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Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload
BACKGROUND: Fluid overload in chronic kidney disease (CKD) is generally controlled by diuretics, with potentially harmful effects on renal function. The efficacy of tolvaptan, a vasopressin V2-receptor antagonist and aquaretic, has not been evaluated for fluid control in CKD with reduced renal funct...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103308/ https://www.ncbi.nlm.nih.gov/pubmed/30147354 http://dx.doi.org/10.2147/IJNRD.S167694 |
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author | Suzuki, Shunji Hanafusa, Norio Kubota, Kenji Tsuchiya, Ken Nitta, Kosaku |
author_facet | Suzuki, Shunji Hanafusa, Norio Kubota, Kenji Tsuchiya, Ken Nitta, Kosaku |
author_sort | Suzuki, Shunji |
collection | PubMed |
description | BACKGROUND: Fluid overload in chronic kidney disease (CKD) is generally controlled by diuretics, with potentially harmful effects on renal function. The efficacy of tolvaptan, a vasopressin V2-receptor antagonist and aquaretic, has not been evaluated for fluid control in CKD with reduced renal function. METHODS: Each patient from a group of 24 CKD patients on tolvaptan 15 mg/d plus conventional diuretics (T group) was matched by age and sex with a patient from a group of 24 CKD patients on conventional nonaquaretic diuretics alone not associated to tolvaptan other than tolvaptan (C group). Changes in renal function were compared between the groups for 1 year. RESULTS: There were no significant differences in blood pressure, hemoglobin levels, cardiac function, urine specific gravity, and urinary sodium concentration between the 2 groups at the beginning of the follow-up period and 1 year after. The estimated glomerular filtration rate (eGFR) by the formula developed by Japanese Society of Nephrology (in mL/min/1.73 m(2)) decreased: C group (from 28.3±13.6 to 23.0±12.3, p=0.09), T group (from 22.7±12.4 to 19.4±12.2, p=0.18), but both did not reach significance. A 50% reduction in eGFR was observed in 4 patients in the C group and 1 in the T group (p<0.05). A subgroup analysis performed on the patients with stage 3–4 CKD demonstrated a significant reduction in eGFR in the C group (n=17, p=0.04), but not in T group (n=17, p=0.07). CONCLUSION: These results suggest that tolvaptan may have less effects on CKD progression among stage 3–4 CKD patients who are on conventional diuretics. |
format | Online Article Text |
id | pubmed-6103308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61033082018-08-24 Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload Suzuki, Shunji Hanafusa, Norio Kubota, Kenji Tsuchiya, Ken Nitta, Kosaku Int J Nephrol Renovasc Dis Original Research BACKGROUND: Fluid overload in chronic kidney disease (CKD) is generally controlled by diuretics, with potentially harmful effects on renal function. The efficacy of tolvaptan, a vasopressin V2-receptor antagonist and aquaretic, has not been evaluated for fluid control in CKD with reduced renal function. METHODS: Each patient from a group of 24 CKD patients on tolvaptan 15 mg/d plus conventional diuretics (T group) was matched by age and sex with a patient from a group of 24 CKD patients on conventional nonaquaretic diuretics alone not associated to tolvaptan other than tolvaptan (C group). Changes in renal function were compared between the groups for 1 year. RESULTS: There were no significant differences in blood pressure, hemoglobin levels, cardiac function, urine specific gravity, and urinary sodium concentration between the 2 groups at the beginning of the follow-up period and 1 year after. The estimated glomerular filtration rate (eGFR) by the formula developed by Japanese Society of Nephrology (in mL/min/1.73 m(2)) decreased: C group (from 28.3±13.6 to 23.0±12.3, p=0.09), T group (from 22.7±12.4 to 19.4±12.2, p=0.18), but both did not reach significance. A 50% reduction in eGFR was observed in 4 patients in the C group and 1 in the T group (p<0.05). A subgroup analysis performed on the patients with stage 3–4 CKD demonstrated a significant reduction in eGFR in the C group (n=17, p=0.04), but not in T group (n=17, p=0.07). CONCLUSION: These results suggest that tolvaptan may have less effects on CKD progression among stage 3–4 CKD patients who are on conventional diuretics. Dove Medical Press 2018-08-17 /pmc/articles/PMC6103308/ /pubmed/30147354 http://dx.doi.org/10.2147/IJNRD.S167694 Text en © 2018 Suzuki et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Suzuki, Shunji Hanafusa, Norio Kubota, Kenji Tsuchiya, Ken Nitta, Kosaku Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title | Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title_full | Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title_fullStr | Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title_full_unstemmed | Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title_short | Effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
title_sort | effects of tolvaptan on renal function in chronic kidney disease patients with volume overload |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103308/ https://www.ncbi.nlm.nih.gov/pubmed/30147354 http://dx.doi.org/10.2147/IJNRD.S167694 |
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