11 Respiratory and Cardiac Disorders
Respiratory Problems
Dyspnea
Dyspnea (also called respiratory distress) is an inappropriate degree of breathing effort based on respiratory rate, rhythm, and character. Dyspnea is a common sign associated with a wide variety of respiratory and nonrespiratory disorders. Physical examination is the first step in diagnosis. Patients with obstructive respiratory diseases have a breathing pattern characterized by increased depth, rate, and effort. Dynamic obstruction (e.g., laryngeal paralysis) cranial to the thoracic inlet (i.e., the upper airway) causes increased inspiratory effort. Dynamic obstruction (e.g., collapsing trachea) caudal to the thoracic inlet (i.e., lower airway) causes increased expiratory effort. Fixed obstructions (e.g., tracheal tumor) often are associated with increased inspiratory and expiratory effort. Nasal cavity obstruction only causes an obstructive breathing pattern if the animal does not breathe through the mouth. Auscultation of wheezes suggests obstruction, but wheezes are not always found in obstructed patients. Monophonic wheezes (i.e., single tone) may be noted with an elongated soft palate. Alternatively, wheezes can have multiple tones (i.e., polyphonic wheezes), as heard in asthmatic cats.
Dyspnea due to extra-respiratory causes (e.g., severe anemia, severe metabolic acidosis) can have what appears to be an obstructive breathing pattern with an increased intensity of normal lung sounds (i.e., bronchovesicular sounds) but without wheezes.
Diseases limiting ability of the lungs to expand cause a restrictive breathing pattern characterized by an increased rate but a normal to decreased depth with or without increased inspiratory effort. Auscultation may reveal crackles, particularly inspiratory, or a complete absence of lung sounds with certain restrictive lung diseases (e.g., pneumothorax, hydrothorax). It may be difficult to auscultate pulmonary parenchymal abnormalities, especially in small patients with low tidal volumes. Thoracic radiographs of these patients can reveal substantial pulmonary parenchymal disease despite apparently normal lung sounds. Distinction between obstructive and restrictive breathing patterns is not always clear; the pattern of breathing exhibited depends on the relative amount of pathologic change in affected tissues. For example, a dog with severe pulmonary edema may have obstructive (airway fluid) and restrictive (interstitial fluid) disease.
Patients with disorders such as flail chest occasionally have paradoxical movements (i.e., a section of the chest wall collapsing during inspiration and expanding during expiration). Pulmonary vascular diseases can be associated with either inspiratory or mixed inspiratory and expiratory dyspnea.
Common causes of dyspnea are listed in Box 11-1.
Box 11-1 Causes of Dyspnea (Respiratory Distress)
Respiratory Disorders
Obstructive Disease
Nasal (only if patient does not breathe through mouth)
Chondromesenchymal hamartoma (cats)
Elongated/edematous soft palate
Extraluminal compression (tumor or granuloma)
Extraluminal compression (tumor, granuloma, hilar lymphadenopathy, left atrial enlargement)
Lower airways and pulmonary parenchyma
Pneumonia (viral, bacterial, fungal)
Hypersensitivity (allergic) lung disease
Eosinophilic bronchopneumopathy
Useful Tests
After the site of an abnormal breathing pattern has been localized by physical examination, tracheal and thoracic radiographs are typically the most useful next diagnostic step (Figure 11-1).

FIGURE 11-1 Approach to respiratory distress and tachypnea in dogs and cats. CBC, Complete blood count; CT, computed tomography; ECG, electrocardiogram.
Note
Although a collapsed trachea can be diagnosed radiographically, it cannot be ruled out by such, even if inspiratory and expiratory films are made. Fluoroscopy or tracheobronchoscopy may be needed to establish the diagnosis.
Transtracheal aspiration (TTA), bronchoalveolar lavage (BAL), or transthoracic fine-needle aspiration (see subsequent sections) may follow if radiography suggests the need for cytologic analysis or culture of the lower airway, especially if coughing is present. Pharyngoscopy, nasopharyngoscopy, and laryngoscopy are useful in patients with upper airway obstruction. Tracheobronchoscopy is useful in tracheal and bronchial disorders, especially for diagnosing obstructive disease such as collapsed trachea, and it is mandatory in most pharyngeal and laryngeal abnormalities (see Figure 11-1). Pleural effusion is always an indication for fluid analysis (see Chapter 10). If dirofilariasis is suspected, a Knott’s test, filter test, or Dirofilaria immitis antigen (or antibody in cats) test is indicated (see Chapter 15). Although they rarely provide a diagnosis, fecal flotation and Baermann’s fecal analysis are inexpensive and noninvasive and can definitively diagnose respiratory parasites. Serologic testing for systemic mycoses (except histoplasmosis) may be useful in dogs (see Chapter 15). Tests for detecting Histoplasma and Blastomyces antigens in the urine are now available (http://www.miravistalabs.com) and might be better than serology.
