CO14 - Pulmonary Hypertension Screening in Interstitial Lung Disease: Interim Comparison of Clinician Suspicion vs Right Heart Catheterization in the PHINDER Study
Claire Thrasher (United States)1; Sandeep Sahay (United States)2; Tejaswini Kulkarni (United States)3; Oksana Shlobin (United States)4; Abhijit Raval (United States)5; David Kiely (UK)6; Maral DerSarkissian (United States)7; Matthew Hunsucker (United States)8; David Zisman (United States)9; Meredith Broderick (United States)1; Dasom Lee (United States)1; Kevin Maher (United States)1; Mary Beth Scholand (United States)10;
1 - United Therapeutics, NC, USA; 2 - Houston Methodist Hospital, TX, USA; 3 - University of Alabama at Birmingham, AL, USA; 4 - Inova Fairfax Hospital, VA, USA; 5 - AnMed, SC, USA; 6 - University of Sheffield, UK; 7 - Analysis Group, CA, USA; 8 - Lebauer Pulmonary Care, NC, USA; 9 - Cleveland Clinic, FL, USA; 10 - University of Utah, UT, USA;
Keywords: Hemodynamics; Screening; Gestalt;
Select the theme: Idiopathic Pulmonary Fibrosis
Type: Original Papers
Presentation: Oral Communication

Introduction: Despite the poor prognosis of interstitial lung disease (ILD) with pulmonary hypertension (PH), evidence-based guidelines for PH screening in ILD are lacking. PHINDER (NCT05776225) aims to develop a validated PH screening tool in patients with ILD.

Objectives: This PHINDER interim analysis assessed the accuracy of study clinicians’ suspicion of PH compared to hemodynamically confirmed PH.

Materials and Methods: PHINDER is a prospective, multicenter study where ILD patients undergo routine non-invasive assessments followed by right heart catheterization (RHC) to confirm pre-capillary PH (mPAP>20 mmHg, PVR>2 WU, PCWP≤15 mmHg). After reviewing all non-invasive test results but prior to RHC, study clinicians are asked to rank their suspicion of PH as low, medium, or high.

Results: At the time of this interim analysis (May 2025), data were available for 189 patients, of whom 15% were deemed low suspicion for PH, 46% deemed medium suspicion, and 39% deemed high suspicion by their clinician prior to RHC. Parameters that trended along with and may have driven suspicion of PH, included 6-minute walk distance, natriuretic peptide levels, supplemental oxygen requirements, peripheral edema or loud second heart sounds, FEV, FVC, DLCO, FVC/DLCO, RV pressure, tricuspid regurgitant velocity, pulmonary artery (PA) enlargement, PA/aorta diameter, and RV/LV diameter. Pre-capillary PH was then confirmed by RHC in 32% of the low-suspicion group (median mPAP 29 mmHg), 51% of the medium-suspicion group (mPAP 26 mmHg), and 69% of the high-suspicion group (mPAP 28 mmHg).

Conclusions: A high level of discrepancy was observed between clinicians’ gestalt assessment of PH likelihood and RHC hemodynamics. Pre-capillary PH was confirmed in almost a third of patients believed to have low likelihood of PH and was ruled out in almost a third of patients believed to have high likelihood of PH. These results underscore the need for more objective PH screening in patients with ILD.

Figure 1. Clinician suspicion of pre-capillary PH vs RHC-confirmed pre-capillary PH.