TY - JOUR
T1 - The efficacy of tolvaptan as a diuretic for chronic kidney disease patients
AU - Tanaka, Akihito
AU - Katsuno, Takayuki
AU - Ozaki, Takenori
AU - Sakata, Fumiko
AU - Kato, Noritoshi
AU - Suzuki, Yasuhiro
AU - Kosugi, Tomoki
AU - Kato, Sawako
AU - Tsuboi, Naotake
AU - Sato, Waichi
AU - Yasuda, Yoshinari
AU - Mizuno, Masashi
AU - Ito, Yasuhiko
AU - Matsuo, Seiichi
AU - Maruyama, Shoichi
N1 - Publisher Copyright:
© 2015 Acta Cardiologica. All rights reserved.
PY - 2015
Y1 - 2015
N2 - Background Tolvaptan selectively binds to the vasopressin V2 receptor and inhibits reabsorption of free water. Although its effi cacy for heart failure has been proven, its effi cacy for chronic kidney disease (CKD) patients has not been assessed in detail. Methods We examined 20 CKD patients (13 men and 7 women) who presented with volume overload and who were administered tolvaptan. We assessed urine volume (UV) and blood biochemistry before administration (d0), 1 day after administration (d1), and 7 to 14 days after administration (d7-14). Results The mean age was 74.0 ± 13.1 years. Besides CKD, there were 9, 8, and 5 patients with heart failure, liver failure or liver cirrhosis, and severe oedema, respectively. UV signifi cantly increased from 959.0 ± 503.8 mL/day at d0 to 1605.4 ± 964.0 mL/day at d7-14 (P < 0.01). Serum creatinine levels were not exacerbated (3.89 ± 3.43 mg/dL at d0 and 3.66 ± 3.02 mg/dL at d7-14). Serum albumin (ALB) levels and urinary protein creatinine ratio (uPCR) did not correlate with UV change. Estimated glomerular fi ltration rate (eGFR) correlated with UV change from d0 to d1 (r = 0.6619, P < 0.01). Serum sodium elevation correlated with increased UV (r = 0.4951, P < 0.05). Conclusion Tolvaptan is useful to reduce volume overload without exacerbation of the renal function; its effect does not depend on ALB or uPCR. The eGFR correlated with the effi cacy of tolvaptan. If UV increases drastically after tolvaptan administration, serum Na levels should be carefully monitored.
AB - Background Tolvaptan selectively binds to the vasopressin V2 receptor and inhibits reabsorption of free water. Although its effi cacy for heart failure has been proven, its effi cacy for chronic kidney disease (CKD) patients has not been assessed in detail. Methods We examined 20 CKD patients (13 men and 7 women) who presented with volume overload and who were administered tolvaptan. We assessed urine volume (UV) and blood biochemistry before administration (d0), 1 day after administration (d1), and 7 to 14 days after administration (d7-14). Results The mean age was 74.0 ± 13.1 years. Besides CKD, there were 9, 8, and 5 patients with heart failure, liver failure or liver cirrhosis, and severe oedema, respectively. UV signifi cantly increased from 959.0 ± 503.8 mL/day at d0 to 1605.4 ± 964.0 mL/day at d7-14 (P < 0.01). Serum creatinine levels were not exacerbated (3.89 ± 3.43 mg/dL at d0 and 3.66 ± 3.02 mg/dL at d7-14). Serum albumin (ALB) levels and urinary protein creatinine ratio (uPCR) did not correlate with UV change. Estimated glomerular fi ltration rate (eGFR) correlated with UV change from d0 to d1 (r = 0.6619, P < 0.01). Serum sodium elevation correlated with increased UV (r = 0.4951, P < 0.05). Conclusion Tolvaptan is useful to reduce volume overload without exacerbation of the renal function; its effect does not depend on ALB or uPCR. The eGFR correlated with the effi cacy of tolvaptan. If UV increases drastically after tolvaptan administration, serum Na levels should be carefully monitored.
UR - http://www.scopus.com/inward/record.url?scp=84926460322&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84926460322&partnerID=8YFLogxK
U2 - 10.1080/ac.70.2.3073514
DO - 10.1080/ac.70.2.3073514
M3 - Article
C2 - 26148383
AN - SCOPUS:84926460322
SN - 0001-5385
VL - 70
SP - 217
EP - 223
JO - Acta Cardiologica
JF - Acta Cardiologica
IS - 2
ER -