Terminally ill patients are very susceptible to infections, which are the r
esult of disease-related processes and/or therapy-induced mechanisms. These
patients are already subject to multiple severe symptoms and associated co
morbid conditions, with much resultant distress. Infection increases this s
ymptom burden and further reduces quality of life. We have retrospectively
investigated the prevalence of infection and clinical course in 102 consecu
tive patients who died after admission to at tertiary palliative care unit
and assessed the site-specific frequency of infection, pathogenic organisms
involved, and the pattern of antibiotic agents used. The prevalence of sym
ptoms and comorbid conditions on admission and during the progress phase of
care were noted. Median overall survival of the total cohort was 12 days.
The median survival of patients with infections was 22 days. Thirty-seven p
atients (36.3%) were diagnosed with 42 separate infections. The sites of in
fections were the urinary tract (42.5%), the respiratory tract (22.9%), blo
od (12.5%), skin and subcutaneous tissues (12.5%), and the eyes (10.0%). Th
ere were 20 separate positive cultures isolated from specimens obtained fro
m 13 individual patients. Three isolates were obtained from 1 patient, 2 is
olates obtained from 5 patients, and 1 isolate was obtained from each of th
e 7 remaining patients. Escherichia coli was the most common pathogen isola
ted. Eleven patients with infections (31.4%) were diagnosed on admission, a
nd antibiotic treatment was commenced within 48 hours of admission in 21 pa
tients (60%). Overall antibiotic response and symptom control of infections
was observed to be a minimum of 40%. Psychological distress was common in
this group of patients (P = 0.001) as were disabling symptoms on admission,
such as pain, immobility, and weakness. Symptoms indicating poor survival,
such as severe pain and dyspnea, were not significantly associated with in
fection. Decreased patient survival in this cohort was not significantly as
sociated with the presence of bacterial infection (P = 0.07), irrespective
of whether or not a positive culture isolate was obtained. We conclude that
appropriate management of infection resulted in enhanced palliative sympto
m control. J Pain Symptom Manage 2000;20:326-334. (C) U.S. Cancer Pain Reli
ef Committee, 2000.