Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2023 Apr;182(4):1741-1747.
doi: 10.1007/s00431-023-04804-9. Epub 2023 Feb 9.

Single vs split dose of prednisolone in the treatment of relapses of childhood nephrotic syndrome

Affiliations
Randomized Controlled Trial

Single vs split dose of prednisolone in the treatment of relapses of childhood nephrotic syndrome

W A L K Weerasooriya et al. Eur J Pediatr. 2023 Apr.

Abstract

Nephrotic syndrome is the commonest glomerular disease in childhood. It usually follows a relapsing and remitting course. Corticosteroids are the mainstay of treatment for both the first episode and subsequent relapses. This study was conducted at a single centre to compare the clinical response to a single dose vs. split dose of prednisolone in the treatment of relapses of childhood nephrotic syndrome. Children between the ages of 1 and 14 years admitted with a relapse of idiopathic steroid sensitive nephrotic syndrome from August 2019 to February 2020 were considered for recruitment. A block randomization method based on age was used for allocation. Patients randomised to group A received oral prednisolone at 60 mg/m2 as a single morning dose, while those randomised to group B received the same total dose as two divided doses, of which 2/3 was given in the morning and the rest in the evening. Treatment was continued until remission was achieved following which all patients were switched to alternate day prednisolone. An independent sample t test was used to compare the two groups. One hundred and four episodes of relapse occurring in 96 children were included of which 49 were treated with prednisolone as a split dose and 55 were treated with a single dose of prednisolone. The mean duration to achieve remission for the split-dose group was 8.02 days (SD 1.58) while it was 9.74 days (SD 3.72) for the single-dose group. This difference was statistically highly significant (t(102) = 3.004; p = 0.001; CI 0.58 to 2.86). There was no difference in the adverse events profile of the two groups. Conclusion: The use of prednisolone as a split dose results in a shorter duration to achieve remission when compared to a single morning dose, resulting in a lower cumulative dose of prednisolone to achieve remission. What is Known: • Corticosteroids are the mainstay of treatment for childhood nephrotic syndrome. • Corticosteroids are given as a single dose in the morning to minimise adrenocortical suppression. What is New: • A more rapid attainment of remission can be achieved with a split dose of corticosteroids.

Keywords: Nephrotic syndrome; Paediatrics; Relapses; Split dose; Steroid.

PubMed Disclaimer

References

    1. Schnaper HW (1989) The immune system in minimal change nephrotic syndrome. Pediatr Nephrol 3(1):101–110. https://doi.org/10.1007/BF00859637 - DOI - PubMed
    1. Shalhoub R (1974) Pathogenesis of lipoid nephrosis: a disorder of T-cell function. The Lancet 304(7880):556–560. https://doi.org/10.1016/S0140-6736(74)91880-7 - DOI
    1. Czock D, Keller F, Rasche FM, Häussler U (2005) Pharmacokinetics and pharmacodynamics of systemically administered glucocorticoids. Clin Pharmacokinet 44(1):61–98. https://doi.org/10.2165/00003088-200544010-00003 - DOI - PubMed
    1. Ekka BK, Bagga A, Srivastava RN (1997) Single-versus divided-dose prednisolone therapy for relapses of nephrotic syndrome. Pediatr Nephrol 11(5):597–599. https://doi.org/10.1007/s004670050344 - DOI - PubMed
    1. Brodehl J (1981) Alternate-day prednisone is more effective than intermittent prednisone in frequently relapsing nephrotic syndrome. Eur J Pediatr 135(3):229–237. https://doi.org/10.1007/BF00442096 - DOI

Publication types

LinkOut - more resources