2005
DOI: 10.1177/026921630501900221
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Patient choice regarding place of death

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Cited by 7 publications
(6 citation statements)
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“…home death is fulfilled. Public preference for home death has been widely reported (40)(41)(42)(43)(44)(45), with home death rates constituting one indicator of the quality of palliative care (46)(47)(48)(49). A lack of available physical resources in these rural areas also compromised the ability of providers to offer effective palliative care.…”
Section: Inadequate Physical Resourcesmentioning
confidence: 99%
“…home death is fulfilled. Public preference for home death has been widely reported (40)(41)(42)(43)(44)(45), with home death rates constituting one indicator of the quality of palliative care (46)(47)(48)(49). A lack of available physical resources in these rural areas also compromised the ability of providers to offer effective palliative care.…”
Section: Inadequate Physical Resourcesmentioning
confidence: 99%
“…12,13,29 Overall, the number of patients dying in their place of choice in Belgium is quite high compared with other studies, in which percentages between 30% and 94% are found, depending on the methodology used. 12,13,[30][31][32][33][34][35][36][37][38] Since congruence could only be measured for those patients whom GPs were informed about, it can be assumed that the high congruence found in the present study is probably an overestimation. The fact that patients died in hospital more often when GPs were not informed (58% as opposed to 16% where GPs were informed) confirms this hypothesis.…”
Section: Original Papers Original Papersmentioning
confidence: 99%
“…3 It has been found that many patients and their families learn about palliative care services from someone other than their physician, and most learn about valuable features of the service after they have enrolled. 4 Patients who had been newly referred to the SPCS based at St Raphael's Hospice were asked to complete a short questionnaire before their first visit from the community palliative care team (CPCT). The questionnaire sought to identify whether patients knew that they had been referred to SPCS, whether they were aware that the specialist palliative care team (SPCT) is based at the hospice, and whether they felt that they had been given enough information to consent to their referral.…”
mentioning
confidence: 99%