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19 Cards in this Set

  • Front
  • Back

chronic thromboembolic pulm htn is complication from

PE


type of pulm arterial htn

interventricular septum flattened consistent with

RV overload

pulm vascular resistance is what compared to systemic

1/10th

normal pressure valvues

RA 2


RV 25/0


LA 5


LV 120/0

pulmonary arterial htn

elevated mean pulp artery pressure > 25 when normal is 8-20

if you suspect pulm htn what to do?

hemodynamic profile


clinical context



PAH is

subgroup of PH


dz state of small pulm aa vascular narrowing and increased resistance. causes RV failure and death

chronic thrombembolic pulm htn CTEPH

after 3 months of anticoag



mPAP >25 with PCWP <15



V/Q mismatch

PAH causes

genetic- ALK, BMPR2


schistosomiasis


chronic hemolytic anemia


pulm veno-occlusive PVOD

PAH really

imbalance of vasconstriction and vasodilators



endothelin pathway: vasonconstriction


NO: vasodilator


prostacyclin pathwya: vasodilator

how does PAH look in histo

intimal fibrosis


medial thickness increase


pulm arteriolar occlusion


plexiform lesions

CTEPH

small dz, blocks in airways

the central role in severe p HTN

dysfunctional endothelial cells

most PH is from

left heart dz

PAH pts die from

RV failure

who gets PAH

females


HIV


anorexigens


congenital heart dz


portal htn


thyroid disorder


cocaine

CTEPH risks

splenectoy


pacemaker device infxn


thyroid hormone replacement

how to screen PAH



how to dx



CTEPH

echo


biomarkers



right heart catherterization to do PCWP and RAP RVP PAP CO



then try a vasodilator and see if fixes


--


V/Q scan, CT angiography

tests that are a waste

EKG


CXR