Literature DB >> 36032622

Long-Term Study in Children with Steroid-Resistant Nephrotic Syndrome Progressing to End-Stage Renal Disease.

Loredana Popa1, Mihaela Balgradean1, Anca Croitoru1.   

Abstract

Introduction:Steroid-resistant nephrotic syndrome (SRNS) in children is a glomerular disease who often fails to respond to immunosuppressive treatment and is a leading cause for progression to end-stage renal disease (ESRD) and dialysis. Some risk factors, that appear to be common in patients with SRNS and progression to ESRD, have been identified and reported: focal and segmental glomeruloslerosis on kidney biopsy, high range persistent proteinuria, microscopic hematuria, hypertension, episodes of acute kidney injury (AKI) and resistance to immunosuppressive agents. The challenge is to identify these risk factors and improve patients' management, because children with ESRD have many associated complications and a high rate of morbidity and mortality. Objective: The aim of our study is to observe the incidence of SRNS in our patients and identify the presence of common risk factors in those progressing to ESRD with requirement for dialysis or kidney transplant. Material and methods:We studied a total number of 125 pacients who were diagnosed with nephrotic syndrome in the Department of Pediatric Nephrology of "M. S. Curie" Emergency Clinical Hospital for Children, Bucharest, Romania, from January 2013 to December 2020. Twenty six patients diagnosed with SRNS were included in our study; all of them underwent clinical examination and laboratory tests and were regularly monitored to assess the progression of kidney disease to ESRD. Discussion and results:Steroid-resistant nephrotic syndrome is associated with an increased risk for developing ESRD with requirement for dialysis and transplant. Resistance to immunosuppressive agents was associated with ESRD in our patients. Focal segmental glomerulosclerosis (FSGS), the most common histopathologic lesion, had no value for progression to ESRD in our study. Hematuria, persistent high value proteinuria, hypertension and episodes of AKI were found in our patients with SRNS and progressed to ESRD.

Entities:  

Year:  2022        PMID: 36032622      PMCID: PMC9375901          DOI: 10.26574/maedica.2022.17.2.271

Source DB:  PubMed          Journal:  Maedica (Bucur)        ISSN: 1841-9038


  6 in total

1.  Time trends and ethnic patterns of childhood nephrotic syndrome in Yorkshire, UK.

Authors:  P A McKinney; R G Feltbower; J T Brocklebank; M M Fitzpatrick
Journal:  Pediatr Nephrol       Date:  2001-12       Impact factor: 3.714

2.  Validation of the revised Schwartz estimating equation in a predominantly non-CKD population.

Authors:  Amy Staples; Robin LeBlond; Sandra Watkins; Craig Wong; John Brandt
Journal:  Pediatr Nephrol       Date:  2010-07-22       Impact factor: 3.714

3.  Long-term outcome of idiopathic steroid-resistant nephrotic syndrome: a multicenter study.

Authors:  Djalila Mekahli; Aurelia Liutkus; Bruno Ranchin; Anchalee Yu; Lucie Bessenay; Eric Girardin; Rita Van Damme-Lombaerts; Jean-Bernard Palcoux; François Cachat; Marie-Pierre Lavocat; Guylhène Bourdat-Michel; François Nobili; Pierre Cochat
Journal:  Pediatr Nephrol       Date:  2009-03-12       Impact factor: 3.714

4.  Long-term outcome of primary nephrotic syndrome.

Authors:  O Koskimies; J Vilska; J Rapola; N Hallman
Journal:  Arch Dis Child       Date:  1982-07       Impact factor: 3.791

5.  Recurrence of focal segmental glomerulosclerosis posttransplantation: a special report of the North American Pediatric Renal Transplant Cooperative Study.

Authors:  A Tejani; D H Stablein
Journal:  J Am Soc Nephrol       Date:  1992-06       Impact factor: 10.121

Review 6.  Steroid-resistant nephrotic syndrome: past and current perspectives.

Authors:  Noureddin Nourbakhsh; Robert H Mak
Journal:  Pediatric Health Med Ther       Date:  2017-04-11
  6 in total

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