Coughing, Including Hemoptysis
Common causes of coughing in dogs and cats are listed in Box 11-2. History is used first to eliminate self-limiting, contagious, infectious diseases. The owner should be carefully questioned to differentiate cough from gagging, because many owners confuse gagging with coughing. Gagging (not that after a coughing stint) would suggest nasopharyngeal or nonrespiratory disorders (i.e., oropharyngeal, esophageal, or gastrointestinal disease). Differentiation of a productive cough (e.g., bronchopneumonia) from a nonproductive cough (e.g., viral tracheobronchitis) and identification of abnormal breathing patterns (see Box 11-1 and Figure 11-1) are also helpful. Tracheal and thoracic radiographs are essential in patients with chronic cough, hemoptysis, or cardiovascular disease but are less useful in acute infectious tracheobronchial diseases unless secondary pneumonia is suspected. Radiographs can be used to diagnose but not reliably rule out a collapsed trachea. Fluoroscopy may be required to rule in or out tracheal collapse and is often needed for evaluation of extent of tracheal collapse if present. TTA or BAL (especially if combined with bronchoscopy) is often diagnostic of allergic disease, parasitic infections, or bacterial infections and supports a clinical diagnosis of certain chronic bronchial diseases (e.g., chronic bronchitis). Bronchoscopy is often needed to diagnose foreign body or obstructive disease. A CBC is seldom helpful unless marked eosinophilia (e.g., allergic or parasitic disease) is present. Fecal flotation and Baermann’s fecal analysis are rarely revealing but are indicated because they are easy and cost-effective. Arterial blood gas analysis is rarely diagnostic or cost-effective in coughing patients without dyspnea.
Box 11-2 Causes of Coughing in Dogs and Cats
Pharynx/Larynx
Infection (bacterial or viral)
Laryngeal paralysis (congenital or acquired)
Eversion of laryngeal saccules
Trachea/Lower Airway
Allergy (allergic bronchitis/asthma)
Bacterial (Bordetella bronchiseptica)
Parasitic (Filaroides spp., Oslerus osleri, Capillaria aerophilia)
Anomalies (collapse, hypoplasia, primary ciliary dyskinesia, segmental stenosis, extraluminal compression [left atrium, tumor])
Neoplasia (osteochondral dysplasia [osteochondroma])
Pulmonary Parenchymal Disease
Allergy (pulmonary infiltrates with eosinophilia)
Fungal (Blastomyces dermatitidis, Histoplasma capsulatum, Coccidioides immitis, Cryptococcus neoformans, Aspergillus spp.)
Protozoal (Toxoplasma gondii, Pneumocystis carinii)
Parasitic (Filaroides hirthi, Filaroides milksi, Dirofilaria immitis, Angiostrongylus vasorum, Paragonimus kellicotti)
Degenerative disease (emphysema)
Neoplasia (primary or metastatic)
Noninfectious granulomatous disorders (eosinophilic pulmonary granulomatosis, pulmonary lymphomatoid granulomatosis)
Cardiovascular Disease
Left atrial enlargement causing bronchial compression
Thromboembolism (dirofilariasis, hyperadrenocorticism, protein-losing nephropathy, neoplasia, cardiac disease)
Nasal Discharge, Sneezing, and Epistaxis
Nasal discharge and sneezing may be the result of primary nasal cavity disease or secondary to bronchopulmonary disease (e.g., pneumonia). Epistaxis may be the result of a primary nasal problem (e.g., neoplasia) or a systemic problem (e.g., coagulopathy). Common causes of these problems are listed in Box 11-3.
