Pericardial disease: Pathology review

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Pericardial disease: Pathology review

ETP Cardiovascular System

ETP Cardiovascular System

Introduction to the cardiovascular system
Anatomy of the heart
Anatomy of the coronary circulation
Anatomy clinical correlates: Heart
Anatomy of the superior mediastinum
Anatomy of the inferior mediastinum
Anatomy clinical correlates: Mediastinum
Development of the cardiovascular system
Fetal circulation
Cardiac muscle histology
Artery and vein histology
Arteriole, venule and capillary histology
Cardiovascular system anatomy and physiology
Lymphatic system anatomy and physiology
Coronary circulation
Blood pressure, blood flow, and resistance
Pressures in the cardiovascular system
Laminar flow and Reynolds number
Resistance to blood flow
Compliance of blood vessels
Control of blood flow circulation
Microcirculation and Starling forces
Measuring cardiac output (Fick principle)
Stroke volume, ejection fraction, and cardiac output
Cardiac contractility
Frank-Starling relationship
Cardiac preload
Cardiac afterload
Law of Laplace
Cardiac and vascular function curves
Altering cardiac and vascular function curves
Cardiac cycle
Cardiac work
Pressure-volume loops
Changes in pressure-volume loops
Physiological changes during exercise
Cardiovascular changes during hemorrhage
Cardiovascular changes during postural change
Normal heart sounds
Abnormal heart sounds
Action potentials in myocytes
Action potentials in pacemaker cells
Excitability and refractory periods
Cardiac excitation-contraction coupling
Electrical conduction in the heart
Cardiac conduction velocity
ECG basics
ECG rate and rhythm
ECG intervals
ECG QRS transition
ECG axis
ECG normal sinus rhythm
ECG cardiac infarction and ischemia
ECG cardiac hypertrophy and enlargement
Baroreceptors
Chemoreceptors
Renin-angiotensin-aldosterone system
Arterial disease
Angina pectoris
Stable angina
Unstable angina
Myocardial infarction
Prinzmetal angina
Coronary steal syndrome
Peripheral artery disease
Subclavian steal syndrome
Aneurysms
Aortic dissection
Vasculitis
Behcet's disease
Kawasaki disease
Hypertension
Hypertensive emergency
Renal artery stenosis
Coarctation of the aorta
Cushing syndrome
Conn syndrome
Pheochromocytoma
Polycystic kidney disease
Hypotension
Orthostatic hypotension
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Chronic venous insufficiency
Thrombophlebitis
Deep vein thrombosis
Lymphedema
Lymphangioma
Shock
Vascular tumors
Human herpesvirus 8 (Kaposi sarcoma)
Angiosarcomas
Truncus arteriosus
Transposition of the great vessels
Total anomalous pulmonary venous return
Tetralogy of Fallot
Hypoplastic left heart syndrome
Patent ductus arteriosus
Ventricular septal defect
Atrial septal defect
Atrial flutter
Atrial fibrillation
Premature atrial contraction
Atrioventricular nodal reentrant tachycardia (AVNRT)
Wolff-Parkinson-White syndrome
Ventricular tachycardia
Brugada syndrome
Premature ventricular contraction
Long QT syndrome and Torsade de pointes
Ventricular fibrillation
Atrioventricular block
Bundle branch block
Pulseless electrical activity
Tricuspid valve disease
Pulmonary valve disease
Mitral valve disease
Aortic valve disease
Dilated cardiomyopathy
Restrictive cardiomyopathy
Hypertrophic cardiomyopathy
Heart failure
Cor pulmonale
Endocarditis
Myocarditis
Rheumatic heart disease
Pericarditis and pericardial effusion
Cardiac tamponade
Dressler syndrome
Cardiac tumors
Acyanotic congenital heart defects: Pathology review
Cyanotic congenital heart defects: Pathology review
Atherosclerosis and arteriosclerosis: Pathology review
Coronary artery disease: Pathology review
Peripheral artery disease: Pathology review
Valvular heart disease: Pathology review
Cardiomyopathies: Pathology review
Heart failure: Pathology review
Supraventricular arrhythmias: Pathology review
Ventricular arrhythmias: Pathology review
Heart blocks: Pathology review
Aortic dissections and aneurysms: Pathology review
Pericardial disease: Pathology review
Endocarditis: Pathology review
Hypertension: Pathology review
Shock: Pathology review
Vasculitis: Pathology review
Cardiac and vascular tumors: Pathology review
Dyslipidemias: Pathology review
Sympatholytics: Alpha-2 agonists
Adrenergic antagonists: Presynaptic
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
ACE inhibitors, ARBs and direct renin inhibitors
Thiazide and thiazide-like diuretics
Calcium channel blockers
cGMP mediated smooth muscle vasodilators
Class I antiarrhythmics: Sodium channel blockers
Class II antiarrhythmics: Beta blockers
Class III antiarrhythmics: Potassium channel blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Lipid-lowering medications: Statins
Lipid-lowering medications: Fibrates
Miscellaneous lipid-lowering medications
Positive inotropic medications
Cardiomyopathies: Clinical
Congenital heart defects: Clinical
Valvular heart disease: Clinical
Infective endocarditis: Clinical
Pericardial disease: Clinical
Chest trauma: Clinical
Hypertension: Clinical
Pulmonary hypertension
Aortic aneurysms and dissections: Clinical
Raynaud phenomenon
Peripheral vascular disease: Clinical
Heart failure: Clinical
Coronary artery disease: Clinical
Deep vein thrombosis and pulmonary embolism: Pathology review
Fascia, vessels and nerves of the upper limb
Vessels and nerves of the forearm
Vessels and nerves of the hand
Anatomy of the abdominal viscera: Blood supply of the foregut, midgut and hindgut
Fascia, vessels, and nerves of the lower limb
Vessels and nerves of the gluteal region and posterior thigh
Anatomy of the popliteal fossa
Ventilation
Ventilation-perfusion ratios and V/Q mismatch
Gas exchange in the lungs, blood and tissues
Oxygen binding capacity and oxygen content
Oxygen-hemoglobin dissociation curve
Carbon dioxide transport in blood
Trypanosoma cruzi (Chagas disease)
Yellow fever virus
Rickettsia rickettsii (Rocky Mountain spotted fever) and other Rickettsia species
Arteriovenous malformation
Cerebral circulation

