Care on a hospital ward
Someone with dementia may be admitted to a general or specialist hospital ward either as part of a planned procedure, such as a cataract operation, or following an accident, such as a fall. Hospital environments can be disorientating and frightening for a person with dementia and may make them more confused than usual. The person might find the ward loud and unfamiliar, and may not understand why they are there. However, there is much that can be done to help them adapt to the new environment. This factsheet covers some of the issues that friends, family and carers should consider when a person with dementia goes into hospital and gives tips on how the person can be reassured and supported during their stay.
Help from hospital staff
Ward staff will not necessarily know that the person has dementia, or may lack experience in working with people with dementia, so it is helpful if relatives and friends can give them information on how dementia is affecting the individual and suggest ways of assisting and communicating with the person. This will make it easier for ward staff to ensure that the person with dementia is comfortable.
Staff should answer any questions and discuss any issues you may have. If they seem too busy to talk, ask to make an appointment - ideally with the named nurse. The named nurse (who is always a trained nurse) will be responsible for co-ordinating the person's care. This meeting will be an opportunity to discuss any concerns and should provide a good basis for future communication. If any problems arise later, they can then usually be sorted out through the named nurse. If you want to discuss the person's condition or treatment in more depth, ask to make an appointment to see the doctor or consultant.
Some hospital trusts provide a mental health service (sometimes referred to as a 'hospital liaison team'). Members of this team might include psychologists, mental health nurses and mental health specialist doctors. Assessment and advice from a member of this team can help nursing and medical staff manage any difficulties the person may be experiencing as a consequence of their dementia. If you are concerned that the person's dementia is deteriorating or not being considered fully, you may want to make an appointment with the mental health team.
You may also want to make an appointment to see the hospital social worker. The social worker can advise on a range of matters, such as:
- problems getting to and from the hospital to visit
- residential and nursing care
- help at home
- difficulties experienced by carers or friends or family, such as illness, disability, stress or other commitments that may affect their ability to visit or continue to care for the person. These should also be discussed with the named nurse.
Information about the person with dementia
It is important that all staff are aware of the person's dementia. Any further information that carers can add is also valuable as it will help staff to see and respond to the person as an individual. The named nurse should explain to other members of staff how the person's dementia can affect their behaviour and communication. They should also tell staff how the person prefers to be addressed - for example, informally, such as 'Charlie', or formally, such as 'Mr Cohen'.
As information can become lost or forgotten, it can help if a friend, carer or family member writes down some important facts about the person with dementia. This written information can be given to the named nurse at the first meeting and should be held in the person's medical notes. One side of A4 paper is usually enough.
Alzheimer's Society has produced a leaflet called This is me which can be used to record this information. When completed, it provides a snapshot of the person with dementia, giving information about them as an individual, such as needs, preferences, likes, dislikes and interests. The leaflet can be downloaded from alzheimers.org.uk/thisisme or ordered from Xcalibre on 01628 529 240.
The information should include:
- the name by which the person wishes to be known
- brief details of their normal routines, including whether they need reminders or support with washing, dressing, going to the toilet, eating and drinking or taking medication
- information about foods they particularly like or dislike, or any difficulties they have eating
- illness or pain that may bother them
- any cultural or religious needs
- information about sleeping patterns
- whether the person likes to be active or inactive - for example, if they walk about - and what can calm them when they are agitated
- whether the person has an advance decision or a personal welfare Lasting Power of Attorney (LPA).
It may be helpful to include some tips for staff. For example:
- 'Mr Cohen finds it helpful if people talk slowly and give one piece of information at a time.'
- 'Saul is more likely to understand if people maintain eye contact while they are talking to him.'
- 'Miss Sellers can feed herself with a spoon if someone cuts her food up.'
- 'Ravi often rocks and holds his tummy if he is in discomfort or pain.'
It may also help staff to communicate and gain more insight into the person with dementia if they have details of the person's:
- close family members or friends
- living situation - for example, whether they live with others or alone
- past occupation
- particular interests.
If the person with dementia frequently walks around the ward, this may make staff anxious. If this is likely, explain that the person finds it comforting to walk around and that staff will need to accommodate this. It may help to point out that preventing the person from doing an activity they wish to do, such as walking, may make them feel threatened or angry. You could also emphasise the benefit of involving the person in suitable activities on or away from the ward. Activities may include chair-based exercises and some wards have day rooms where people can watch a film. You may need to describe how much supervision would be required for this.
Tips: how you can help
If you choose, you may be able to help with the individual's personal care (for example, taking them to the toilet or supporting them at mealtimes). If you would like to do this, discuss it with the named nurse. Other ways in which you can help might include:
- making sure clothes are discreetly labelled in case they are mislaid
- cleaning spectacles and checking on hearing aids
- checking the person's mouth for signs of soreness
- thinking of enjoyable pastimes or items to occupy the person's time.
