National Survey of Patient Activity Data for Specialist Palliative Care Services

MDS full report for the year 2009-2010

May 2011

Patient Activity Data cover

The aim of the end of life care Minimum Data Set (MDS) is to provide good quality, comprehensive data about hospice and specialist palliative care services on a continuing basis. This report is the 15th since the original collection in 1995/96 and it is the first to report on activities since the rollout of additional investment associated with the End of Life Care Strategy in England.

 

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