Peer-reviewed veterinary case report
Clot-busting drug TPA used to treat sudden aortic blood clots in cats
By Guillaumin, Julien et al.·Published in Journal of feline medicine and surgery·2019·1 Department of Clinical Sciences, United States·View original on PubMed →
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Original publication title: Thrombolysis with tissue plasminogen activator (TPA) in feline acute aortic thromboembolism: a retrospective study of 16 cases.
- Species:
- cat
Plain-English summary
A 5-year-old male domestic shorthair cat was brought in for sudden weakness in both back legs, a sign of a serious condition called feline aortic thromboembolism (FATE). The cat was treated with a medication called tissue plasminogen activator (TPA), which helps dissolve blood clots, and also received pain relief and other supportive treatments. While the cat experienced some complications, like kidney issues and injury from blood flow restoration, the overall survival rate and improvement in condition were similar to cats treated with standard care. Ultimately, 44% of the cats treated with TPA were discharged, showing that this treatment can be a viable option for FATE.
People also search for: cat sudden weakness back legs · feline aortic thromboembolism treatment · TPA for cats blood clots
Abstract
OBJECTIVES: Thrombolytic therapy is a treatment of choice for people with acute ischemic events, but is uncommonly administered for feline aortic thromboembolism (FATE). This study reports selected clinical data and outcomes of acute FATE treated with tissue plasminogen activator (TPA). A reference group treated with current standard of care (SOC) was analyzed for comparison. METHODS: This was a retrospective study of FATE in two academic hospitals. TPA-treated cats with two or more limbs (n = 16) affected were compared with a SOC-treated group with two or more limbs affected (n = 38). A limb score based on motor function and pulse quality was calculated for each group. RESULTS: Limb score and proportion of congestive heart failure at admission was similar in both groups. Time from FATE to admission was shorter in the TPA group, with a median of 3 h (range 0-6 h) vs 6 h (range 0-48 h; P = 0.0004). The most common regimen received for TPA was 1 mg/kg over 1 h. Other treatments were similar to those of the SOC group and included analgesia, thromboprophylaxis and furosemide. Documented complications for TPA-treated cats included reperfusion injury (5/10) and acute kidney injury (AKI; 3/10). Discharge proportion rate was 44% (TPA) vs 29% (SOC; P = 0.351). There were no differences in short-term survival rate (56.2% vs 39.5%; P = 0.369), clinical improvement (56.2% vs 31%; P = 0.122), rates of reperfusion injury (50% vs 50%; P = 1.00) or AKI (30% vs 27%; P = 1.00) between the TPA-treated and SOC groups, respectively. CONCLUSIONS AND RELEVANCE: Survival and complication rates of TPA-treated cats and SOC-treated cats for acute FATE were similar.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/29807505/