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Erschienen in: Pediatric Nephrology 10/2014

01.10.2014 | Brief Report

Fludrocortisone as a new tool for managing tubulopathy after pediatric renal transplantation: a series of cases

Erschienen in: Pediatric Nephrology | Ausgabe 10/2014

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Abstract

Background

The management of tubulopathies after renal transplantation (RTx) may require high doses of sodium and bicarbonate, reducing the quality of life and therapeutic compliance of the patient. Some studies on adult patients have highlighted the benefits of fludrocortisone (fludro) in the treatment of severe tubulopathies.

Methods

This study was a retrospective review of the medical charts of 15 children, aged 12.4 (range 3.6–17.4) years who received fludro after RTx.

Results

With the administration of fludro, both sodium bicarbonate and chloride supplementation decreased, from 10 (range 0–14) to 0 (0–5) g/day, and from 9 (0–20) to 0 (0–3) g/day, respectively (both p < 0.001). Serum potassium also significantly decreased (4.6 ± 0.4 vs. 3.3 ± 0.6 mmol/L; p < 0.001), but there was no significant effect on renal function. Both systolic and diastolic blood pressure increased significantly. Fludro therapy was stopped in six patients due to side-effects (arterial hypertension, hypokalemia during acute diarrhea, gastric pain, n = 3), parental decision (n = 1), inefficacy and/or non-compliance (n = 1) and scheduled withdrawal (n = 1). Four of these patient had subsequent increasing requirements for bicarbonate and/or sodium supplementation, which ultimately required the re-introduction of fludro in two of these patients.

Conclusions

Based on our findings, fludro would appear to be an effective therapy in most cases of severe tubulopathy after RTx. Further prospective studies are required to validate this indication and to determine the optimal dose and timing of treatment to avoid side-effects as well as the clinical and biological follow-up.
Literatur
1.
Zurück zum Zitat Deppe CE, Heering PJ, Viengchareun S, Grabensee B, Farman N, Lombes M (2002) Cyclosporine a and FK506 inhibit transcriptional activity of the human mineralocorticoid receptor: a cell-based model to investigate partial aldosterone resistance in kidney transplantation. Endocrinology 143:1932–1941PubMedCrossRef Deppe CE, Heering PJ, Viengchareun S, Grabensee B, Farman N, Lombes M (2002) Cyclosporine a and FK506 inhibit transcriptional activity of the human mineralocorticoid receptor: a cell-based model to investigate partial aldosterone resistance in kidney transplantation. Endocrinology 143:1932–1941PubMedCrossRef
2.
Zurück zum Zitat Kramer HJ, Goldman R, Gonick HC (1972) Salt-losing syndromes following renal transplantation. Am J Med 53:368–376PubMedCrossRef Kramer HJ, Goldman R, Gonick HC (1972) Salt-losing syndromes following renal transplantation. Am J Med 53:368–376PubMedCrossRef
3.
Zurück zum Zitat Higgins R, Ramaiyan K, Dasgupta T, Kanji H, Fletcher S, Lam F, Kashi H (2004) Hyponatraemia and hyperkalaemia are more frequent in renal transplant recipients treated with tacrolimus than with cyclosporin. Further evidence for differences between cyclosporin and tacrolimus nephrotoxicities. Nephrol Dial Transplant 19:444–450PubMedCrossRef Higgins R, Ramaiyan K, Dasgupta T, Kanji H, Fletcher S, Lam F, Kashi H (2004) Hyponatraemia and hyperkalaemia are more frequent in renal transplant recipients treated with tacrolimus than with cyclosporin. Further evidence for differences between cyclosporin and tacrolimus nephrotoxicities. Nephrol Dial Transplant 19:444–450PubMedCrossRef
4.
Zurück zum Zitat Katari SR, Magnone M, Shapiro R, Jordan M, Scantlebury V, Vivas C, Gritsch HA, McCauley J, Starzl T, Demetris AJ, Randhawa PS (1997) Tacrolimus nephrotoxicity after renal transplantation. Transplant Proc 29:311PubMedCrossRefPubMedCentral Katari SR, Magnone M, Shapiro R, Jordan M, Scantlebury V, Vivas C, Gritsch HA, McCauley J, Starzl T, Demetris AJ, Randhawa PS (1997) Tacrolimus nephrotoxicity after renal transplantation. Transplant Proc 29:311PubMedCrossRefPubMedCentral
5.
Zurück zum Zitat Bagchi S, Husain Zaidi S, Prasad Mathur R (2011) Severe symptomatic hyponatremia–an uncommon presentation of tacrolimus nephrotoxicity. Nephrol Dial Transplant 26:2042–2044PubMedCrossRef Bagchi S, Husain Zaidi S, Prasad Mathur R (2011) Severe symptomatic hyponatremia–an uncommon presentation of tacrolimus nephrotoxicity. Nephrol Dial Transplant 26:2042–2044PubMedCrossRef
6.
Zurück zum Zitat Rokaw MD, West ME, Palevsky PM, Johnson JP (1996) FK-506 and rapamycin but not cyclosporin inhibit aldosterone-stimulated sodium transport in A6 cells. Am J Physiol 271:C194–C202PubMed Rokaw MD, West ME, Palevsky PM, Johnson JP (1996) FK-506 and rapamycin but not cyclosporin inhibit aldosterone-stimulated sodium transport in A6 cells. Am J Physiol 271:C194–C202PubMed
7.
Zurück zum Zitat Aker S, Heering P, Kinne-Saffran E, Deppe C, Grabensee B, Kinne RK (2001) Different effects of cyclosporine a and FK506 on potassium transport systems in MDCK cells. Exp Nephrol 9:332–340PubMedCrossRef Aker S, Heering P, Kinne-Saffran E, Deppe C, Grabensee B, Kinne RK (2001) Different effects of cyclosporine a and FK506 on potassium transport systems in MDCK cells. Exp Nephrol 9:332–340PubMedCrossRef
8.
Zurück zum Zitat Navar LG (2014) Intrarenal renin-angiotensin system in regulation of glomerular function. Curr Opin Nephrol Hypertens 23:38–45PubMedCrossRef Navar LG (2014) Intrarenal renin-angiotensin system in regulation of glomerular function. Curr Opin Nephrol Hypertens 23:38–45PubMedCrossRef
Metadaten
Titel
Fludrocortisone as a new tool for managing tubulopathy after pediatric renal transplantation: a series of cases
Publikationsdatum
01.10.2014
Erschienen in
Pediatric Nephrology / Ausgabe 10/2014
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-014-2842-3

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