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May 17, 2026Journal of Veterinary Internal Medicine1 citationsOpen Access

Descriptive assessment of cardiac changes in cats with feline infectious peritonitis

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PČPetra ČernáEREvan RossLVLance Visser

Key Result

Feline infectious peritonitis in cats was associated with left ventricular wall thickening in up to 55% of cases and elevated cardiac troponin I, which normalized after 12 weeks of antiviral therapy.

Key Points

  • To prospectively document the cardiac changes in cats with feline infectious peritonitis (FIP) using echocardiography and cardiac troponin I levels.
  • Twenty cats with FIP underwent echocardiographic examinations and cTnI testing.
  • Concurrent infections associated with myocarditis were tested using serum samples.
  • Serum cTnI concentrations were reassessed after 12 weeks of antiviral treatment.
  • 55% of cats showed thickening of the left ventricular posterior wall.
  • 40% exhibited pleural effusion and 25% had pericardial effusion.
  • cTnI normalized to < 0.20 ng/mL in all 6 cats after treatment.

Study Design

Type

Observational (n=20)

Structured PICO

Do cats with feline infectious peritonitis exhibit echocardiographic and biomarker evidence of myocardial injury?

P
Population
20 cats with naturally occurring feline infectious peritonitis (FIP) without previous history of heart disease.
I
Intervention
Antiviral drugs for 12 weeks
O
Outcome
Frequency of cardiac changes using echocardiography and cardiac troponin I (cTnI) concentrationssurrogate

Cats with feline infectious peritonitis frequently exhibit increased cardiac troponin I and ventricular wall thickening, suggesting myocarditis or myocardial injury that may resolve with antiviral treatment.

Abstract

Abstract Background Myocarditis and myocardial injury associated with feline infectious peritonitis (FIP) recently are being recognized. Hypothesis/Objectives Prospectively document the frequency of cardiac changes in cats with FIP using echocardiography and cardiac troponin I (cTnI) concentrations. Animals Twenty cats with naturally occurring FIP without previous history of heart disease. Methods Cats diagnosed with FIP were tested for common concurrent infections associated with myocarditis by testing serum for feline immunodeficiency virus (FIV) antibodies, feline leukemia virus antigen (FeLV), Dirofilaria immitis antigen, Bartonella spp. immunoglobulin G (IgG), and Toxoplasma gondii IgG and immunoglobulin M (IgM) as well as by testing blood for nucleic acids of Bartonella spp. and coronavirus (SARS-COV-2). Each cat also was tested for serum cTn1 concentration and underwent an echocardiographic examination. After 12 weeks of treatment with antiviral drugs, serum cTnI concentrations were reassessed. Results All echocardiographic measurements were normalized to patient body weight. The left ventricular posterior wall from right parasternal long axis and short axis was thickened in 55% (11/20) and 25% (5/20) of cats, respectively. Pleural effusion was present in 40% (8/20) of cats and pericardial effusion in 25% (5/20) of cats, but a cardiac cause was not identified for these effusions. Median cTnI at initial evaluation was 0.37 ng/ml (interquartile range IQR, 0.20-0.83; upper reference interval, 0.20 ng/ml). Repeat cTnI was performed after 12 weeks of antiviral treatment in 6 cats that initially had increased cTnI (median initial cTnI, 0.75 ng/mL) and, in all 6 cats, cTnI normalized to 0.20 ng/mL. Conclusions and clinical importance Cats with FIP can present with increases in cTnI and ventricular wall thickening, findings suggestive of myocarditis or myocardial injury.

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Cite This Study

Černá et al. (2026) conducted an observational in Feline infectious peritonitis (FIP) (n=20). Antiviral drugs was evaluated on Frequency of cardiac changes (echocardiography and cTnI concentrations). Feline infectious peritonitis in cats was associated with left ventricular wall thickening in up to 55% of cases and elevated cardiac troponin I, which normalized after 12 weeks of antiviral therapy.

synapsesocial.com/papers/6a095bdd7880e6d24efe1c49https://doi.org/10.1093/jvimsj/aalag083
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