- Familiar objects, such as photographs on the bedside table of family members or a much-loved pet, can be very reassuring for a person with dementia on an unfamiliar hospital ward. They can also provide staff with a good talking point. If the person still reads, you could provide a notebook, so staff and visitors can write messages, reminders and details of when they are next visiting.
- Familiar faces may also bring the person comfort and reassurance. Because of this, it has been recommended that hospitals encourage flexible visiting times for families of people with dementia.
- Noise and bustle on the ward can add to the person's confusion and heighten their levels of anxiety or agitation - particularly at busy times, such as ward rounds or visiting hours. You could ask if there is a quiet room or day room that the person can visit to get away from the bustle.
Eating and drinking
- Mealtimes in a busy hospital environment can be difficult and stressful for a person with dementia. Make staff aware of any difficulties that the person has at mealtimes and how they can help. Make sure the person is given the option of eating in the dining room, if there is one, or at their bedside if they prefer.
- Make sure staff help the person with dementia to eat and choose food if necessary, and don't assume that the person isn't hungry or doesn't want their food if they don't seem keen to eat it. Some people with dementia cannot eat their food without reminders and prompts at mealtimes. Staff are often particularly busy at mealtimes and may be grateful for any help you can offer in helping the person to eat. You may like to discuss this with the named nurse.
- If the person has difficulty swallowing, ask if they can be assessed by a speech and language therapist, or if food can be provided in a soft or puréed texture. If the person is not eating well, or is losing weight, the named nurse should contact the hospital dietitian. The dietitian will co-ordinate a nutritional care plan with nursing and catering staff, which may involve prescribing high-energy drinks or specific foods.
- If the person with dementia is very unwell they may not want to eat or drink. Tube feeding may be suggested as a means to help a person receive food and fluids. The terms 'nasogastric' or 'gastrostomy' (PEG) tubes are often used. The decision to tube feed should only be made respecting the wishes of the patient and in full discussion with carers or relatives.
- Doctors should discuss the person's medication, and any changes, with the person with dementia and their carer or relatives.
- If the person is prescribed sedative medication, this may make them more confused. It may be possible to reduce the dose or stop the medication altogether. If you have any concerns, discuss these with the doctor. (For more information about avoiding drugs unless they are really necessary, see our booklet Reducing the use of antipsychotic drugs: A guide to the treatment and care of behavioural and psychological symptoms of dementia.)
If you have any problems with the person's treatment or care, discuss these first with the named nurse. He or she should explain why things went wrong and how they will be put right. Use the following tips to complain effectively:
- Try to start on a positive note by mentioning something you have appreciated about the person's care.
- Try to make the complaint specific - for example, on three occasions you came in and saw that the drugs on the table had not been taken. It may help you to have the details written down.
- Try to stay calm.
If it is not possible to sort the problem out on the spot, keep brief notes, as it is easy to forget details. The notes should include:
- what occurred and when
- who you contacted or discussed it with
- what their response was.
If the problem still cannot be resolved, ask to see the ward manager or make an appointment with the consultant. Alternatively, you may prefer to contact the Patient Advice and Liaison Service (PALS) based at the hospital. PALS acts on behalf of patients and families, and liaises with hospital staff to help resolve problems and concerns quickly.
Leaving hospital after treatment, known as discharge, should be planned and carers or family should receive advance notice. However, decisions can often be made quickly, so you should begin preparations as soon as the person goes into hospital. The social worker can advise on the suitability of residential or nursing care, or on ways of helping when the person returns home. An occupational therapist can assess the home environment to advise on any aids to help support the person living at home. For more information, see our factsheet on Hospital discharge (453).
If the person has received specific advice and input from a specialist (for example, a dietitian) while on the ward, make sure follow-up care is arranged. Ask for contact numbers for further review once the person is back in the community.
At the end of life
- If the person is in the last stages of life, those who are close to them may want to stay with them outside visiting hours. Discuss possible arrangements with staff.
- Depending on the nature of the person's illness - for example, if the doctor feels the person is likely to have a heart attack - you may need to consider your views on resuscitation. The medical team and consultant should always discuss such issues and decisions with the main carer or family members. It may help to talk it through with family or friends. If anything is unclear, ask them to explain any terminology they use.
- Most UK hospitals use the 'Liverpool Care Pathway' at the end of life. This is a guide for staff that aims to improve care quality by involving family members and making sure that unnecessary and intrusive treatments are not carried out.
- The person may have set out their own wishes regarding resuscitation in an advance decision and these should be followed (see factsheet 463, Advance decision).
Last updated: December 2011
Next review due: December 2013
Reviewed by: Dr Liz Sampson, Senior Lecturer, UCL Medical School, London and Ms Jane Buswell, Nurse Consultant, University Hospitals Bristol NHS Foundation Trust, Bristol
Order a free copy of this publication by contacting us on 0300 3030 5933 or email@example.com
If you have any questions about the information on this factsheet, or require further information, please contact the Alzheimer’s Society helpline.
0300 222 11 22
Visit our section about care services.
Find out how you can request permission to use our information beyond this site.
Visit Talking Point and take part in the discussions