The World Health Organisation defines palliative care as "an approach which improves the quality of life of patients and their families facing life threatening illness, through the prevention and relief of suffering by means of early identification, impeccable assessment and treatment of pain and other problems, physical, psychosocial and spiritual".

Palliative care aims to relieve physical symptoms and emotional pain and to support patients and their families when they have life-limiting illnesses including those associated with old age.

Palliative care is truly holistic. Its specialists "walk with" the patient and family right through the illness and up to the death of the patient and then they carry on with bereavement support for those closely affected by the loss. They are serious about care. Palliative care is delivered by a team of professionals, doctors, nurses, social workers, physiotherapists, occupational therapists, speech therapists, chaplains and volunteers.

There are times when non-specialists; GPs, community nurses and others are part of the palliative care team and they must understand and use a palliative approach. This approach means that the patient and family are the centre of attention, their myriad concerns are paramount and every effort is made to support them through the often difficult though frequently rewarding time which characterises the end of a person's life. It requires careful attention to detail and regular follow-up.

We should have sufficient palliative care specialists to regularly visit people in their homes, in hospices, acute hospitals and aged-care facilities. They must consult and plan management aimed at keeping patients comfortable. They must have time to teach GPs, generalist nurses and other medical specialists about symptom control and the palliative approach.

Specialist social workers and psychologists should visit to support patients and their families. Every aged care facility must have an end-of-life plan for each patient. GPs and nurses must be trained to recognise the approach of death and must know how to keep the patient comfortable. And the necessary medications must be there when needed. We should all be assured that the quality of care which is currently only available to a fortunate few in the community is available to all.

What can be done? More funding is needed from all governments.

Dr Yvonne McMaster, Retired palliative care specialist

Join Yvonne McMaster on Twitter

Comments  

#1 Christine Hamilton 2016-04-21 01:35
My Dad died in a Nursing Home, he had dementia but died of pneumonia, I had been sitting with him for about 5 hours the night before, but I couldnt have another night off work so I wasnt there when he died. I got the call from the Nursing home at 5am to tell me he had died, I specifically asked them to NOT phone my Mum, that I would wait until she got up and had breakfast and I would go to see her in person to tell her at about 9am.

At 8.30am the phone rang, my Mum very upset, to tell me my Dad had died during the night, . how did you know this I asked her, THE FUNERAL DIRECTOR HAD CALLED TO TELL HER.. to the day I die, I am angry about that, THAT SHOULD NEVER HAVE HAPPENED, after like 50 years of marriage, you should not get the news that your husband has died from a complete stranger, funeral director that you have never spoken to before. My Mum was ok about it, he died, nothing could change that, but to me maybe just a lack of communication or I think that someone was in a hurry, too much of a hurry just to wait another half an hour? I just thought this comment might be useful insight into our experience.
Quote