Lynelle R. Johnson - Canine and Feline Respiratory Medicine

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This comprehensive reference provides readers with everything they need to know about diagnosing and treating canine and feline respiratory disease. Significantly updated and expanded, it focuses on localization of disease, efficient diagnostic testing, and appropriate therapy. With more images, discussion, and diagrams, this
includes more detail and new information throughout, particularly in the areas of antimicrobial guidelines, anti-fungal therapies, and ant-viral medications in cats.
Logically organized for ease of use in the practice setting,
features problem-based learning to enhance working knowledge of the topics discussed. Chapters cover localization of disease, respiratory diagnostics, respiratory therapeutics, nasal disorders, and diseases of airways. Sections on parenchymal disease; pleural and mediastinal disease; and vascular disorders are also presented. 
Offers a complete guide to the diagnosis and treatment of respiratory conditions in canine and feline patients—now expanded to include more detailed and advanced information Focuses on localization of disease, diagnostic testing, and appropriate therapy Thoroughly updated with new antimicrobial guidelines, the latest information on anti-fungal therapy, and new advances in ant-viral medications in cats Includes many new images and topics for discussion Features problem-based learning to support a working understanding of the topics discussed
is an essential resource for veterinary internal medicine specialists, general practitioners, and veterinary students.

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Table 2.1 Normal blood gas values for dogs and cats.

Dog Cat
P aO 2(mmHg) 90 (80–105) 100 (95–105)
P aCO 2(mmHg) 37 (32–43) 31 (26–36)
pH 7.35–7.45 7.35–7.45
HCO 3(mmol/l) 22 (18–26) 18 (14–22)

HCO 3, bicarbonate; P aCO 2, partial pressure of carbon dioxide; P aO 2, partial pressure of oxygen.

Alveolar–Arterial Oxygen Gradient and PF Ratio

The alveolar–arterial (A–a) oxygen gradient estimates the difference between the calculated alveolar oxygen level expected for the animal and the measured arterial oxygen level. Thus, the A–a gradient corrects for the level of ventilation performed by the animal and allows comparison of blood gas data through the course of disease that is not impacted by the effect of an increase or a decrease in P aCO 2on P aO 2. The A–a oxygen gradient is calculated as:

where F iO 2is the fraction of inspired oxygen 021 on room air PB is the - фото 10

where F iO 2is the fraction of inspired oxygen (0.21 on room air), PB is the barometric pressure (in mmHg), PH 2O is the water vapor pressure (47 mmHg at 37 °C), and R is the respiratory quotient (ratio of CO 2production to O 2consumption, usually assigned a value between 0.8 and 1.0). P aO 2and P aCO 2are obtained from blood gas analysis. Normal value for the A–a oxygen gradient is < 15.

The PaO 2/FiO 2ratio (PF or oxygenation ratio) provides a measure of the ability of the lung to oxygenate as the fraction of inspired oxygen changes from room air to 100% oxygen. This is calculated by dividing arterial oxygen by FiO 2(ranging from 0.21 to 1.0). Normal animals have a PF ratio of > 500 at sea level. Values between 300 and 500 indicate mild impairment of oxygenation, while values < 200 indicate serious decrements in oxygenation. A PF ratio < 200–300 is one of the criteria for a diagnosis of acute respiratory distress syndrome.

Causes of Hypoxemia

Obtaining an arterial blood gas, calculating the A–a gradient, and assessing response of hemoglobin saturation or P aO 2to exogenous oxygen supplementation allow assumptions to be made about the most likely mechanism causing hypoxemia ( Table 2.2). This can help determine the most likely cause of hypoxemia, although ventilation/perfusion mismatch underlies the pathophysiology of hypoxemia in almost all lung diseases, and many clinical disorders have multiple contributors to hypoxemia.

Diagnostic Imaging

Radiography

Radiography is often the key to creating an appropriate list of differential diagnoses for the respiratory case and for determining the type of sampling method that is most likely to achieve a final diagnosis, such as endoscopy, fine‐needle aspiration (FNA), or a tracheal wash ( Table 2.3). It will also help determine the need for advanced imaging, including fluoroscopy, ultrasound, nuclear scintigraphy, or computed tomography (CT). The widespread use of digital radiography has enhanced the evaluation of pulmonary patterns, although overlying structures can still confuse interpretation. Specific features of these tests are presented in the relevant disease sections.

