The need to sedate terminally ill patients for uncontrolled symptoms h
as been previously documented in a few reports. A retrospective consec
utive chart review was undertaken at a hospice in Cape Town, South Afr
ica, to develop an understanding of the local experience and assess th
e potential for improved patient management. Twenty-three of seventy-s
ix (30%) patients received sedating therapies: twenty patients for del
irium, two patients for delirium and dyspnea, and one patient for dysp
nea alone. Fourteen patients were sedated with a continuous subcutaneo
us infusion of midazolam, seven patients with intermittent doses of be
nzodiazepines, and two patients with chlorpromazine and lorazepam. The
mean midazolam dose was 29 mg per day (median 30 mg; range 15-60 mg p
er clay). Patients were sedated on average 2.5 days before death (medi
an 1 day; range 4 hours-12 days). The mean equivalent daily dose of pa
renteral morphine in the last week of life showed significantly higher
mean for the sedated group, as compared to the nonsedated group. Ther
e was minimal investigation of reversible causes for delirium, none of
the patients underwent an opioid rotation, and the opioid dose was se
ldom decreased. None of the patients received parenteral hydration. Th
e prevalence for the use of sedating treatment is consistent with the
range of other literature reports. Nevertheless, the wide disparity in
the reported prevalence of these problems, and the ethical concerns r
aised by the relative frequency of this sedative approach, cannot be i
gnored. (C) U.S. Cancer Pain Relief Committee, 1998.