Am J Perinatol 2023; 40(11): 1208-1216
DOI: 10.1055/s-0041-1733957
Original Article

Early Neonatal Mortality among Babies Born with Spina Bifida in Finland (2000–2014)

Vijaya Kancherla
1   Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia
,
Sanjida Mowla
1   Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia
,
Sari Räisänen
2   School of Health, Tampere University of Applied Sciences, Tampere, Finland
,
Mika Gissler
3   Information Services Department, THL Finnish Institute for Health and Welfare, Helsinki, Finland; Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden, Academic Primary Health Care Centre, Region Stockholm, Sweden
› Institutsangaben

Abstract

Objective We examined early neonatal mortality risk, temporal trends, and selected infant and maternal factors associated with early neonatal mortality among all spina bifida-affected live births in Finland.

Study Design We linked multiregistry population-based data from the national registers in Finland for infants born with spina bifida from 2000 to 2014. Early neonatal mortality was defined as death in 0 to 6 days after birth. Early neonatal mortality risk and 95% confidence intervals (CI) was estimated by using the Poisson approximation of binomial distribution. Poisson regression was used to examine temporal trend in early neonatal mortality from 2000 to 2014 for spina bifida cases and all births in Finland. Selected infant and maternal characteristics were compared between cases that experienced early neonatal mortality and cases that did not. Exact logistic regression was used to estimate unadjusted odds ratios (uORs) and 95% confidence intervals (CIs).

Results A total of 181 babies were born alive with spina bifida in Finland during the study period; 61% had isolated spina bifida. Pooling all study years, 7.2% (95% CI: 4.2–12.4%) of all live-born cases experienced early neonatal death. There was a significant increase in early neonatal mortality among spina bifida births over the study period (p < 0.0001). Low gestational age (<37 weeks; uOR = 6.96; 95% CI: 1.86–29.01), cases occurring as a part of a syndrome (uOR = 125.67; 95% CI: 14.90 to >999.999), and advanced maternal age at gestation (≥35 years; uOR = 5.33; 95% CI: 1.21–21.87) were positively associated with early neonatal mortality.

Conclusion Using national data from Finland, we found high early neonatal mortality with increasing trend over birth period spanning 15 years (2000–2014), and unadjusted positive associations with some infant and maternal factors. Future studies should pool data from Nordic countries to increase study size allowing multivariable analysis.

Key Points

  • Early neonatal mortality in babies affected by spina bifida is 7% in Finland.

  • Early neonatal mortality trend showed a significant increase from 2000 to 2014.

  • Low gestational age, syndrome case status, and advanced maternal age increased early neonatal mortality risk in spina bifida.

Note

The data that support the findings of this study are available in multiple data sources with permission from the Finnish Institute for Health and Welfare and Statistics Finland. The Finnish register data have been given for this specific study, and the data cannot be shared without authorization from the register keepers. More information on the authorization application to researchers who meet the criteria for access to confidential data can be found at https://www.findata.fi/en/services/services-for-customers/ (Health and Social Data Permit Authority Findata), https://thl.fi/fi/web/thlfi-en/statistics/information-for-researchers/authorisation-application (THL), and https://www.stat.fi/meta/tietosuoja/kayttolupa_en.html (Statistics Finland).




Publikationsverlauf

Eingereicht: 31. März 2021

Angenommen: 08. Juli 2021

Artikel online veröffentlicht:
24. August 2021

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