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Table 1 Characteristics of patients admitted to the Queen Elizabeth II Palliative Care Program between Jan 1, 1998 and Dec 31, 2002 and died during the same period

From: Transitions in care during the end of life: changes experienced following enrolment in a comprehensive palliative care program

Characteristic

Number of patients* (%)

Sex

 

   Female

1925 (48.5)

   Male

2047 (51.5)

Age, years

 

< 60

992 (25.1)

60–69

873 (22.1)

70–79

1208 (30.6)

≥ 80

878 (22.2)

Year of admission to PCP

 

1998

883 (22.2)

1999

824 (20.8)

2000

876 (22.1)

2001

771 (19.4)

2002

618 (15.6)

Year of death

 

1998

645 (16.2)

1999

820 (20.7)

2000

858 (21.6)

2001

824 (20.8)

2002

824 (20.8)

Survival (days)

 

0–30

1605 (40.4)

31–60

723 (18.2)

61–90

432 (10.9)

91–120

251 (6.3)

121+

960 (24.2)

Location of death

 

   Hospital death (not in PCP unit)

2009 (50.6)

   Inpatient PCP unit

635 (16.0)

Home

1218 (30.7)

Long-term care facility

110 (2.8)

Diagnoses, summarized

 

Lung cancer

1025 (26.1)

All other cancers

2525 (64.3)

Other disease, no cancer

375 (9.6)

Caregiver relationship

 

Spouse

2165 (57.8)

Child

1017 (27.2)

Parents / other relations

448 (12.0)

Other

116 (3.1)

Primary reasons for referral to PCP

 

(responses are not exclusive)

 

Pain

1630 (41.0)

Other symptoms

1868 (47.0) 1729 (43.5)

Patient support

1729 (43.5)

Family support

1620 (40.8)

Staff support

317 (8.0)

Home consultation

1067 (26.9)

Terminal care

345 (8.7)

Respite care

5 (0.1)

Grief

19 (0.5)

  1. * N = 3,972. Smaller n by characteristic due to missing values.