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314  Section 4  Respiratory Disease

            Table 32.1  Recognized risk factors for PTE disease processes with a known association with thromboembolic disease in the dog. Those
  VetBooks.ir  included
            conditions also associated with an increased risk in the cat are marked by an asterisk. Proposed mechanisms for these risk factors are

                                               Hypercoagulable        Vascular flow            Endothelial injury/
             Disease process risk factor       state                  abnormalities/stasis     dysfunction
             *Corticosteroid administration    ✓
             Diabetes mellitus                 ✓
             Dirofilariasis                    ✓                                               ✓
             *DIC (secondary to other disease)  ✓
             Endocarditis                      ✓                                               ✓
             (tricuspid/pulmonic)
             *Feline infectious peritonitis    ✓                                               ✓
             Hyperadrenocorticism              ✓
             Hypothyroidism                    ✓
             *IMHA                             ✓                                               ?
             *Indwelling venous catheters                             ✓                        ✓
             Myocardial disease                ✓                      ✓                        ✓
             *Neoplasia                        ✓                      ✓
             *Pancreatitis                     ✓                                               ✓
             *Protein‐losing enteropathy       ✓
             *Renal amyloidosis/PLN            ✓
             *Sepsis                           ✓                                               ✓
             *Surgery/trauma                   ✓                      ✓                        ✓
            Source: Adapted from Goggs et al. [1].
            DIC, disseminated intravascular coagulation; IMHA, immune‐mediated hemolytic anemia; PLN, protein‐losing nephropathy.



              Clinical Signs                                  may be clinical signs attributable to the predisposing
                                                              intercurrent disease.
            The clinical signs of PTE are variable, inconsistent, and   Clinicians should suspect PTE in patients with no
            nonspecific. The degree of physiologic impairment and   history of cardiopulmonary disease who develop res­
            thus the severity of clinical signs reflect both the mag­  piratory distress acutely, particularly where known risk
            nitude of the PTE and the patient’s ability to compen­  factors exist.
            sate. The most common signs are dyspnea, tachypnea,
            and depression. Other signs include coughing, hemop­    Diagnosis
            tysis, cyanosis, syncope, collapse, and sudden death. In
            dyspneic patients, physical examination may reveal   Suggested Diagnostic Approach
            harsh lung sounds and crackles suggestive of pulmo­
            nary edema. Occasionally, lung and heart sounds may   Pulmonary thromboembolism is commonly  suspected
            be muffled due to pleural effusion or in very rare cases   but infrequently conclusively diagnosed, probably
            pneumothorax. In eupneic patients, lung field ausculta­  because of variability in clinical signs, low test specific­
            tion will likely be normal. On cardiac auscultation,   ity,  and limited availability of definitive diagnostics.
            tachycardia with a split second heart sound may be   Establishing a clear diagnosis of PTE remains a challenge
            noted or, more commonly, a loud second heart      in veterinary medicine, even with a logical approach. In
            sound associated with pulmonary hypertension. Signs   human medicine, where definitive diagnostics are widely
            compatible with backward heart failure (jugular disten­  available, the major challenge is to identify which patients
            sion or pulsation, ascites) or forward heart failure (poor   to prioritize for definitive imaging studies. This need has
            peripheral pulse quality, pallor, prolonged capillary   driven the development of clinical prediction rules and
            refill time) may be present. Complicating the picture   diagnostic algorithms.
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