Childhood Steroid-resistant Nephrotic Syndrome: Long-term Outcomes from a Tertiary Care Center

被引:5
|
作者
Agrwal, Shipra [1 ]
Mantan, Mukta [2 ,3 ]
Dabas, Aashima [2 ,3 ]
Batra, Vineeta V. [4 ]
机构
[1] Army Coll Med Sci, Dept Pediat, New Delhi, India
[2] Maulana Azad Med Coll, Dept Pediat, New Delhi, India
[3] Lok Nayak Hosp, New Delhi, India
[4] Govind Ballabh Pant Inst Postgrad Med Educ & Res, Dept Pathol, New Delhi, India
关键词
Calcineurin inhibitors; CKD; MCD; remission; SRNS; steroids; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; CYCLOSPORINE-A; CHILDREN; CYCLOPHOSPHAMIDE; TACROLIMUS; EFFICACY; SAFETY; TRIAL;
D O I
10.4103/ijn.ijn_258_21
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Steroid-resistant nephrotic syndrome (SRNS) is a rare condition that accounts for about 10% to 20% of all nephrotic syndromes in children. While calcineurin inhibitors induce remission in the majority, the data on long-term outcomes are limited. This retrospective study aimed to look at the clinical profile, biopsy findings, and long-term treatment outcomes in children with SRNS. Methods: The records of all children (1-18 years) with SRNS with biopsy findings of minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), or mesangioproliferative glomerulonephritis, who received treatment for a minimum period of 12 months and were in follow-up during the years 2007-2018 at a tertiary care teaching hospital were retrieved. The clinical, histopathological, and biochemical factors and treatment outcomes were recorded and analyzed. Results: Ninety-one (72 boys) children with a median (interquartile range [IQR]) age of onset of nephrotic syndrome as 48 (24-87) months were included. MCD and FSGS were the most common histopathological types (57.1% and 36.3%, respectively) and 62 (68.1%) patients had late steroid resistance. Calcineurin inhibitors (CNIs) were used in 86.8% of the children, and response rates with cyclosporine and tacrolimus for complete remission (CR) were 80% and 73.7%, respectively, with median (IQR) time to response being 3 (2-4) months. The presence of MCD on histology and the use of CNIs were significantly associated with CR (P < 0.01). At a median (IQR) follow-up of 5 (3-7) years, 76 (83.5%) children had either CR or partial remission, four (4.4%) developed chronic kidney disease and five (5.5%) died (three due to end-stage renal disease and two of infective complications). Conclusion: SRNS children with MCD on biopsy, late resistance, and response to CNIs have better long-term outcomes. Most patients respond to CNIs within the first 6 months of use and need therapy for at least 24 to 36 months.
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收藏
页码:320 / 326
页数:7
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