Evidence map›Paper›PMID 42171541›Full record

ArticleJACC. Heart failure2026

Refining the Definition for "Low Risk" in Pulmonary Arterial Hypertension: Time to Reduce Morbidity and Mortality.

Charles Fauvel, Priscilla Correa Jaque, Yongqi Liu, Sang Wan Lee, Sandeep Sahay, Nelson A Villasmil Hernandez, Jason Weatherald, James White, Allen Everett, Megan Griffith and 7 more

Abstract read
In one paragraph

Article in JACC. Heart failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

17 authors.

Charles FauvelDepartment of Cardiology, Rouen University Hospital, French National Institute for Health and Medical Research (INSERM) U1096, F-76000, Rouen, France.
Priscilla Correa JaqueDepartment of Cardiology, Eastern Virginia Medical School, Old Dominion University, Sentara Health, Norfolk, Virginia, USA.
Yongqi LiuDepartment of Statistics, The Ohio State University, Columbus, Ohio, USA.
Sang Wan LeeDepartment of Statistics, The Ohio State University, Columbus, Ohio, USA.
Sandeep SahayDivision of Pulmonary, Critical Care & Sleep Medicine, Houston Methodist Hospital, Houston, Texas, USA.
Nelson A Villasmil HernandezDivision of Pulmonary, Critical Care & Sleep Medicine, Houston Methodist Hospital, Houston, Texas, USA.
Jason WeatheraldDepartment of Medicine, Division of Pulmonary Medicine, University of Alberta, Edmonton, Canada.
James WhiteDivision of Pulmonary and Critical Care Medicine, University of Rochester, New York, USA.
Allen EverettBlalock-Taussig-Thomas Congenital Heart Center, Johns Hopkins University, Baltimore, Maryland, USA.
Megan GriffithDepartment of Pediatrics, Division of Cardiology, University of Texas Southwestern, Dallas, Texas, USA.
Thomas M CascinoDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Adam PererHuman-Computer Interaction Institute, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
Katelyn MorrisonHuman-Computer Interaction Institute, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
Michael LewisDepartment of Medicine, Division of Pulmonary/Critical Care Medicine, Cedars Sinai Medical Center, Los Angeles, California, USA; Smidt Heart Institute, Cedars Sinai Medical Center, Los Angeles, California, USA.
Yuri MatusovDepartment of Medicine, Division of Pulmonary/Critical Care Medicine, Cedars Sinai Medical Center, Los Angeles, California, USA.
Shili LinDepartment of Statistics, The Ohio State University, Columbus, Ohio, USA.
Raymond L BenzaDepartment of Cardiology, Eastern Virginia Medical School, Old Dominion University, Sentara Health, Norfolk, Virginia, USA. Electronic address: rbenza@odu.edu.

Funding

PHORA-Pulmonary Hypertension Outcome Risk AssessmentR01HL164906 · NHLBI · SENTARA HEALTH · PI RAYMOND Louis Benza · 2022 to 2026
$3.0M
NHLBI NIH HHS R01 HL164906
6 · The paper itself

Abstract

background"Low-risk" pulmonary arterial hypertension (PAH) patients are defined as having a risk of death <5% within 1 year. As treatment improves, accounting for the negative impact of short-term morbidity and considering extending the duration of <5% mortality in this definition seem prudent.

objectivesThis study sought to propose a more stringent definition of low risk that extends the low mortality risk to 3 years and specifies a low risk of morbidity at 1 year.

methodsThis study used patient-level data from a harmonized data set of 8 PAH randomized controlled trials that included patients with a REVEAL (Registry to Evaluate Early and Long-Term PAH Disease Management) 2.0 risk score ≤6 (ie, low risk using contemporary scores). Low risk was a priori defined as "risk of death <5% at 3 years and risk of clinical worsening <10% at 1 year." Clinical worsening was defined at the individual trial level and included any of the following: lung transplantation, hospitalization for PAH, initiation of long-term oxygen therapy, 15% decrease in 6-minute walking distance (6MWD) from baseline with a worsening of NYHA functional class, or the addition of a new PAH medication.

resultsA total of 1,925 PAH patients were included: median age, 46 years (Q1-Q3: 34-57 years); mean pulmonary artery pressure, 47 mm Hg (Q1-Q3: 37-58 mm Hg); pulmonary vascular resistance, 8 WU (Q1-Q3: 6-12 WU), 6MWD, 409 m (Q1-Q3: 363-423 m); and N-terminal pro-B-type natriuretic peptide, 227 pg/mL (Q1-Q3: 101-621 pg/mL). Compared with patients with a REVEAL 2.0 score equal to 5 or 6, patients with a score ≤4 had a better clinical and hemodynamic presentation and met the definition of "refined low risk" (3-year mortality of 2.6% and 1-year clinical worsening of 6.4%). Idiopathic PAH, 6MWD, N-terminal pro-B-type natriuretic peptide, NYHA functional class I to II, heart rate, and the absence of previous atrial fibrillation were associated with refined low risk.

conclusionsThis study is the first to embed both morbidity and mortality within the definition of low -risk for PAH and suggests that patients with a REVEAL 2.0 risk score ≤4 define this condition.

Indexed as

Hypertension, PulmonaryPulmonary Arterial HypertensionDisease ProgressionFemaleHumansLung TransplantationMaleMiddle AgedMorbidityNatriuretic Peptide, BrainPeptide FragmentsRandomized Controlled Trials as TopicRisk AssessmentTime FactorsWalk TestNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)clinical worseningdeathlow riskprognosisREVEAL 2.0

Identifiers

PMID42171541
PMCPMC13352415

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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.