Box 11-3 Causes of Nasal Discharge, Sneezing, and Epistaxis in Dogs and Cats
Bleeding Disorders
Factor deficiency (congenital and acquired)
Thrombocytopenia (infectious and immune mediated)
Vessel wall (trauma and vasculitis)
Infections
Viral: distemper, parainfluenza, adenovirus type 2 (dogs); herpesvirus, calicivirus (cats)
Bacterial: including dental disease, chronic feline rhinosinusitis, Bordetella bronchiseptica (dog)
Fungal: Aspergillus spp., Penicillium spp., Cryptococcus neoformans, Rhinosporidium seeberi; other opportunistic fungi are rare (e.g., Trichosporon)
Rickettsial: Ehrlichia canis, Rocky Mountain spotted fever
Parasitic: Pneumonyssoides caninum, Linguatula serrata, Capillaria aerophila, Syngamus ierei, Cuterebra spp.
When epistaxis occurs, evaluation for coagulopathy should be the initial diagnostic step (see Chapter 5). Radiography, but preferably computed tomography (CT) or magnetic resonance imaging (MRI) of the nasal cavity, is usually performed next (Figure 11-2); however, these studies may not be diagnostic in acute disease. If a mass lesion or bone lysis is identified, biopsy via the naris is indicated. Rhinoscopy to look for foreign objects is done following diagnostic imaging studies and can be performed while a patient is anesthetized for imaging. Direct examination may reveal adult Pneumonyssoides caninum. Serologic testing for nasal aspergillosis can be falsely negative and should not be relied on for a diagnosis (see Chapter 15). Direct examination of the nasal cavity (dorsal and ventral meatus) can be performed with rigid or flexible scopes (see under Rhinoscopy). The nasopharynx and posterior portion of the nasal cavity can be visualized with a dental mirror and penlight or more efficiently with a flexible endoscope. Endoscopy of the anterior portion of the nasal cavity in small dogs and cats is limited by the endoscope’s diameter. Nasal lavage is rarely diagnostic. Bacterial culture is not routinely recommended; interpretation is difficult because of the large normal bacterial population of the nasal cavity (see Chapter 15). Fungal culture for aspergillosis can have both false-positive and false-negative results (see Chapter 15). Cultures for fungi are generally more reliable if performed on nasal biopsy specimens rather than nasal cavity swabs. Nasal biopsy samples can be obtained with alligator-type clamshell instruments, with uterine or colonic biopsy forceps, or bone curettes (described later). If these procedures are not diagnostic and the condition persists, exploratory rhinotomy should be considered providing nasal CT or MRI has also been performed.
Nasal Radiography
Common Indications
Nasal radiography is indicated for chronic nasal discharge, epistaxis, severe acute undiagnosed sneezing, facial deformity, nasal obstruction, or pawing at the face or nose (see Box 11-3).
Advantages
Nasal radiography is noninvasive. Neoplasia and aspergillosis often cause bone lysis, which is seldom present in other disorders.
Disadvantages
General anesthesia is required, and excessive fluid (e.g., nasal hemorrhage, exudate) may obscure soft tissue abnormalities. In addition, the procedure provides low resolution of fine detail (except occasionally for high-detail dental films in cats and small dogs).
Readers are referred to a radiology text for additional information.20 CT and MRI are preferred imaging modalities and provide superior detail for evaluating the nasal cavity.
Computed Tomography
Common Indications
CT has the same indications as nasal radiography. It is essential for planning radiation therapy for nasal tumors and highly recommended before topical clotrimazole therapy for nasal aspergillosis to ensure that the cribriform plate has not been eroded. MRI can be used instead of CT. It gives more soft tissue detail than CT, but CT is typically sufficient, quicker, and less expensive.
Advantages
CT requires less anesthetic time and provides much more detail than even well-positioned nasal radiographs.13,15 CT is excellent at determining extent of disease, finding “caverns” where aspergillosis has caused destruction and loss of turbinate structures, and it is far superior at finding tumors. CT readily detects involvement of the orbital region, frontal sinuses, calvarium, and cribriform plate in both aspergillosis and tumors.
Disadvantages
The need for specialized equipment and the slightly greater cost compared with radiographs are the major drawbacks. Occasionally, contrast media are needed to distinguish between nonenhancing soft tissue density due to nasal discharge and enhancing density due to tumor or inflammation. Readers are referred to a radiology text for additional information.
Rhinoscopy
Advantages
Rhinoscopy is relatively noninvasive, may be done after nasal imaging during the same anesthetic procedure, and may provide definitive diagnosis.6 It is especially useful for diagnosing nasal aspergillosis.
