Although it’s something we all do at some point, the topic of dying has traditionally been a difficult and uncomfortable one to discuss. That’s changing as people understand and embrace the objectives of end of life and palliative care: addressing physical, emotional and spiritual needs, maximizing quality of life and helping satisfy individuals’ desires and preferences - including how and where they want to spend their final days and where they want to die.
For the majority of people, that means being cared for, and dying, in their own homes (1;2). Home palliative care services make it possible to respect those wishes, while ensuring patients in the advanced stage of an illness – and their family caregivers – receive the help and support they need.
A well-done systematic review of relevant studies attempted to determine whether home palliative care does actually increase the chance of patients dying at home (3).
What the research tells us
There is strong evidence that compared with usual care (i.e. in hospitals, hospices and nursing homes), home palliative care increases the likelihood of a patient dying at home (3;4). Home palliative care did not have any significant impact on caregivers’ grief in the first 13 months following their loved one’s death (3). There was not enough evidence to draw conclusions about quality of life or the effects on caregiver burden (3;4).
Further research is warranted, including additional investigation into the cost-effectiveness of services. Meanwhile home palliative care offers important benefits and appears to be an alternative option for patients, their families and caregivers whose end of life wishes include dying at home.