i would be grateful for views on the legal framework governing the continued use of zopiclone in a care‑home setting for a person with Alzheimer’s disease who lacks capacity and is subject to a DoLS authorisation.
Background
• Zopiclone 3.75 mg was prescribed in hospital as a short‑term (14‑day) measure.
• The discharge summary stated it should be reviewed by the GP.
• The person was admitted directly to a care home under a court‑approved placement and remains there.
• It is unclear whether any GP review has taken place since admission.
Questions
1. Medication review:
Who is responsible for reviewing a short‑term sedative when someone moves from hospital to a care home, and what are the expected timescales?
2. MCA / best interests:
What MCA processes are required if a sedative‑hypnotic is continued beyond the original short‑term period (capacity assessment, best‑interests decision, documentation)?
3. DoLS / restraint:
At what point could ongoing use of a sedative for behavioural management amount to chemical restraint under MCA/DoLS, and what safeguards are required?
4. Covert medication:
If such medication were given covertly, what authorisation and documentation would be required?
I am seeking clarification of the legal and regulatory framework, not medical advice.
Thank you.