Literature DB >> 15206026

Bartter syndrome: benefits and side effects of long-term treatment.

Maria Helena Vaisbich1, Maria Danisi Fujimura, Vera H Koch.   

Abstract

The present study reports clinical and laboratory data of patients with Bartter syndrome at diagnosis and follow-up with emphasis on the long-term benefits and side effects of the pharmacological therapy, which includes indomethacin and potassium supplementation. We followed 12 children, 6 boys, with a median age at diagnosis of 24.5 months (range 7-137 months) and at the end of the study 157.5 months (range 26.0-224.0 months). All children presented with polyuria and polydipsia, dehydration, and metabolic and electrolyte disturbances with failure to thrive. However, at study entry 5 of 12 patients also had hypophosphatemia, which disappeared after a mean time of 50+/-22.4 months, 3 of 12 had nephrocalcinosis, and 2 of 12 had typical renal cysts. Despite treatment, hypokalemia was persistent in some patients. During long-term follow-up we observed recovery of growth velocity and adequate metabolic and electrolyte balance. However, we noticed renal and gastrointestinal complications: 2 patients had a perforated gastric ulcer, 1 had a gastric ulcer, and gastritis was detected in 3 children. A decreased glomerular filtration rate was observed in 2 patients during follow-up. Our data emphasize the need for regular surveillance of renal function and gastrointestinal endoscopy in these patients. As an alternative to indomethacin, we present our satisfactory preliminary results with rofecoxib.

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Year:  2004        PMID: 15206026     DOI: 10.1007/s00467-004-1527-8

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  22 in total

1.  Successful management of an extreme example of neonatal hyperprostaglandin-E syndrome (Bartter's syndrome) with the new cyclooxygenase-2 inhibitor rofecoxib.

Authors:  Nikolaus A Haas; Robert Nossal; Christoph H Schneider; Martin A G Lewin; Volker Ocker; Martin Holder; Frank Uhlemann
Journal:  Pediatr Crit Care Med       Date:  2003-04       Impact factor: 3.624

2.  Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Authors:  D B Simon; R S Bindra; T A Mansfield; C Nelson-Williams; E Mendonca; R Stone; S Schurman; A Nayir; H Alpay; A Bakkaloglu; J Rodriguez-Soriano; J M Morales; S A Sanjad; C M Taylor; D Pilz; A Brem; H Trachtman; W Griswold; G A Richard; E John; R P Lifton
Journal:  Nat Genet       Date:  1997-10       Impact factor: 38.330

3.  Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Authors:  D B Simon; F E Karet; J Rodriguez-Soriano; J H Hamdan; A DiPietro; H Trachtman; S A Sanjad; R P Lifton
Journal:  Nat Genet       Date:  1996-10       Impact factor: 38.330

4.  Treatment of Bartter's syndrome in early childhood with prostaglandin synthetase inhibitors.

Authors:  J M Littlewood; M R Lee; S R Meadow
Journal:  Arch Dis Child       Date:  1978-01       Impact factor: 3.791

5.  Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs.

Authors:  L A García Rodríguez; H Jick
Journal:  Lancet       Date:  1994-03-26       Impact factor: 79.321

6.  Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

Authors:  Melanie Peters; Nikola Jeck; Stephan Reinalter; Andreas Leonhardt; Burkhard Tönshoff; G ünter Klaus G; Martin Konrad; Hannsjörg W Seyberth
Journal:  Am J Med       Date:  2002-02-15       Impact factor: 4.965

7.  Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Authors:  D B Simon; C Nelson-Williams; M J Bia; D Ellison; F E Karet; A M Molina; I Vaara; F Iwata; H M Cushner; M Koolen; F J Gainza; H J Gitleman; R P Lifton
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

8.  The neonatal variant of Bartter syndrome and deafness: preservation of renal function.

Authors:  Hanna Shalev; Melly Ohali; Leonid Kachko; Daniel Landau
Journal:  Pediatrics       Date:  2003-09       Impact factor: 7.124

9.  Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome.

