[Sustained effectiveness of osmotic-release methylphenidate: a study of 266 cases]

A Fernández-Jaén1, D Martín Fernández-Mayoralas, B Calleja-Pérez

  • 1Servicio de Neurología Pediátrica, Hospital de La Zarzuela, Madrid, España. aferjaen@telefonica.net

Revista De Neurologia
|March 26, 2009
PubMed
Abstract

Insights

Osmotic-release methylphenidate (MTF-O) effectively manages attention deficit/hyperactivity disorder (ADHD) symptoms. This treatment sustained improvements in attention and behavior throughout the day, as reported by families.

Area of Science:

  • Pharmacology
  • Neuroscience
  • Pediatrics

Context:

  • Attention deficit/hyperactivity disorder (ADHD) significantly impacts children's daily functioning.
  • Methylphenidate (MTF) is a common pharmacotherapy for ADHD.
  • Osmotic-release formulations (MTF-O) aim to provide sustained symptom control.

Purpose:

  • To evaluate the sustained effectiveness of osmotic-release methylphenidate (MTF-O) in pediatric ADHD patients.
  • To assess MTF-O's impact on attention, hyperactivity, and impulsivity within a family context.

Summary:

  • A study involving 266 ADHD patients (ages 5-17) assessed MTF-O treatment over four days, alternating between on and off treatment weekends.
  • Validated scales (DSM-IV-TR, ICG-M, Depremb-R) were used to quantify symptom changes.
  • Results showed statistically significant reductions in inattention, hyperactivity, and impulsivity (p < 0.01) with MTF-O.

Impact:

  • MTF-O demonstrated sustained clinical improvement in ADHD symptoms from morning to bedtime, according to family-reported outcomes.
  • The findings support MTF-O as an effective treatment for improving attention and behavior in children with ADHD throughout the day.

Related Concept Videos

Oral Drug Delivery Systems: Continuous-Release Systems01:26

Oral Drug Delivery Systems: Continuous-Release Systems

Continuous-release drug delivery systems offer a strategic approach to maintaining therapeutic drug levels over extended periods following oral administration. By modulating the release rate of active pharmaceutical ingredients, these systems minimize fluctuations in plasma concentrations, which enhances clinical efficacy and reduces the need for frequent dosing. Such characteristics make them particularly advantageous in managing chronic diseases where patient adherence and stable drug...
Ophthalmic Drug Delivery Systems01:23

Ophthalmic Drug Delivery Systems

Ophthalmic drug delivery faces major limitations due to poor absorption across the corneal membrane. This process is primarily driven by diffusion and is influenced by two main factors: the physicochemical properties of the drug and tear drainage. Most ophthalmic drugs, such as pilocarpine, epinephrine, atropine, and local anesthetics, are weak bases. They are typically formulated at an acidic pH to enhance chemical stability. However, this leads to high ionization, reducing their ability to...
Modified-Release Drug Delivery Systems: Classification01:23

Modified-Release Drug Delivery Systems: Classification

Modified-release drug delivery systems improve drug efficacy and minimize side effects by controlling the rate and location of drug release. These systems fall into three categories: rate-programmed, stimuli-activated, and site-targeted.Rate-programmed systems release drugs at a predetermined rate, maintaining consistent therapeutic levels and reducing fluctuations that could lead to toxicity or subtherapeutic effects. These systems use polymeric matrices, reservoir-based designs, or osmotic...
Modified-Release Drug Delivery Systems: Influencing Factors01:20

Modified-Release Drug Delivery Systems: Influencing Factors

Modified-release drug delivery systems are designed to optimize the therapeutic effect of drugs by minimizing side effects, reducing the dosage required, and controlling drug release to align with pharmacokinetic and pharmacodynamic needs. The system depends on two key factors: the drug's release from the formulation and its movement through the body to the target site. Unlike conventional dosage forms, where absorption is the limiting step, the rate of drug release is the key determinant in...
Modified-Release Drug Delivery Systems: Overview01:19

Modified-Release Drug Delivery Systems: Overview

Modified-release dosage forms are designed to address the limitations of drugs with short biological half-lives. These forms maintain stable therapeutic drug concentrations over extended periods, reducing the need for frequent dosing. A consistent drug level helps minimize peak-trough fluctuations, which can reduce adverse effects, lower the risk of drug resistance, and improve overall treatment effectiveness.One common type of modified-release form is the extended-release (ER) formulation. ER...
Modified-Release Drug Delivery Systems: Drug Release Characteristics01:22

Modified-Release Drug Delivery Systems: Drug Release Characteristics

Drug release from modified-release dosage forms is designed to achieve specific therapeutic effects by controlling the rate and extent of drug release. The classification of these drug release systems is based on key pharmacokinetic assumptions: drug disposition follows first-order kinetics, drug release is the rate-limiting step in absorption, and the released drug is rapidly and completely absorbed.There are four major models of drug release patterns. The first model is the slow zero-order...