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A retrospective Aliskiren and Losartan study in non-diabetic chronic kidney disease 被引量:1
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作者 Keng-Thye Woo Hui-Lin Choong +7 位作者 Kok-Seng Wong Han-Kim Tan marjorie foo fook-Chong Stephanie Evan JC Lee Vathsala Anantharaman Grace SL Lee Choong-Meng Chan 《World Journal of Nephrology》 2013年第4期129-135,共7页
AIM: To assess the effcacy 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 pa-tients with non-diabetic CK... AIM: To assess the effcacy 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 pa-tients 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 medi-cal 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 com-pared to the other two treatment groups had signifcantly less proteinuria at the end of 36 mo ( P 〈 0.007). All 3 groups had signifcant reduction of proteinuria ( P 〈 0.043, P 〈 0.001). Total urinary protein was signifcantly differ-ent 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 signifcantly different be-tween 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 pa-tients showed that Combination therapy with Aliskiren and ARB was effective but was not safe as it was asso-ciated with a high prevalence of hyperkalaemia. 展开更多
关键词 ALISKIREN Chronic kidney disease disease Clinical trial
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