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. 2020 May 17;10(5):e036465. doi: 10.1136/bmjopen-2019-036465

Table 1.

Cohort characteristics at time of the health assessment, summarised overall and by death status during the follow-up period

Variable Statistics/groups All participants
(n=961)
Deceased participants
(n=294)
Alive participants
(n=667)
Age (years) Mean (SD) 44.1 (14.6) 52.4 (13.6) 40.5 (13.6)
Min, max 16–83 18–83 16–77
Age group 16–25 years 127 (13.2%) 10 (3.4%) 117 (17.5%)
26–35 years 153 (15.9%) 26 (8.8%) 127 (19.0%)
36–45 years 246 (25.6%) 49 (16.7%) 197 (29.5)
46–55 years 205 (21.3%) 85 (28.8%) 120 (18.0%)
>55 years 230 (23.9%) 124 (42.0%) 106 (15.9%)
Sex Male 525 (54.6%) 154 (52.4%) 371 (55.6%)
Female 436 (45.3%) 140 (47.5%) 296 (44.4%)
Ability level Mild ID 382 (39.7%) 92 (31.2%) 290 (43.5%)
Moderate ID 236 (24.5%) 73 (24.7%) 163 (24.4%)
Severe ID 180 (18.7%) 67 (22.7%) 113 (16.9%)
Profound ID 163 (17.0%) 62 (21.1%) 101 (15.1%)
Accommodation type Family carer 374 (38.9%) 70 (23.8%) 304 (45.6%)
Independent 93 (9.7%) 36 (12.2%) 57 (8.5%)
Paid support 435 (45.2%) 161 (54.6%) 274 (41.1%)
Congregate care 59 (6.1%) 27 (9.2%) 32 (4.8%)
Down syndrome No 782 (81.4%) 230 (78.2%) 552 (82.8%)
Yes 179 (18.6%) 64 (21.7%) 115 (17.2%)

ID, intellectual disabilities.