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. 2014 Jul 23;6(7):54. doi: 10.1186/s13073-014-0054-x

Table 1.

Living participants by re-contact status and consent

Contacted a (n = 1,820) Status of consent b (n = 871)
Yes No p-value Given Refused p-value
Study <0.0001 0.76
  FHS 138 (48.6%) 146 (51.4%) 98 (90.7%) 10 (9.3%)
  WELD 551 (73.3%) 201 (26.7%) 423 (88.7%) 54 (11.3%)
  INHALE 456 (58.2%) 328 (41.8%) 252 (88.1%) 34 (11.9%)
Sex <0.0001 0.05
  Male 238 (48.5%) 253 (51.5%) 122 (84.1%) 23 (15.9%)
  Female 907 (68.3%) 422 (31.7%) 651 (89.7%) 75 (10.3%)
Age (years) <0.0001 0.07
  <49 229 (51.0%) 220 (49.0%) 163 (92.6%) 13 (7.4%)
  50+ 916 (66.8%) 455 (33.2%) 610 (87.8%) 85 (12.2%)
Race <0.0001 0.43
  White 578 (72.2%) 223 (27.8%) 448 (89.8%) 51 (10.2%)
  Black 550 (55.6%) 439 (44.4%) 312 (87.2%) 46 (12.9%)
  Other 17 (56.7%) 13 (43.3%) 13 (92.9%) 1 (7.1%)
Status 0.0009 0.48
  Case 362 (68.8%) 164 (31.2%) 248 (89.9%) 28 (10.1%)
  Control 783 (60.5%) 511 (39.5%) 525 (88.2%) 70 (11.8%)

aExcludes 13 people for whom contact status was unclear/still pending.

bExcludes 274 people who were successfully contacted and verbally agreed but never sent back the form (n = 252), individuals who were contacted but too sick to give informed consent (n = 30), and n = 2 individuals who were deceased but had next of kin return a consent form.