Effects of Tolvaptan Addition to Furosemide in Normo- and Hyponatremia Patients with Heart Failure and Chronic Kidney Disease Stages G3b-5: A Subanalysis of the K-STAR Study

Background: Tolvaptan increases free water clearance (aquaresis) and thereby improves hyponatremia. Although hyponatremia on admission is common in patients with congestive heart failure (CHF), little is known regarding the response to tolvaptan in those who also have chronic kidney disease (CKD) wi...

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Veröffentlicht in:American journal of nephrology 2017-11, Vol.46 (5), p.417-426
Hauptverfasser: Tominaga, Naoto, Kida, Keisuke, Inomata, Takayuki, Sato, Naoki, Izumi, Tohru, Akashi, Yoshihiro J., Shibagaki, Yugo
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container_end_page 426
container_issue 5
container_start_page 417
container_title American journal of nephrology
container_volume 46
creator Tominaga, Naoto
Kida, Keisuke
Inomata, Takayuki
Sato, Naoki
Izumi, Tohru
Akashi, Yoshihiro J.
Shibagaki, Yugo
description Background: Tolvaptan increases free water clearance (aquaresis) and thereby improves hyponatremia. Although hyponatremia on admission is common in patients with congestive heart failure (CHF), little is known regarding the response to tolvaptan in those who also have chronic kidney disease (CKD) with or without hyponatremia. The aim of this subanalysis was to investigate the differences in treatment response between normo- and hyponatremia patients with CHF and CKD stages G3b-5. Methods: The Kanagawa Aquaresis Investigators Trial of Tolvaptan on HF Patients with Renal Impairment (K-STAR) was a multicenter, open-label, randomized, controlled prospective clinical trial that included 81 Japanese patients with CHF and residual signs of congestion despite oral furosemide treatment (≥40 mg/day). All patients were randomly assigned to 7-day treatment with either ≤15 mg/day of new add-on tolvaptan or ≤40 mg/day of increased furosemide. A subanalysis was conducted for 73 patients, who were classified into 2 groups according to their assigned treatment, then further stratified into 2 subgroups according to their serum sodium concentration [Na + ]. The differences between the urine and serum parameters from day 1 to 3 were compared between the groups and between the subgroups in each group. Results: The change (Δ) in urine volume (ΔUV) and Δurine osmolality were greater in the tolvaptan group than in the furosemide group; however, ΔUV and Δurine osmolality did not show significant differences between the normonatremia subgroup and the hyponatremia subgroup in each group. In addition, Δserum [Na + ] was greater in the tolvaptan group, although the change was not clinically significant. In contrast, Δserum [Na + ] did not show significant differences between the normo- and hyponatremia subgroups in each group. Conclusion: Tolvaptan added to furosemide resulted in a greater diuretic effect than increased furosemide, even in normonatremia patients with CHF complicated by CKD stages G3b-5 in the very early treatment phase.
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Although hyponatremia on admission is common in patients with congestive heart failure (CHF), little is known regarding the response to tolvaptan in those who also have chronic kidney disease (CKD) with or without hyponatremia. The aim of this subanalysis was to investigate the differences in treatment response between normo- and hyponatremia patients with CHF and CKD stages G3b-5. Methods: The Kanagawa Aquaresis Investigators Trial of Tolvaptan on HF Patients with Renal Impairment (K-STAR) was a multicenter, open-label, randomized, controlled prospective clinical trial that included 81 Japanese patients with CHF and residual signs of congestion despite oral furosemide treatment (≥40 mg/day). All patients were randomly assigned to 7-day treatment with either ≤15 mg/day of new add-on tolvaptan or ≤40 mg/day of increased furosemide. A subanalysis was conducted for 73 patients, who were classified into 2 groups according to their assigned treatment, then further stratified into 2 subgroups according to their serum sodium concentration [Na + ]. The differences between the urine and serum parameters from day 1 to 3 were compared between the groups and between the subgroups in each group. Results: The change (Δ) in urine volume (ΔUV) and Δurine osmolality were greater in the tolvaptan group than in the furosemide group; however, ΔUV and Δurine osmolality did not show significant differences between the normonatremia subgroup and the hyponatremia subgroup in each group. In addition, Δserum [Na + ] was greater in the tolvaptan group, although the change was not clinically significant. In contrast, Δserum [Na + ] did not show significant differences between the normo- and hyponatremia subgroups in each group. 