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. Author manuscript; available in PMC: 2017 Aug 1.
Published in final edited form as: Am J Hosp Palliat Care. 2014 Sep 12;33(2):130–135. doi: 10.1177/1049909114550392

Table 1.

Caregiver Demographics and Outcomes among EOL Caregivers, by Hospice Status

Measure EOL Caregivers, non-
Hospice
(n=214)a
EOL Caregivers With
Hospice
(n=238)a
P Valueb
Age, frequency (weighted percent)
18–49 58 (36.9%) 71 (39.3%) .67
    50+ 156 (63.1%) 167 (60.7%)
Race, frequency (weighted percent)
White 146 (79.0%) 180 (84.2%) .15
African-American 68 (21.0%) 58 (15.8%)
Gender, frequency (weighted percent)
Male 60 (39.2%) 71 (39.2%) .99
Female 154 (60.8%) 167 (60.8%)
Level of Education, frequency (weighted percent)
  ≤High School 80 (39.3%) 90 (41.1%) .74
>High School 134 (60.7%) 148 (58.9%)
Income, frequency (weighted percent)
<$25,000 95 (40.0%) 81 (30.2%) .05
≥$25,000 119 (60.0%) 157 (69.8%)
Kessler-6 Score, frequency (weighted percent)
≥13 18 (8.5%) 17 (8.7%) .95
<13 193 (91.5%) 221 (91.3%)
Days in month where mental health was not good, frequency (weighted percent)
> 4 days 71 (34.4%) 77 (34.1%) .96
≤ 4 days 143 (65.6%) 161 (65.9%)
Administered Medications in the Period before Death, frequency (weighted percent) 56 (33.3%) 85 (46.4%) .03
Rated Care at End-of-Life as Excellent, frequency (weighted percent) 52 (26.1%) 117 (51.2%) <.0001
Satisfied with Decisions about Care or Treatment, frequency (weighted percent) 161 (71.2%) 204 (86.4%) .03
Non-Hospital Location of Death, frequency (weighted percent) 96 (45.3%) 181 (74.1%) <.0001
a

Excluding missing, “don’t know”, and “refused” responses

b

Based on the Rao-Scott χ2 test.