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Internal illnesses. Chronic cor pulmonale (lecture notes)

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LECTURE No. 36. Chronic cor pulmonale

Hypertrophy and (or) dilatation of the right heart due to pulmonary arterial hypertension due to a respiratory disease.

Etiology. Etiological factors include bronchopulmonary disorders - obstructive and restrictive processes: polycystic lung disease, chronic bronchitis, bronchial asthma, pulmonary emphysema, diffuse pneumofibrosis, pulmonary granulomatosis, vascular lesions - primary pulmonary arterial hypertension, arteritis, repeated pulmonary vascular embolism, lung resection, thoracic lesions -diaphragmatic apparatus; lesions of the spine, chest, their deformation, pleural moorings, obesity.

Pathogenesis. Pathogenetic stages: precapillary hypertension in the pulmonary circulation, right ventricular hypertrophy, right ventricular heart failure, development of pulmonary arterial hypertension, an increase in cardiac output due to an increase in catecholamines caused by hypoxia, an increase in blood viscosity due to erythrocytosis in response to chronic hypoxia, the development of bronchopulmonary anastomoses, an increase in intraalveolar pressure in broncho-obstructive lung diseases.

Classification. The disease is classified as follows:

1) by etiology: bronchopulmonary, thoracophrenic, vascular;

2) downstream: acute (minutes, hours), subacute (days, weeks), chronic (months, years);

3) according to the degree of compensation: compensated, decompensated.

Clinic. The main manifestations of the disease are the following: shortness of breath, cyanosis (appears with II and III degrees of respiratory failure), swelling of the jugular veins, epigastric pulsation, tachycardia, expansion of the boundaries of the heart, especially to the right, deafness of heart tones, emphasis of the II tone over the pulmonary artery, increase and soreness liver, peripheral edema, small diuresis (in a decompensated state).

Additional diagnostic study. A complete blood count (erythrocytosis, normal or reduced ESR), a general urinalysis (the appearance of protein, cylinders during decompensation), a biochemical blood test (dysproteinemia), a functional study of the lungs (allows to distinguish between the degree of respiratory failure) are carried out. On the ECG - signs of cor pulmonale: high P waves in II and III standard leads (P - pulmonale), rightogram, pronounced S wave in I standard lead and left chest leads, the appearance of Q in lead III. A study of hemodynamics is carried out (increased central venous pressure, slowing down the speed of blood flow, increasing the volume of circulating blood). On echocardiography: an increase in thickness in the compensated state and cavity in the decompensated state of the right ventricle. An X-ray examination is also carried out.

Complications. Complications of the disease are pulmonary-cardiac coma (hypercapnic encephalopathy), cough-fainting syndrome (loss of consciousness with convulsions), gastric and duodenal ulcers.

Treatment. Treatment is aimed at treating the underlying disease. In case of infection of the bronchopulmonary apparatus, antibiotics are used, in case of broncho-obstruction - bronchodilators, in case of PE - anticoagulants, fibrinolytic drugs, in case of thoracodiaphragmatic pulmonary heart - artificial ventilation of the lungs. Peripheral vasodilators are used to reduce pulmonary arterial hypertension (nitrates, apressin, calcium channel blockers, β2adrenomimetics). Oxygen therapy is carried out, bloodletting of 200-300 ml with infusion of low-viscosity solutions (rheopolyglucin) to reduce erythrocytosis, infusion of sodium bicarbonate solution to reduce acidosis. Diuretics are administered, it is possible to use diuretics of different classes simultaneously, vasodilators, antiplatelet drugs, non-steroidal anabolic agents (ATP, riboxin). Remedial gymnastics, massage, postural drainage are shown.

Prevention. Prevention is the prevention and timely treatment of respiratory diseases.

Flow. The course of the disease is chronic and progressive.

Forecast. Adverse.

Author: Myshkina A.A.

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