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Karger AG, Basel</rights><rights>2017 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2017 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-c36735fe930669c761dfa9784fe98d10792ae0f477642717b11e8a649409a8663</citedby><cites>FETCH-LOGICAL-c404t-c36735fe930669c761dfa9784fe98d10792ae0f477642717b11e8a649409a8663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2429,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29130954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tominaga, Naoto</creatorcontrib><creatorcontrib>Kida, Keisuke</creatorcontrib><creatorcontrib>Inomata, Takayuki</creatorcontrib><creatorcontrib>Sato, Naoki</creatorcontrib><creatorcontrib>Izumi, Tohru</creatorcontrib><creatorcontrib>Akashi, Yoshihiro J.</creatorcontrib><creatorcontrib>Shibagaki, Yugo</creatorcontrib><title>Effects of Tolvaptan Addition to Furosemide in Normo- and Hyponatremia Patients with Heart Failure and Chronic Kidney Disease Stages G3b-5: A Subanalysis of the K-STAR Study</title><title>American journal of nephrology</title><addtitle>Am J Nephrol</addtitle><description>Background: Tolvaptan increases free water clearance (aquaresis) and thereby improves hyponatremia. Although hyponatremia on admission is common in patients with congestive heart failure (CHF), little is known regarding the response to tolvaptan in those who also have chronic kidney disease (CKD) with or without hyponatremia. The aim of this subanalysis was to investigate the differences in treatment response between normo- and hyponatremia patients with CHF and CKD stages G3b-5. Methods: The Kanagawa Aquaresis Investigators Trial of Tolvaptan on HF Patients with Renal Impairment (K-STAR) was a multicenter, open-label, randomized, controlled prospective clinical trial that included 81 Japanese patients with CHF and residual signs of congestion despite oral furosemide treatment (≥40 mg/day). All patients were randomly assigned to 7-day treatment with either ≤15 mg/day of new add-on tolvaptan or ≤40 mg/day of increased furosemide. 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Although hyponatremia on admission is common in patients with congestive heart failure (CHF), little is known regarding the response to tolvaptan in those who also have chronic kidney disease (CKD) with or without hyponatremia. The aim of this subanalysis was to investigate the differences in treatment response between normo- and hyponatremia patients with CHF and CKD stages G3b-5. Methods: The Kanagawa Aquaresis Investigators Trial of Tolvaptan on HF Patients with Renal Impairment (K-STAR) was a multicenter, open-label, randomized, controlled prospective clinical trial that included 81 Japanese patients with CHF and residual signs of congestion despite oral furosemide treatment (≥40 mg/day). All patients were randomly assigned to 7-day treatment with either ≤15 mg/day of new add-on tolvaptan or ≤40 mg/day of increased furosemide. A subanalysis was conducted for 73 patients, who were classified into 2 groups according to their assigned treatment, then further stratified into 2 subgroups according to their serum sodium concentration [Na + ]. The differences between the urine and serum parameters from day 1 to 3 were compared between the groups and between the subgroups in each group. Results: The change (Δ) in urine volume (ΔUV) and Δurine osmolality were greater in the tolvaptan group than in the furosemide group; however, ΔUV and Δurine osmolality did not show significant differences between the normonatremia subgroup and the hyponatremia subgroup in each group. In addition, Δserum [Na + ] was greater in the tolvaptan group, although the change was not clinically significant. In contrast, Δserum [Na + ] did not show significant differences between the normo- and hyponatremia subgroups in each group. Conclusion: Tolvaptan added to furosemide resulted in a greater diuretic effect than increased furosemide, even in normonatremia patients with CHF complicated by CKD stages G3b-5 in the very early treatment phase.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>29130954</pmid><doi>10.1159/000481995</doi><tpages>10</tpages></addata></record>
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subjects Administration, Oral
Aged
Aged, 80 and over
Analysis
Antidiuretic Hormone Receptor Antagonists - therapeutic use
Benzazepines - therapeutic use
Cardiac patients
Care and treatment
Chronic kidney failure
Clinical trials
Dose-Response Relationship, Drug
Drug Therapy, Combination - methods
Female
Furosemide
Furosemide - adverse effects
Heart failure
Heart Failure - blood
Heart Failure - drug therapy
Heart Failure - urine
Humans
Hyponatremia
Hyponatremia - blood
Hyponatremia - chemically induced
Hyponatremia - prevention & control
Hyponatremia - urine
Kidney diseases
Kidney Failure, Chronic - blood
Kidney Failure, Chronic - drug therapy
Kidney Failure, Chronic - urine
Male
Original Report: Patient-Oriented, Translational Research
Potassium - blood
Potassium - urine
Prospective Studies
Sodium - blood
Sodium - urine
Sodium Potassium Chloride Symporter Inhibitors - adverse effects
Treatment Outcome
title Effects of Tolvaptan Addition to Furosemide in Normo- and Hyponatremia Patients with Heart Failure and Chronic Kidney Disease Stages G3b-5: A Subanalysis of the K-STAR Study
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