R. Voltz et al., END-OF-LIFE DECISIONS AND ADVANCE DIRECTIVES IN PALLIATIVE CARE - A CROSS-CULTURAL SURVEY OF PATIENTS AND HEALTH-CARE PROFESSIONALS, Journal of pain and symptom management, 16(3), 1998, pp. 153-162
In order to explore possible differences in the scope of end-of-life d
ecisions and attitudes toward advance directives (AD) in palliative ca
re, we conducted a survey of 159 patients in palliative care instituti
ons and 93 health-care professionals experienced in palliative care in
the United States, Germany, and Japan. Giving an AD in this clinical
setting was considered important by patients and professionals. The pr
evalence of a formal written Ao was 79% in the United States, 18% in G
ermany, and 9% in Japan. In Japan, there was a high prevalence of entr
usting all decisions to the family (known as omakase). More than 80% o
f the patients had negative feelings toward their future decisions in
the United States and Germany, in contrast to only 45% in Japan. Altho
ugh favored by the professionals, there were no specific instruments f
or obtaining ADs. In Germany and Japan, some patients had given an inf
ormal AD. As a pilot content validity step, survey results were used t
o derive a checklist for content and procedural aspects in end-of-life
decision-making. This checklist may provide the basis for developing
an instrument to guide physicians, especially non-palliative care spec
ialists, in communication with their patients and their families in th
is difficult clinical situation. (C) U.S. Cancer Pain Relief Committee
, 1998.