RT Journal Article SR Electronic T1 G400(P) How useful is recording preferred place of end of life care and place of death as outcome measure in paediatric palliative care? JF Archives of Disease in Childhood JO Arch Dis Child FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health SP A164 OP A164 DO 10.1136/archdischild-2015-308599.354 VO 100 IS Suppl 3 A1 Brook, LA YR 2015 UL http://adc.bmj.com/content/100/Suppl_3/A164.1.abstract AB Aims To evaluate the preferred place for end of life care and place of death as an outcome measure in paediatric palliative care Methods Medical records of children dying under the care of the Paediatric Palliative Care team from January 2009 to December 2013 were audited. Results 187 deaths were identified: mean 37.5 deaths per year. Deaths per year increased over the 5 year period (p > 0.05). 53% of deaths were in the 0–4 years age range and 5% were over 18 years. 58% of deaths were non oncology palliative care, 38% oncology palliative care and 5% oncology on active treatment. Oncology deaths on active treatment increased over the 5 year period (p > 0.05). Preferred place for end of life care was recorded in 77% children dying during palliative care. 57% oncology and 33% non oncology patients identified home as their preferred setting for end of life care. 25% non oncology and 12% oncology patients identified hospice as their preferred place of care. Increasing numbers of non oncology families chose home and oncology families chose hospice over the 5 year period. Overall 92% children died in their preferred setting for end of life care. The number of rapid discharges required to achieve preferred place for end of life care increased (p < 0.05). Ten children did not die in the preferred setting for end of life care. In 3 cases the palliative care team was not aware that the patients had been admitted to hospital until after the child had died, three rapid discharges were abandoned due to rapid deterioration. Four children died suddenly. When statistics were broken down by quarter the small numbers of deaths overall resulted in large but not statistically significant swings in the percentage of children achieving death in the preferred setting for end of life care. Conclusions Recording of preferred setting for end of life care and death in the setting of choice for end of life care is achievable. Small numbers of patients, result in large but not statistically significant swings by quarter. This measure is not appropriate for me intervals of less than a year.