Evidence map›Paper›PMID 29938590›Full record

ArticlePulmonary circulation

Non-invasive right ventricular load adaptability indices in patients with scleroderma-associated pulmonary arterial hypertension.

Sarah French, Myriam Amsallem, Nadia Ouazani, Shufeng Li, Kristina Kudelko, Roham T Zamanian, Francois Haddad, Lorinda Chung

Open access · goldAbstract read
In one paragraph

Article in Pulmonary circulation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. sPAP/PAAT Ratio as a New Index of Pulmonary Vascular Load: A Study in Normal Subjects and Ssc Patients with and without PH.Pathophysiology : the official journal of the International Society for Pathophysiology · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Right ventricular pressure-volume loop shape and systolic pressure change in pulmonary hypertension.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. 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 4 institutions in 2 countries.

Sarah French1 Division of Internal Medicine, Stanford University Medical Center, USA.
Myriam Amsallem2 Division of Cardiovascular Medicine, Stanford University Medical Center, USA.
Nadia Ouazani2 Division of Cardiovascular Medicine, Stanford University Medical Center, USA.
Shufeng Li4 Division of Biostatistics, Stanford University Medical Center, USA.
Kristina Kudelko5 Division of Pulmonary and Critical Care Disease, Stanford University Medical Center, USA.
Roham T Zamanian5 Division of Pulmonary and Critical Care Disease, Stanford University Medical Center, USA.
Francois Haddad2 Division of Cardiovascular Medicine, Stanford University Medical Center, USA.
Lorinda Chung7 Division of Rheumatology, Stanford University Medical Center, USA.
Stanford University · USStanford Medicine · USCardiovascular Institute of the South · USUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scleroderma-associated pulmonary arterial hypertension (SSc-PAH) is associated with worse outcome than idiopathic pulmonary arterial hypertension (IPAH), potentially due to worse right ventricular adaptation to load as suggested by pressure-volume loop analysis. The value of non-invasive load-adaptability metrics has not been fully explored in SSc-PAH. This study sought to assess whether patients with incident SSc-PAH have worse echocardiographic load-adaptability metrics than patients with IPAH. Twenty-two patients with incident SSc-PAH were matched 1:1 with IPAH based on pulmonary vascular resistance. Echocardiographic load-adaptability indices were divided into: surrogates of ventriculo-arterial coupling (e.g. right ventricular area change/end-systolic area), indices reflecting the proportionality of load adaptation (e.g. tricuspid regurgitation velocity-time integral normalized for average right ventricular radius), and simple ratios (e.g. tricuspid annular plane systolic excursion/right ventricular systolic pressure). The prognostic value of these indices for clinical worsening (i.e. death, transplant, or hospitalization for heart failure) at one year was explored. The two groups were comprised of patients of similar age, with similar cardiac index, pulmonary resistance, capacitance and NT-proBNP levels ( p > 0.10). There was no difference in baseline right ventricular dimension, function or load-adaptability indices. At one year, eight (36.4%) SSc-PAH patients had experienced clinical worsening (eight hospitalizations and two deaths) versus one hospitalization in the IPAH group. Load adaptation at one year in survivors was not worse in SSc-PAH ( p > 0.33). Patients with IPAH responded better to therapy than SSc-PAH in terms of reduction of right ventricular areas at one year ( p < 0.05). Right ventricular load-adaptability echocardiographic indices do not appear to capture the increased risk of negative outcomes at one year associated with SSc-PAH.

Indexed as

connective tissue diseaseechocardiographyoutcomespulmonary arterial hypertensionright ventriclescleroderma

Identifiers

PMID29938590
PMCPMC6056794
OpenAlexW2810395606

What OpenQuestion holds

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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.