Journal of Clinical Medicine (Nov 2022)

Left Heart Disease Phenotype in Elderly Patients with Pulmonary Arterial Hypertension: Insights from the Italian PATRIARCA Registry

  • Matteo Toma,
  • Roberta Miceli,
  • Edoardo Bonsante,
  • Davide Colombo,
  • Marco Confalonieri,
  • Andrea Garascia,
  • Stefano Ghio,
  • Mariangela Lattanzio,
  • Carlo Maria Lombardi,
  • Giuseppe Paciocco,
  • Cristina Piccinino,
  • Irene Rota,
  • Caterina Santolamazza,
  • Laura Scelsi,
  • Piermario Scuri,
  • Davide Stolfo,
  • Antonella Vincenzi,
  • Lorenzo Volpiano,
  • Marco Vicenzi,
  • Pietro Ameri

DOI
https://doi.org/10.3390/jcm11237136
Journal volume & issue
Vol. 11, no. 23
p. 7136

Abstract

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Pulmonary arterial hypertension (PAH) in the elderly is often associated with left heart disease (LHD), prompting concerns about the use of pulmonary vasodilators. The PATRIARCA registry enrolled ≥70 year-old PAH or chronic thromboembolic pulmonary hypertension (CTEPH) patients at 11 Italian centers from 1 December 2019 through 15 September 2022. After excluding those with CTEPH, post-capillary PH at the diagnostic right heart catheterization (RHC), and/or incomplete data, 23 (33%) of a total of 69 subjects met the criteria proposed in the AMBITION trial to suspect LHD. Diabetes [9 (39%) vs. 6 (13%), p = 0.01] and chronic kidney disease [14 (61%) vs. 12 (26%), p = 0.003] were more common, and the last RHC pulmonary artery wedge pressure [14 ± 5 vs. 10 ± 3 mmHg, p p = 0.02] was lower in LHD than non-LHD patients. However, PAH therapy was similar, with 13 (57%) and 23 (50%) subjects, respectively, taking two oral drugs. PAH medication patterns remained comparable between LHD and non-LHD patients also when the former [37, 54%] were identified by atrial fibrillation and echocardiographic features of LHD, in addition to the AMBITION criteria. In this real-world snapshot, elderly PAH patients were treated with pulmonary vasodilators, including combinations, despite a remarkable prevalence of a LHD phenotype.

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