Department of Clinical Sciences, Kansas State University College of Veterinary Medicine, Manhattan, Kansas, USA.
Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
J Vet Intern Med. 2021 Jan;35(1):456-461. doi: 10.1111/jvim.15991. Epub 2020 Dec 6.
To characterize urinary isolates, the Clinical and Laboratory Standards Institute (CLSI) uses an amoxicillin breakpoint for cats based on plasma (not urine) drug concentrations (≤0.25 μg/mL), but a urine-specific breakpoint for dogs exists (≤8 μg/mL).
To measure urine concentrations of amoxicillin and clavulanate after PO administration of amoxicillin-clavulanate to cats, and to suggest updated urine-specific susceptibility breakpoints for PO amoxicillin and amoxicillin-clavulanate in cats.
Eleven healthy purpose-bred cats.
Cats were given 3 62.5 mg doses of amoxicillin-clavulanate PO q12h. After the third dose, urine was collected over 28 hours, recording urination time and volume. At least 3 urine samples were collected per cat. Liquid chromatography with mass spectrometry was used to determine the urine concentrations of amoxicillin and clavulanate.
Amoxicillin concentrations were >8 μg/mL in all urine samples collected within 12 hours after administration (range, 31.6-1351 μg/mL), with means of 929 μg/mL (0-6 hours) and 532 μg/mL (6-12 hours). The mean half-life of amoxicillin in urine was 1.99 hours, and mean recovery was 30%. Clavulanate was detected in all urine samples, with mean half-life of 2.17 hours.
Orally administered amoxicillin-clavulanate resulted in urine amoxicillin concentrations above the cutoff (8 μg/mL) for wild-type Escherichia coli in all cats. Because urine-specific susceptibility testing breakpoints can be determined using urine concentrations, this information should allow new CLSI uropathogen susceptibility breakpoints for amoxicillin and amoxicillin-clavulanate in healthy cats, increasing the urine breakpoint from ≤0.25 to ≤8 μg/mL.
为了对尿液分离株进行特征描述,临床和实验室标准协会(CLSI)使用基于猫血浆(非尿液)药物浓度(≤0.25μg/mL)的阿莫西林折点,但存在用于狗的尿液特异性折点(≤8μg/mL)。
测量猫口服阿莫西林克拉维酸钾后尿液中的阿莫西林和克拉维酸浓度,并为猫的口服阿莫西林和阿莫西林克拉维酸钾提出更新的尿液特异性药敏折点。
11 只健康的纯种猫。
猫口服 3 次 62.5mg 阿莫西林克拉维酸钾,每 12 小时 1 次。在第三次给药后,收集 28 小时的尿液,记录排尿时间和尿量。每只猫至少收集 3 份尿液样本。采用液相色谱-质谱法测定尿液中阿莫西林和克拉维酸的浓度。
给药后 12 小时内收集的所有尿液样本中,阿莫西林浓度均>8μg/mL(范围为 31.6-1351μg/mL),给药后 0-6 小时和 6-12 小时的平均值分别为 929μg/mL 和 532μg/mL。阿莫西林在尿液中的平均半衰期为 1.99 小时,平均回收率为 30%。所有尿液样本中均检测到克拉维酸,其平均半衰期为 2.17 小时。
口服阿莫西林克拉维酸钾后,所有猫的尿液中阿莫西林浓度均高于野生型大肠埃希菌的药敏截止值(8μg/mL)。由于可以使用尿液浓度来确定尿液特异性药敏试验折点,因此这一信息应能为健康猫的阿莫西林和阿莫西林克拉维酸钾提供新的 CLSI 尿病原体药敏折点,将尿液折点从≤0.25μg/mL 提高到≤8μg/mL。