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Pulmonary hypertension in Saudi Arabia: First data from the SAUDIPH registry with a focus on pulmonary arterial hypertension.

Abdullah M AldalaanSarfraz A SaleemiIhab WehebaAbeer AbdelsayedMaha M AleidFatima AlzubiHamdeia ZaytounNadeen Alharbi
Published in: Respirology (Carlton, Vic.) (2020)
PAH was the most frequent aetiology and patients were younger at diagnosis compared to other cohorts. Most patients showed improvement in FC and NT-proBNP. The estimated 1-year survival was better than previous studies, possibly reflecting wider use of combination therapy and the high prevalence of CHD-PAH.
Keyphrases
  • pulmonary arterial hypertension
  • pulmonary hypertension
  • end stage renal disease
  • combination therapy
  • ejection fraction
  • newly diagnosed
  • pulmonary artery
  • machine learning
  • electronic health record
  • big data