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Table 3 Caregiver and caregiver-reported MS characteristics

From: A forgotten aspect of the NICE reference case: an observational study of the health related quality of life impact on caregivers of people with multiple sclerosis

Characteristic

Distribution

Length of time as caregiver (years)

Mean (SD)

9.57 (8.47)

Length of time individual has had MS (years)

Mean (SD)

14.93 (12.83)

Type of MS

Relapsing Remitting MS (RRMS)

N (%)

50 (25.0%)

Secondary Progressive MS (SPMS)

87 (43.5%)

Primary Progressive MS (PPMS)

63 (31.5%)

PDDS Level*

0

N (%)

12 (6.0%)

1

16 (8.0%)

2

15 (7.5%)

3

9 (4.5%)

4

20 (10.0%)

5

26 (13.0%)

6

27 (13.5%)

7

62 (31.0%)

8

13 (6.5%)

Relationship between caregiver and individual with MS

Partner/Spouse

N (%)

153 (76.5%)

Parent

13 (6.5%)

Child

4 (2.0%)

Family Other

19 (9.5%)

Friend

11 (5.5%)

Live with the person you provide care for?

Yes

N (%)

168 (84.0%)

Number of hours a day providing care

1 - 4

N (%)

55 (27.5%)

5 - 9

46 (23.0%)

10 - 24

99 (49.5%)

Help with activities of daily living

Getting in/out of bed

N (%)

116 (58.0%)

Dressing

116 (58.0%)

Washing

102 (51.0%)

Cooking

157 (78.5%)

Eating

59 (29.5%)

Getting around inside the home

104 (52.0%)

Getting around outside the home

156 (78.0%)

Help with caregiving?

None

N

93

Friends/Relatives

85

 

External formal care giver

 

51

  1. N = Sample Size; SD = Standard Deviation; * See Table 1 for description of PDDS levels.