Evidence map›Paper›PMID 39076250›Full record

ArticlePulmonary circulation2024

Selexipag in patients with pulmonary arterial hypertension associated with connective tissue disease (PAH-CTD): Real-world experience from EXPOSURE.

Sean Gaine, Pilar Escribano-Subias, Audrey Muller, Catarina C Fernandes, Martina Fontana, Tatiana Remenova, Stefan Söderberg, Tobias J Lange

Abstract read
In one paragraph

Article in Pulmonary circulation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

8 authors.

Sean GaineNational Pulmonary Hypertension Unit, Mater Misericordiae University Hospital Dublin Ireland.ORCID 0000-0002-5941-684X
Pilar Escribano-SubiasPulmonary Hypertension Unit, Cardiology Department CIBERCV, Hospital 12 de Octubre Madrid Spain.
Audrey MullerActelion Pharmaceuticals Ltd, a Johnson & Johnson Company, Global Epidemiology Allschwil Switzerland.
Catarina C FernandesActelion Pharmaceuticals Ltd, a Johnson & Johnson Company, Global Medical Affairs Allschwil Switzerland.
Martina FontanaJanssen-Cilag S.p.A, a Johnson & Johnson Company, Statistics and Decision Sciences Milan Italy.
Tatiana RemenovaActelion Pharmaceuticals Ltd, a Johnson & Johnson Company, Global Medical Safety Allschwil Switzerland.
Stefan SöderbergDepartment of Public Health and Clinical Medicine, Cardiology and Heart Centre Umeå University Umeå Sweden.ORCID 0000-0001-9225-1306
Tobias J LangeDepartment of Pulmonology Kreisklinik Bad Reichenhall Bad Reichenhall Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selexipag is indicated for the treatment of pulmonary arterial hypertension (PAH), including PAH associated with connective tissue disease (CTD), and further insights into the management of selexipag-treated PAH-CTD patients in clinical settings are needed. These analyses of the ongoing, multicenter, prospective EXPOSURE (EUPAS19085) study describe characteristics, treatment patterns, tolerability, and outcomes of PAH-CTD patients initiating selexipag in Europe/Canada. All analyses were descriptive, with idiopathic PAH patients who typically display better prognosis included for context. Six hundred ninety-eight selexipag-treated patients had follow-up information; 178 (26%) had PAH-CTD. The median age was 68 years, patients were predominantly female (88%), and with WHO functional class III symptoms (63%); the median time since diagnosis was 1.7 years. There were 5% patients at low, 25% intermediate-low, 40% intermediate-high, and 30% high risk of 1-year mortality, according to the ESC/ERS 4-strata risk score. Most (80%) initiated selexipag as a triple oral therapy, and most of these (62%) remained on triple therapy 6 months post-baseline. Over a median (Q1-Q3) selexipag exposure period of 8.6 (2.5-17.2) months, 79 (44%) patients discontinued selexipag; 36 (20%) due to tolerability/adverse events. Sixty (34%) patients were hospitalized at least once; 120 hospitalizations occurred, with 49 (48%) deemed PAH-related. Survival at 1 year was 85%, and at 2 years was 71%; 29 (16%) patients died. These results describe the use of combination therapy with selexipag for patients with PAH-CTD. These findings suggest an opportunity to optimize the benefits of selexipag among patients with PAH-CTD by moving from escalating after years in response to clinical deterioration to escalating sooner to prevent clinical deterioration.

Indexed as

real‐world evidenceregistrysclerodermasurvivaltreatment patterns

Identifiers

PMID39076250
PMCPMC11284239

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Registered trials

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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.