HYPOXEMIA
HYPOXEMIA: Excerpt from Differential Diagnosis in Primary Care
In developing the list of possible causes of hypoxemia, the physiologic model of intake, absorption, transport, excretion, and regulation is most useful.

HYPOXEMIA
Intake
Both upper airway obstruction (laryngotracheitis, foreign body, etc.) and lower airway obstruction (bronchial asthma, emphysema, etc.) may inhibit the intake of oxygen causing hypoxemia. In addition, conditions that affect the chest wall such as kyphoscoliosis, ankylosing, spondylitis, and myasthenia gravis reduce the intake of oxygen by decreasing the vital capacity.
Absorption
Absorption of oxygen in the lungs may be inhibited by atelectasis, pneumothorax, or pneumonia where the alveolar sacs are blocked or collapsed or by a diffusion defect as occurs in Haman Rich disease, silicosis, sarcoidosis, and scleroderma. Absorption is also impeded by a pulmonary embolism or pulmonary hemangioma, which interferes with the perfusion of a segment of a lung. Large venous–arterial shunts such as tetralogy of Fallot can produce the same picture.
Transport
The cardiovascular system transports oxygen to the tissue. When blood flow is slowed because of CHF or shock, oxygen is not picked up in the lungs and transported to the tissues fast enough to keep pace with the demand resulting in hypoxemia. CHF also decreases absorption by the accumulation of fluid in the lungs blocking the diffusion of oxygen across the alveoli.
Excretion
Blocking the excretion of oxygen does not cause hypoxemia. However, blockage of the excretion of carbon dioxide, as in pulmonary emphysema and asthmatic bronchitis, contributes to hypoxemia by not allowing the blood to pick up oxygen in exchange for carbon dioxide.
Regulation
Respirations are regulated by the central nervous system. Consequently, drugs, such as phenobarbital that decrease the respiratory rate cause hypoxemia. Diseases that affect the respiratory center such as poliomyelitis or Guillain–Barré syndrome can suppress respiration, causing hypoxemia.
Approach to the Diagnosis
The clinical picture of obstructive lung disease is usually obvious. Other causes of hypoxemia may require more extensive laboratory evaluation to diagnose. Arterial blood gases are the most important study. An increased carbon dioxide will suggest pulmonary emphysema or asthma. Pulmonary function tests can assist in the diagnosis in these conditions as well. If the carbon dioxide level is normal or decreased, a perfusion or defusion defect must be looked for. A lung scan will help rule out a pulmonary embolism. A chest x-ray will help reveal pneumothorax, atelectasis, sarcoidosis, and pulmonary fibrosis. An arm-to-tongue circulation time will help rule out CHF. A consult with a pulmonologist or cardiologist is always wise when faced with hypoxemia.
Other Useful Tests
- CBC (shock, infection)
- Urinalysis (collagen disease)
- Sedimentation rate (infection)
- Chemistry panel (shock, myocardial infarction)
- Blood volume (shock, CHF)
- Sulfhemoglobin and methemoglobin (sulfhemoglobinemia, methemoglobinemia)
- Carboxyhemoglobin (carbon monoxide poisoning)
- Serial ECGs and cardiac enzymes (myocardial infarct)
- CT scan of the chest (pulmonary aneurysm, bronchiectasis)
- Lung biopsy (neoplasm, pulmonary fibrosis)
- Bronchoscopy (neoplasm, bronchiectasis)
Book Source Details
- Book Title: Differential Diagnosis in Primary Care
- Author(s): R. Douglas Collins
- Year of Publication: 2007
- Copyright Details: Differential Diagnosis in Primary Care, Copyright © 2007 Lippincott Williams & Wilkins.
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- "Algorithmic Diagnosis of Symptoms and Signs" (2003)
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- HYPOXEMIA
- "Differential Diagnosis in Primary Care" (2007)
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- HYPOXEMIA
- "Differential Diagnosis in Primary Care" (2007)
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Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
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