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Table 3 Demographic characteristics of survey participants (n = 536)

From: What are the information needs and concerns of individuals with Polycystic Kidney Disease? Results of an online survey using Facebook and social listening analysis

Disease status

The person with PKD

495 (92.4 %)

Parent of someone who has PKD

15 (2.8 %)

Carer of someone who has PKD

15 (2.8 %)

Sibling of someone with PKD

1 (0.2 %)

Friend of someone with PKD

3 (0.6 %)

Other

16 (3.0 %)

Gender

 Female

380 (70.9 %)

 Male

156 (29.1 %)

 Prefer not to say

0 (0.0 %)

Age

 Less than 18 years of age

12 (2.2 %)

 18–34 years of age

73 (13.6 %)

 35–54 years of age

238 (44.4 %)

 55–70 years of age

177 (33.0 %)

 70 + years of age

36 (6.7 %)

Length of time since diagnosis of person with PKD (years)

 

 Less than 1 year ago

17 (3.2 %)

 1–5 years ago

79 (14.7 %)

 5–10 years ago

64 (11.9 %)

 More than 10 years ago

376 (70.2 %)

Stage of PKD

 Unsure

53 (9.9 %)

 Stage 1 or 2

150 (28.0 %)

 Stage 3

121 (22.6 %)

 Stage 4 (predialysis)

85 (15.9 %)

 Stage 5 (dialysis or have had a transplant)

116 (21.7 %)

 Other comments

31 (5.8 %)

 No response

1 (0.2 %)

Location of respondent

 USA

308 (57.5 %)

 Australia

134 (25 %)

 United Kingdom

53 (9.9 %)

 Europe

11 (2.1 %)

 New Zealand

8 (1.5 %)

 Canada

8 (1.5 %)

 South East Asia

8 (1.5 %)

 Middle East

3 (0.6 %)

 South or Central America

2 (0.4 %)

 Africa

1 (0.2 %)

  1. Legend: PKD Polycystic Kidney Disease. Stage of PKD had n = 525 responses