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      Efficacy of combination therapy with natriuretic and aquaretic drugs in cirrhotic ascites patients: A randomized study

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          Abstract

          AIM

          To assess the effects of a combination therapy with natriuretic and aquaretic drugs in cirrhotic ascites patients.

          METHODS

          A two-center, randomized, open-label, prospective study was conducted. Japanese patients who met the criteria were randomized to trial group and the combination diuretic group (received 7.5 mg of tolvaptan) or the conventional diuretic group (received 40 mg of furosemide) for 7 d in addition to the natriuretic drug which was used prior to enrolment in this study. The primary endpoint was the change in body weight from the baseline. Vital signs, fluid intake, and laboratory and urinary data were assessed to determine the pharmacological effects after administration of aquaretic and natriuretic drugs.

          RESULTS

          A total of 56 patients were randomized to receive either tolvaptan ( n = 28) or furosemide ( n = 28). In the combination and conventional diuretic groups, the average decrease in body weight from the baseline was 3.21 ± 3.17 kg ( P < 0.0001) and 1.75 ± 2.36 kg ( P = 0.0006), respectively, when measured on the final dosing day. Following 1 wk of treatment, a significantly greater reduction in body weight was observed in the combination diuretic group compared to that in the conventional diuretic group ( P = 0.0412).

          CONCLUSION

          Compared to a conventional diuretic therapy with only a natriuretic drug, a combination diuretic therapy with natriuretic and aquaretic drugs is more effective for patients with cirrhotic ascites.

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          Most cited references23

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          Prediction of creatinine clearance from serum creatinine.

          A formula has been developed to predict creatinine clearance (Ccr) from serum creatinine (Scr) in adult males: (see article)(15% less in females). Derivation included the relationship found between age and 24-hour creatinine excretion/kg in 249 patients aged 18-92. Values for Ccr were predicted by this formula and four other methods and the results compared with the means of two 24-hour Ccr's measured in 236 patients. The above formula gave a correlation coefficient between predicted and mean measured Ccr's of 0.83; on average, the difference predicted and mean measured values was no greater than that between paired clearances. Factors for age and body weight must be included for reasonable prediction.
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            Diuretic strategies in patients with acute decompensated heart failure.

            Loop diuretics are an essential component of therapy for patients with acute decompensated heart failure, but there are few prospective data to guide their use. In a prospective, double-blind, randomized trial, we assigned 308 patients with acute decompensated heart failure to receive furosemide administered intravenously by means of either a bolus every 12 hours or continuous infusion and at either a low dose (equivalent to the patient's previous oral dose) or a high dose (2.5 times the previous oral dose). The protocol allowed specified dose adjustments after 48 hours. The coprimary end points were patients' global assessment of symptoms, quantified as the area under the curve (AUC) of the score on a visual-analogue scale over the course of 72 hours, and the change in the serum creatinine level from baseline to 72 hours. In the comparison of bolus with continuous infusion, there was no significant difference in patients' global assessment of symptoms (mean AUC, 4236±1440 and 4373±1404, respectively; P=0.47) or in the mean change in the creatinine level (0.05±0.3 mg per deciliter [4.4±26.5 μmol per liter] and 0.07±0.3 mg per deciliter [6.2±26.5 μmol per liter], respectively; P=0.45). In the comparison of the high-dose strategy with the low-dose strategy, there was a nonsignificant trend toward greater improvement in patients' global assessment of symptoms in the high-dose group (mean AUC, 4430±1401 vs. 4171±1436; P=0.06). There was no significant difference between these groups in the mean change in the creatinine level (0.08±0.3 mg per deciliter [7.1±26.5 μmol per liter] with the high-dose strategy and 0.04±0.3 mg per deciliter [3.5±26.5 μmol per liter] with the low-dose strategy, P=0.21). The high-dose strategy was associated with greater diuresis and more favorable outcomes in some secondary measures but also with transient worsening of renal function. Among patients with acute decompensated heart failure, there were no significant differences in patients' global assessment of symptoms or in the change in renal function when diuretic therapy was administered by bolus as compared with continuous infusion or at a high dose as compared with a low dose. (Funded by the National Heart, Lung, and Blood Institute; ClinicalTrials.gov number, NCT00577135.).
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              Management of adult patients with ascites due to cirrhosis: an update.

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                Author and article information

                Contributors
                Journal
                World J Gastroenterol
                World J. Gastroenterol
                WJG
                World Journal of Gastroenterology
                Baishideng Publishing Group Inc
                1007-9327
                2219-2840
                7 December 2017
                7 December 2017
                : 23
                : 45
                : 8062-8072
                Affiliations
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Kanagawa 252-0375, Japan. kiruha555@ 123456yahoo.co.jp
                Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Kanagawa 252-0375, Japan
                Department of Gastroenterology, Shonan Atsugi Hospital, Kanagawa 243-8551, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan
                Author notes

                Author contributions: Uojima H, Hidaka H, Nakayama T, Sung JH, Ichita C, Tokoro S, Masuda S, Sasaki A, Koizumi K, Egashira H and Kako M contributed equally to this work; Uojima H and Nakayama T collected and analyzed the data; Uojima H drafted the manuscript; Kako M designed and supervised the study; Sung JH, Ichita C, Tokoro S, Masuda S, Sasaki A, Koizumi K and Egashira H offered technical or material support; all authors have read and approved the final version to be published.

                Correspondence to: Haruki Uojima, MD, Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0375, Japan. kiruha555@ 123456yahoo.co.jp

                Telephone: +81-42-7788111 Fax: +81-42-7788390

                Article
                jWJG.v23.i45.pg8062
                10.3748/wjg.v23.i45.8062
                5725301
                29259382
                9ee1be7c-d376-44d0-aeca-20814fe5966f
                ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved.

                This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.

                History
                : 13 September 2017
                : 25 October 2017
                : 8 November 2017
                Categories
                Randomized Clinical Trial

                tolvaptan,liver cirrhosis,diuretic effect,ascites,hepatic edema

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