-
1دورية أكاديمية
المؤلفون: Veltkamp, Floor, Pistorius, Marcel C. M., Mak‐Nienhuis, Elske M., Schreuder, Michiel F., Bouts, Antonia H. M., Mathôt, Ron A. A.
المساهمون: Nierstichting
المصدر: British Journal of Clinical Pharmacology ; ISSN 0306-5251 1365-2125
الوصف: Aims Prednisolone is the cornerstone of treatment for idiopathic nephrotic syndrome in children, but is associated with marked side‐effects. Therapeutic drug monitoring using saliva would be a patient‐friendly option to monitor prednisolone treatment. To assess the feasibility of saliva monitoring, we described the pharmacokinetics (PK) of unbound prednisolone in plasma and saliva of children with first onset steroid‐sensitive nephrotic syndrome (SSNS). Methods Children (age 2–16 years) with SSNS participating in a randomized, placebo‐controlled trial with levamisole were treated with an 18‐week tapering schedule of prednisolone. Five serial samples were collected at 4 (saliva) and 8 weeks (saliva and plasma) after first onset. A nonlinear mixed‐effects model was used to estimate the PK parameters of unbound prednisolone and the saliva‐to‐plasma ratio. Monte Carlo simulations were performed to assess the predictive performance of saliva monitoring. Results From 39 children, 109 plasma and 275 saliva samples were available. Estimates (relative squared error) of unbound plasma clearance and volume of distribution were 93 (5%) L h −1 70 kg −1 and 158 (7%) L 70 kg −1 , respectively. Typical saliva‐to‐plasma ratio was 1.30 (8%). Monte Carlo simulations demonstrated that on basis of 4 saliva samples and a single plasma sample unbound plasma area‐under‐the‐concentration–time curve can be predicted within 20% imprecision in 79% of the patients compared to 87% based on 4 plasma samples. Conclusion Saliva proved to be a reliable and patient‐friendly option to determine prednisolone plasma exposure in children with SSNS. This opens opportunities for further PK and pharmacodynamics studies of prednisolone in a variety of paediatric conditions.
-
2دورية أكاديمية
المؤلفون: Veltkamp, Floor, Pistorius, Marcel C M, Mak-Nienhuis, Elske M, Schreuder, Michiel F, Bouts, Antonia H M, Mathôt, Ron A A
المصدر: Br J Clin Pharmacol ; ISSN:1365-2125 ; Volume:90 ; Issue:7
مصطلحات موضوعية: clinical pharmacology, paediatric nephrology, pharmacokinetics
الوصف: Prednisolone is the cornerstone of treatment for idiopathic nephrotic syndrome in children, but is associated with marked side-effects. Therapeutic drug monitoring using saliva would be a patient-friendly option to monitor prednisolone treatment. To assess the feasibility of saliva monitoring, we described the pharmacokinetics (PK) of unbound prednisolone in plasma and saliva of children with first onset steroid-sensitive nephrotic syndrome (SSNS).
