.5%). EQ-5D-5L scores were low with nearly a quarter of patients reporting problems with usual activities and mobility, and 26.4% needing to change work patterns.

conclusionsThough treatment patterns generally followed guidelines, BPA was potentially underutilized. Dyspnea was common, despite treatment, with patients experiencing reduced quality of life, highlighting an unmet need.

Indexed as

Accredited settingsBurdenChronic thromboembolic pulmonary hypertensionReal-world evidenceTreatment patterns

Identifiers

PMID41410826
PMCPMC12992756

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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.