Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Neurosurgery, Children's Wisconsin, Milwaukee, WI, USA.
Childs Nerv Syst. 2023 Sep;39(9):2413-2421. doi: 10.1007/s00381-022-05704-3. Epub 2022 Oct 29.
The early care of children with spina bifida has changed with the increasing availability of fetal surgery and evidence that fetal repair improves the long-term outcomes of children with myelomeningocele. We sought to determine current trends in the prevalence and early care of children with myelomeningocele using a national administrative database.
This is a retrospective, cross-sectional cohort study of infants with spina bifida admitted within the first 28 days of life using the 2012-2018 Healthcare Cost and Utilization Project National Inpatient Database. Patients with spina bifida were identified by ICD code and stratified into a cohort with a coded neonatal repair of the defect and those without a coded repair. This database had no identifier specific for fetal surgery, but it is likely that a substantial number of infants without a coded repair had fetal surgery.
We identified 5,090 patients with a coded repair and 5,715 without a coded repair. The overall prevalence of spina bifida was 3.94 per 10,000 live births. The percentage of patients without neonatal repair increased during the study period compared to those with repair (p = 0.0002). The cohort without neonatal repair had a higher risk of death (p < 0.001), prematurity (p < 0.001), and low birth weight (p < 0.001). More shunts were placed in patients who underwent neonatal repair (p < 0.001). Patients without neonatal repair were less likely to have public insurance (p = 0.0052) and more likely to reside in zip codes within the highest income quartile (p = 0.0002).
The prevalence of spina bifida from 2012 to 2018 was 3.94 per 10,000 live births, with an increasing number of patients without neonatal repair of the defect, suggesting increased utilization of fetal surgery. Patients without neonatal repair had a higher risk of death, prematurity, and low birth weight but were more likely to have commercial insurance and reside in high-income zip codes.
随着胎儿手术的普及和证据表明胎儿修复可以改善脊髓脊膜膨出患儿的长期预后,对患有脊髓脊膜膨出的患儿的早期护理发生了改变。我们试图通过国家行政数据库确定使用脊髓脊膜膨出患儿的患病率和早期护理的当前趋势。
这是一项使用 2012-2018 年医疗保健成本和利用项目国家住院患者数据库对出生后 28 天内入院的患有脊髓脊膜膨出的婴儿进行的回顾性、横断面队列研究。通过 ICD 编码识别患有脊髓脊膜膨出的患者,并将其分为接受缺陷新生儿修复的队列和未接受编码修复的队列。该数据库没有特定于胎儿手术的标识符,但很可能有相当数量的未编码修复的婴儿接受了胎儿手术。
我们确定了 5090 例接受编码修复的患者和 5715 例未接受编码修复的患者。脊髓脊膜膨出的总体患病率为每 10000 例活产 3.94 例。与接受修复的患者相比,在研究期间未接受新生儿修复的患者比例增加(p<0.001)。未接受新生儿修复的队列死亡风险更高(p<0.001)、早产风险更高(p<0.001)、出生体重较低(p<0.001)。接受新生儿修复的患者中放置的分流器更多(p<0.001)。未接受新生儿修复的患者更有可能没有公共保险(p=0.0052),而更有可能居住在收入最高四分位数的邮政编码中(p=0.0002)。
2012 年至 2018 年脊髓脊膜膨出的患病率为每 10000 例活产 3.94 例,越来越多的患者未对缺陷进行新生儿修复,这表明胎儿手术的使用率增加。未接受新生儿修复的患者死亡、早产和低出生体重的风险更高,但更有可能拥有商业保险并居住在高收入邮政编码中。