Key result
GS-441524 combined with cardiac therapy resolves feline infectious peritonitis-induced transient myocardial thickening.
Why the study?
Transient myocardial thickening associated with feline infectious peritonitis is extremely rare, with clinical signs overlapping with congestive heart failure.
Does GS-441524 combined with cardiac therapy improve transient myocardial thickening and congestive heart failure in a cat with feline infectious peritonitis?
Case Report (n=1)
No
Does GS-441524 combined with cardiac therapy improve transient myocardial thickening and congestive heart failure in a cat with feline infectious peritonitis?
This case demonstrates that specific antiviral treatment with GS-441524, alongside standard cardiac care, can lead to complete and sustained resolution of transient myocardial thickening and congestive heart failure secondary to feline infectious peritonitis.
Answers are grounded in this paper and cite their sources.
May warrant antiviral consideration in FIP with myocardial thickening; leaves open confirmation in controlled feline studies.
This case report provides a thorough description of the clinical assessment and management of an extremely rare case of transient myocardial thickening associated with feline infectious peritonitis (FIP) and highlights the overlap of clinical signs secondary to FIP or congestive heart failure. An 11-year-old male Norwegian cat was presented with a 3-week history of weakness, dysorexia, tachypnea, dyspnea, and weight loss. Thoracic point-of-care ultrasound (POCUS) revealed severe bilateral pleural effusion without cardiac chamber enlargement. Blood work including serum protein electrophoresis (demonstrating polyclonal gammopathy) was suggestive of FIP. Analyses of pleural effusion consisted of real-time PCR being positive for FCoV nucleic acids with a high viral load and slightly equivocal increased NT-proBNP. Together with the noncardiogenic nature of the effusion, these findings were consistent with a diagnosis of FIP. Three days after the presentation, the cat exhibited progressive dyspnea secondary to newly collected pleural effusion with markedly increased NT-proBNP. At that time, echocardiography revealed left ventricular wall thickening and left atrial enlargement, thus suggesting hypertrophic cardiomyopathy or myocarditis with left-sided congestive heart failure. Cardiac troponin I concentration was increased. Nine days after admission, the patient was discharged on cardiac therapy and nucleoside analog GS-441524. Fifteen days after initiation of GS treatment, echocardiography showed a decrease in left ventricular wall thickness. No long-term complications or recurrences of FIP or myocardial hypertrophy were observed at the 1.5-, 4-, and 18-month follow-ups, with normalization of cardiac troponin I concentration and echocardiographic variables, thus supporting the hypothesis of FIP-related transient myocardial thickening. To the authors' knowledge, this is one of the rare reports of transient myocardial thickening in the FIP setting, following GS-441524 treatment. Cardiac POCUS and NT-proBNP dosage in pleural effusion should systematically be performed in order to unmask congestive heart failure.
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Dhunputh et al. (2026) conducted a case report in Feline infectious peritonitis (FIP) and transient myocardial thickening (n=1). GS-441524 and cardiac therapy was evaluated on Resolution of clinical signs, myocardial hypertrophy, and normalization of cardiac biomarkers. Treatment with GS-441524 and cardiac therapy resolved feline infectious peritonitis and transient myocardial thickening in an 11-year-old cat, with normal echocardiogram at 18-month follow-up.
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