A case report on cor pulmonale

Introduction

Cor pulmonale is a condition in which an alteration in the function and structure of the right ventricle of heart occurs, primarily as a result of respiratory disease which leads to increased blood flow resistance in the pulmonary circulation. The most common link between the heart and lung dysfunction in Cor pulmonale is the pulmonary hypertension.^[1], ^[2]

The mean pulmonary arterial pressure is usually more than 20mmhg for Cor pulmonale to occur. A complete failure of right ventricle happen if the mean pulmonary arterial pressure is ≥ 40mmg hg. It is considered that the chronic hypoxia often leads to pulmonary arteriolar constriction due to the increased action of the physiological mechanism which occurs in order to maintain the balance of ventilation and perfusion in lungs.

The other mechanisms that has the potential to increase mean pulmonary arterial pressure in Cor pulmonale include chronic hypercapnia and respiratory acidosis which leads to pulmonary vasoconstriction and an anatomical disruption of the pulmonary vascular bed which may occur as a result of primary lung disease such as in the cases of pulmonary fibrosis, pulmonary thromboembolic disease and emphysema.

Cor pulmonale may also occur due to an increase in the blood viscosity which occur as a result of lung disease and its associated complications such as in secondary polycythemia. It is generally a progressive chronic process but may also occur acutely in some cases due to an acute case of pulmonary hypertension, often following a pulmonary embolism.^[3]

Cor pulmonale can be generally classified as acute, subacute and chronic types. Massive pulmonary emboli is the most common cause of Acute Cor Pulmonale and it occurs when > 60 % occlusion of the vascular bed occurs which can often result in immediate death. The most common cause of subacute Cor pulmonale is secondary endolymphatic carcinomatosis of lungs in which the metastatic carcinoma may diffusely infiltrate the perivascular lymphatics and further includes the pulmonary arterioles. This can interfere with the blood flow through the pulmonary circuit and often results in right ventricular failure.^[4]

Case Report

A 55 year old female patient was admitted in the General medicine department with complaints of Anasarca since 1 month, decreased urine output since 5 days and breathlessness since 3 days. She has a medical history of COPD and was evaluated by a cardiologist 15 days back for Cor pulmonale, severe pulmonary artery hypertension, dyslipidemia and COPD. On physical examination, the respiratory system showed reduced air entry and bilateral rhonchi.

Her lab parameters included an elevated BNP, CRP, FBS and HbA1C. She was admitted in medical ICU and managed with Injection Furosemide, Methylprednisolone, Pantoprazole, Cefoperazone, Enoxaparin, Neb Ipratropium bromide, Levosalbutamol, oral doses of Sildenafil, Intermittent oxygen therapy and other supportive measures. Patient’s condition improved with treatment and hence was discharged with oral doses of Furosemide, Methylprednisolone, Sildenafil, Gliclazide and intermittent oxygen therapy at home.

Discussion

Cor Pulmonale can be described as a condition in which failure of right ventricle occurs due to an increase in the resistance to blood flow in pulmonary circulation. Here the patient was a 55 year old female patient, presented with similar symptoms as that of Cor Pulmonale with a history of COPD and a recent case of severe pulmonary artery hypertension. She had anasarca and elevated BNP which indicated the right ventricle failure of heart associated with Cor pulmonale.

The most common drugs used for management of Cor Pulmonale includes diruretics, oxygen therapy, vasodilators, theophylline, digitalis and anticoagulation therapy.^[5] Phosphodiesterase type 5 (PDE 5) inhibitors such as sildenafil are also used in Cor Pulmonale and are found to have beneficial effects in managing the pulmonary hypertension by widening and relaxing the blood vessels in lungs thus allowing the blood to flow more easily. In COPD, the synthesis of nitric oxide in pulmonay arteries are usually impaired. The inhibition of PDE 5 can act on the nitric oxide signalling pathway in pulmonary vessels and can delay the cyclic guanosine monophosphate degradation which in turn improves the vasodilator action of Nitric oxide. Thus the use of PDE 5 inhibitors such as sildenafil can be useful in such conditions for managing pulmonary hypertension related to COPD.^[6]

A loop diuretic known as furosemide was prescribed to manage anasarca and fluid overload associated with Cor pulmonale. The use of diuretics must be done cautiously as it has the potential to cause adverse acid-base effects and electrolyte imbalance which can lead to cardiac arrythmias that may alter the cardiac output.^[7] Anticoagulants are also beneficial in some cases of Cor Pulmonale and their use have shown to reduce the mortality in patients with Cor pulmonale and pulmonary artery hypertension.^[8] Administration of systemic steroids have been shown to improve dyspnea, pulmonary function, reduce hospitalization length and relapse rate.^[9], ^[10], ^[11], ^[12], ^[13]

Conclusion

Cor Pulmonale was managed efficiently at the earliest with suitable interventions. The symptoms associated with Cor Pulmonale, COPD and Pulmonary artery hypertension were treated appropriately and subsided. The patient showed improvement in health and hence was discharged with appropriate medications.

Source of Funding

None.

Conflict of Interest

The author(s) declare that there is no conflict of interest.