Clinical outcome of children with primary distal renal tubular acidosis.

J Med Assoc Thai

Division of Nephrology, Department of Pediatrics, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Published: October 2011

Objective: To evaluate the clinical course of children with primary distal renal tubular acidosis and to determine parameters correlated with the outcomes.

Material And Method: A retrospective review of medical records was carried out. The parameters at initial diagnosis and the last visit were collected including height standard deviation score (SDS), weight SDS, ultrasonography of kidneys, serum electrolytes, urine electrolytes, urine calcium to urine creatinine ratio (urine Ca/Cr), serum creatinine, bicarbonate dosage and glomerular filtration rate estimated by Schwartz's formula (eGFR).

Results: Fifteen patients were included with median follow-up time of 12 years (range 4.5 to 19 years). Median age at diagnosis was 3 years (range 0.25 to 9 years). At the last visit, median height SDS increased significantly from -3.1 to -0.8 (p = 0.04). Height SDS at the last visit correlated with age at diagnosis (r = -0.54, p = 0.038) and serum bicarbonate at the last visit (r = 0.68, p = 0.008). Moreover, at the last visit, eGFR correlated with urine Ca/Cr (r = -0.84, p = 0.001).

Conclusion: After treatment, growth of patients improved satisfactorily. The outcomes were associated with age at diagnosis, compliance of bicarbonate therapy and urine Ca/Cr at the last visit.

Download full-text PDF

Source

Publication Analysis

Top Keywords

urine ca/cr
12
age diagnosis
12
children primary
8
primary distal
8
distal renal
8
renal tubular
8
tubular acidosis
8
electrolytes urine
8
years range
8
height sds
8

Similar Publications

Background: X-linked hypophosphatemic rickets (XLH) is associated with uninhibited FGF23 activity, which leads to phosphaturia, hypophosphatemia and depressed active vitamin D (1,25OH2D) levels. Conventional treatment with phosphate supplements and vitamin D analogs may lead to hypercalciuria (HC), nephrocalcinosis (NC) and hyperparathyroidism. We investigated the effects of burosumab treatment, an anti-FGF23 monoclonal antibody recently approved for XLH, on these complications.

View Article and Find Full Text PDF

Background/aim: Nocturnal enuresis can be frustrating for children and their families as the child ages. Our aim is to evaluate urine aquaporin 2 (AQP-2) as a noninvasive biomarker of water balance in children with primary monosymptomatic nocturnal enuresis (PMNE).

Material And Methods: The study included 90 children; sixty-eight children suffering from PMNE aged (9.

View Article and Find Full Text PDF

Background: Reference values for urinary calcium (Ca) and other solutes/creatinine (Cr) ratios in infants and young children are scarce. Its variation with type of lactation administered, breastfed (BF) or formula (F), is incompletely known.

Methods: A total of 511 spot urine samples from 136 children, aged 6 days to < 5 years, was collected.

View Article and Find Full Text PDF

Background: Bartter syndrome (BS) is a rare congenital salt-losing renal tubular transport disorder, characterized by salt wasting, polyuria, biochemical abnormalities, and acid-base homeostasis imbalance. The syndrome has five different genetic forms, and novel mutations of CLCNKB gene lead to type 3 BS also known as classic BS. In this case, we report clinical and molecular findings from a newborn baby with BS.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!