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A retrospective Aliskiren and Losartan study in non-diabetic chronic kidney disease

机译:非糖尿病慢性肾脏病回顾性Aliskiren和Losartan研究

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摘要

AIM: To assess the efficacy of combined Aliskiren and Losartan vs high dose Losartan and Aliskiren alone in chronic kidney disease (CKD).METHODS: This is a retrospective study of 143 patients with non-diabetic CKD comparing combined Aliskiren (150 mg/d) with Losartan (100 mg/d) therapy vs High dose Angiotensin receptor blockers (ARB) (Losartan 200 mg/d) and the third group Aliskiren (150 mg/d) alone. This study involved only patient medical records. Entry criteria included those patients who had been treated with the above drugs for at least 36 mo within the 5 years period; other criteria included proteinuria of 1 g or more and or CKD Stage 3 at the start of the 36 mo period. The study utilised primary renal end points of estimated Glomerular Filtration Rate (eGFR) < 15 mL/min or end stage renal failure.RESULTS: Patients treated with high dose ARB compared to the other two treatment groups had significantly less proteinuria at the end of 36 mo (P < 0.007). All 3 groups had significant reduction of proteinuria (P < 0.043, P < 0.001). Total urinary protein was significantly different between the 3 groups over the 3-year study period (P = 0.008), but not eGFR. The changes in eGFR from baseline to each year were not significantly different between the 3 therapeutic groups (P < 0.119). There were no significant differences in the systolic and diastolic blood pressure between the 3 drug groups throughout the 3 years. The incidence of hyperkalemia (> 5.5 mmol/L) was 14.2% (7/49) in the Combined Aliskiren and ARB group, 8.7% (4/46) in the Aliskiren alone group and 6.3% (3/48) in the High dose ARB group (P < 0.001).CONCLUSION: This study in non-diabetic CKD patients showed that Combination therapy with Aliskiren and ARB was effective but was not safe as it was associated with a high prevalence of hyperkalaemia.
机译:目的:评估阿利吉仑和氯沙坦联用与单独使用大剂量氯沙坦和阿利吉仑的组合在慢性肾脏疾病(CKD)中的疗效。方法:这是一项对143例非糖尿病性CKD患者的回顾性研究,比较了阿利吉仑联合(150 mg / d)分别使用氯沙坦(100 mg / d)和高剂量血管紧张素受体阻滞剂(ARB)(洛沙坦200 mg / d)和第三组阿利吉仑(150 mg / d)。该研究仅涉及患者病历。入组标准包括那些在5年内接受上述药物治疗至少36个月的患者;其他标准包括1 g或更大的蛋白尿和/或36 mo周期开始时的CKD 3期。该研究利用估计肾小球滤过率(eGFR)<15 mL / min或终末期肾功能衰竭的主要肾脏终点。结果:与其他两个治疗组相比,高剂量ARB治疗的患者在36岁末的蛋白尿明显减少mo(P <0.007)。所有3组蛋白尿均明显减少(P <0.043,P <0.001)。在3年研究期间,三组之间的总尿蛋白显着不同(P = 0.008),但eGFR没有差异。 3个治疗组之间从基线到每年的eGFR变化无显着差异(P <0.119)。在过去的3年中,这3个药物组之间的收缩压和舒张压没有显着差异。 Aliskiren和ARB联合治疗组高钾血症(> 5.5 mmol / L)的发生率为14.2%(7/49),Aliskiren单独治疗组的高钾血症发生率为8.7%(4/46),High组为6.3%(3/48)结论:对非糖尿病性CKD患者进行的这项研究表明,与Aliskiren和ARB联合治疗是有效的,但不安全,因为它与高钾血症的高患病率有关。

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