Summary
Precapillary pulmonary hypertension (PH) is diagnosed when mean pulmonary arterial
pressure (mPAP) equals or exceeds 25 mmHg and the pulmonary capillary wedge pressure
(PCWP) is equal or lower than 15 mmHg. Because both parameters can only be derived
from invasive hemodynamic assessment, right heart catheter (RHC) is still a gold standard
for the diagnosis of PH. Severe precapillary PH corresponds to pulmonary vascular
disease and carries a poor prognosis. Unfortunately, due to a generally low specificity
of non-invasive estimates of systolic pulmonary pressure, at least 50% of patients
with suspicion of PH need to undergo invasive RHC for exclusion of precapillary PH.
Therefore, and also in order to manage the growing number of postcapillary PH due
to heart and lung disease in the general population, pulmonary and cardiologic diagnostic
algorithms combining multiple parameters have been developed. Recent disease scores
are reviewed, and an outlook is given on emerging evidence from the DETECT clinical
study holding the promise to non-invasively predict precapillary PH in vulnerable
patients. These diagnostic trees help limit unnecessary procedures and help differentiate
the current categories of PH. However, one has to keep in mind that the diagnosis
of PH is still made by hemodynamic assessment.
Keywords
Diagnosis management - Cardiology - clinical studies