The Yellow Cat: Diagnostic & Therapeutic StrategiesCE Article
Craig B. Webb, PhD, DVM, Diplomate ACVIM (Small Animal Internal Medicine)
Colorado State University
There is no mystery when it comes to a “yellow” cat. Icterus and jaundice—both of which describe a yellowish pigmentation of the skin—indicate hyperbilirubinemia, a 5- to 10-fold elevation in serum bilirubin concentration.
However, this is where the certainty ends and the diagnostic challenge begins. The icteric cat presentation is not a sensitive or specific marker of disease, despite the visually obvious and impressive clinical sign (Figure 1).1
The objective of this article is to briefly review differentials for hyperbilirubinemia in the cat, and present a diagnostic and therapeutic strategy that will help practitioners approach this problem in an efficient and effective manner.
Hyperbilirubinemia results when serum bilirubin concentrations reach 2 to 3 mg/dL (35–50 mcmol/L).
HYPERBILIRUBINEMIA: ORGANIZATION BY LOCATION
The differentials for hyperbilirubinemia should be organized by location: prehepatic, hepatic, and posthepatic. While, in cats, it is common to find concurrent disease processes, starting from this foundation is the first step toward an effective and efficient diagnostic workup of icteric cats.
Hemolysis releases hemoglobin, which is then metabolized through biliverdin to bilirubin in the liver. Hepatocytes in the healthy feline liver have a large capacity for uptake, conjugation, and excretion of bilirubin.
Prehepatic icterus is most likely due to the combination of a large increase in bilirubin from hemolysis and a degree of intrahepatic cholestasis secondary to hypoxia.2 In dogs, the most common cause of prehepatic hyperbilirubinemia is immune-mediated hemolytic anemia (IMHA), but that condition appears to be quite rare in cats. The list of prehepatic causes of hyperbilirubinemia in cats is extensive (Table 1).
A significant decrease, or loss, of hepatocellular function effects bilirubin metabolism, and frequently results in intrahepatic cholestasis (Table 1). Unconjugated bilirubin from damaged hepatocytes is present, although the majority of bilirubin that appears in the cat’s circulation is conjugated, having completed the metabolic step prior to encountering the cholestatic overflow into the vasculature.2
Extrahepatic biliary disease interferes with the normal flow of bile and the final steps in bilirubin excretion, resulting in extrahepatic cholestasis (Table 1). As with intrahepatic disease, both unconjugated and conjugated bilirubin appear in the serum, rendering the biochemical distinction between conjugated and unconjugated serum bilirubin of minimal diagnostic importance.
COMMON CAUSES OF PREHEPATIC HYPERBILIRUBINEMIA
Infectious disease is a relatively common cause of prehepatic hemolysis in cats.
Mycoplasma species, particularly Mycoplasma haemofelis, can cause significant erythrocyte destruction, anemia, hyperbilirubinemia, and clinical disease. Outdoor, male, and/or shelter cats appear to be at increased risk, and coinfection with feline immunodeficiency virus (FIV) is common.3-5
Concurrent diseases, immunosuppression, and stress appear to impact the course and severity of disease and outcome of treatment. An eventual recurrence of disease is seen with some frequency in those cats that show a clinical response to treatment.
Feline leukemia virus (FeLV) infection can trigger a host immune response that results in immune-mediated prehepatic erythrocyte destruction. This may be the result of a virus-induced expression of antigens on the red blood cell (RBC) surface. Immune-mediated thrombocytopenia may accompany IMHA in cats with underlying FeLV infection.6
Cytauxzoon felis is transmitted by ticks (Amblyomma americanum) and appears to be increasing in prevalence and geographical distribution in the United States, expanding from the southeastern portion of the country. Risk for infection increases with increased exposure to the tick vector, and the progression of clinical disease is rapid and often fatal.
Babesia felis can cause severe prehepatic hemolysis and anemia in cats, but appears to be rare outside of costal South Africa.7
Immune-Mediated Hemolytic Anemia
Primary IMHA appears to be quite rare in cats. It is difficult to characterize feline IMHA or determine risk factors because of the paucity of cases in the literature, but younger male cats may be overrepresented. The prognosis is guarded, with a mortality rate of 25%.8
Inherited Erythrocyte Disorders
Erythrocyte pyruvate kinase (PK) deficiency is a very rare inherited disorder transmitted as an autosomal recessive trait, causing prehepatic hemolysis.
