Torsemide can be used for long-term management of congestive heart failure in equids: a description of 12 cases (2019-2024).

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Tác giả: Marc S Kraus, Virginia B Reef, Kavita Shroff, Cristobal Navas de Solis, Darko Stefanovski

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Journal of the American Veterinary Medical Association , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 65261

 OBJECTIVE: Information about congestive heart failure (CHF) treatment in the horse is limited. Torsemide, an oral loop diuretic, is increasingly used in humans, dogs, and cats with CHF. Torsemide is well absorbed and induces diuresis in healthy horses, and its use in a horse with CHF has been reported. This retrospective descriptive study aimed to describe the use of torsemide in equids with CHF. ANIMALS: 12 equids (10 horses, 1 miniature donkey, and 1 mule). CLINICAL PRESENTATION: Horses presented to a referral practice with clinical signs of congestive heart failure. Diagnosis was confirmed with echocardiography. Treatment with torsemide as well as other cardiac medications was instituted. The cases were evaluated and monitored with physical examinations, clinicopathologic data, and repeat echocardiograms. RESULTS: Torsemide (PO, q 12 h [median 0.5 mg/kg
  IQR, 0.5 to 0.5 mg/kg
  range, 0.25 to 1 mg/kg]) was well tolerated in the 12 cases. There were improvements in heart rate and respiratory rate and increases in plasma creatinine concentration (median, 1.3 vs 1.9 mg/dL) that followed therapeutic interventions that included torsemide. Median survival time of equids with CHF treated with torsemide was 189 days (IQR, 10 to 348.25 days
  range, 2 to 806 days), with 2 distinct clusters. Four cases were euthanized within 2 weeks after starting treatment, while 8 survived longer than 137 days or are currently alive. CLINICAL RELEVANCE: Torsemide can be used in equids diagnosed with CHF without serious adverse events and has the potential to be a useful oral diuretic. The nature of the study does not allow us to conclude that torsemide had a causal relationship with clinical progression.
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