Authors:  Stephan C Reinalter; Nikola Jeck; Christoph Brochhausen; Bernhard Watzer; Rolf M Nüsing; Hannsjörg W Seyberth; Martin Kömhoff
Journal:  Kidney Int       Date:  2002-07       Impact factor: 10.612

10.  Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome.

Authors:  Rosa Vargas-Poussou; Chunfa Huang; Philippe Hulin; Pascal Houillier; Xavier Jeunemaître; Michel Paillard; Gabrielle Planelles; Michèle Déchaux; R Tyler Miller; Corinne Antignac
Journal:  J Am Soc Nephrol       Date:  2002-09       Impact factor: 10.121

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  24 in total

Review 1.  Understanding Bartter syndrome and Gitelman syndrome.

Authors:  Oliver T Fremont; James C M Chan
Journal:  World J Pediatr       Date:  2012-01-27       Impact factor: 2.764

2.  Female ROMK null mice manifest more severe Bartter II phenotype on renal function and higher PGE2 production.

Authors:  Qingshang Yan; Xinbo Yang; Alessandra Cantone; Gerhard Giebisch; Steven Hebert; Tong Wang
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2008-06-25       Impact factor: 3.619

Review 3.  The long-term complications of the inherited tubulopathies: an adult perspective.

Authors:  Maryam Khosravi; Stephen B Walsh
Journal:  Pediatr Nephrol       Date:  2014-02-25       Impact factor: 3.714

4.  Effect of nonsteroidal anti-inflammatory drugs in children with Bartter syndrome.

Authors:  Gaël Gasongo; Larry A Greenbaum; Olivier Niel; Theresa Kwon; Marie-Alice Macher; Anne Maisin; Véronique Baudouin; Claire Dossier; Georges Deschênes; Julien Hogan
Journal:  Pediatr Nephrol       Date:  2018-11-13       Impact factor: 3.714

Review 5.  Salt-Losing Tubulopathies in Children: What's New, What's Controversial?

Authors:  Robert Kleta; Detlef Bockenhauer
Journal:  J Am Soc Nephrol       Date:  2017-12-13       Impact factor: 10.121

6.  Nephrotoxicity with cyclooxygenase 2 inhibitor use in children.

Authors:  Jeffery T Fletcher; Nicole Graf; Anthony Scarman; Hamda Saleh; Stephen I Alexander
Journal:  Pediatr Nephrol       Date:  2006-09-06       Impact factor: 3.714

7.  Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features.

Authors:  Rezan Topaloglu; Esra Baskın; Elif Bahat; Salih Kavukcu; Nilgun Cakar; Osman Donmez; Ayfer Gur Guven; Salim Calıskan; Ozlem Erdogan; Fatos Yalcınkaya
Journal:  Clin Exp Nephrol       Date:  2010-11-20       Impact factor: 2.801

8.  Transfer of rofecoxib into human milk.

Authors:  Sharon J Gardiner; Evan J Begg; Mei Zhang; Ruth C E Hughes
Journal:  Eur J Clin Pharmacol       Date:  2005-06-10       Impact factor: 2.953

Review 9.  Longitudinal growth in chronic hypokalemic disorders.

Authors:  Helena Gil-Peña; Natalia Mejia; Oscar Alvarez-Garcia; Vanessa Loredo; Fernando Santos
Journal:  Pediatr Nephrol       Date:  2009-11-10       Impact factor: 3.714

10.  Genetic analysis in Bartter syndrome from India.

Authors:  Pradeep Kumar Sharma; Bhaskar Saikia; Rachna Sharma; Kumar Ankur; Praveen Khilnani; Vinay Kumar Aggarwal; Hae Cheong
Journal:  Indian J Pediatr       Date:  2014-04-04       Impact factor: 1.967

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