Efficacy and safety of tolvaptan after pediatric congenital heart disease surgery

It is not clear whether tolvaptan is safe and effective irrespective of various underlying clinical conditions including the functional ventricle morphology, chromosomal abnormalities, and renal function after complex pediatric congenital heart disease surgery. Also, the appropriate dose of tolvapta...

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Veröffentlicht in:Heart and vessels 2021-05, Vol.36 (5), p.717-723
Hauptverfasser: Kojima, Takuro, Kanai, Azusa, Yoshiba, Shigeki, Kobayashi, Toshiki, Sumitomo, Naokata
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container_issue 5
container_start_page 717
container_title Heart and vessels
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creator Kojima, Takuro
Kanai, Azusa
Yoshiba, Shigeki
Kobayashi, Toshiki
Sumitomo, Naokata
description It is not clear whether tolvaptan is safe and effective irrespective of various underlying clinical conditions including the functional ventricle morphology, chromosomal abnormalities, and renal function after complex pediatric congenital heart disease surgery. Also, the appropriate dose of tolvaptan in these patients has not been previously identified. We retrospectively assessed the urine volume, body weight, patient clinical characteristics, laboratory data, and vital signs before and on days 1 and 7 of the tolvaptan administration after congenital heart disease surgery. Also, we assessed the relationship between the tolvaptan dose and its effects. A total of 86 patients were included the study. The mean time from the surgery to the tolvaptan administration was 23.5 ± 3.7 days. After administering tolvaptan, the urine volume significantly increased and body weight significantly decreased from baseline by days 1 and 7 ( p  
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Also, the appropriate dose of tolvaptan in these patients has not been previously identified. We retrospectively assessed the urine volume, body weight, patient clinical characteristics, laboratory data, and vital signs before and on days 1 and 7 of the tolvaptan administration after congenital heart disease surgery. Also, we assessed the relationship between the tolvaptan dose and its effects. A total of 86 patients were included the study. The mean time from the surgery to the tolvaptan administration was 23.5 ± 3.7 days. After administering tolvaptan, the urine volume significantly increased and body weight significantly decreased from baseline by days 1 and 7 ( p  &lt; 0.0001). The urine volume significantly increased more in the survivors than the deceased. Of the 22 patients who had low serum sodium concentrations at baseline, 20 had an increased serum sodium concentration on day 7. The clinical effect of tolvaptan was not affected by the functional ventricle morphology, chromosomal abnormalities, or renal function. There was a positive correlation between the tolvaptan dose and change in the urine volume until a tolvaptan dose of up to 0.3 mg/kg/day but not at more than 0.3 mg/kg/day. Tolvaptan administration is safe and effective after congenital heart disease surgery irrespective of various underlying clinical conditions. 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Also, the appropriate dose of tolvaptan in these patients has not been previously identified. We retrospectively assessed the urine volume, body weight, patient clinical characteristics, laboratory data, and vital signs before and on days 1 and 7 of the tolvaptan administration after congenital heart disease surgery. Also, we assessed the relationship between the tolvaptan dose and its effects. A total of 86 patients were included the study. The mean time from the surgery to the tolvaptan administration was 23.5 ± 3.7 days. After administering tolvaptan, the urine volume significantly increased and body weight significantly decreased from baseline by days 1 and 7 ( p  &lt; 0.0001). The urine volume significantly increased more in the survivors than the deceased. Of the 22 patients who had low serum sodium concentrations at baseline, 20 had an increased serum sodium concentration on day 7. The clinical effect of tolvaptan was not affected by the functional ventricle morphology, chromosomal abnormalities, or renal function. There was a positive correlation between the tolvaptan dose and change in the urine volume until a tolvaptan dose of up to 0.3 mg/kg/day but not at more than 0.3 mg/kg/day. Tolvaptan administration is safe and effective after congenital heart disease surgery irrespective of various underlying clinical conditions. 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Kanai, Azusa ; Yoshiba, Shigeki ; Kobayashi, Toshiki ; Sumitomo, Naokata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-908b71d865cfffd73b056d3fab9b66de0838837ea5554cd82adbf7249cc49f713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Abnormalities</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Body weight</topic><topic>Cardiac &amp; Cardiovascular Systems</topic><topic>Cardiac Surgery</topic><topic>Cardiology</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular System &amp; Cardiology</topic><topic>Congenital diseases</topic><topic>Coronary artery disease</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Morphology</topic><topic>Original Article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Peripheral Vascular Disease</topic><topic>Renal function</topic><topic>Science &amp; 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subjects Abnormalities
Biomedical Engineering and Bioengineering
Body weight
Cardiac & Cardiovascular Systems
Cardiac Surgery
Cardiology
Cardiovascular disease
Cardiovascular diseases
Cardiovascular System & Cardiology
Congenital diseases
Coronary artery disease
Heart
Heart diseases
Life Sciences & Biomedicine
Medicine
Medicine & Public Health
Morphology
Original Article
Patients
Pediatrics
Peripheral Vascular Disease
Renal function
Science & Technology
Sodium
Surgery
Urine
Vascular Surgery
Ventricle
title Efficacy and safety of tolvaptan after pediatric congenital heart disease surgery
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