Scholarlink

Pulmonary hypertension (PH) is diagnosed by finding a mean pulmonary arterial pressure (mPAP) of more than 20 mmHg at rest when measured invasively at right heart catheterisation (RHC) (Humbert et al. 2022). The haemodynamics of mPAP at RHC are a function of both diastolic and systolic pulmonary artery pressure (dPAP and sPAP, respectively) and are calculated as mPAP = (2/3 × dPAP) + (1/3 × sPAP).

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

CT and MR Measurements in Pulmonary Hypertension

  • 章节

  • 发表日期：

    2025年

查看全文
  • Gabriel Galea,
  • Nick Screaton

摘要

Pulmonary hypertension (PH) is diagnosed by finding a mean pulmonary arterial pressure (mPAP) of more than 20 mmHg at rest when measured invasively at right heart catheterisation (RHC) (Humbert et al. 2022). The haemodynamics of mPAP at RHC are a function of both diastolic and systolic pulmonary artery pressure (dPAP and sPAP, respectively) and are calculated as mPAP = (2/3 × dPAP) + (1/3 × sPAP).