Cats usually present as young adults, and the severity of the anemia and clinical signs is variable and may change over time, ranging from asymptomatic to hemolytic crisis.
The disease is most frequently described in Abyssinian and Somali breeds but may also be present in a variety of other purebred and domestic shorthair cats.9 Interestingly, Abyssinian and Somali breeds have also been shown to suffer from another inherited cause of prehepatic hemolysis: increased erythrocyte osmotic fragility. Genetic testing has been developed for screening cats for PK deficiency and is commercially available (vgl.ucdavis.edu/services/pkdeficiency.php)
Other Causes of Hemolysis
Hemolysis secondary to hypophosphatemia has become rare due to heightened awareness, diligent monitoring, and proactive intervention during the treatment of diabetic ketoacidosis.
Disseminated intravascular coagulation is also a rare occurrence, seen predominantly in the critical care setting, but serving as a reminder that prehepatic hemolysis can occur as a secondary consequence in a variety of diseases.
Feline erythrocytes are susceptible to oxidative stress, and a large variety of toxins and drugs (including acetaminophen, benzocaine, methylene blue, phenazopyridine, onions/onion powder, propylene glycol, and propylthiouracil) can cause Heinz body anemia or hemolytic destruction of RBC membranes.
COMMON CAUSES OF HEPATIC HYPERBILIRUBINEMIA
Feline Hepatic Lipidosis
Hepatic lipidosis appears to be a unique feline phenomenon, highlighting that hepatic metabolism in the cat is different from many other species.10 Although feline hepatic lipidosis may be an idiopathic (Figure 2) and, therefore, primary problem, it quite frequently occurs secondary to another disease that caused the cat to stop eating.
In contrast to dogs—in which hepatic disease is usually located in the liver parenchyma—feline liver disease typically targets the biliary system, and is most commonly seen as cholangitis. The World Small Animal Veterinary Association Liver Standardization Group clarified the terminology, defining feline cholangitis as neutrophilic (acute or chronic), lymphocytic, or secondary to liver flukes.11
COMMON CAUSES OF POSTHEPATIC HYPERBILIRUBINEMIA
Extrahepatic Bile Duct Obstruction
Cholelithiasis may be obstructive and is, thus, approached as a cause of extrahepatic bile duct obstruction (EHBO). Other causes of EHBO include tumors, nonneoplastic masses, cholecystitis, inspissated bile, cholangitis, and pancreatitis. The prognosis, even following successful surgery, is guarded.
Feline Triaditis Syndrome
Feline triaditis describes the concurrent conditions of cholangitis, pancreatitis, and inflammatory bowel disease in cats.
There is a common outflow track for the feline pancreas and bile duct as they approach the major duodenal papilla. This anatomic association makes it likely that inflammatory disease or infection in one of these tissues impacts the health and function of the associated tissues.
At this time it is unclear if the underlying etiology of triaditis is immune-mediated process, infectious, or multifactorial, making treatment decisions difficult. Significant local inflammation may create a functional EHBO that is not amenable to surgical removal, but must be addressed medically.
Feline liver fluke infection is geographical and found in tropical environments, such as Florida, the Caribbean, and Hawaii, where land snails, lizards, and toads are the hosts. Infection is usually subclinical, although cats may present with nonspecific signs (Table 1).
DIAGNOSTIC APPROACH TO AN ICTERIC CAT
As with any diagnostic approach, the clinical evaluation of an icteric cat begins with signalment, history, and physical examination.
The list of differentials for hyperbilirubinemia (Table 1) include breed-specific entries (eg, Abyssinian) and diseases that occur in certain age groups (eg, feline infectious peritonitis [FIP]). For many differentials the patient history is similar.
History & Clinical Signs
Anorexia is a key component in the presentation of cats with hepatic lipidosis and appears to be an early clinical manifestation of anemia in cats. Lethargy can be difficult to appreciate in sedentary cats, and sick cats often hide, further delaying the owner’s observation of more obvious clinical signs.
