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替米沙坦与贝那普利长期口服治疗猫慢性肾病的疗效比较

Comparison of Efficacy of Long-term Oral Treatment with Telmisartan and Benazepril in Cats with Chronic Kidney Disease.

作者信息

Sent U, Gössl R, Elliott J, Syme H M, Zimmering T

机构信息

Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.

Department of Comparative Biomedical Sciences, Royal Veterinary College, London, UK.

出版信息

J Vet Intern Med. 2015 Nov-Dec;29(6):1479-87. doi: 10.1111/jvim.13639. Epub 2015 Oct 16.

Abstract

BACKGROUND

The efficacy and benefits of telmisartan in cats with chronic kidney disease (CKD) have not previously been reported.

HYPOTHESIS

Long-term treatment of cats with CKD using telmisartan decreases urine protein-to-creatinine ratio (UP/C) similar to benazepril.

ANIMALS

Two-hundred and twenty-four client-owned adult cats with CKD.

METHODS

Prospective, multicenter, controlled, randomized, parallel group, blinded clinical trial with noninferiority design. Cats were allocated in a 1:1 ratio to either telmisartan (1 mg/kg; n = 112) or benazepril (0.5-1.0 mg/kg; n = 112) PO q24 h. The primary endpoint was prospectively defined as the change in proteinuria (benazepril:telmisartan) based on a log transformed weighted average of UP/C change from baseline (AUC 0→t/t) as a percentage compared using a confidence interval (CI) approach. Changes of UP/C from baseline were assessed on all study days and corrected for multiple comparisons.

RESULTS

Telmisartan proved noninferior to benazepril in controlling proteinuria (CI, -0.035 to 0.268). At Day 180, UP/C compared to baseline in the telmisartan group was significantly lower (-0.05 ± 0.31; P = .016), whereas in the benazepril group the change (-0.02 ± 0.48) was not statistically significant (P = .136). Similar results were obtained at all assessment points with significant decrease in UP/C occurring with telmisartan but not benazepril.

CONCLUSION AND CLINICAL IMPORTANCE

Both telmisartan and benazepril were well tolerated and safe. Telmisartan proved to be noninferior to benazepril and significantly decreased proteinuria relative to baseline at all assessment points whereas benazepril did not.

摘要

背景

此前尚未报道替米沙坦对患有慢性肾病(CKD)的猫的疗效和益处。

假设

使用替米沙坦对患有CKD的猫进行长期治疗可降低尿蛋白肌酐比(UP/C),效果与贝那普利相似。

动物

224只客户拥有的成年CKD猫。

方法

采用非劣效性设计的前瞻性、多中心、对照、随机、平行组、盲法临床试验。猫按1:1的比例随机分为替米沙坦组(1mg/kg;n = 112)或贝那普利组(0.5 - 1.0mg/kg;n = 112),口服,每24小时一次。主要终点前瞻性定义为基于从基线开始的UP/C变化的对数转换加权平均值(AUC 0→t/t)作为百分比的蛋白尿变化(贝那普利:替米沙坦),使用置信区间(CI)方法进行比较。在所有研究日评估UP/C相对于基线的变化,并对多重比较进行校正。

结果

在控制蛋白尿方面,替米沙坦被证明不劣于贝那普利(CI,-0.035至0.268)。在第180天,替米沙坦组的UP/C与基线相比显著降低(-0.05±0.31;P = 0.016),而贝那普利组的变化(-0.02±0.48)无统计学意义(P = 0.136)。在所有评估点均获得类似结果,替米沙坦使UP/C显著降低,而贝那普利则未。

结论及临床意义

替米沙坦和贝那普利耐受性良好且安全。替米沙坦被证明不劣于贝那普利,并且在所有评估点相对于基线均显著降低蛋白尿,而贝那普利则未。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5312/4895689/b2bec9ac44bd/JVIM-29-1479-g001.jpg

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