Abstract
Methylphenidate is the most frequently used medicine for the treatment of ADHD. While its short-term effects are well-known, long-term effects are much less clear.
In the first part of my thesis I investigated the effects of stopping methylphenidate (i.e., switching to a placebo) after approximately one year of use. Methylphenidate generally remained more effective than a placebo, based on teacher ratings. However, a large subgroup of children could stop using methylphenidate without deteriorating. Still, many of these children continued to use methylphenidate. Either stopping their medication or a critical reexamination of the dosage would be more fitting. Furthermore, I found that continued use of methylphenidate beyond two years has a beneficial effect on working memory.
In the second part of my thesis I investigated how well clinicians adhere to guidelines when prescribing methylphenidate. I found that guideline adherence can be improved, both during the initial dose finding phase and follow-up visits. More frequent follow-ups, better registration of height and weight, and using validated questionnaires could all contribute to reducing potential risks and overall unnecessary use of methylphenidate.
Finally, in a large database I found that better adherence to ADHD medication reduces the risk of minor offenses in adolescents, underscoring the importance of regular monitoring.
My thesis shows that optimizing methylphenidate is delicate: after one year, many children benefit from a dosage review or may stop their medication. However, methylphenidate may also reduce delinquent behavior. Thus, we need a practical, systematic evaluation method for clinical use that assesses multiple domains and helps create personalized treatment plans.
In the first part of my thesis I investigated the effects of stopping methylphenidate (i.e., switching to a placebo) after approximately one year of use. Methylphenidate generally remained more effective than a placebo, based on teacher ratings. However, a large subgroup of children could stop using methylphenidate without deteriorating. Still, many of these children continued to use methylphenidate. Either stopping their medication or a critical reexamination of the dosage would be more fitting. Furthermore, I found that continued use of methylphenidate beyond two years has a beneficial effect on working memory.
In the second part of my thesis I investigated how well clinicians adhere to guidelines when prescribing methylphenidate. I found that guideline adherence can be improved, both during the initial dose finding phase and follow-up visits. More frequent follow-ups, better registration of height and weight, and using validated questionnaires could all contribute to reducing potential risks and overall unnecessary use of methylphenidate.
Finally, in a large database I found that better adherence to ADHD medication reduces the risk of minor offenses in adolescents, underscoring the importance of regular monitoring.
My thesis shows that optimizing methylphenidate is delicate: after one year, many children benefit from a dosage review or may stop their medication. However, methylphenidate may also reduce delinquent behavior. Thus, we need a practical, systematic evaluation method for clinical use that assesses multiple domains and helps create personalized treatment plans.
Original language | English |
---|---|
Qualification | Doctor of Philosophy |
Awarding Institution |
|
Supervisors/Advisors |
|
Award date | 4-Sept-2024 |
Place of Publication | [Groningen] |
Publisher | |
Print ISBNs | 978-94-6506-248-8 |
DOIs | |
Publication status | Published - 2024 |