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Combination of echocardiography and pulmonary function tests could predict no complication of pulmonary hypertension during 5 years in patients with systemic sclerosis.

Katsuhiko YonedaSoshi TakahashiKazuhiko NakayamaMasanori IwahashiNoriaki EmotoShunichi Kumagai
Published in: International journal of rheumatic diseases (2023)
The conventional screening tests may be useful for detecting pre-capillary PH with SSc, and both esPAP < 35.0 mm Hg and DLCO% > 70% indicated a lower risk of developing PH for at least 5 years.
Keyphrases
  • systemic sclerosis
  • pulmonary hypertension
  • interstitial lung disease
  • pulmonary artery
  • pulmonary arterial hypertension
  • computed tomography
  • rheumatoid arthritis
  • living cells
  • aqueous solution