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  4. Dosing Variability and Clinical Outcomes of Oxybutynin: A Pediatric Cohort of Patients With Neurogenic Bladder

Dosing Variability and Clinical Outcomes of Oxybutynin: A Pediatric Cohort of Patients With Neurogenic Bladder

Top Spinal Cord Inj Rehabil, 2022 · DOI: 10.46292/sci21-00091 · Published: July 1, 2022

UrologyPediatrics

Simple Explanation

Neurogenic bladder is a common issue for children with spinal cord problems, leading to potential kidney damage if not treated early. Oxybutynin is a common medication used to manage this condition. This study looked at how oxybutynin is used in children with neurogenic bladder, focusing on the dose given, other medications they take, and bladder function tests. The study found that there's a wide range in the amount of oxybutynin prescribed and that some children still had high bladder pressures even on the highest recommended dose, which suggests the need to understand why some children respond differently to the medication.

Study Duration
Retrospective data collected between October 7, 2015, and December 30, 2015
Participants
100 pediatric patients with neurogenic bladder
Evidence Level
Not specified

Key Findings

  • 1
    There was significant variability in oxybutynin dosing among the pediatric patients with neurogenic bladder, with the median daily dose being 0.36 mg/kg.
  • 2
    A considerable proportion of patients (38%) with a detrusor leak point pressure (DLPP) greater than 40 cm H2O were on or exceeding the maximum guideline-recommended dose of oxybutynin.
  • 3
    The wide dosing variability and high DLPPs despite maximal dosing indicate a need for further investigation of oxybutynin’s bioavailability in this population compared to its side effects and clinical outcomes.

Research Summary

This retrospective study examined the real-world practice patterns of medical management of neurogenic bladder in a pediatric cohort, focusing on oxybutynin use, dosing variability, and potential drug interactions. The study found a wide range in oxybutynin dosing, which may be influenced by patient-specific differences in bioavailability and tolerance, as well as potential drug-drug interactions. The findings suggest a need for further research to understand the relationship between oxybutynin dose, exposure, and effect, particularly in patients with high detrusor leak point pressures despite maximal dosing.

Practical Implications

Personalized Dosing

Future research could focus on developing precision-dosing models based on patient genomics to optimize oxybutynin therapy.

Bioavailability Investigation

Further investigation into oxybutynin's bioavailability in the pediatric population is needed to understand the variability in clinical outcomes.

Drug Interaction Awareness

Clinicians should be aware of potential drug-drug interactions with oxybutynin, especially in patients on multiple medications.

Study Limitations

  • 1
    Retrospective nature of the study
  • 2
    Absence of serum concentrations of oxybutynin or its metabolites
  • 3
    Single-center study, potentially limiting generalizability

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