|LETTER TO EDITOR
|Year : 2020 | Volume
| Issue : 1 | Page : 53-55
Therapy with the combination of tolvaptan and furosemide for refractory edema in nephrotic syndrome
Jitendra Meena, Aditi Sinha, Pankaj Hari, Arvind Bagga
Division of Nephrology, Department of Pediatrics, ICMR Center for Advanced Research in Nephrology, All India Institute of Medical Sciences, New Delhi, India
|Date of Submission||14-Nov-2018|
|Date of Acceptance||17-May-2019|
|Date of Web Publication||06-Sep-2019|
Prof. Pankaj Hari
Room No. 3061, Division of Nephrology, Department of Pediatrics, ICMR Center for Advanced Research in Nephrology All India Institute of Medical Sciences, New Delhi
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Meena J, Sinha A, Hari P, Bagga A. Therapy with the combination of tolvaptan and furosemide for refractory edema in nephrotic syndrome. Indian J Nephrol 2020;30:53-5
|How to cite this URL:|
Meena J, Sinha A, Hari P, Bagga A. Therapy with the combination of tolvaptan and furosemide for refractory edema in nephrotic syndrome. Indian J Nephrol [serial online] 2020 [cited 2020 Jan 22];30:53-5. Available from: http://www.indianjnephrol.org/text.asp?2020/30/1/53/266085
Edema, the chief clinical manifestation of nephrotic syndrome, often can be severe, more so in patients with steroid-resistant nephrotic syndrome (SRNS). Severe edema requires prolonged therapy with furosemide, which may be associated with adverse effects. While patients with hypovolemia benefit from administration of intravenous (IV) albumin with or without furosemide, the former is expensive and carries the risk of pulmonary edema in patients with oligouria. Tolvaptan, an antagonist of the arginine vasopressin receptor, increases free water excrection and diuresis. Shimizu et al.first reported use of tolvaptan in an 8 year-old girl with nephrotic syndrome and refractory edema. We report our experience with the combination of oral tolvaptan and IV furosemide in patients with nephrotic syndrome in whom the edema was refractory to IV furosemide alone.
We studied 10 patients (6 boys) with a median age of 7 (6–14) years, who received therapy with oral tolvaptan (0.5–1 mg/kg/day) and IV furosemide (3–4 mg/kg/day) for 48 h. Combination therapy was associated with significant increase in urine volume, from 1.2 (0.9–2.7) mL/kg/h at baseline to 2.4 (2.0–3.3) mL/kg/h at 48 h of therapy. There was a small but significant reduction in body weight from baseline 20.5 to 19.9 kg after 48 h. Serum sodium increased significantly from 133 mEq/L at baseline to 140.5 mEq/L after combination therapy. Three patient showed hypernatremia (serum sodium >145 mEq/L). [Table 1] shows other parameters before and after combination therapy. None of the patients developed clinical evidence of hypovolemia during the study.
|Table 1: Clinical parameters before and 48 h after therapy with oral tolvaptan and intravenous furosemide|
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Our study demonstrates that combination therapy with oral tolvaptan and IV furosemide increases the urine output, without affecting renal function. Hypoalbuminemia in nephrotic syndrome results in impaired furosemide delivery to the tubular lumen at its site of action in thick ascending loop of Henle contributing to furosemide resistance. Since tolvaptan acts on the basolateral side of collecting duct and does not require secretion into the tubular lumen, its aquaretic action is not affected by the blood level of albumin. The therapeutic efficacy of vasopressin receptor antagonist is well demonstrated in the management of fluid retention in congestive heart failure and cirrhosis. Recently, in a case series of 14 patients with nephrotic proteinuria secondary to diabetic nephropathy, improvement in furosemide refractory edema with tolvaptan therapy was described.
Finding from this study shows that coadministration of tolvaptan and furosemide is effective in increasing urine output in patients with furosemide resistant edema due to nephrotic syndrome. While therapy is safe, careful monitoring of serum sodium is essential. Prospective controlled studies are required to examine whether tolvaptan is an effective and safe oral therapy for management of edema in nephrotic syndrome.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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