Skip to main content

Table 1 Characteristics of patients and carers

From: A patient-centred approach to health service delivery: improving health outcomes for people with chronic illness

Categories

Sub-categories

Patient (N = 52)

§Carer (N = 14)

Residence

ACT

26 (50.0%)

6 (42.9%)

Sydney West

26 (50.0%)

8 (57.1%)

Gender

Male

28 (53.8%)

1 (07.1%)

Female

24 (46.2%)

13 (92.9%)

Age

Less than 45 yrs

^1 (1.9%)

2 (14.3%)

45-64 yrs

16 (30.8%)

5 (35.7%)

65-85 yrs

35 (67.3%)

7 (50.0%)

Culturally and linguistically diverse (CALD)

CALD background

11 (21.2%)

5 (35.7%)

Indigenous

Indigenous background

7 (13.5%)

0

Finance

Experiencing financial difficulties

31 (59.6%)

11 (78.6%)

Marital Status

Married/de facto/living with a partner

29 (55.8%)

13 (92.9%)

Work Status

Employed

5 (9.6%)

2 (14.3%)

Not employed

47 (90.4%)

12 (85.7%)

Diagnosis

Type 2 diabetes

16 (30.8%)

*4 (28.6%)

CHF

15 (28.8%)

*2 (14.3%)

COPD

10 (19.2%)

*5 (35.7%)

More than one index condition

11 (21.2%)

*3 (21.3%)

Average length of illness

16.5 years

*21.4 years

Other co-morbid conditions

43 (86.5%)

*11 (85.7%)

Visit to GP

Weekly

4 (7.7%)

*1 (7.1%)

Fortnightly

8 (15.4%)

*6 (42.9%)

Monthly

23 (44.2%)

*5 (35.7%)

Bi-monthly

3 (5.8%)

*0

Quarterly

7 (13.5%)

*1 (7.1%)

Half-yearly

2 (3.8%)

*0

Only when necessary

5 (9.6%)

*1 (7.1%)

Family Carer

Have a family carer

#22 (42.3%)

NA

Average length of caring

#14.7 years

12.5 years

Relationship of carer to patient

  

Offspring

6 (27.3%)

4 (28.6%)

Spouse/partner

14 (63.6%)

10 (71.4%)

Other

2(9.1%)

0

Carer receives financial assistance

#5 (22.7%)

5 (35.7%)

Carer receives informal support

#14 (63.6%)

9 (64.3%)

  1. § Nine carers were spouses or offspring of the patients interviewed, ^ One Indigenous participant was younger than 45 years old (given a gap of approximately 20 years shorter life expectancy than non-Indigenous Australian it was deemed to be appropriate to be included in the study), * Denotes the carer’s account about the patient’s condition and management.
  2. # Denotes the patient’s account about the carer.