Skip to main content

Table 3 Characteristics of the carers and patients included in the analysis, n = 23

From: Adaptation of the Ambulatory and Home Care Record for collecting palliative care service utilisation data from family carers in the UK: a pilot study

  

n (%)

Carer (participant)

 Gender

Female

16 (69.6)

 Age

Median (range)

63 (44–81)

 Relationship to patient

Spouse/partner

17 (73.9)

Child

4 (17.4)

Parent

1 (4.3)

Other

1 (4.3)

 Lives with/staying with patient

21 (91.3)

 In full or part time work (vs retired)

6 (26.0)

 College or university educated

11 (47.8)

  

Baseline; last recorded

 Carer burden during end-of-life care [26], range 0 (best)–100 (worst)

Mean

34.78; 40.83

Standard deviation

25.16; 26.89

Median

29.17; 35.00

Range

0–90; 0–100

Best quartile, n %

11(47.8); 8(34.8)

2nd quartile, n %

7(30.5); 9(39.1)

3rd quartile, n %

3(13.0); 3(13.0)

Worst quartile, n %

2(8.6); 3(13.0)

Patient

 

 Gender

Female

10 (43.5)

 Age

Median (range)

70 (43–93)

 Lives alone (vs with spouse/other)

3 (13.0)

 College or university educated

9 (45.0)

 Receives attendance allowancea

11 (47.8)

 Diagnosis

Cancer

20 (87.0)

Non-cancer

3 (13.0)

 Place of death

Hospice

4 (17.4)

Hospital

4 (17.4)

Home

2 (8.7)

Unknown or alive at end of study

13 (56.5)

  

Baseline; last recorded

 Functional status—ECOG [25]

0. Fully active

0; 0

1. Restricted in strenuous activity

1(4.3); 2(8.7)

2. Ambulatory, capable of self-care but not work

11(47.8); 5(21.7)

3. Limited self-care

7(30.4); 8(34.8)

4. Completely disabled

4(17.4); 3(13.0)

5. Dead

0; 5(21.7)

 Service satisfaction

 

Baseline; last recorded

Exceeds expectations

10(43.5); 10(43.5)

Meets expectations

10(43.5); 12(52.2)

Falls short of expectations

3(13.0); 1(4.3)

  1. aBenefit available in the UK