Pulmonary shunts

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Pulmonary shunts

Respiratory Exam 1

Respiratory Exam 1

Pleural effusion, pneumothorax, hemothorax and atelectasis: Pathology review
Obstructive lung diseases: Pathology review
Pneumothorax
Pleural effusion
Lung volumes and capacities
Anatomy clinical correlates: Pleura and lungs
Anatomy of the lungs and tracheobronchial tree
Bronchioles and alveoli histology
Trachea and bronchi histology
Anatomic and physiologic dead space
Alveolar surface tension and surfactant
Alveolar gas equation
Acute respiratory distress syndrome
Emphysema
Asthma
Bronchiectasis
Chronic bronchitis
Alpha 1-antitrypsin deficiency
Pulmonary embolism
Respiratory distress syndrome: Pathology review
Cystic fibrosis: Pathology review
Restrictive lung diseases: Pathology review
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Sarcoidosis
Restrictive lung diseases
Idiopathic pulmonary fibrosis
Reading a chest X-ray
Compliance of lungs and chest wall
Ventilation
Regulation of pulmonary blood flow
Ventilation-perfusion ratios and V/Q mismatch
Zones of pulmonary blood flow
Airflow, pressure, and resistance
Diffusion-limited and perfusion-limited gas exchange
Gas exchange in the lungs, blood and tissues
Oxygen-hemoglobin dissociation curve
Oxygen binding capacity and oxygen content
Carbon dioxide transport in blood
Upper respiratory tract infection
Bacterial epiglottitis
Congenital pulmonary airway malformation
Neonatal respiratory distress syndrome
Transient tachypnea of the newborn
Pulmonary hypoplasia
Tracheoesophageal fistula
Croup
Bacterial tracheitis
Pulmonary hypertension
Pulmonary edema
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Respiratory acidosis
Respiratory alkalosis
Acid-base disturbances: Pathology review
Pulmonary shunts
Pulmonary chemoreceptors and mechanoreceptors
Methemoglobinemia
Deep vein thrombosis and pulmonary embolism: Pathology review
Pulmonary changes at high altitude and altitude sickness
Pulmonary changes during exercise
Breathing control
Sleep apnea
Goodpasture syndrome

Transcript

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Pulmonary circulation starts with oxygen (O2) poor and carbon dioxide (CO2) rich blood in the right atrium that flows into the right ventricle.

From there - blood is pumped into the large pulmonary trunk, which splits to form the two pulmonary arteries – one for each lung.

The pulmonary arteries divide into smaller arteries known as pulmonary arterioles and then eventually into pulmonary capillaries which surround the alveoli - which are the millions of tiny air sacs where gas exchange happens.

At that point, O2 enters the blood and CO2 enters the alveoli.

The pulmonary capillaries drain into small veins known as pulmonary venules that flow into two pulmonary veins exiting each lung, and these pulmonary veins complete the circuit by delivering O2-rich and CO2-poor blood into the left atrium, which flows into the left ventricle and then into the aorta where it enters systemic circulation.

Normally, about 2% of the blood follows a slightly different path. It’s diverted, or shunted, so that it bypasses the pulmonary capillaries, and this is called a physiologic shunt.

There are two main ways this happens. First, when blood goes out to the heart muscle itself - it returns through tiny veins called thebesian veins.

Rather than draining into the venous system and going into the right atrium, these veins sometimes dump that blood into the closest chamber of the heart.

So, for example, if blood that goes out the aorta and through the coronary arteries to the muscle in the left ventricle of the heart, then the deoxygenated blood might then drain directly into the left ventricle chamber of the heart. At that point it would mix with the rest of the oxygenated blood and get squeezed right back out through the aorta.

So - this blood basically bypasses the pulmonary circulation.

Second, the conducting airways of the lungs, like the bronchi, receive systemic arterial blood from the bronchial arteries.

But the deoxygenated blood can flow, or anastomose, right into nearby pulmonary veins which are carrying oxygenated blood that has already travelled through the pulmonary capillaries.

So, once again, deoxygenated blood might flow right into the pulmonary veins and mix in with the rest of the oxygenated blood, bypassing the pulmonary circulation.

Now, in addition to these naturally occurring physiologic shunts, there are also some pathological defects that can lead to more shunting of blood.

In most left-to-right shunts, blood flows from the left side of the heart to the right side of the heart. This can happen when there is a gap in the wall, or septa, that divides the left and right chambers of the heart.

So, for example, a ventricular septal defect allows blood to flow down its pressure gradient from the high-pressure left ventricle into the lower pressure right ventricle.

And an atrial septal defect allows for the same thing, only blood is shunted from the left atrium to the right atrium.

Another type of left-to-right shunt happens with a patent ductus arteriosus.

The ductus arteriosus is a fetal blood vessel that creates a pathway for blood to flow from the pulmonary artery into the aorta. During fetal development, this is important because the lungs are not working, and are fluid-filled and compressed.

So oxygenated blood coming from the placenta bypasses the lungs and goes directly into fetal systemic circulation.

This pathway is supposed to close at birth, and allow blood to flow normally from the right ventricle into the pulmonary artery and into the lungs.

But in some babies, it remains open, or patent, and that allows blood to flow from the high-pressure aorta into the lower-pressure pulmonary artery.

The end result of any of these left-to-right shunts is that oxygenated blood is making a second loop through pulmonary circulation, which means the right ventricle is doing a bit of extra work - moving blood around that’s already oxygenated.

On the flip side, in a right-to-left shunt, blood flows from the right side of the heart to the left. Normally this wouldn’t happen because blood would not want to flow up its pressure gradient.

But, right-to-left shunts typically involve changing pressures in the chambers of the heart which reverse the gradient.

So, for example, in the congenital heart condition called Tetralogy of Fallot, there is a large ventricular septal defect and stenosis, or narrowing, of the right ventricular outflow tract into the pulmonary artery.

The right ventricular outflow tract stenosis increases the resistance to blood going into the pulmonary circulation, and that increases right ventricular pressure.

If the right ventricular pressure exceeds left ventricular pressure, then blood can flow down the new pressure gradient, and a right to left shunt occurs.

Key Takeaways

A pulmonary shunt occurs when there is re-diversion of blood from its usual path through pulmonary circulation. This can occur when there is an abnormal flow of blood from the right side of the heart to the left side of the heart, bypassing the lungs. Examples include conditions like patent ductus arteriosus, ventricular septal defect, and atrial septal defect. Sometimes a pulmonary shunt may be said when the alveoli fill with fluid, causing parts of the lung to be unventilated although they are still perfused. This is because even though blood from the right ventricles passes through the lungs before reaching the left atria, it is still unoxygenated.

Sources

  1. "Medical Physiology" Elsevier (2016)
  2. "Physiology" Elsevier (2017)
  3. "Human Anatomy & Physiology" Pearson (2018)
  4. "Principles of Anatomy and Physiology" Wiley (2014)
  5. "Gas exchange and ventilation–perfusion relationships in the lung" European Respiratory Journal (2014)
  6. "Simulations Reveal Adverse Hemodynamics in Patients With Multiple Systemic to Pulmonary Shunts" Journal of Biomechanical Engineering (2015)