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Table 2 Characteristics of next-of-kin and information about patients

From: Assessment of the quality of end-of-life care: translation and validation of the German version of the “Care of the Dying Evaluation” (CODE-GER) - a questionnaire for bereaved relatives

 

Main sample (N = 237)

Interrater (N = 38)

T2 (N = 55)

Number (%)

Number (%)

Number (%)

Gender

 Female

153 (65)

27 (71)

36 (66)

 Male

84 (35)

11 (29)

19 (34)

Age

 20–29

6 (3)

4 (11)

2 (4)

 30–39

20 (8)

5 (9)

 40–49

34 (14)

10 (26)

10 (18)

 50–59

69 (29)

15 (40)

17 (31)

 60–69

56 (24)

5 (13)

15 (27)

 70–79

33 (14)

2 (5)

5 (9)

 80+

19 (8)

2 (5)

1 (2)

Relation to patient

 Husband / Wife / Partner

101 (43)

11 (30)

21 (38)

 Son / Daughter

96 (41)

15 (39)

23 (42)

 Brother / Sister

13 (6)

4 (10)

3 (5)

 Son-in-law / Daughter-in-law

4 (2)

6 (16)

2 (4)

 Parent

9 (3)

1 (2)

 Friend

3 (1)

 Other

11 (4)

2 (5)

5 (9)

Nationality

 Germany

213 (90)

35 (92)

52 (94)

 Austria

1 (0.3)

 Croatia

1 (0.3)

 Greece

1 (0.3)

 Italy

2 (1)

 Missing

19 (8)

3 (8)

3 (6)

Religion

 Roman Catholic

101 (43)

18 (47)

22 (40)

 Protestant

89 (38)

12 (32)

24 (44)

 Muslim

 None

43 (18)

6 (16)

8 (14)

 New apostolic

2 (0.5)

1 (2.5)

1 (2)

 Buddhist

1 (2.5)

 Missing

2 (0.5)

Main diagnosis of patient assessed by relativea

 Cancer

134 (57)

24 (63)

35 (64)

 Kidney disease

48 (20)

8 (21)

6 (11)

 Heart failure

41 (17)

6 (16)

4 (7)

 Stroke

33 (14)

5 (13)

7 (13)

 COPD

19 (8)

3 (8)

4 (7)

 Dementia

19 (8)

6 (16)

7 (13)

 Motor neurone disease

2 (1)

 Don’t know

5 (2)

1 (2)

 Something else

51 (22)

12 (32)

13 (24)

Ward on which patient had died

 Palliative Care Unit

120 (51)

24 (64)

32 (58)

 Internal medicine and neurology

60 (25)

7 (18)

10 (18)

 Intensive care unit

57 (24)

7 (18)

13 (24)

  1. aMultiple selection was possible. Percentage rates reflect the amount of one diagnosis per sample.; T2 = Participants of repeated measurement