Table 2.2 Respiratory causes of hypoxemia.

Mechanism Clinical attributes Causes
Hypoventilation High P aCO 2Normal A–a gradient Improved by oxygen supplementation Improved by increasing alveolar ventilation Anesthesia Upper airway obstruction Neuromuscular weakness CNS disease
V/Q mismatch Increased A–a gradient Mildly increased P aCO 2Markedly improved by oxygen supplementation Virtually any lung disease
Shunt Increased A–a gradient Not improved by oxygen supplementation Not improved by increasing alveolar ventilation Congenital right to left cardiac shunts Acute respiratory distress syndrome
Diffusion impairment Increased A–a gradient Seldom a major cause of hypoxemia at rest Causes hypoxemia during exercise or with low inspired oxygen Improved by oxygen supplementation Interstitial lung disease Pulmonary edema
Reduced inspired oxygen Improved by oxygen supplementation Causes hypoxemia during exercise or when diffusion is impaired High altitude

A–a, alveolar–arterial; CNS, central nervous system; P aO 2, partial pressure of oxygen.

Table 2.3 Airway sampling techniques for various lung patterns.

Radiographic pattern Differential diagnoses Sampling technique
Interstitial Viral pneumonia Rickettsial pneumonia Protozoal pneumonia Hemorrhage Vasculitis Pulmonary fibrosis Neoplasia Early pulmonary edema Aspiration pneumonia Fine‐needle aspirate Lung biopsy Bronchoscopy Tracheal wash
Bronchial Chronic bronchitis Feline bronchitis/asthma Bronchiectasis Parasitic bronchitis Early bronchopneumonia Tracheal wash Bronchoscopy
Alveolar Bronchopneumonia Aspiration pneumonia Fungal pneumonia Hemorrhage Pulmonary edema Neoplasia Non‐cardiogenic pulmonary edema Tracheal wash Bronchoscopy
Consolidation Neoplasia Lung lobe torsion Consolidating pneumonia Granuloma Bronchial obstruction Feline bronchitis Foreign body inhalation Bronchoscopy Fine‐needle aspirate Tracheal wash
Vascular Congenital heart disease Congestive heart failure Heartworm disease Pulmonary hypertension Pulmonary thromboembolism Echocardiography
Effusion Hydrothorax Pyothorax Hemothorax Chylothorax Neoplasia Diaphragmatic hernia Thoracocentesis

Orthogonal views are always recommended for evaluation of thoracic contents, and assessment of the thorax is improved by obtaining both left and right lateral views, as well as a dorsoventral or ventrodorsal image. Lateral views provide an optimized view of the lung closest to the radiographic unit, therefore a left lateral projection would be more likely to identify infiltrates in the right middle lung lobe in a patient with aspiration pneumonia. A right lateral projection might be preferred to investigate airway collapse at the left cranial lobar bronchus (cranial and caudal segments). The dorsoventral view provides better imaging of the cardiac silhouette and pulmonary vessels, although the ventrodorsal view allows better assessment of small volumes of pleural effusion, as well as infiltrates in the ventral or lateral portions of the lung. Importantly, attempts should be made to confirm the presence of pulmonary nodules on both a lateral and an orthogonal view.

In some patients, cervical radiographs can provide valuable information on the extrathoracic respiratory tract and its potential role in thoracic disease. Loss of the nasal air column from the nasal cavity into the nasopharynx, elongation or thickening of the soft palate, the suggestion of laryngeal edema or mass, air in the laryngeal saccules, or caudal retraction of the larynx are clues to the presence of an upper airway obstructive lesion that could be contributing to disordered breathing or a lower respiratory tract process.

Ultrasound

Ultrasound of the larynx can be used to evaluate patients for laryngeal paralysis or mass lesions, and cervical tracheal collapse can also be identified with ultrasound. However, these studies can be technically challenging because soft tissues are adjacent to air‐filled structures, which causes marked attenuation of the ultrasound beam. However, valuable information can be gained by an experienced ultrasonographer.

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