Evidence map›Paper›PMID 37336527›Full record

ArticleESC heart failure2023

Transitioning intravenous epoprostenol to oral selexipag in idiopathic pulmonary arterial hypertension: a case report.

André Alexandre, Inês Furtado, Luísa Carvalho, Fabienne Gonçalves, Alzira Melo, Joana Alves, Mário Santos, Abílio Reis

Open access · goldAbstract readCase Reports
In one paragraph

Article in ESC heart failure, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% of its field
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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

8 authors at 2 institutions in 1 country.

André AlexandreDepartment of Cardiology, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.ORCID 0000-0003-2465-2217
Inês FurtadoPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.ORCID 0000-0003-3985-0718
Luísa CarvalhoPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.
Fabienne GonçalvesPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.ORCID 0000-0002-3439-5093
Alzira MeloPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.
Joana AlvesPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.
Mário SantosDepartment of Cardiology, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.ORCID 0000-0002-4509-0260
Abílio ReisPulmonary Vascular Disease Unit, Centro Hospitalar Universitário de Santo António (CHUdSA), Porto, Portugal.ORCID 0000-0002-9932-3736
Hospital de Santo António · PTUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intravenous (i.v.) prostacyclin is the cornerstone treatment in high-risk pulmonary arterial hypertension (PAH) patients. Selexipag is an orally available prostacyclin receptor agonist. Limited data are available regarding the feasibility of transitioning from i.v. epoprostenol to selexipag. A 50-year-old woman with idiopathic PAH was diagnosed in a World Health Organization (WHO) Functional Class (FC) IV. She improved with upfront triple combination therapy, including i.v. epoprostenol. Over 2 years of follow-up, the patient remained at low risk and expressed strong preference towards oral therapies. After careful risk-benefit clinical consideration, she was transitioned from i.v. epoprostenol to selexipag. Selexipag was started at dosage of 200 μg twice daily (b.i.d.) and titrated up to 1600 μg b.i.d. over 8 weeks (up-titration of 200 μg b.i.d. every week). Simultaneously, i.v. epoprostenol was down-titrated 3.0 ng/kg/min every week from a dosage of 27.5 ng/kg/min. The transition occurred under strict medical surveillance and was well tolerated. One year after discontinuation of epoprostenol, the patient remains in WHO FC I and has no signs of clinical deterioration. Although not generalizable to most PAH patients, this case highlights that a carefully planned transition from epoprostenol to selexipag is feasible in selected low-risk patients within a shared medical decision-making framework.

Indexed as

Hypertension, PulmonaryPulmonary Arterial HypertensionAcetamidesAntihypertensive AgentsEpoprostenolFamilial Primary Pulmonary HypertensionFemaleHumansMiddle AgedPyrazinesAcetamidesAntihypertensive AgentsEpoprostenolPyrazinesselexipagIdiopathic pulmonary arterial hypertensionIntravenous epoprostenolOral selexipagPulmonary hypertensionSwitchback therapyTransition therapy

Identifiers

PMID37336527
PMCPMC10375174
OpenAlexW4381251429

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.