ArticleJACC. Case reports2025
Facilitating Earlier Diagnosis of Pulmonary Hypertension Using a Novel Noninvasive Diagnostic.
Article in JACC. Case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Critical Appraisal of "A Machine Learning-Based Model to Estimate the Risk of Pulmonary Hypertension in Chronic Kidney Disease Patients".Journal of clinical hypertension (Greenwich, Conn.) · 2025Article
Corrections and comments
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPulmonary hypertension (PH) is frequently underdiagnosed due to limitations of transthoracic echocardiography, particularly when tricuspid regurgitant velocity (TRV) is unmeasurable. CorVista PH (point-of-care test for pulmonary hypertension [POC-PH]) is a novel, Food and Drug Administration-cleared point-of-care diagnostic with 82% sensitivity and 92% specificity for identifying mean pulmonary artery pressure elevation. SUMMARY: We present a patient who underwent multiple transthoracic echocardiograms negative for PH. POC-PH testing prompted right heart catheterization, revealing group 2 PH, and enabling the diagnosis of heart failure with preserved ejection fraction. We also present 3 patients with measurable TRV, all of whom tested positive on POC-PH and were confirmed to have PH via right heart catheterization. These included both precapillary and postcapillary PH phenotypes. DISCUSSION: An average of 3 transthoracic echocardiograms are required to diagnose pulmonary arterial hypertension spanning a period exceeding 2 years. TAKE-HOME MESSAGE: POC-PH demonstrated clinical utility in identifying PH where transthoracic echocardiography failed to raise suspicion.
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Registered trials
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 Socratic graph.