Dog owners may notice changes in the color of urine or feces, but it is much less likely for cat owners to report pigmenturia or acholic feces in this fastidious species. It is also relatively unusual for cats to have dietary indiscretion of toxins, household products, medications, or human food, but certainly the potential for exposure should be investigated during the anamnesis.
The prevalence of multi-cat households also confounds the owner’s ability to appreciate changes in appetite, water consumption, or elimination habits.
A complete physical examination, including body temperature, pulse, respiratory rate, fundic examination, cardiovascular auscultation, and abdominal palpation, is essential. Physical findings may indicate potential underlying etiologies, such as hepatomegaly with hepatic lipidosis, cranial abdominal discomfort with pancreatitis, and tachycardia with anemia.
The physical examination is often dominated by the color of the cat. Icterus is best appreciated as a discoloration of the mucous membranes, the sclera (Figure 3), and/or the inner aspect of the pinnae (Figure 4). The intensity and actual color may be influenced by the normal tissue color, degree of anemia, and perfusion.
The clinical condition and color of the cat are influenced by both the degree of anemia—mild to severe—and the time course of RBC destruction—acute or chronic.
Changes on the serum biochemical profile are nonspecific. The degree of elevation in total bilirubin is cited as a nonspecific but generally guides to the most likely location or etiology of the problem:
- 3 to 6 mg/dL is associated with prehepatic hemolysis, FIP, pancreatitis, and sepsis
- Greater than 12 mg/dL is associated with hepatic lipidosis and EHBO.
PREHEPATIC HYPERBILIRUBINEMIA DIAGNOSTICS
The laboratory diagnostic workup for the vast majority of icteric cats starts with determining whether prehepatic hemolysis is present.
Complete Blood Count
Hemolysis can often be an extravascular antibody-mediated process in which the serum turns icteric. A simple hematocrit tube can be expected to identify a significant degree of anemia and a relatively normal serum total protein. Less frequently, the hemolysis occurs within the vasculature itself, in which case the serum may appear pink, while both the plasma (hemoglobinemia) and urine (hemoglobinuria) appear red.
A complete blood count (CBC) more accurately and completely characterizes the anemia as regenerative or nonregenerative; however, the regenerative process may take up to 5 days to manifest as an appropriate increase in the absolute reticulocyte count (> 40,000–60,000/mcL, depending on the laboratory). A CBC also identifies other potentially important erythrocyte characteristics.
The degree of anemia is cited as a nonspecific but general indictor of the likelihood that feline icterus is the result of prehepatic hemolysis. As a rule of thumb, prehepatic hemolysis usually results in a packed cell volume (PCV) of less than 13% to 20%; however, the cat’s baseline or normal PCV, hydration status, and the time frame over which the hemolysis occurred may all impact the clinical signs, measured PCV, and elevation in total bilirubin.
Careful examination of the blood smear is a critical step in any attempt to identify infectious organisms or indicators of immune-mediated agglutination.
Infectious disease testing is commonly used for prehepatic hyperbilirubinemia (Table 2).
In addition to hyperbilirubinemia, cats with mycoplasmosis are frequently hyperglobulinemic as a result of chronic immune stimulation, and they may have mild to moderate elevations in liver enzyme activity as a result of anemic—hypoxia-induced hepatocyte necrosis.
Feline Leukemia Virus
There are a variety of technologies available to easily test for the FeLV p27 antigen, which is present in the majority of infected cats.
Biochemical changes with Cytauxzoon felis are nonspecific, while anemia, pancytopenia, and thrombocytopenia may be seen on the CBC.
Diagnosing IMHA using persistent RBC agglutination, a positive Coombs’ test, RBC characteristics, and reticulocytosis can be challenging in cats; other potential causes of prehepatic hemolysis must be carefully considered.
Agglutination can be difficult to distinguish from normal rouleaux formation in the cat, but true RBC autoagglutination can be identified by mixing one drop of potassium ethylenediaminetetraacetic acid (K-EDTA) whole blood with 1 to 4 drops of 0.9% sodium chloride on a microscope slide. Macroscopic slide erythrocyte agglutination is seen in all IMHA cats, although it rarely persists following RBC washing.
