Ensuring the Least Restrictive Medication

June 27, 2025

A Guide for Carers Using the Maudsley Deprescribing Guidelines

The overuse of psychotropic drugs is a significant concern in healthcare, aged care, and disability services. This issue has been highlighted during several Disability Royal Commission hearings, bringing to light the need for more responsible prescribing practices and better support for individuals affected by these medications.


On Wednesday, 12 March 2025, the Striking the Balance forum featured keynote speakers Dr. Mark Horowitz, an expert in psychotropic drugs and author of the Maudsley Deprescribing Guidelines, and Professor Julian Trollor, Director of the National Centre of Excellence in Intellectual Disability Health. These experts shared valuable insights into the challenges and solutions related to the overuse of psychotropic drugs.

Deprescribing: Is the process of tapering or stopping medications that may no longer be necessary or beneficial. It aims to minimise medication burden and reduce the risk of side effects and dependency

Dr. Horowitz emphasised the importance of deprescribing guidelines to help healthcare providers reduce the reliance on psychotropic medications. His Maudsley Deprescribing Guidelines offer a structured approach to safely tapering off these drugs, ensuring that patients receive appropriate care without unnecessary medication.

Professor Trollor highlighted the need for comprehensive health assessments and personalised care plans for individuals with intellectual disabilities. He stressed that psychotropic drugs should not be the first line of treatment and that alternative therapies and supports should be considered to address behavioural and mental health issues.


Steps for Carers to Ensure Least Restrictive Medication


  1. Comprehensive Assessment:
    Begin with a thorough assessment of your loved one's current medications, health status, and behavioural needs. Collaborate with healthcare professionals to understand the necessity of each medication and identify potential candidates for deprescribing.

  2. Educate Yourself and Your Loved One:
    Familiarise yourself with the Maudsley Deprescribing Guidelines and educate your loved one about the benefits and process of deprescribing. Understanding the guidelines can empower both of you to make informed decisions about medication management.

  3. Collaborate with Healthcare Providers:
    Work closely with doctors, pharmacists, and other healthcare providers to develop a personalised deprescribing plan. Ensure that the plan includes gradual tapering schedules, monitoring for withdrawal symptoms, and strategies for managing any challenges that may arise.
     
  4. Monitor and Support:
    Regularly monitor your loved one's progress during the deprescribing process. Be vigilant for any signs of withdrawal or changes in behaviour. Provide emotional support and reassurance to help them cope with the transition.
     
  5. Use Non-Pharmacological Interventions:
    Explore non-pharmacological interventions that can support your loved one's health and well-being. This may include behavioural therapies, lifestyle changes, and other supportive measures that can reduce the need for medication.

  6. Advocate for Your Loved One:
    Advocate for your loved one's right to receive the least restrictive medication. Ensure that healthcare providers consider their preferences and needs when making decisions about medication management.
     

The overuse of psychotropic drugs in healthcare, aged care, and disability services is a pressing issue that requires immediate attention. By adopting deprescribing guidelines and personalised care plans, carers and healthcare providers can work together to ensure that individuals receive the most appropriate and effective care.

News & Insights

Check Our Latest Resources

September 10, 2025
Understanding Megalocornea-Intellectual Disability Syndrome
September 10, 2025
The NDIS Quality and Safeguards Commissio n has released a new suite of resources titled "Restrictive Practices and Me", designed to support meaningful conversations with participants when regulated restrictive practices are included in their behaviour support plans. These resources aim to uphold participants' rights and ensure that discussions around restrictive practices are accessible, respectful, and tailored to individual needs. Developed in collaboration with people with disability, NDIS providers, authorisation bodies, and advocacy organisations, the materials reflect a commitment to person-centred practice and transparency. What’s Included? The Restrictive Practices and Me toolkit features: A tip sheet for practitioners and providers Plain English and Easy Read discussion books A case study illustrating practical application A set of icons to visually represent different types of restrictive practices These resources are editable and adaptable, allowing practitioners to tailor content to each participant’s circumstances. For example, pages not relevant to a participant’s situation can be removed, and images can be reused in other formats. Why It Matters Under Section 20 of the NDIS (Restrictive Practices and Behaviour Support) Rules 2018, participants must be informed when restrictive practices are proposed. These conversations must be conducted in a way that is easy to understand and respectful of the participant’s autonomy. The Commission emphasises that restrictive practices should only be used as a last resort, and must be the least restrictive option available. They must be included in a behaviour support plan and follow the appropriate authorisation processes. Regulatory Priorities for 2025–26 This initiative aligns with the NDIS Commission’s broader regulatory priorities for 2025–26, which include: Reducing and eliminating regulated restrictive practices Strengthening oversight of unregistered providers Improving management of high-risk health concerns Ensuring providers support and train skilled workers Commissioner Louise Glanville reaffirmed the Commission’s commitment to human rights, stating that “practices that restrict the rights or freedom of movement of people with disability can be traumatic, dangerous and breach basic human rights." Accessing the Resources The Restrictive Practices and Me resources are available for download on the NDIS Commission website . Providers are encouraged to use, adapt, and share these tools to foster informed, respectful, and rights-based conversations with participants. Link : Talking to participants about Restrictive Practices Reference: NDIS Commision 2025-26 priorities focus: participant rights and safer services
September 10, 2025
 By Tharon Neurodivergent Consultant at helpz