Exam 4: Hypertension Part II (Mar) Flashcards
World Health Organization (WHO) classifications on Pulmonary hypertension
- Pulmonary arterial hypertension (PAH)
- PH due to left heart disease
- PH due to lung diseases and/or hypoxia
- Chronic Thromboembolic pulmonary hypertension (CTEPH)
- PH with unclear multifactorial mechanisms
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Plumonary HTN
* definition
* S/S
* 3 hemodynamic profiles
mean pulmonary artery pressure (mPAP) >20 mmHg
* S/S: Accentuated S2 & S4 “gallop” heart sounds, LE swelling
* 3 hemodynamic profiles based on PAWP and PVR:
1. isolated precapillary PH
2. isolated postcapillary PH
3. combined pre & postcapillary PH
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Precapillary PH definition
defined as PVR of ≥3.0 wood units w/o elevated LAP or PAWP (PAWP <15mmHg = normal)
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Isolated postcapillary PH definition
- results from increased pulmonary venous pressure, usually d/t elevated LAP caused by valve disease or LV dysfunction
- Isolated postcapillary PH is characterized by a PAWP >15mmHg, w/normal PVR
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Combined pre- and postcapillary PH definition
- (aka reactive PH) reflects chronic pulmonary venous HTN with secondary pulmonary arterial vasoconstriction and remodeling
- Characterized by a PAWP >15mmHg and a PVR > 3.0 WU
- Can be subcategorized as fixed or vasoreactive d/o the response to vasodilators, diuretics, or mechanical assistance
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High flow PH definition
occurs w/o an elevation in PAWP or PVR and results from increased pulmonary blood flow caused by a systemic-to-pulmonary shunt or high cardiac output
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Chart for hemodynamic definitions of PH
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Pulmonary Artery HTN
* Diagnosis
* 4 mechanisms that increase mPAP
- Right heart catheterization is required for a dx, classification and tx plan
- Mechanisms that increase mPAP
1) elevated resistance to blood flow within the arterial circulation
2) increased pulmonary venous pressure from left heart disease
3) chronically increased pulmonary blood flow
4) a combination of these processes
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PVR equation:
PH can result from abnormalities in the _ or _ components of the _ _ sometimes both
PVR = (mPAP − PAWP)/COP
* PH can result from abnormalities in the arterial or venous components of the lung circulation, sometimes includes contributions from both
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Pulmonary Artery HTN
* what does a TEE show?
* Why get an Echo? whats the limitations?
- TTE reveals RA & RV enlargement
- Echocardiogram is commonly used to estimate pulmonary arterial systolic pressure (PASP) as a screening tool for PH
- Although echocardiographic PASP > 41 mmHg is relatively sensitive and specific for PH, it cannot provide the accurate mPAP for definitive diagnosis
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Severity of PH classifications
- Once right heart cath is performed, the severity of PH determined:
- Mild PH (mPAP = 20–30 mmHg)
- Moderate PH (mPAP = 31–40 mmHg)
- Severe PH (mPAP >40 mmHg)
- normal pulmonary circulation can accommodate a fourfold increase in COP without a marked change in mPAP
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- How many people does PH affect?
- Nearly 1:8 PAH pts have long term improvements with ___
15 ppl per million per year
- calcium channel blockers
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- 3% of PAH cases are deemed _ , with mutations in __ __ _ receptor type 2 (BMPR2)
- The remaining cases are designated “__ __ ,” since they can be ascribed to manifestations of drugs, toxins, or other diseases
- 3% of PAH cases are deemed inheritable, with mutations in bone morphogenetic protein receptor type 2 (BMPR2)
- The remaining cases are designated “associated PAH,” since they can be ascribed to manifestations of drugs, toxins, or other diseases
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- PAH was traditionally a disease of __ __, with median survival rate of 3 yrs, current data shows a demographic shift, now with __ __ and more ____ being diagnosed
- Despite improved diagnosis and therapy, 1-year mortality is ̴____%
- PAH was traditionally a disease of young women, with median survival rate of 3 yrs, current data shows a demographic shift, now with older pts and more men being diagnosed
- Despite improved diagnosis and therapy, 1-year mortality is ̴15%
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Pulmonary Artery HTN
* development
* 3 main classifications of pulmonary vasodialator drugs
* What kind of therapy is often required?
- Sustained vasoconstriction and remodeling
- There are 3 main classes of pulmonary vasodilator drugs for PAH: Prostanoids, Endothelin receptor antagonists (ERAs), nitric oxide/guanylate cyclase pathways
- Combination therapy is often required for adequate tx of PAH
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