Biochemical abnormalities are varied and inconsistent, although the majority of cats have a positive direct Coombs’ test, further supporting the diagnosis of IMHA. However, Coombs’ testing should be interpreted with caution and related to other clinical and hematologic findings.12
Inherited Erythrocyte Disorders
Biochemical and CBC parameters of cats with erythrocyte PK deficiency are nonspecific and inconsistent among patients, although hyperglobulinemia was frequently seen. Genetic testing and responsible breeding are clearly important considerations.
HEPATIC HYPERBILIRUBINEMIA DIAGNOSTICS
Hepatic hyperbilirubinemia is caused by significant primary hepatic disease. A minimum diagnostic database includes a CBC, serum biochemical profile, urinalysis, and FeLV/FIV status.
Once the cat is icteric, and prehepatic causes have been ruled out, the serum bilirubin is elevated to the point where a bile acids test for liver function is redundant; the results will be abnormal. With mild hyperbilirubinemia (< 2 mg/dL), a bile acids test may be warranted to assess liver function.
Ultrasonographic imaging of the entire abdomen by a board-certified specialist is an essential step in the assessment of the feline hepatobiliary system. Ultrasound is a powerful tool for assessing the liver parenchyma, visualizing the biliary system, and searching for EHBO.
Fine Needle Aspiration
Ultrasound-guided fine needle aspiration (FNA) is also a minimally invasive technique for acquiring samples of certain tissue, such as the liver, pancreas, and lymph nodes, and masses for cytology and culture. Coagulation parameters and clotting times should be determined prior to FNA.
In cats that present with hepatic lipidosis, it is critical to put diagnostic effort into identifying the disease that led to the cat’s anorexia in the first place, whether that is as simple as dental disease or as complex as feline pancreatitis. Failure to identify and address the concurrent condition is very likely to result in the cat being presented to the hospital again with the same complaint.
The diagnostic effort of feline cholangitis is directed toward identification of the predominant inflammatory cell type present in the cat’s hepatobiliary system: acute neutrophilic, chronic neutrophilic, or lymphocytic.
FNA of the liver is a relatively simple procedure that may produce a cytologic sample suggestive of cholangitis, but this technique has significant limitations. It may be of low yield, resulting in a nondiagnostic sample, the nonspecific report of hepatocellular vacuolization, or an interpretation that would be different than that obtained by histopathology.13
Technically more challenging techniques, best performed by board-certified specialists with ample experience, are ultrasound-guided cholecystocentesis and laparoscopy-assisted gallbladder aspiration. For both procedures, samples are collected for cytology and culture, since bile has been shown to be the sample most likely to yield an informative bacterial culture result.14,15
Liver biopsy is required for a definitive diagnosis of hepatic disease.1
The most common infectious organisms found in patients with neutrophilic cholangitis are enteric bacteria (eg, E coli, Enterobacter, Clostridia) and antibiotics for treatment should be selected based on sensitivity.
POSTHEPATIC HYPERBILIRUBINEMIA DIAGNOSTICS
Extrahepatic Bile Duct Obstruction
Abdominal ultrasound of cats with EHBO frequently identifies distension of the gallbladder, common bile duct, and intrahepatic ducts (Figure 5).
Diagnosis of triaditis is based on identification of disease in each of the 3 tissues involved; the gold standard for diagnosis is histopathology. Less invasive diagnostics include the feline pancreatic lipase immunoreactivity (fPLI) blood test, abdominal ultrasound, liver FNA, cholecystocentesis, cytology, culture and sensitivity, and small intestinal endoscopic biopsy; however, these patients may have increased anesthetic risks.
Although not widely available in private practice, feline abdominal laparoscopy can be performed with equipment sized for pediatrics and allows the collection of tissue for histopathology (liver and pancreas) as well as direct aspiration of the gallbladder (Figure 6).
Liver fluke eggs can sometimes be found in the feces or by bile cytology. A recent study assessing the use of percutaneous ultrasound-guided cholecystocentesis in cats known to be infected with Platynosomum species flukes found the technique to be technically feasible and safe in cats with cholangitis.17
Detailed treatment protocols for specific differentials are beyond the scope of this article. However, some selected therapies are described.
