Pulmonary hypertension resident survival guide

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vidit Bhargava, M.B.B.S [2], Rim Halaby, M.D. [3]

Overview

Pulmonary hypertension (PH) is defined by mean pulmonary artery pressure > 25, pulmonary capillary wedge pressure (PCWP), left atrial pressure, or left ventricular end diastolic pressure (LVEDP) ≤ 15 mm Hg; and a pulmonary vascular resistance (PVR) > than 3 Wood units. [1]

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Click here for the complete list of causes.

Management

Diagnosis

A complete diagnostic approach should be carried out after a focused initial rapid evaluation is conducted and following initiation of any urgent intervention. [2] [3]


 
 
 
Characterize the symptoms:
❑ Progressive dyspnea
❑ Exertional dizziness and syncope
Edema of the extremities
Angina
Palpitations
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Inquire about past medical history

❑ Cardiovascular disease

Congenital heart disease
❑ Left heart disease

❑ Pulmonary disease

❑ Previous PE
COPD
Interstitial lung disease
Sleep apnea
Asthma

❑ Recent surgery (<3 months) (suggestive of PE)
❑ Conective tissue disease
HIV infection
Portal hypertension
Chronic hemolytic anemia
Myeloproliferative disorders
Splenectomy
❑ Systemic diseases

Sarcoidosis
Pulmonary Langerhans histiocytosis

Lung tumors
Chronic kidney disease in dialysis

Thyroid disorders
 
 
 
 
 
 
 
 
 
 
 
 
 
Inquire about risk factors

❑ Family history of pulmonary hypertension
❑ Drugs

❑ Anorectic drugs
Amphetamines
Cocaine
Phenylpropanolamine
Saint John's wort
Chemotherapeutic agents
Selective serotonin reuptake inhibitors
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

Vitals ❑ Pulse

❑ Tachycardia

❑ Respiratory rate

❑ Tachypnea

Physical signs that reflect severity of PH:
Loud pulmonary second heart sound (P2)
Systolic murmur suggestive of tricuspid regurgitation
❑ Raised jugular venous pressure (JVP)
❑ Early systolic click
❑ Left parasternal heave
❑ Right ventricular S4


Physical signs suggestive of moderate to severe PH:
Holosystolic murmur that increases with inspiration
❑ Increased jugular v waves
❑ Pulsatile liver
Diastolic murmur
Hepatojugular reflux


Physical signs suggestive of advanced PH with right ventricular failure:
❑ Right ventricular S3
❑ Distension of jugular veins
Hepatomegaly
Peripheral edema
Ascites
Hypotension


Physical signs suggestive of possible underlying causes:
Central cyanosis → Abnormal V/Q, shunt
ClubbingCongenital heart disease
❑ Cardiac auscultatory findings → Congenital or acquired heart disease
Rales, decreased breath sounds, dullness → Pulmonary congestion
❑ Fine rales, excessive muscle use, wheezing, protracted respiration, cough → Pulmonary parenchymal disease
Obesity, kyphoscoliosis, enlarged tonsils → Disordered ventilation
Sclerodactyly, arthritis, telengiectasia, Raynaud phenomenon, rash → Connective tissue disorder
❑ Peripheral venous insufficiency → Possible venous thrombosis
❑ Venous stasis ulcers → Possible sickle cell disease
❑ Pulmonary vascular bruits → Chronic thromboembolic PH
Splenomegaly, spider angiomata, palmar erythema, icterus, caput medusaeportal hypertension
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order tests:

Chest X-ray

❑ Pulmonary artery dialation

EKG
Echocardiogram

Right heart catherization
 
 
 
 
 


Treatment

 
 
 
Anticoagulation +/-
Diuretics +/-
Oxygen therapy +/-
Digoxin
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Acute vasoreactivity testing

Epoprostenol IV 2ng/Kg/min every 10 to 15 min, OR
Adenosine IV 50 mcg/Kg/min every 2 min, OR

Nitric oxide (inhaled)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Positive
 
 
 
Negative
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Oral calcium channel blocker (CCB)
 
Lower risk
 
Higher risk
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Follow closely for efficacy and safety
❑ Sustained response?
 
❑ Oral endothelin receptor antagonists: Bostenan 125 mg BD, OR
Oral phospodiesterase-5 inhibitors: Sildenafil 20 mg TDS
❑ IV epoprostenol (started at 2 ng/Kg/min - 25-40 ng/kg/min), OR
IV treprostinil (83 ng/Kg/min)
Iloprost (inhaled)
❑ Treprostinil (SC)
 
❑ IV epoprostenol (started at 2 ng/Kg/min - 25-40 ng/kg/min), OR
IV treprostinil (83 ng/Kg/min)
Iloprost (inhaled)
❑ Oral endothelin receptor antagonists: Bostenan 125 mg BD, OR
Oral phospodiesterase-5 inhibitors: Sildenafil 20 mg TDS
Treprostinil (SC)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
 
 
❑ Reassess
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Response to the monotherapy

