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Dietary Sodium Intake in Children on Chronic Dialysis (PeDialysis)

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

Chronic Dialysis in Children

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Cardiovascular disease is common in patients with end-stage renal disease that began in childhood, and volume overload plays a key role in the development of hypertension, left ventricular hypertrophy (LVH) and alterations. cardiovascular disease in this population. Thus, inter-dialytic weight gain is correlated with blood pressure and left ventricular mass index in children on hemodialysis (HD). Significant inter-dialytic weight gain in dialysis patients is largely due to thirst secondary to salt ingestions: attempts at water restriction without concomitant sodium restriction will probably be in vain. Additionally, sodium overload negatively affects blood pressure and cardiovascular status through various mechanisms unrelated to volume expansion.

Soda extraction by dialysis is often difficult, and sodium control is largely dependent on restricting dietary sodium intake. Some studies in adults have shown that a low sodium diet reduced inter-dialytic weight gain, reduced intra-dialytic complications, improved blood pressure values, and lowered index. left ventricular mass and mortality in dialysis patients.

For children with chronic kidney disease, data from the American Chronic Kidney Disease (CKiD) study show that the median sodium intake in children without dialysis with chronic kidney disease exceeds the maximum recommended intakes for all patients. age groups.

No study to date has investigated the average dietary sodium intake of children on dialysis. And, more importantly, the relationship between dietary sodium intake and cardiovascular morbidity has never been studied in children on dialysis.

Enrollment

4 estimated patients

Sex

All

Ages

3 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

  • Minor patient (≥ 3 months and <18 years)
  • Under the care of the University Hospitals of Strasbourg
  • Having benefited from chronic dialysis (> 3 months)
  • Having undergone hemodialysis (HD) or hemodiafiltration (HDF), 3 sessions / week, or automated peritoneal dialysis (PD)
  • Subject (and / or his parental authority) not having expressed, after being informed, his opposition to the reuse of his data for the purposes of this research.

Non-Inclusion Criteria :

  • Patient or one of the parents who expressed their opposition to participating in the study
  • Intensive hemodialysis (HD at home, HD at night, ≥ 4 sessions / week)
  • Intercurrent illness or clinical instability (left to the judgment of the physician)
  • Non-nephrological diseases causing loss of salt (eg cystic fibrosis, etc.)
  • Any physical or psychosocial situation that prevented the 24-hour ambulatory BP measurement from being taken, or poor compliance with the dietetic collection, etc.).

Trial contacts and locations

1

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Central trial contact

Ariane ZALOSZYC, MD

Data sourced from clinicaltrials.gov

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