Pulmonary Hypertension Flashcards
Pulmonary Hypertension
mean pa more then 25 mmHg right heart cath
normal 8-20 mmHg
uncertain 21-24 mmHg
heritable PAH types:
heritable
bmpr2 - induces apoptsis, excessive endo growth- auto dom
alk1- endoglin with or without hemohaggic telangectaisa
Pul veno occlusive disease
may account for 10% pphtn
fibrosis of veins-
lung bx defin diagnosis
Pulmonary hypertension CTE
VQ distinguishes from primary pah- more sensitive than ct scan
Pulmonary Artery Hypertension rx
diuretics, O2 (in hypoxemia), anticoag inr 2, exercise-
>class 1 then invasive (adenosine, epoprostenol, nitr oxide)
if mean pap falls 10mmHg with increased or unchanged co
trial of ccb, dihydropyridines
5 yr survival advantage
advanced pulmonary hypertension therapy
prostanoids: epoprostenol, treprostinil, iloprost
endothelin receptor antagonists: endothelin 1, bostentan, ambrisentan
phosphodiesterase type 5 inhibitor- only sildenafil improved oxygenation- can be added to bostentan and epoprostanol
Pulmonary Embolism types
score for pretest prob
massive (hypotension) submassive (all others)
score high>6, <2 low
dvt symptom (3), no dx to explain (3), tachycard (1.5),immobil (1.5), prior dvt, pe (1.5), malig (1), hemoptysis (1)
acute pulmonary embolism treatment
reversible risk factor
unprovoked
recurrent
reversible risk factor: 3mth inr 2.5 goal
unprovoked:consider indef if no bleeding risk- reassess after 3 mths
recurrent- indefinite warfarin rx
thrombolytics in pulmonary embolism/ mortality
no mortality benefit
may improve short term physiology
Obstructive Sleep apnea
cpap
> 15 AHI cpap
apnea hypopnea index