Skip to main content
Top
Published in: The Journal of Obstetrics and Gynecology of India 3/2020

01-06-2020 | Hydrocephalus | Original Article

Relative Prevalence and Outcome of Fetal Neural Tube Defect in a Developing Country

Authors: Manisha Kumar, Aayushi Hasija, Nikita Garg, Ramya Mishra, S. C. Roy Chaudhary

Published in: The Journal of Obstetrics and Gynecology of India | Issue 3/2020

Login to get access

Abstract

Objectives

To find out the relative prevalence of fetal neural tube defect (NTD) and its outcome in terms of survival at birth and beyond 2 years of age.

Methods

A 10-year prospective (2008–2018) observational study was performed, which included all prenatally detected fetal NTD. Two-year follow-up was done in cases of pregnancies resulting in live birth, in terms of their survival, physical morbidity and developmental delay.

Results

NTD was seen in 401/648 (62%) cases among the central nervous system malformations. More than half of the cases (54.1%) presented after 20 weeks of gestation, and 42.8% of the mothers were primiparous. Spina bifida was seen in 206 cases, anencephaly in 144, encephalocele in 43, whereas iniencephaly was seen in only eight cases. Associated anomalies were present in 51.2%. Only 19.0% cases were live-born, and merely 11% were alive beyond 2 years of age. Among types of spina bifida, lumbosacral meningomyocele was the most common (41.6%), whereas thoracic was the rarest (8.7%). After 2 years, physical disability was observed in more than half of the cases who survived.

Conclusions

NTD is one of the commonest malformations with high mortality, and the physical and mental sub-normality is high among those who survive.
Literature
1.
go back to reference Hans JTD, Martin L, Akira H. Clinical neuroembryology: development and developmental disorders of the human central nervous system. 2nd ed. Heidelberg: Springer; 2014. Hans JTD, Martin L, Akira H. Clinical neuroembryology: development and developmental disorders of the human central nervous system. 2nd ed. Heidelberg: Springer; 2014.
2.
go back to reference Greene ND, Stanier P, Copp AJ. Genetics of human neural tube defects. Hum Mol Genet. 2009;18:R113–29.CrossRef Greene ND, Stanier P, Copp AJ. Genetics of human neural tube defects. Hum Mol Genet. 2009;18:R113–29.CrossRef
3.
go back to reference Hunter A. Brain and spinal cord. Oxford Monogr Med Genet. 2006;52:715. Hunter A. Brain and spinal cord. Oxford Monogr Med Genet. 2006;52:715.
4.
go back to reference Mahapatra A. Spinal dysraphism controversies: AIIMS experiences and contribution. Indian J Neurosurg. 2012;1:4–8.CrossRef Mahapatra A. Spinal dysraphism controversies: AIIMS experiences and contribution. Indian J Neurosurg. 2012;1:4–8.CrossRef
5.
go back to reference Busby A, Abramsky L, Dolk H, et al. Preventing neural tube defects in Europe: a missed opportunity. Reprod Toxicol. 2005;20(3):393–402.CrossRef Busby A, Abramsky L, Dolk H, et al. Preventing neural tube defects in Europe: a missed opportunity. Reprod Toxicol. 2005;20(3):393–402.CrossRef
6.
go back to reference Lorber J. Spina bifida cystica. Results of treatment of 270 consecutive cases with criteria for selection for the future. Arch Dis Child. 1972;47(256):854–73.CrossRef Lorber J. Spina bifida cystica. Results of treatment of 270 consecutive cases with criteria for selection for the future. Arch Dis Child. 1972;47(256):854–73.CrossRef
7.
go back to reference Kandasamy V, Subramanian M, Rajilarajendran H, et al. A study on the incidence of neural tube defects in a tertiary care hospital over a period of five years. J Clin Diagn Res JCDR. 2015;9(7):QC01–4.PubMed Kandasamy V, Subramanian M, Rajilarajendran H, et al. A study on the incidence of neural tube defects in a tertiary care hospital over a period of five years. J Clin Diagn Res JCDR. 2015;9(7):QC01–4.PubMed
8.
go back to reference Adeleye AO, Olowookere KG. Central nervous system congenital anomalies: a prospective neurosurgical observational study from Nigeria. Congenit Anom (Kyoto). 2009;49(4):258–61.CrossRef Adeleye AO, Olowookere KG. Central nervous system congenital anomalies: a prospective neurosurgical observational study from Nigeria. Congenit Anom (Kyoto). 2009;49(4):258–61.CrossRef
9.
go back to reference Kumar R, Singhal N. Outcome of meningomyelocele/lipomeningomyelocele in children of northern India. Pediatr Neurosurg. 2007;43(1):7–14.CrossRef Kumar R, Singhal N. Outcome of meningomyelocele/lipomeningomyelocele in children of northern India. Pediatr Neurosurg. 2007;43(1):7–14.CrossRef
10.
go back to reference Netto JM, Bastos AN, Figueiredo AA, et al. Spinal dysraphism: a neurosurgical review for the urologist. Rev Urol. 2009;11:71–81.PubMedPubMedCentral Netto JM, Bastos AN, Figueiredo AA, et al. Spinal dysraphism: a neurosurgical review for the urologist. Rev Urol. 2009;11:71–81.PubMedPubMedCentral
11.
go back to reference Thompson DN. Postnatal management and outcome for neural tube defects including spina bifida and encephalocoeles. Prenat Diagn. 2009;29(4):412–9.CrossRef Thompson DN. Postnatal management and outcome for neural tube defects including spina bifida and encephalocoeles. Prenat Diagn. 2009;29(4):412–9.CrossRef
12.
go back to reference Kuo BJ, Vissoci JR, Egger JR, et al. Perioperative outcomes for pediatric neurosurgical procedures: analysis of the National Surgical Quality Improvement Program-Pediatrics. J Neurosurg Pediatr. 2017;19(3):361–71.CrossRef Kuo BJ, Vissoci JR, Egger JR, et al. Perioperative outcomes for pediatric neurosurgical procedures: analysis of the National Surgical Quality Improvement Program-Pediatrics. J Neurosurg Pediatr. 2017;19(3):361–71.CrossRef
13.
go back to reference Shin M, Kucik JE, Siffel C, et al. Improved survival among children with spina bifida in the United States. J Pediatr. 2012;161(6):1132–7.CrossRef Shin M, Kucik JE, Siffel C, et al. Improved survival among children with spina bifida in the United States. J Pediatr. 2012;161(6):1132–7.CrossRef
14.
go back to reference Hunt GM. Open spina bifida: outcome for a complete cohort treated unselectively and followed into adulthood. Dev Med Child Neurol. 1990;32:108–18.CrossRef Hunt GM. Open spina bifida: outcome for a complete cohort treated unselectively and followed into adulthood. Dev Med Child Neurol. 1990;32:108–18.CrossRef
Metadata
Title
Relative Prevalence and Outcome of Fetal Neural Tube Defect in a Developing Country
Authors
Manisha Kumar
Aayushi Hasija
Nikita Garg
Ramya Mishra
S. C. Roy Chaudhary
Publication date
01-06-2020
Publisher
Springer India
Published in
The Journal of Obstetrics and Gynecology of India / Issue 3/2020
Print ISSN: 0971-9202
Electronic ISSN: 0975-6434
DOI
https://doi.org/10.1007/s13224-020-01311-x

Other articles of this Issue 3/2020

The Journal of Obstetrics and Gynecology of India 3/2020 Go to the issue