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. Author manuscript; available in PMC: 2021 Nov 19.
Published in final edited form as: Dev Med Child Neurol. 2021 Jan 2;63(11):1294–1301. doi: 10.1111/dmcn.14792

Table 1:

Unadjusted comparisons of demographic characteristics, categories of spinal segmental level of motor function, and the age at last visit recorded in the NSBPR between fetal surgery patients (n=298) and postnatal surgery patients matched for date of birth (±3mo) (n=648), assessed when patients in both cohorts were at least 12 months of age

Covariate Fetal surgery, n (%) Postnatal surgery, n (%) IRR (95% CI); p
Male sex 147/298 (49) 321/648 (50) 1.00 (0.76–1.32); 0.99
Female sex 151/298 (51) 327/648 (50)
Non-Hispanic white 236/285 (83) 404/631 (64) 3.06 (2.07–4.54); <0.01
Non-Hispanic black 10/285 (4) 75/631 (12) 0.30 (0.15–0.58); <0.01
Hispanic 34/287 (12) 136/641 (21) 0.41 (0.26–0.66); <0.01
Private insurance 218/298 (73) 335/648 (52) 2.76 (2.00–3.81); <0.01
Sacral level 102 (34) 163 (25) Reference
Low lumbar level 81 (27) 151 (23) 0.94 (0.64–1.37); 0.75
Mid-lumbar level 79 (27) 176 (27) 0.75 (0.50–1.11); 0.15
High lumbar level 16 (5) 87 (13) 0.30 (0.16–0.55); <0.01
Thoracic level 20 (7) 71 (11) 0.47 (0.26–0.84); 0.01
Age at last visit in years 3.67 (1.42–11.09) 4.08 (2.00–11.50) 0.02 (−0.13 to 0.17); 0.82

All patients had myelomeningocele, were born 1997 through 2017, and were enrolled in the National Spina Bifida Patient Registry (NSBPR) 2009 through 2017. The significance of differences between cohorts in demographic characteristics was assessed by univariable Poisson regression. The significance of differences in frequencies of patients in categories of spinal segmental level of motor function was assessed by Poisson univariable regression, and the significance of differences in age at last visit recorded in the NSBPR was assessed by univariable Poisson linear regression. Percentages may not total 100% because of rounding. IRR, incidence rate ratio; CI, confidence interval.