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Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study

BACKGROUND: Following the Thalidomide disaster, the Medical Birth Registry of Norway (MBRN) was established in 1967, with epidemiological surveillance of congenital anomalies as one main aim. Limb reduction defects (LRD) constitute a rare and heterogeneous anomaly group, where correct registration a...

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Autores principales: Klungsøyr, Kari, Nordtveit, Tone Irene, Kaastad, Trine Sand, Solberg, Sigrun, Sletten, Ida Neergård, Vik, Anne-Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636750/
https://www.ncbi.nlm.nih.gov/pubmed/31314783
http://dx.doi.org/10.1371/journal.pone.0219930
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author Klungsøyr, Kari
Nordtveit, Tone Irene
Kaastad, Trine Sand
Solberg, Sigrun
Sletten, Ida Neergård
Vik, Anne-Karin
author_facet Klungsøyr, Kari
Nordtveit, Tone Irene
Kaastad, Trine Sand
Solberg, Sigrun
Sletten, Ida Neergård
Vik, Anne-Karin
author_sort Klungsøyr, Kari
collection PubMed
description BACKGROUND: Following the Thalidomide disaster, the Medical Birth Registry of Norway (MBRN) was established in 1967, with epidemiological surveillance of congenital anomalies as one main aim. Limb reduction defects (LRD) constitute a rare and heterogeneous anomaly group, where correct registration and classification is important for surveillance and research. We aimed at reviewing and recoding LRD cases in the MBRN using the same classification system for all years, and evaluate time trends, characteristics and risk factors, 1970–2016. METHODS: After reviewing and recoding LRD cases using International Classification of Diseases (ICD), 10(th) version, for all years, time trends, association with major anomalies, risk factors and infant outcomes were calculated. Generalized linear models for the binomial family with log link gave relative risks (RR) with 95% confidence intervals (CI). Classification of LRD as suggested by European surveillance of congenital anomalies (EUROCAT) was attempted. RESULTS: Overall LRD prevalence, 1970–2016, was 4.4 per 10 000, slightly increasing during 1970–1981, followed by relatively stable rates. There were more defects in upper than lower limbs. Defects in hands/fingers were most common, but unspecific descriptions prevented classification of LRD according to EUROCAT. A majority of cases had associated anomalies, the most common being other limb defects, followed by cardiac defects and anomalies in the nervous and digestive systems. From 1999, 26% of LRD cases were terminated, more than 90% of these had associated major anomalies. Stillbirth, neonatal and infant mortality were higher among infants with LRD, also related to associated anomalies. Pre-gestational diabetes was associated with a more than three times increased risk of offspring total LRD, while no association with maternal epilepsy was found. Taking folate/multivitamin supplements before and/or during pregnancy was associated with lower risk of offspring LRD (adjusted RR 0.7; 95% CI 0.6–0.9), while daily smoking did not significantly increase the risk. CONCLUSION: The MBRN now has information on LRD coded by ICD-10 from 1970, but information is not specific enough to use other recommended classification systems. Collecting radiographic descriptions and/or more details from hospital records would improve the quality of the registry data. Taking folate supplements before/during pregnancy may reduce the risk of offspring LRD.
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spelling pubmed-66367502019-07-25 Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study Klungsøyr, Kari Nordtveit, Tone Irene Kaastad, Trine Sand Solberg, Sigrun Sletten, Ida Neergård Vik, Anne-Karin PLoS One Research Article BACKGROUND: Following the Thalidomide disaster, the Medical Birth Registry of Norway (MBRN) was established in 1967, with epidemiological surveillance of congenital anomalies as one main aim. Limb reduction defects (LRD) constitute a rare and heterogeneous anomaly group, where correct registration and classification is important for surveillance and research. We aimed at reviewing and recoding LRD cases in the MBRN using the same classification system for all years, and evaluate time trends, characteristics and risk factors, 1970–2016. METHODS: After reviewing and recoding LRD cases using International Classification of Diseases (ICD), 10(th) version, for all years, time trends, association with major anomalies, risk factors and infant outcomes were calculated. Generalized linear models for the binomial family with log link gave relative risks (RR) with 95% confidence intervals (CI). Classification of LRD as suggested by European surveillance of congenital anomalies (EUROCAT) was attempted. RESULTS: Overall LRD prevalence, 1970–2016, was 4.4 per 10 000, slightly increasing during 1970–1981, followed by relatively stable rates. There were more defects in upper than lower limbs. Defects in hands/fingers were most common, but unspecific descriptions prevented classification of LRD according to EUROCAT. A majority of cases had associated anomalies, the most common being other limb defects, followed by cardiac defects and anomalies in the nervous and digestive systems. From 1999, 26% of LRD cases were terminated, more than 90% of these had associated major anomalies. Stillbirth, neonatal and infant mortality were higher among infants with LRD, also related to associated anomalies. Pre-gestational diabetes was associated with a more than three times increased risk of offspring total LRD, while no association with maternal epilepsy was found. Taking folate/multivitamin supplements before and/or during pregnancy was associated with lower risk of offspring LRD (adjusted RR 0.7; 95% CI 0.6–0.9), while daily smoking did not significantly increase the risk. CONCLUSION: The MBRN now has information on LRD coded by ICD-10 from 1970, but information is not specific enough to use other recommended classification systems. Collecting radiographic descriptions and/or more details from hospital records would improve the quality of the registry data. Taking folate supplements before/during pregnancy may reduce the risk of offspring LRD. Public Library of Science 2019-07-17 /pmc/articles/PMC6636750/ /pubmed/31314783 http://dx.doi.org/10.1371/journal.pone.0219930 Text en © 2019 Klungsøyr et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Klungsøyr, Kari
Nordtveit, Tone Irene
Kaastad, Trine Sand
Solberg, Sigrun
Sletten, Ida Neergård
Vik, Anne-Karin
Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title_full Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title_fullStr Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title_full_unstemmed Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title_short Epidemiology of limb reduction defects as registered in the Medical Birth Registry of Norway, 1970-2016: Population based study
title_sort epidemiology of limb reduction defects as registered in the medical birth registry of norway, 1970-2016: population based study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6636750/
https://www.ncbi.nlm.nih.gov/pubmed/31314783
http://dx.doi.org/10.1371/journal.pone.0219930
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