Disadvantages
Anesthesia is required. If an otoscope cone is used, only the rostral nares can be visualized. Even with a fiberscope, arthroscope, or cystoscope, overall visualization is limited, necessitating a careful, methodical examination that does not always allow diagnosis. Copious nasal discharge or hemorrhage will obstruct visualization of nasal structures. In small dogs, rhinoscopy is difficult unless an arthroscope is available. Care must be taken to avoid causing hemorrhage, which can obscure the field of view.
Procedure
Imaging should be performed first. Next, posterior rhinoscopy is performed by placing a flexible scope into the posterior pharynx and retroflexing it to look above the soft palate. If a flexible scope is not available, one may retract the soft palate with an ovariectomy hook and visualize the area with a dental mirror and nasopharyngeal illuminator. Anterior rhinoscopy is then performed, preferably with a rigid arthroscope or cystoscope, or a small-diameter flexible bronchoscope or ureteroscope. If these are not available, an otoscope or nasal speculum will allow some visualization of the rostral nares. Tissue or brush biopsies can be obtained for cytologic analysis, histopathologic examination, or culture.
Nasal Lavage
Procedure
Under general anesthesia with endotracheal intubation, the nasopharynx is packed off with gauze sponges and the nasal cavity is vigorously lavaged with lactated Ringer’s solution via a soft rubber tube (Rob-Nel catheter; Sherwood Medical, St. Louis, MO). The fluid is recovered in a dish placed at the nares. A foreign body may occasionally be dislodged and recovered from the naris or gauze sponges in the nasopharynx.
Analysis
Recovered fluid is centrifuged, and the sediment is stained and examined. A Wright-type (Giemsa) or Gram stain is preferred when looking for organisms (e.g., Cryptococcus spp.). If lavaged material appears to be an exudate, it can be cultured for fungi. Bacterial culture is rarely useful. Direct examination of lavage fluid may reveal adult or larval P. caninum.
Nasal Biopsy
Common Indications
Indications are the same as for nasal lavage. Nasal biopsy is performed to further characterize the nature of nasal disease present, with or without radiographic evidence of masses or bone lysis. The procedure may also be performed to obtain tissue for culture if indicated.
Advantage
Tissue can be obtained for histopathologic evaluation (and culture if indicated). Diseases other than neoplasia or fungal rhinitis that may be diagnosed by this method are (1) various idiopathic inflammatory diseases,8,14 and (2) primary ciliary dyskinesia (i.e., immotile cilia syndrome), although the latter requires electron microscopy to be definitive.
Disadvantages
The procedure often causes bleeding, which may be profuse. Although unlikely, penetration of the cribriform plate is possible if the endoscopist is not careful.
Procedure
If the animal’s coagulation status is questionable, a platelet count, mucosal bleeding time, activated clotting time, or prothrombin time (PT) and partial thromboplastin time (PTT) should be performed (see Chapter 5). Nasal biopsy is performed under general anesthesia with endotracheal intubation. The head should be positioned so that the nose points downward. The nasopharynx can be packed off as for nasal lavage. The biopsy instrument can be either small clamshell forceps for smaller patients or uterine or colonic biopsy forceps, or bone curettes, for larger patients. Direct biopsy of lesions may also be accomplished during rhinoscopy using biopsy forceps suitable for the scope. The distance from the naris to the medial canthus of the eye is marked on the biopsy forceps because this approximates the distance to the cribriform plate. The biopsy instrument is advanced with the jaws open slightly in advance of reaching the affected tissue; the jaws are then closed once the area of interest is penetrated, and the biopsy instrument with tissue is withdrawn. Caution: The biopsy instrument must not be advanced beyond the level of the medial canthus because of potential cribriform plate perforation.
Specimens are fixed in formalin (or other appropriate fixative if electron microscopy is desired) and submitted. A portion of the biopsy specimen can be submitted for fungal or bacterial culture if indicated (see Chapter 15). Impression smears can be made for cytologic examination, and the remaining tissue can be submitted for histopathologic evaluation. Bleeding from the naris after biopsy is expected but usually subsides within 30 minutes. Occasionally, bleeding is profuse, prolonged, or both, in which case the affected area can be packed with cotton-tipped applicator sticks dipped in dilute (1 : 10,000) epinephrine solution while the animal is maintained under anesthesia until bleeding stops. Alternatively, nasal tampons (Merocel Standard Nasal Dressing with drawstring; Medtronic Xomed, Jacksonville, FL) may be used. In extreme cases, ligation of the ipsilateral internal carotid artery can be life saving.

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