Hydration status, pain (buprenorphine, 0.01 mg/kg sublingual Q 8 H), and vomiting (maropitant, 1 mg/kg SC Q 24 H) can all be addressed in a relatively effective manner and can significantly impact the clinical outcome.
Ursodeoxycholic acid (5−15 mg/kg Q 24 H) is an adjunct therapy that has been used in the successful treatment of bilirubin cholelithiasis, EHBO, and a Somali cat with PK deficiency, but it should not be used in place of antibiotics or prednisolone for lymphocytic cholangitis and neutrophilic cholangitis, respectively.18
Adjunct therapy may include S-adenosyl-methionine (90 mg/cat Q 24 H), silimarin (2−5 mg/kg Q 24 H), and/or vitamin E (50 IU Q 24 H); however, there may be a limit to the number of medications an owner can administer to a cat.
Selected Prehepatic Hyperbilirubinemia Treatment Options
Immune-Mediated Hemolytic Anemia
In addition to supportive care, including blood products, cats with IMHA appeared to respond to prednisolone therapy, although additional immunosuppressive drugs have also been used.
Anecdotal and case reports discuss the addition of cyclosporine (5 mg/kg Q 24 H), chlorambucil (2 mg/cat every 3 days), and mycophenolate mofetil (10 mg/kg Q 12 H) to treatment protocols, especially if prednisolone fails to improve the cat’s anemia.19,20
Feline Leukemia Virus
Although immunosuppression in FeLV positive cats is best avoided, in those patients with clear evidence of IMHA secondary to FeLV infection, blood transfusions are indicated and, if those fail, prednisolone (2.2 mg/kg Q 12 H) may be used as with primary IMHA patients.8,21
Erythrocyte PK Deficiency
Therapy for erythrocyte PK deficiency is supportive and nonspecific, and outcome depends, in large part, on the severity of presentation and use of transfusions to stabilize critical patients.
Selected Hepatic Hyperbilirubinemia Treatment Options
Treatment of hepatic causes of hyperbilirubinemia is best guided by histopathology, when possible, or cytology and culture.
The foundation of treatment for hepatic lipidosis is relatively simple: provide nutrition to the cat. The logistics may be challenging but the advent of esophagostomy tubes (E-tube) makes both nutrition and medication administration easier (Figure 7). Nutrition is critical; therefore, placement of an E-tube should be encouraged early in the disease process if the cat is anorectic.
Vitamin K1 (1 mg SC Q 12 H) should be administered prior to E-tube placement if evidence of a coagulopathy is present.
Degenerative neutrophils with pleomorphic bacteria from the bile of an acutely ill cat is consistent with acute neutrophilic cholangitis (Figure 8), and treatment is initiated with 2 months of antibiotics aimed at enteric bacteria: cephalosporins, amoxicillin and clavulanic acid (62.5 mg/cat Q 12 H), enrofloxacin (5 mg/kg Q 24 H), and metronidazole (7.5 mg/kg Q 12 H).
A mixed population of inflammatory cells or cytology dominated by lymphocytes in a cat presenting with a more chronic history of illness, or failure of initial antibiotic therapy, is consistent with chronic neutrophilic cholangitis or lymphocytic cholangitis, and prednisolone (2 mg/kg Q 24 H initially; taper to 0.5−1 mg/kg Q 48 H) is the foundation of treatment.22
Lymphocytic cholangitis is believed to be immune-mediated, and treatment includes prednisolone with or without a period of concurrent antibiotics, although other immunosuppressive medications, such as cyclosporine, have been used in these patients.
Selected Posthepatic Hyperbilirubinemia Treatment Options
Extrahepatic Biliary Obstruction
Posthepatic causes, such as EHBO, often require surgical intervention—laparotomy may be the only viable therapeutic option—and carry a poor prognosis. Nonsurgical causes, such as pancreatitis and cholangitis, are medically managed and the prognosis is impacted by the severity of disease, response to treatment, and owner commitment.
The effective treatment of triaditis is complicated, but is initiated with supportive care targeting hydration, perfusion, electrolyte and acid–base balance, pain, and vomiting; then targets the aspect of the disease constellation that appears to be having the greatest impact on the patient.
Antibiotics are administered in patients in which there is the potential for sepsis, gastrointestinal translocation, positive bacterial cultures, or a left shift with band neutrophils on the CBC.