❑ No evidence of heart failure on physical exam
❑ Functional class I/II
❑ 6 minute walk distance >400 m
❑ Normal RV size on echocardiogram
❑ Normal right atrial pressure and cardiac index

❑ Near normal or stable BNP
 
Unstable clinical course

❑ Signs of heart failure
❑ Functional class IV
❑ 6 minute walk distance <400 m
❑ RV enlargement on echocardiogram
❑ High right atrial pressure and low cardiac index

❑ Elevated/increasing BNP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Continue CCB
 
 
 
 
 
❑ Consider combo-therapy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
In case of progress despite optimal medical treatment:
❑ Investigational protocols, OR
Atrial septostomy, OR
Lung transplant

The algorithm is based on Expert consensus document on pulmonary hypertension published by ACCF/AHA in 2009.[4]

Follow Up Testing

Shown below is a table depicting the follow up testing after etiology for pulmonary hypertension is established.

Condition Follow up testing
BMPR2 mutation ❑ Yearly echocardiogram
❑ Right heart catheterization if evidence of PH
1st degree relative of patient with BMPR2 mutation or with 2 or more relatives with PH ❑ Genetic counseling for BMPR2 testing
❑ Proceed as above if positive
Systemic sclerosis ❑ Yearly echocardiogram
❑ Right heart catheterization if evidence of PH
HIV infection ❑ Do echocardiogram if signs & symptoms are suggestive of PH
❑ Right heart catheterization if evidence of PH on echocardiography
Portal hypertension ❑ If considering liver transplant perform echocardiogram
❑ Right heart catheterization if evidence of PH
CHD with shunt ❑ Echocardiogram and right heart catheterization at the time of diagnosis
❑ Repair any significant defect
Recent acute pulmonary embolism ❑ If symptomatic 3 months after event, perform ventilation perfusion scintigraphy
❑ Do a pulmonary angiogram if positive
Prior fenfluramine use (appetite suppressant) ❑ Echocardiogram only if symptomatic
Sickle cell disease ❑ Yearly echocardiogram
❑ Right heart catheterization if evidence of PH

Do's

  • Monitor liver function tests monthly in patients being treated with endothelin receptor antagonists.
  • Follow up on patients with advanced symptoms, right heart failure, advanced hemodynamics and those on parenteral or combination therapy every 3 months.

Don'ts

References

  1. Kiely, DG.; Elliot, CA.; Sabroe, I.; Condliffe, R. (2013). "Pulmonary hypertension: diagnosis and management". BMJ. 346: f2028. PMID 23592451.
  2. McLaughlin, V. V.; Archer, S. L.; Badesch, D. B.; Barst, R. J.; Farber, H. W.; Lindner, J. R.; Mathier, M. A.; McGoon, M. D.; Park, M. H.; Rosenson, R. S.; Rubin, L. J.; Tapson, V. F.; Varga, J. (2009). "ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension: A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association: Developed in Collaboration With the American College of Chest Physicians, American Thoracic Society, Inc., and the Pulmonary Hypertension Association". Circulation. 119 (16): 2250–2294. doi:10.1161/CIRCULATIONAHA.109.192230. ISSN 0009-7322.
  3. Galie, N.; Hoeper, M. M.; Humbert, M.; Torbicki, A.; Vachiery, J.-L.; Barbera, J. A.; Beghetti, M.; Corris, P.; Gaine, S.; Gibbs, J. S.; Gomez-Sanchez, M. A.; Jondeau, G.; Klepetko, W.; Opitz, C.; Peacock, A.; Rubin, L.; Zellweger, M.; Simonneau, G.; Vahanian, A.; Auricchio, A.; Bax, J.; Ceconi, C.; Dean, V.; Filippatos, G.; Funck-Brentano, C.; Hobbs, R.; Kearney, P.; McDonagh, T.; McGregor, K.; Popescu, B. A.; Reiner, Z.; Sechtem, U.; Sirnes, P. A.; Tendera, M.; Vardas, P.; Widimsky, P.; Sechtem, U.; Al Attar, N.; Andreotti, F.; Aschermann, M.; Asteggiano, R.; Benza, R.; Berger, R.; Bonnet, D.; Delcroix, M.; Howard, L.; Kitsiou, A. N.; Lang, I.; Maggioni, A.; Nielsen-Kudsk, J. E.; Park, M.; Perrone-Filardi, P.; Price, S.; Domenech, M. T. S.; Vonk-Noordegraaf, A.; Zamorano, J. L. (2009). "Guidelines for the diagnosis and treatment of pulmonary hypertension: The Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT)". European Heart Journal. 30 (20): 2493–2537. doi:10.1093/eurheartj/ehp297. ISSN 0195-668X.
  4. McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR; et al. (2009). "ACCF/AHA 2009 expert consensus document on pulmonary hypertension: a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association: developed in collaboration with the American College of Chest Physicians, American Thoracic Society, Inc., and the Pulmonary Hypertension Association". Circulation. 119 (16): 2250–94. doi:10.1161/CIRCULATIONAHA.109.192230. PMID 19332472.