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Questions

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A 35-year-old woman is brought to the emergency department following a motor vehicle accident. At the scene, she was in severe pain and pointed to her chest. Soon after arrival, the patient loses consciousness. Temperature is 37.0°C (98.6°F), pulse is 120/min, respirations are 22/min, and blood pressure is 75/55 mmHg. On physical examination, there are multiple lacerations over the torso and face. Significant bruising is noted over the chest. Neck veins are distended. On chest auscultation, lung fields are clear bilaterally and heart sounds are weak. Echocardiography is obtained and shows a large pericardial effusion. Which of the following sets of hemodynamic parameters are most likely to be seen in this patient?  

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Two people came to the emergency department. One of them is 55 year old Pamela who has sharp retrosternal chest pain that gets worse when she breathes in. On chest auscultation, a friction rub can be heard. The other person is 43 year old Thomas, who had been in a car accident and now presents severe hypotension and on physical examination, his neck veins are distended, his heart rate is really high. On chest auscultation there’s barely audible heart sounds. An ECG was ordered for both individuals. Pamela had ST-segment elevation in several leads and also PR depression, while Thomas has low-voltage QRS complexes.

Okay, based on what we know about the individuals, we can assume that both suffer from pericardial disease. But first, a bit of physiology. The pericardium is a sac that covers the heart and the roots of the great vessels. The pericardium has two layers, an inner serous layer and an outer fibrous layer. The space between the two layers is the pericardial cavity that cushions the heart from any kind of external jerk or shock - like a shock absorber. The pericardium also fixes the heart to the mediastinum, to prevent it from twisting, so that the large vessels don’t get pinched shut.

Now for pericardial disease, we should start by talking about inflammation in the pericardium, which is called pericarditis. People who develop pericarditis are also at risk of developing a pericardial effusion where the inflammation causes fluid to accumulate around the heart.

