Evidence map›Paper›PMID 34206876›Full record

ReviewJournal of clinical medicine2021

Echocardiography in Pulmonary Arterial Hypertension: Is It Time to Reconsider Its Prognostic Utility?

Ioannis T Farmakis, Eftychia Demerouti, Panagiotis Karyofyllis, George Karatasakis, Maria Stratinaki, Dimitrios Tsiapras, George Athanassopoulos, Vassilios Voudris, George Giannakoulas

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Right heart reverse remodeling:International journal of cardiology. Congenital heart disease · 2025
    Article
  4. Article
  5. Assessing the role of tracheostomy placement in bronchopulmonary dysplasia with pulmonary hypertension.Journal of perinatology : official journal of the California Perinatal Association · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
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

9 authors at 3 institutions in 1 country.

Ioannis T FarmakisCardiology Department, AHEPA University Hospital, Aristotle University of Thessaloniki, PC 54621 Thessaloniki, Greece.
Eftychia DemeroutiNon-Invasive Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.ORCID 0000-0003-2032-7775
Panagiotis KaryofyllisInvasive-Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.
George KaratasakisNon-Invasive Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.
Maria StratinakiDepartment of Cardiology, General Hospital Venizeleio, PC 71409 Irákleion, Greece.ORCID 0000-0001-8720-1830
Dimitrios TsiaprasNon-Invasive Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.
George AthanassopoulosNon-Invasive Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.
Vassilios VoudrisInvasive-Cardiology Department, Onassis Cardiac Surgery Center, PC 17674 Athens, Greece.
George GiannakoulasCardiology Department, AHEPA University Hospital, Aristotle University of Thessaloniki, PC 54621 Thessaloniki, Greece.ORCID 0000-0001-7491-6319
Onassis Cardiac Surgery Center · GRAristotle University of Thessaloniki · GRThe General Hospital of Heraklion "Venizeleio-Pananio" · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is characterized by an insult in the pulmonary vasculature, with subsequent right ventricular (RV) adaptation to the increased afterload that ultimately leads to RV failure. The awareness of the importance of RV function in PAH has increased considerably because right heart failure is the predominant cause of death in PAH patients. Given its wide availability and reduced cost, echocardiography is of paramount importance in the evaluation of the right heart in PAH. Several echocardiographic parameters have been shown to have prognostic implications in PAH; however, the role of echocardiography in the risk assessment of the PAH patient is limited under the current guidelines. This review discusses the echocardiographic evaluation of the RV in PAH and during therapy, and its prognostic implications, as well as the potential significant role of repeated echocardiographic assessment in the follow-up of patients with PAH.

Indexed as

echocardiographypulmonary arterial hypertensionright ventricle

Identifiers

PMID34206876
PMCPMC8268493
OpenAlexW3176609613

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.