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Table 5 Participants’ demands after undergoing the genetic screening

From: Current attitudes and preconceptions on newborn genetic screening in the Chinese reproductive-aged population

 

Is it necessary to undergo genetic screening?

Value

P

Total (n = 1141, 100%)

Yes (n = 989, 86.68%)

No/I don’t know (n = 152, 13.32%)

Which ways would you like to learn more about NBGS? (Multiple options)

 Consult doctors face to face

1047 (91.76%)

917 (92.72%)

130 (85.53%)

  

 Brochure or education video of outpatient waiting area

683 (59.86%)

599 (60.57%)

84 (55.26%)

  

 Get online and research by oneself

319 (27.96%)

274 (27.70%)

45 (29.61%)

1.781

P > 0.05

 Study or lecture for pregnant women

622 (54.51%)

549 (55.51%)

73 (48.03%)

  

 The official account of hospital

571 (50.04%)

507 (51.26%)

64 (42.11%)

  

Will you actively obtain a genetic diagnosis after a positive genetic screening result?

 Yes, actively carry out a genetic diagnosis to clarify the disease

1124 (98.51%)

986 (99.70%)

138 (90.79%)

71.218

P < 0.05

 No need, genetic screening is equal to genetic diagnosis

17 (1.49%)

3 (0.30%)

14 (9.21%)

  

If your child's genetic screening results reveal other suspected pathogenic genes, but are not related to the clinical phenotype, would you like to be informed?

 Yes, I need to know

1119 (98.07%)

978 (98.89%)

141 (92.76%)

26.135

P < 0.05

 Don’t want to know, to reduce the anxiety after knowing the result

22 (1.93%)

11 (1.11%)

11 (7.24%)

  

If you know that your children have carried pathogenic genes through genetic screening, will you tell them when they become adults?

 Yes, and recommend them to do a carrier screen with their partner before giving birth to their child

1069 (93.69%)

935 (94.54%)

134 (88.16%)

9.077

P < 0.05

 Will not tell them, to reduce their anxiety after knowing the results

72 (6.31%)

54 (5.46%)

18 (11.84%)