Table 2 Compliance of participants with NBS
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%) | |||
Do you think if both couples do not have genetic diseases, their child will not have a genetic disease? | |||||
Yes | 117 (10.25%) | 93 (9.40%) | 24 (15.79%) | ||
No | 738 (64.68%) | 673 (68.05%) | 65 (42.76%) | 37.038 | P < 0.05 |
I don't know | 286 (25.07%) | 223 (23.56%) | 63 (41.45%) | ||
If the NBS results are negative, does it mean that the baby will not have an IMD? | |||||
Yes | 127 (11.13%) | 108 (10.92%) | 19 (12.50%) | ||
No | 647 (56.70%) | 594 (60.06%) | 53 (34.87%) | 37.879 | P < 0.05 |
I don't know | 367 (32.17%) | 287 (29.02%) | 80 (52.63%) | ||
Do you know what it means to be suspiciously positive for NBS? | |||||
It means that there have abnormal indicators and needs to be further re-examined | 1052 (92.20%) | 935 (94.54%) | 117 (76.97%) | 67.085 | P < 0.05 |
It means that a disease has been diagnosed | 15 (1.31%) | 13 (1.31%) | 2 (1.31%) | ||
I don't know, it’s probably meaningless | 74 (6.49%) | 41 (4.15%) | 33 (21.71%) | ||
If your child's neonatal disease screening is suspiciously positive, how would you treat it? | |||||
No treatment until the child has symptoms | 5 (0.44%) | 3 (0.30%) | 2 (1.31%) | ||
Search information on the Internet and treat by oneself | 5 (0.44%) | 4 (0.40%) | 1 (0.66%) | 3.296 | P > 0.05 |
Go to the appointed hospital or department immediately | 1131 (99.12%) | 982 (99.30%) | 149 (98.03%) | ||