The blood goes from right to left side of the heart through the pulmonary circulation, which is low-resistance, low-pressure circulation. The mean pulmonary vascular pressure is normally between 10 to 18 mm Hg. During exercise, this low-pressure circulation can accommodate high blood flow. The resistance in the pulmonary vasculature depends on the pressure in the pulmonary arteries, left atrial pressure, and cardiac output.
The increase in resistance due to any cause that leads to an abnormal increase in pressures in pulmonary artery can lead to pulmonary hypertension. Pulmonary hypertension is a persistent increase in the mean pulmonary arterial pressure of more than 25 mm Hg at rest and greater than 30 mm Hg during exercise on cardiac catheterization.
Pulmonary hypertension (PH) can be classified as idiopathic/primary when the cause is unknown. Secondary pulmonary hypertension occurs due to underlying diseases or known risk factors, underlying heart and lung disease being the most common.
WHO classification based on the mechanism or underlying etiology:
Idiopathic pulmonary arterial hypertension (IPAH) is a rare form of PH that is more common in females. The incidence of the other groups is similar to the particular underlying diseases.
The prevalence of group 3 pulmonary hypertension (PH) appears to be high in older patients. However, prevalence varies among COPD patients due to genetic polymorphisms, with higher mean pulmonary pressures in COPD patients with LL serotonin transporter gene polymorphism when compared to LS or SS variants.
Pulmonary hypertension irrespective of the cause occurs due to restricted blood flow in a pulmonary artery. The major pathology in Group 1 and Group 4 is obstruction of pulmonary vessels. Some diseases such as sarcoidosis, schistosomiasis, and HIV infection directly affect pulmonary vessels.
Group 1 PH (Pulmonary artery hypertension): This group includes diseases that alter the pulmonary vasculature structurally. Bone morphogenetic protein receptor 2 gene (BMRP2 gene) belongs to the TGF-b family. It normally controls the proliferation of vascular smooth muscle cells. Mutation in BMRP2 gene can result in hypertrophy of smooth muscle along with dysfunction of the endothelium. This causes a decrease in the inner diameter of the lumen of the pulmonary artery that leads to an increase in pulmonary vascular resistance and an increase in right ventricular afterload resulting in high PA pressures.
Group 2 PH (Pulmonary venous hypertension or postcapillary pulmonary hypertension): The left heart disease causes back pressure and increases the hydrostatic pressure in the pulmonary veins which eventually results in increased pressure in pulmonary arteries.
Group 3 PH: Advanced chronic lung conditions lead to lung tissue destruction and a decrease in the capillary area. The common mechanisms that lead to pulmonary hypertension in this group are hypoxic vasoconstriction and vascular remodeling of the pulmonary vasculature.
Hypoxic pulmonary vasoconstriction is a compensatory mechanism that occurs to preserve the ventilation-perfusion matching by limiting the blood flow to hypoxic alveoli. The primary mechanism for vasoconstriction is through mitochondrial signaling and inhibition of potassium channels and pulmonary vascular smooth muscle membrane depolarization, thereby increasing calcium entry in muscle cells. Vascular remodeling also occurs which affects the pulmonary arterioles. These changes occur due to increased expression of endothelin 1, platelet-derived growth factors, vascular endothelial growth factor, and angiotensin 2 and a reduction in nitric oxide synthase.
In Group 4 PH, thromboembolic occlusion or narrowing of pulmonary arteries, proximal and distal both can lead to an increase in back pressure in the pulmonary circulation. This eventually leads to vascular remodeling due to shear stress. The combination of vessel occlusion and vasculopathy increase the resistance and pressure within the pulmonary circulation.
Group 5 PH is multifactorial.
Dyspnea on exertion, lethargy, and fatigue are the initial symptoms due to inability to maintain cardiac output, especially during exercise. Exertional dyspnea progresses to dyspnea at rest as the disease advances.
Orthopnea and paroxysmal nocturnal dyspnea can be seen in Group 2 PH patients. Patients can also complain of a nonproductive cough, hemoptysis, hoarseness. Exertional anginal pain, syncope, and peripheral edema can occur due to right ventricular hypertrophy and heart failure as the disease progresses.
The severity is based on New York Heart Association (NYHA) Functional Classification.
Signs include loud second heart sound pulmonary component, which is the initial physical finding, followed by tricuspid regurgitation murmur, jugular venous distention, hepatomegaly, and edema of lower extremities.
Pulmonary hypertension can be suspected on clinical presentation. However, it is important to rule out other causes as the signs and symptoms of pulmonary hypertension are non-specific. Baseline functional class of the patient can be determined by 6-minute walk test.
If the pulmonary hypertension is suspected, a presumptive diagnosis of pulmonary hypertension can be made with echocardiography, which estimates the systolic pressure of the pulmonary artery and right heart function. Further tests are done to exclude heart and lung diseases that are the common causes of pulmonary hypertension. These tests include ECG, pulmonary function test (PFT) with diffusing capacity of the lungs for carbon monoxide (DLCO), arterial blood gas (ABG), chest x-ray, and high-resolution computed tomography (HRCT).
ECG shows right ventricular hypertrophy, right atrial enlargement, right axis deviation, increased amplitude of P wave in lead II in all groups. It may show left ventricular hypertrophy in left heart disease.
The chest radiograph may show signs of left heart disease such as pulmonary vascular congestion and pleural effusion. Increased right ventricular size and cardiomegaly in all patients can be seen in PAH.
