Pulm HTN Flashcards
How is pulmonary hypertension (PH) different from systemic hypertension?
Complex diagnosis and treatment
What is the mean pulmonary artery pressure (mPAP) threshold for defining pulmonary hypertension?
> 20 mmHg
What are some symptoms of pulmonary hypertension?
Accentuated S2 & S4, LE swelling
How is pulmonary hypertension classified based on PA wedge pressure and pulmonary vascular resistance?
3 hemodynamic profiles
-Isolated precapillary PH
-isolated postcapillary PH
-Combined pre and postcapillary PH
What is precapillary PH defined as?
PVR ≥3.0 wood units w/o elevated LAP or PAWP
What characterizes isolated postcapillary PH?
PAWP >15mmHg, normal PVR
What defines combined pre- and postcapillary PH?
PAWP >15mmHg, PVR >3.0 WU
How is high-flow PH characterized?
No elevation in PAWP or PVR
What are the three Groups of Pulmonary Hypertension?
Isolated precapillary, Isolated postcapillary, Combined pre- and postcapillary
What is required for diagnosis, classification, and treatment planning of Pulmonary Artery HTN?
Right heart catheterization
What can elevate mean pulmonary arterial pressure (mPAP)?
1) elevated resistance within arterial circulation 2) increased pulmonary venous pressure 3) chronically increased pulmonary blood flow 4) a combination of processes
How is Pulmonary Vascular Resistance (PVR) calculated?
(mPAP - PAWP)/COP
What components of lung circulation can contribute to Pulmonary Hypertension?
Arterial or venous abnormalities, sometimes both
What can TTE reveal in pulmonary hypertension?
RA & RV enlargement, elevated tricuspid-regurgitation velocity
Why is an echocardiogram commonly used in PH?
Estimate PASP as screening tool
How is the severity of PH determined after a right heart catheterization?
By mPAP values
What are the classifications based on mPAP values in PH?
Mild, moderate, severe
How much can normal pulmonary circulation accommodate in terms of COP increase without a notable change in mPAP?
Fourfold increase
What does PH stand for?
Pulmonary Artery HTN
What is the classification of PAH according to the World Health Organization?
Rare disease affecting 15 people per million per year
What is the significance of Idiopathic PAH?
No identifiable risk factor
What percentage of PAH cases are inheritable and what is the associated mutation?
3%, mutations in BMPR2
How are the remaining cases of PAH designated?
Associated PAH” due to drugs
What is the demographic shift seen in PAH patients according to current data?
Now more older patients and men being diagnosed
What is the 1-year mortality rate despite improved diagnosis and therapy for PAH?
Approximately 15%
What are the 3 main classes of pulmonary vasodilator drugs for PAH?
Prostanoids, Endothelin receptor antagonists (ERAs), Nitric oxide/guanylate cyclase pathway drugs
What leads to pathologic distortion of small pulmonary arteries in PAH?
Sustained vasoconstriction and remodeling processes
Is combination therapy often needed for the treatment of PAH?
Yes