Pericarditis is in most cases idiopathic. It can also be due to a viral infection, like Coxsackie B virus. Pericarditis can also be seen in autoimmune diseases, like rheumatoid arthritis or systemic lupus erythematosus, because the immune system attacks our own tissues, including the pericardium. For your exams, other high yield causes include myocardial infarction and Dressler syndrome which occurs several weeks after a myocardial infarction. Basically, when heart cells die in a myocardial infarction, it attracts white blood cells to the area, leading to massive inflammation that also involves the serous pericardium. Another cause is uremia, which is when blood levels of urea gets really high and this usually happens due to kidney failure. The high levels of urea irritate the serous pericardium, making it secrete a thick pericardial fluid that’s full of fibrin strands and white blood cells. Cancers like lung cancer and lymphoma can also lead to pericarditis, due to metastasis that reach the pericardium, irritating it. Finally, there’s radiation therapy that can also lead to pericarditis.

Now, inflammation of the pericardium causes the fluid and immune cells in tiny blood vessels in the fibrous and serous pericardium to leak into the interstitium of those layers, making the layer itself a bit thicker and more boggy; think of how a piece of dry sponge thickens as it soaks up fluid.

Now, sometimes, when the inflammation persists, immune cells can initiate fibrosis of the serous pericardium which can produce an inelastic shell around the heart, making it hard for the chambers to expand and this is called constrictive pericarditis. For your tests, remember that the most common cause of constrictive pericarditis in high- and middle-income countries is idiopathic or viral infection, while in lower-income countries, it’s tuberculosis. In a test question, it might often also appear as a consequence of chest radiotherapy. Now, both ventricles can’t fully expand and fill with blood. So, from the left ventricle, all that blood backs up into the lungs, specifically in the pulmonary veins and capillary beds which can increase the pressure in these vessels. This leads to fluid moving from the blood vessels to the interstitial space causing pulmonary edema, or congestion. In the alveoli of the lungs, all the extra fluid makes oxygen and carbon dioxide exchange a lot harder, and therefore patients have dyspnea or trouble breathing. And from the right ventricle, blood accumulates in the veins of the systemic circulation. One common manifestation of this is jugular venous distention, where the jugular vein that’s relatively close to the heart becomes enlarged and distended. One fact that you have to remember here is that normally, during inspiration, the jugular venous pressure falls, because blood returns to the right ventricle. However, in constrictive pericarditis, the right ventricle isn’t as compliant. So, in this case, during inspiration, the jugular venous pressure will paradoxically rise and this is called Kussmaul’s sign. Also in the body, when blood backs up to the liver and portal circulation, it causes hepatomegaly or liver distention, as well as portal hypertension and ascites, which is the accumulation of fluid in the peritoneal cavity. Finally, fluid that backs up into the interstitial space in the soft tissues of the legs causes pitting edema, which means that the tissue is visibly swollen and when you apply pressure to it it leaves a “pit” and takes awhile to come back to its original place.

The main symptom of pericarditis, which is extremely high yield, is severe, sharp retrosternal chest pain, that radiates to the neck, shoulders, and back, and it typically happens with each breath during inspiration. That’s because the lungs expand during inspiration, filling the thoracic cavity and compressing the pericardium. The pain typically worsens when a person is supine and improves when a person is sitting upright and leaning forward, because less pressure is put on the heart.

For diagnosis, the most important clue is that upon auscultation, there’s a pericardial friction rub which is a scratchy, grating, high-pitched rub resembling the sound of leather rubbing against leather. On ECG, there’s widespread ST segment elevation in several leads. This will help you distinguish it from the myocardial infarction which also presents with chest pain and ST elevation, but in myocardial infarction the ST elevation is only present in the leads that correspond to the infarcted tissue. Also, for your tests, remember that PR segment depression is a very specific ECG finding in pericarditis. On imaging, pericarditis can show up as an enlarged heart on chest X-ray, and an echocardiogram can show fluid in the pericardium. In constrictive pericarditis, a CT can detect calcifications and thickening of the pericardium seen in a CT scan.

Sources

  1. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  2. "Diagnosis and treatment of pericarditis" Heart (2015)
  3. "Acute Cardiac Tamponade" New England Journal of Medicine (2003)
  4. "2015 ESC Guidelines for the diagnosis and management of pericardial diseases: The Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC)Endorsed by: The European Association for Cardio-Thoracic Surgery (EACTS)" Eur Heart J. (2015)
  5. "Pathophysiology of Heart Disease" Wolters Kluwer Health (2015)