V/Q Scans are done to rule out chronic thromboembolic pulmonary hypertension (CTEPH) once the common causes are excluded. Patients with perfusion defects are further evaluated by CT pulmonary angiography and right heart catheterization.
Pulmonary hypertension diagnosis can be confirmed with right heart catheterization that measures the hemodynamic parameters accurately. Pulmonary artery catheter can directly measure central venous pressure, right heart intracardiac pressure, pulmonary artery pressure, pulmonary capillary wedge pressure/PA occlusion pressure, cardiac output, mixed venous oxyhemoglobin saturation. These direct measures such as mean PAP, pulmonary capillary wedge pressure (PCWP) and, cardiac output (CO) can be used to calculate pulmonary vascular resistance indirectly. Pulmonary vascular resistance (PVR) helps in determining the prognosis of pulmonary hypertension. Mean PAP is high in both PAH and Group 2 PH, but PCWP greater than 15 mm Hg is typically seen in PH due to left heart disease.
Before initiating the therapy, baseline disease severity should be assessed. Disease severity is determined by assessing functional impairment based on exercise capacity and hemodynamic derangement.
The goal of the management of pulmonary hypertension is primary therapy to treat the underlying cause of pulmonary hypertension. Following primary therapy, the disease severity is reassessed.
Patients with WHO Functional class II, III and, IV with persistent pulmonary hypertension despite primary therapy require advanced therapy which targets pulmonary hypertension itself and not the underlying cause). Advanced therapy is used in most Group 1 PAH cases and some patients with group 3, 4, and 5 on a case-by-case basis. However, it is almost never used for Group 2 patients.
Advanced therapy includes prostacyclin agonists, endothelin receptor antagonists, NO-cGMP enhancers, and rarely, calcium channel blockers.
Combination or alternate therapy is used in patients with refractory PAH.
Group 1 PH: None of the primary therapies have been proven to be successful for most types. Often, advanced therapy is required.
Group 2 PH: Medications or valve repair to optimize left heart function in these patients. In patients with volume overload, diuretics can be considered. Thiazides followed by loop diuretics can be used. However, over diuresis should be avoided. Sodium restriction can be helpful.
Heart failure should be managed according to ejection fraction. Beta blockers, nitrates, and digoxin should be avoided in a preserved ejection fraction, until very necessary. Treatment of coexisting conditions (hypertension, valvular heart disease, ischemic heart disease, diabetes, thyroid disease) and lifestyle modification. Remote monitoring strategies such as weight and symptoms can help reduce hospitalizations in heart failure patients with reduced or preserved ejection fraction.
Group 3 PH: Supplemental oxygen to correct hypoxemia and management the underlying cause of hypoxemia.
Group 4 PH: The most effective step in effectively reducing the resistance of pulmonary vessels secondary to chronic thrombo-emboli is pulmonary thromboendarterectomy. Small vessel disease is a contraindication as the reduction in the pulmonary vascular resistance post-thromboendarterectomy is not as expected. Pulmonary artery steal syndrome and, reperfusion pulmonary edema are the common negative sequelae. After initial improvement post-thromboendarterectomy, late adverse events such as residual pulmonary hypertension and recurrent pulmonary hypertension can take place.
If the disease is inoperable and thrombectomy cannot be performed, Balloon pulmonary-artery angioplasty is an alternative.
If the thromboembolism is surgically inaccessible or there is recurrent or persistent pulmonary hypertension post-thromboendarterectomy, advanced medical therapy can be considered. Advanced medical therapy includes anticoagulants and pulmonary vasodilators. However, there is no approved medical therapy.
The non-specific clinical picture leads to delay in diagnosis of pulmonary hypertension due to overlap with common heart and lung diseases. The diagnosis of pulmonary hypertension can be made by evaluating and excluding the following-
The mean survival of people with evidence of right heart failure or severe pulmonary hypertension (greater than 55 mm Hg mean pulmonary artery pressure) is about a year. People with preserved right heart function and with mean pulmonary artery pressure less than 55 mm Hg survive for approximately 3 years.
Complications include cor pulmonale and right heart failure.
Secondary pulmonary hypertension is a complex, life-threatening disease that significantly affects the quality of life and over time leads to right heart failure. A timely evaluation, proper treatment, regular follow up and patient education can positively affect the outcome of the disease. For this, integrated, interprofessional care with involvement of different subspecialties is required. The physicians with a team of nurse specialists, pharmacists and, social workers coordinate closely to provide the best possible care and counsel these patients.
Non-specific symptoms of the disease usually result in the delay in diagnosis. The family physician suspects the disease based on non-invasive tests (echocardiogram, x-ray). Once the presumptive diagnosis of pulmonary hypertension has been made, it is very critical to classify the type of pulmonary hypertension as the treatment for one group may cause deleterious effects if used for another group. These patients are, therefore, referred to different subspecialty physicians to determine the cause. A referral to the pulmonologist is essential for the sleep studies and pulmonary function tests to exclude lung disease as a cause. To rule out left heart disease, patients are referred to a cardiologist. Right heart catheterization to confirm the diagnosis is also done by the cardiologist. Similarly, to rule out other causes the patients are also referred to rheumatologists, and, other doctors. It is also important to counsel the patients so that they can live with this disease.
Treatment of the cause of pulmonary hypertension is the key to manage the disease. Hence, collaboration with physicians, physician assistants, and nurse practitioners in different specialties is essential to manage secondary pulmonary hypertension. (Level V)
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