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Published: 30 May 2017

Research into palliative care top priority for cancer patients

How and when people are referred to palliative care should be prioritised according to cancer patients. In the first study of its kind, researchers from the Surrey, with funding from the UK Oncology Nursing Society, surveyed cancer patients and nurses to help identify priorities for future research into oncology nursing and how it should be delivered.

Patients identified palliative and end-of-life care as top areas for future examination with particular focus on models of end-of-life care in the community and access to specialist palliative care within oncology services. The identification of this as a matter of importance for patients suggests that improvements on how and when palliative care services are introduced is required.

Those affected by cancer also classified cognitive changes associated with cancer treatment as a priority for future research, as such changes are not only distressing for the patient but their families as well.

Unlike patients, oncology nurses placed importance on the use of eHealth and technology to manage cancer symptoms at home as an area of significance for future research. The identification of this priority area shows that nurses are responsive to service changes in the NHS and are increasingly using technology in the delivery of care.

Despite such differences, oncology nurses and patients were in agreement in a number of areas on what should be on future research agendas. They agreed that factors affecting the early presentation of cancer symptoms should be a priority area - keeping with research in this area which shows that early diagnosis of cancer is vital in improving survival rates and delivering effective care.

Both parties also identified the availability of psychosocial support services across the cancer pathway and the management of anxiety and uncertainty following cancer treatment.

Professor Emma Ream, Director of Health Sciences Research, said: “Our study demonstrates the importance of seeking the opinions of cancer patients, as what they consider important may not mirror what the profession considers a priority. Too often the voice of cancer patients is unheard, but if services are to improve we should listen to the very people they are affecting.”

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