Pul 2 - Lung vol and Pulm Circ Flashcards
What is the inspiratory reserve volume (IRV)?
The additional air that can be forcibly inhaled after the inspiration of a normal tidal volume.
What is the expiratory reserve volume (ERV)?
The additional air that can be forcibly exhaled after the expiration of a normal volume.
What is the inspiratory capacity (IC)?
It is tidal volume plus inspiratory reserve volume.
TV + IRV = IC.
What is the vital capacity?
It is the inspiratory capacity plus the expiratory capacity.
IC + ERV : VC
Remember that Inspiratory capacity is Tidal volume + inspiratory reserve volume.
What is residual volume?
It is the amount of air left in you after you exhale as much as you can.
What is functional residual capacity?
It is expiratory reserve volume plus residual volume.
ERV + RV: FRC
What is total lung capacity (TLC)?
All the volume that can be taken, exhaled, and left in the system.
IRV + TV + ERV + RV: TLC or IC + FRC: TLC or VC + RV: TLC
What is the air that isn’t participating in gas exchanged called and what are it’s components?
Physiological dead space.
- Anatomical dead space: Air in the airways.
- Function dead space: capable of gas exchange, but no gas exchange occurs (apices of the lung during relaxed breathing); cannot be directly measured but can be calculated using dead space equation.
What is the equation for dead space?
Vd = Vt x (PaCO2 -PECO2)/ PaCO2.
Vd: Dead space
Vt: Tidal volume
PaCO2: Partial CO2 of arterial blood.
PECO2: PCO2 expired air.
What is tidal volume?
The amount of air that is moved in and out of the lungs during normal, relaxed respiration.
What happens in the lungs in a decrease in alveolar oxygen?
Local vasoconstriction.
What does effect does COPD have on the pulmonary vasculature?
Low alveolar oxygen causes chronic vasoconstriction, which causes pulmonary hypertension. Sustained pulmonary hypertension causes cor pulmonale (lung disease that causes heart failure).
What are the 2 factors that can limit gas exchange?
- Perfusion. (Under normal circumstances, transfer of O2 is limited by perfusion).
- Diffusion.
What causes bronchoconstriction of an airway?
- Anaphylaxis.
- Bronchospasm.
- Asthma.
- Parasympathetic stimulation.
How would sympathetic stimulation of the beta 2 receptors affect the radius of the airway?
It will increase the radius, decreasing resistance.
How can we lower the viscosity/density of air going through the airway?
Have the patient breath a specific mixture of helium and oxygen to lower air viscosity.
What is the normal pulmonary artery pressure?
It is 10 to 15 mmHg.
What is the number that defines pulmonary hypertension?
Pulmonary artery pressure of 25 mmHg or above at rest. Or greater than or equal to 35 during excercise.
What is another name for primary pulmonary hypertension and what are the causes?
Also known as idiopathic pulmonary arterial hypertension, caused by:
- Abnormalities in BMPR2: Bone Morphogenetic Protein Receptor II: normally this gene prevents proliferation of vascular smooth muscle; mutation of this gene leads to reduced vessel radius, increased resistance, and increased pulmonary arterial pressure.
- Associated with HIV and Kaposi sarcoma (HHV-8).
- More common in women, average age is 36.
What is the cause of secondary pulmonary hypertension?
- Chronic lung disease: COPD, pulmonary fibrosis.
- Mitral stenosis.
- Recurrent thromboemboli.
- Autoimmune disease.
- Left-to-Right shutns (VSD).
- Sleep apnea or high altitude: Hypoxic vasoconstriction.
What is the treatment for pulmonary hypertension?
- Bosentan or Ambrisentan: Both end in -sentan, the competitively antagonize endothelian-1 receptors, decreasing pulmonary resistance.
- Iloprost or Epoprostenol (Prostaglandin analogue): They relax smooth muscle.
- Sildenafil (Revatio; not viagra in Pul HTN): fosfodiaesterase inhibitor.
- Nifedipine: dihydropyridine calcium channel blocker.
3.
If a lung collapses, what happens to the intrathoracic volume?
When this happens, the chest wall is allowed to expand, unnaposed by the lungs, increasing intrathoracic volume.
What gene mutation can cause primary pulmonary hypertension?
BMPR 2 mutation.
What is the mechanism of action of Bosentan?
Antagonist at the endothelin-1 receptor.