Abstract
Since the 1970s, the accepted standard of care for children presenting with their first episode of nephrotic syndrome has been a course of oral prednisone comprising 60 mg/m2 (2 mg/kg) daily for 4 weeks followed by 40 mg/m2 (1.5 mg/kg) on alternate days for 4 weeks with or without a tapering dose. A meta-analysis of randomized controlled trials (RCTs) in 2007 concluded that prednisone treatment for ≥3 months compared with 2 months reduced the risk of relapse at 12-24 months. However some included studies were at high risk of bias, which, on average, leads to an overestimation of the treatment effect observed. Subsequently 4 RCTs (3 of which were placebo-controlled) published between 2013 and 2019 that were at low risk of bias and involving 775 children demonstrated no benefit of extended-duration treatment beyond 8-12 weeks (with daily administration followed by alternate-day prednisone) for the outcome of first relapse or frequent relapses...
| Original language | English |
|---|---|
| Pages (from-to) | 433-435 |
| Number of pages | 3 |
| Journal | American Journal of Kidney Diseases |
| Volume | 80 |
| Issue number | 4 |
| Early online date | 1 Aug 2022 |
| DOIs | |
| Publication status | Published - Oct 2022 |
Keywords
- Prednisone
- Nephrotic Syndrome
- Child health