Dispelling some myths about palliative care

Palliative care is not just about dying – patients who access it in the early stages of an illness live longer and with better quality of life

The traditional view that palliative care implies only hospice and end-of-life care no longer holds true. Increasingly, palliative care is recognised as being equally important as a service to support patients esarlier in the course of a serious or life-limiting illness. This can sometimes be from the time of diagnosis, and patients can sometimes receive care and support from palliative care for many years.

So, a referral to palliative care should not be feared. It does not always mean that a patient is imminently dying.

In fact, new research has shown that patients with incurable cancer, who are referred to palliative care at time of diagnosis, live longer than patients who just receive conventional oncology treatment from time of diagnosis.

As well as not just being appropriate for patients with cancer, palliative care also has much to offer patients with other illnesses, such as heart failure, chronic lung conditions, (such as COPD and pulmonary fibrosis), renal failure, MND and MS.


Though most people associate palliative care with care at home or in a hospice, in fact, most patients referred to palliative care avail of the service while they are in an acute hospital. Nationally in 2017, 11,500 new patients received palliative care input in the acute hospital setting, compared to 2,700 in hospice and 9,500 in community palliative care.

Emotional support

It is often while in hospital that patients are sickest, and will have the greatest need for the input of the palliative care service to help with complex symptoms, such as pain, nausea, breathlessness, as well as the need for emotional and psychological support. Palliative care also helps to prepare patients for discharge home again from hospital.

Research in Ireland has confirmed international research showing the earlier a patient is referred to the palliative care service during a hospital admission, the better the outcomes, including clinical outcomes and quality of life – in particular, patients seen within a day or two of admission to the hospital had a much shorter length of stay than those patients seen later in their admission.

My initiative, called PAL.M.ED., is an early referral programme to palliative care in emergency departments. Results include a reduction in the average length of stay of more than 10 days for patients referred early to palliative care in the ED compared with patients referred later during the course of their admission.

So, the key message is: Palliative care is not all about dying – it’s about living, with a life-limiting illness, and putting quality at the centre of that time.

– Dr Eoin Tiernan is a palliative medicine consultant at the Beacon Hospital