Department of Veterinary Clinical Sciences, Iowa State University, Ames, Iowa, USA.
Department of Statistics, Iowa State University, Ames, Iowa, USA.
J Vet Intern Med. 2021 Sep;35(5):2102-2111. doi: 10.1111/jvim.16236. Epub 2021 Aug 13.
Angiotensin-converting enzyme inhibitors (ACEIs) are commonly prescribed in dogs, but the ideal dosage is unknown.
HYPOTHESIS/OBJECTIVES: In dogs with cardiac disease, a dose-response relationship exists for ACEIs with respect to long-term outcome.
One hundred forty-four dogs with cardiac disease, 63 with current or prior congestive heart failure.
Retrospective medical record review. Cox proportional hazards models were used to determine variables associated with 2-year survival or survival from first-onset congestive heart failure (CHF).
Median initial ACEI dosage was 0.84 (interquartile range [IQR], 0.56-0.98) mg/kg/day, and 108/144 (75%) of dogs received q12h dosing. No clinically relevant changes in renal function test results, serum electrolyte concentrations, or blood pressure occurred between initial prescription of ACEI and first reevaluation (median, 14 days later). In univariable analysis, higher ACEI dose was associated with increased survival from first-onset CHF (P = .005), and within the subgroup of dogs in CHF at the time of ACEI prescription, higher ACEI dose was associated with improved survival at 2 years (P = .04). In multivariable analysis, q12h dose frequency of ACEI (hazard ratio [HR], 0.30; 95% CI, 0.10-0.88; P = .03) and higher serum potassium concentration at visit 1 (HR, 0.39; 95% CI, 0.16-0.97; P = .04) were predictive of 2-year survival. The ACEIs were well-tolerated, with only 8/144 (5.6%) dogs having ACEI dose decreased or discontinued because of adverse effects.
Twice daily dose frequency might optimize the cardioprotective benefit of ACEIs.
血管紧张素转换酶抑制剂(ACEI)在犬中常被处方使用,但理想剂量尚不清楚。
假说/目的:在患有心脏疾病的犬中,ACEI 的剂量与长期预后存在剂量反应关系。
144 只患有心脏疾病的犬,其中 63 只患有或曾患有充血性心力衰竭。
回顾性病历审查。使用 Cox 比例风险模型确定与 2 年生存率或首次充血性心力衰竭(CHF)发作后生存率相关的变量。
初始 ACEI 剂量的中位数为 0.84(四分位距[IQR],0.56-0.98)mg/kg/天,144 只犬中有 108 只(75%)接受 q12h 给药。在 ACEI 首次处方和第一次重新评估(中位数为 14 天后)之间,肾功能试验结果、血清电解质浓度或血压没有发生任何临床相关的变化。在单变量分析中,较高的 ACEI 剂量与首次 CHF 发作后的生存率增加相关(P=0.005),并且在 ACEI 处方时患有心力衰竭的犬亚组中,较高的 ACEI 剂量与 2 年生存率的提高相关(P=0.04)。在多变量分析中,ACEI 的 q12h 剂量频率(危险比[HR],0.30;95%CI,0.10-0.88;P=0.03)和第 1 次就诊时较高的血清钾浓度(HR,0.39;95%CI,0.16-0.97;P=0.04)是 2 年生存率的预测因素。ACEI 耐受性良好,仅有 8/144(5.6%)只犬因不良反应而减少或停止 ACEI 剂量。
每日两次的剂量频率可能会优化 ACEI 的心脏保护作用。