Corticosteroids are usually avoided in the face of a positively identified bacterial component, although a single anti-inflammatory dose of glucocorticoid may be used to counter the inflammatory mediators. Without strong evidence of a bacterial infection, corticosteroids are often used to treat each separate component of feline triaditis: inflammatory bowel disease, pancreatitis, and lymphocytic-plasmacytic cholangitis.
Nutritional support in the form of E-tube placement is often implemented.
Medical treatment for liver fluke infection may be attempted with praziquantel (20−30 mg/kg Q 24 H for 3 days), but rare, severe cases may require surgery to remove a posthepatic biliary obstruction as identified with abdominal ultrasound.
A thoughtful approach to hyperbilirubinemia, starting with localization of the disease and including the calculated consideration of differentials unique to that location, greatly enhances the efficient and effective diagnosis and treatment of the “yellow cat.” Organizing the effort in terms of pre-hepatic, hepatic, and post-hepatic conditions is a logical and time-tested approach that has been successfully applied to many icteric cats.
CBC = complete blood count; EBHO = extrahepatic biliary obstruction; E-tube = esophagostomy tube; FeLV = feline leukemia virus; FIP = feline infectious peritonitis; FIV = feline immunodeficiency virus; FNA = fine needle aspiration; IMHA = immune-mediated hemolytic anemia; PCV = packed cell volume; PK = pyruvate kinase; RBC = red blood cell
- Sherding RG. Feline jaundice. J Fel Med Surg 2000; 2(3):165-169.
- Sherding RG. Icterus. In Washabau RJ, Day MJ (eds): Canine and Feline Gastroenterology. St. Louis: Elsevier, 2013, pp 140-147.
- Jenkins KS, Dittmer KE, Marschall JC, et al. Prevalence and risk factor analysis of feline haemoplasma infection in New Zealand domestic cats using a real-time PCR assay. J Feline Med Surg 2013; 15:1063-1069.
- Duarte A, Marques V, Correia JH, et al. Molecular detection of haemotropic Mycoplasma species in urban and rural cats from Portugal. J Feline Med Surg 2015;17:516-522.
- Walker VR, Morera GF, Gómez JM, et al. Prevalence, risk factor analysis, and hematological findings of hemoplasma infection in domestic cats from Valdivia, Southern Chile. Comp Immunol Microbiol Infect Dis 2016; 46:20-26.
- Hartmann K. Clinical aspects of feline retroviruses: A review. Viruses 2012; 4:2684-2710.
- Hartmann K, Addie D, Belák S, et al. Babesiosis in cats: ABCD guidelines on prevention and management. J Feline Med Surg 2013; 15(7):643-646.
- Kohn B, Weingart C, Eckmann V, et al. Primary immune-mediated hemolytic anemia in 19 cats: Diagnosis, therapy, and outcome (1998-2004). J Vet Intern Med 2006; 20(1):159-166.
- Grahn RA, Grahn JC, Penedo MC, et al. Erythrocyte pyruvate kinase deficiency mutation identified in multiple breeds of domestic cats. BMC Vet Res 2012; 8:207-217.
- Verbrugghe A, Bakovic M. Peculiarities of one-carbon metabolism in the strict carnivorous cat and the role in feline hepatic lipidosis. Nutrients 2013; 5:2811-2835.
- Van den Ingh TS, Van Winkle T, Cullen JM, et al. Morphological classification of parenchymal disorders of the canine and feline liver: 2. Hepatocellular death, hepatitis and cirrhosis. In Rothuizen J, Bunch SE, Charles JE, et al: WSAVA Standards for Clinical and Histological Diagnosis of Canine and Feline Liver Diseases. Philadelphia: Elsevier, 2006, pp 85-101.
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- Wang KY, Panciera DL, Al Rukivat RK, et al. Accuracy of ultrasound-guided fine-needle aspiration of the liver and cytologic findings in dogs and cats: 97 cases (1990-2000). JAVMA 2004; 224(1):75-78.
- Wagner KA, Hartmann FA, Trepanier LA. Bacterial culture results from liver, gallbladder, or bile in 248 dogs and cats evaluated for hepatobiliary disease: 1998-2003. J Vet Intern Med 2007; 21:417-424.
