Pulmonary hypertension: Difference between revisions

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==Background==
==Background==
Pulmonary Hypertension = mean PA pressure >25mmHg assessed by right heart cath
*Pulmonary Hypertension (PH) = mean PA pressure >25mmHg assessed by right heart cath
*can be divided into:
*PH divided into 5 groups:
**precapillary PH (normal PCWP)
**Group 1 PAH: Idiopathic pulmonary arterial hypertension, formerly called primary PH
***Includes Pulmonary arterial hypertension (PAH), PH due to due to lung disease, and chronic thromboembolic PH
**Group 2 PH: PH due to left heart disease (systolic/diastolic dysfunction, and valvular heart dz)
**postcapillary PH (elevated PCWP)
**Group 3 PH: PH due to various causes of hypoxemia, such as COPD, ILD, or sleep-disordered breathing
***PH due to left heart disease
**Group 4 PH: PH due to chronic thromboembolic disease
**Group 5 PH: Uncommon and includes PH with unclear multifactorial mechanisms (myeloproliferative dz, sarcoidosis, glycogen storage dz, etc)
 


==Etiology==
==Etiology==

Revision as of 01:56, 27 April 2014

Background

  • Pulmonary Hypertension (PH) = mean PA pressure >25mmHg assessed by right heart cath
  • PH divided into 5 groups:
    • Group 1 PAH: Idiopathic pulmonary arterial hypertension, formerly called primary PH
    • Group 2 PH: PH due to left heart disease (systolic/diastolic dysfunction, and valvular heart dz)
    • Group 3 PH: PH due to various causes of hypoxemia, such as COPD, ILD, or sleep-disordered breathing
    • Group 4 PH: PH due to chronic thromboembolic disease
    • Group 5 PH: Uncommon and includes PH with unclear multifactorial mechanisms (myeloproliferative dz, sarcoidosis, glycogen storage dz, etc)


Etiology

  • PAH can be heritable, idiopathic, or associated with connective tissue disease, HIV, portal HTN, congenital heart dz, schistosomiasis, chronic hemolytic anemia
  • PH can be due to lung disease, left heart disease, chronic exposure to high altitudes, chronic thromboembolic disease, myeloproliferative disorders, sarcoidosis, vasculitis, glycogen storage disease, Gaucher disease, chronic renal failure on dialysis

Diagnosis

  • Consider in undifferentiated patients with dyspnea, fatigue, syncope, chest pain, palpitations
  • Look for JVD, hepatomegaly, ascites, edema, stigmata of liver failure or CTD
  • ECG shows signs of RHD (RAE, RAD, RVH)
  • CXR with vascular congestion, PA dilation, RA enlargement
  • TTE shows fluid status of patient, LV or RV failure, with or without elevated PAP, or pericardial tamponade
  • Need RH cath to definitively diagnose

Chronic Therapies

  • Prostacyclins - vasodilatation, inhibit platelet aggregation
    • Epoprostenol, Iloprost, Treprostinil, Beraprost
    • Complications include acute decompensation if stopped abruptly, diarrhea, edema, headache
  • Phosphodiesterase Type 5 (PDE5) Inhibitors - vasodilation, increases RV contractility
    • Sildenafil
    • Complications include hypotension with administration of nitrates, flushing, epistaxis, headache
  • Endothelin receptor antagonists - vasodilation
    • Bosentan, Ambrisentan
    • Complications include liver failure, supratherapeutic INR,
  • Patients also usually taking digoxin, coumadin, diuretics, home O2. RARELY are they on CCB only if responsive during cath. Consider line infections as complication to chronic infusions.

Acute Treatment for PAH crisis

  1. Decrease preload - no fluids, consider diuretics
  2. O2
  3. Optimize myocardial contractility
    1. Treat relative bradycardia
      1. atropine, pace, low dose dobutamine <5mcg/kg/min to increase contractility
      2. Consider norepinephrine prior to dobutamine if hypotensive
    2. Rhythm control for tachycardias - NO CCB or BB for rate control
      1. Electrical cardioversion or amiodarone
  4. Decrease afterload - pulmonary vasodilation
    1. sildenafil, bostantan, epoprostenol (2ng/kg/min), inhaled NO if intubated
  5. Check INR, dig level and correct
  6. Empiric abx
  7. If intubated, low PEEP, low tidal volumes

Source

  • 4/07 DONALDSON (adapted from Sarver)
  • Critical Decisions in Emergency Medicine, May 2013; 27(5)