Surgical Treatment of Neural Tube Defects

J. Šutovský
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Abstract

Neural tube defects (NTDs) are developmental pathologies associated with undesirable lifelong consequences. Incidence of these pathologies differs between countries and regions depending on socio-economic and healthcare quality. It is also influenced by folic acid and zinc supplementation. Genetic factors influence probability of NTD, increasing risk of defect in siblings up to 3–8%. Estimated incidence in United States is 3–4/10000 live births, and worldwide incidence increases on about 10/10000 live births. Despite various types and localizations of spina bifida, in all of them neural tissue is in danger. This can lead to various types of neurologic disorders. Not only due to direct damaging of spinal cord and nerve roots but also other parts of central nervous system are also endangered by disturbed prenatal development. Other consequences as orthopedic abnormalities, bladder, and bowel dysfunction influence quality of life. Surgical therapy is often the only possibility to preserve existing function of neural tissue, allows its further development and prevents complications. In this chapter surgical techniques with aim to restore spinal cord and nerve roots anatomy, preservation of its function and defect closures are presented. Also, treatment of possible comorbidities and complications is discussed. Spina bifida management requires multi-speciality cooperation and care to monitor, prevent and treat various potential complication that can negatively influence quality of life and even survival. Prenatal diagnosis is based on maternal screening of serum alpha fetoprotein (AFP) levels and prenatal ultrasonography examination. As the suspicion of neural tube defect arises, an amniocentesis is recommended to complete a genetic analysis and obtain amniotic fluid for more precise AFP and acetylcholinesterase examination. Some types of neural tube defects are diagnosed after delivery, some are symptomatic until adulthood and some are diagnosed incidentally. Each of them requires specific management, based on underlying pathology.
神经管缺损的外科治疗
神经管缺陷(NTDs)是一种与不良终身后果相关的发育病理学。这些疾病的发病率因国家和地区的社会经济和卫生保健质量而异。叶酸和锌的补充也会对其产生影响。遗传因素影响NTD的概率,增加兄弟姐妹缺陷的风险达3-8%。据估计,美国的发病率为3 / 4/10000活产,全世界的发病率约为10/10000活产。尽管脊柱裂的类型和部位各不相同,但所有脊柱裂的神经组织都处于危险之中。这会导致各种类型的神经系统疾病。胎儿发育紊乱不仅会直接损害脊髓和神经根,还会危及中枢神经系统的其他部分。其他后果如骨科异常、膀胱和肠功能障碍影响生活质量。手术治疗往往是唯一的可能,以保持现有的神经组织的功能,使其进一步发展和防止并发症。在这一章的手术技术,目的是恢复脊髓和神经根解剖,保存其功能和缺陷关闭提出。此外,还讨论了可能的合并症和并发症的治疗。脊柱裂的治疗需要多专业合作和护理,以监测、预防和治疗各种可能影响生活质量甚至生存的潜在并发症。产前诊断是基于母体血清甲胎蛋白(AFP)水平筛查和产前超声检查。当怀疑神经管缺损时,建议进行羊膜穿刺术以完成基因分析并获得羊水以进行更精确的甲胎蛋白和乙酰胆碱酯酶检查。有些类型的神经管缺陷是在分娩后诊断出来的,有些直到成年才有症状,有些是偶然诊断出来的。每一种都需要基于潜在病理的特殊治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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