- Peters LM, Glanemann B, Garden OA, et al. Cytological findings of 140 bile samples from dogs and cats and associated clinical pathological data. J Vet Intern Med 2016; 30:123-131.
- Rothuizen J, Twedt DC. Liver biopsy techniques. Vet Clin North Am Sm Anim Pract 2009; 39:469-480.8.
- Koster L, Shell L, Illanes O, et al. Percutaneous ultrasound-guided cholecystocentesis and bile analysis for detection of Platynosomum spp.-induced cholangitis in cats. J Vet Intern Med 2016; 30(3):787-793.
- Harvey AM, Holt PE, Barr FJ, et al. Treatment and long-term follow-up of extrahepatic biliary obstruction with bilirubin cholelithiasis in a Somali cat with pyruvate kinase deficiency. J Feline Med Surg 2007; 9(5):424-431.
- Black V, Adamantos S, Barfield D, et al. Feline non-regenerative immune-mediated anaemia: Features and outcome in 15 cases. J Feline Med Surg 2015; 26:1-6.
- Bacek LM, Macintire DK. Treatment of primary immune-mediated hemolytic anemia with mycophenolate mofetil in two cats. J Vet Emerg Crit Care 2011; 21:45-49.
- Hartmann K. Feline leukemia virus infection. In Greene CE. Infectious Diseases of the Dog and Cat, 3rd ed. Philadelphia: Saunders Elsevier, 2006, p 124.
- Otte CM, Penning LC, Rothuizen J, Favier RP. Retrospective comparison of prednisolone and ursodeoxycholic acid for the treatment of feline lymphocytic cholangitis. Vet J 2013; 195(2):205-209.
- Weingart C, Tasker S, Kohn B. Infection with haemoplasma species in 22 cats with anaemia. J Feline Med Surg 2016; 18(2):129-136.
- Sherrill MK, Cohn LA. Cytauxzoonosis: Diagnosis and treatment of an emerging disease. J Feline Med Surg 2015; 17(11):940-948.
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CE Test. The Yellow Cat: Diagnostic & Therapeutic Strategies
This article is RACE-approved for 1 hour of continuing education credit. To receive credit, take the approved test online at vetmedteam.com/tvp.aspx (CE fee of $5/article).
After reading this article clinicians should be able to differentiate the disease processes in cats with hyperbilirubinemia, formulate an efficient diagnostic path, and prepare an effective treatment protocol for these patients.
This article provides an overview of the differentials for feline hyperbilirubinemia, a diagnostic plan for identifying the underlying etiology of the condition, and a number of therapeutic options for these patients.
Questions online may differ from those here; answers are available once CE test is taken at vetmedteam.com/tvp.aspx. Tests are valid for 2 years from date of approval.
- True/False: Icterus is a sensitive marker of the cause of hyperbilirubinemia in cats.
- Locating the source of hyperbilirubinemia is an important diagnostic step. Which of the following is not normally a component of this localizing step?
- Which of the following is the first and most cost-effective step toward the diagnosis of prehepatic hemolysis?
- Hematocrit tube (PCV/TP)
- Complete blood count
- Serum biochemical profile
- Coombs’ test
- Which of the following is not considered a cause of hemolytic anemia in cats?
- Cytauxzoon felis
- Mycoplasma hemofelis
- Which of the following is the single most important component of the treatment plan for idiopathic hepatic lipidosis?
- Vitamin E
- Which of the following is not one of the WSAVA classifications of feline cholangitis?
- Acute neutrophilic
- Chronic neutrophilic
- Acute eosinophilic
- Cytology can be used to guide treatment in cases of feline cholangitis. If ultrasound-guided FNA of the liver revealed degenerative neutrophils with intracellular bacteria, the foundation of treatment would be which of the following?
- Amoxicillin and clavulanic acid
- Ursodeoxycholic acid
- Which of the following is not considered a component of feline triaditis?
- Which of the following is the treatment of choice in a cat in which biliary choleliths are causing an extrahepatic biliary obstruction?
- Ursodeoxycholic acid
- Placement of an esophagostomy feeding tube allows the owner to administer which of the following to an icteric cat at home?
- All of the aboves