Publication, Part of NCARDRS Congenital Anomaly Statistics: Annual Data
NCARDRS Congenital Anomaly Official Statistics Report, 2021
Official statistics
Glossary
Glossary of terms
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Definition |
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The cause, set of causes, or manner of causation of a disease or condition, such as genetic. |
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The period from conception to birth. |
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Proportion of notifications of congenital anomalies reported to NCARDRS out of all cases of congenital anomaly in the population. |
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Babies is used throughout, from the early stages of pregnancy through to the neonatal period and refers to all pregnancy outcomes; live births, stillbirths, late miscarriages between 20-23 complete weeks and terminations at any gestation. |
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Confidence interval (see Technical details document for more information) |
Expresses the uncertainty of a statistic as a range in which the true value would be expected to be found on repeated sampling. Estimates with non-overlapping confidence intervals are considered statistically significantly different. |
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Condition present at delivery, originating before birth, and includes structural, chromosomal, genetic, and biochemical anomalies. |
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European Surveillance of Congenital Anomalies – European network of population-based registries for the epidemiological surveillance of congenital anomalies. |
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National Health Service (NHS) screening programme for specified structural and chromosomal anomalies during pregnancy using laboratory and/or ultrasound tests. |
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NCARDRS codes congenital anomalies according to the paediatric adaptation of ICD-10 produced by the British Paediatric Association (BPA).
The auditable conditions screened under the Fetal Anomaly Screening Programme (FASP):
Anencephaly (Q00*) Spina bifida (Q05*) Transposition of great arteries (Q20.3) Atrioventricular septal defect (Q21.2*) Tetralogy of Fallot (Q21.3, Q21.82) Hypoplastic left heart (Q23.4) Cleft lip +/- palate (Q36*, Q37*) Bilateral renal agenesis (Q60.1) Lethal skeletal dysplasia (Q77.0*, Q77.1, Q77.2, Q77.8*, Q78.0*) Congenital diaphragmatic hernia (Q79.0*) Exomphalos (Q79.2) Gastroschisis (Q79.3) Trisomy 21 (Q90*) Trisomy 18 (Q91*) Trisomy 13 (Q91*) |
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Includes genetic syndromes, hereditary skin disorders, skeletal dysplasias and chromosomal anomalies as defined by EUROCAT. |
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The Index of Multiple Deprivation (IMD) is the official measure of relative deprivation for small areas in England. IMD ranks every small area in England from 1 (most deprived area) to 32,844 (least deprived area). |
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Deaths from birth to under 1 year of age as recorded by Child and infant mortality data from the ONS |
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The number of infant deaths per 10,000 live births. |
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Late fetal deaths from 20 to 23 completed weeks of gestation. |
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A baby showing signs of life at birth as recorded by the Office for National Statistics |
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The total number of babies diagnosed with a congenital anomaly that are live born compared to the total number of live births. |
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The high-level body system and anomaly type groupings of congenital anomalies as defined by the NCARDRS modified version of EUROCAT’s subgroups. |
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Includes anomalies with no known genetic cause. Not all babies undergo genetic testing, so it is likely that some of these anomalies are of genetic origin. |
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Body responsible for collection and production of statistics related to the economy, population, and society of the UK. |
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Outcome of the end of the pregnancy, as distinct to the civil registerable nature of the birth. Stillbirths or live births that have been preceded by a termination procedure are categorised in this report as a termination |
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Medical care for a condition focusing on relief of symptoms rather than treating the underlying condition. |
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Extra genetic material is present, but only from part of the chromosome, not the entire chromosome. To ensure consistency throughout the report and internationally, partial trisomies are also included in the trisomy groups for prevalence reporting. |
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Stillbirths and deaths under 7 days of age as recorded by the Office for National Statistics. |
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The number of perinatal deaths per 10,000 total births. |
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From 28 days of life to 1 year of age. |
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A quintile is a statistical value of a data set that represents 20% of a given population, so the first quintile represents the lowest fifth of the data (1% to 20%); the second quintile represents the second fifth (21% to 40%) and so on. |
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| A rare disease is a life-threatening or chronically debilitating disease that affects 5 people or fewer in 10,000 and requires special, combined efforts to enable patients to be treated effectively. See The UK Strategy for Rare Diseases for further information. | |
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Severe cardiac anomalies are a subgroup comprised of the following congenital heart anomalies:
Common arterial truncus Transposition of great vessels Single ventricle Atrioventricular septal defect Tetralogy of Fallot Tricuspid atresia and stenosis Ebstein’s anomaly Pulmonary valve atresia Aortic valve atresia/stenosis Hypoplastic left heart Hypoplastic right heart Coarctation of aorta Total anomalous pulmonary venous return |
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A baby born after 24 or more completed weeks of gestation and which did not, at any time, breathe or show signs of life as recorded by the Office for National Statistics. |
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Substance or other factor that can cause congenital anomaly by affecting fetal development. |
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Term used to describe the deliberate ending of a pregnancy with the intention that the fetus will not survive.
This includes terminations of pregnancy for fetal anomaly as well as terminations of pregnancy for other medical reasons where a fetal anomaly was present.
Where a pregnancy ends in a termination, the baby may be born dead, or if parents have not opted for prior feticide, the baby may be born alive but die shortly after. Depending on the gestation at which a termination takes place (before or after 24 weeks), it may instead be registered as a stillbirth. |
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Live births and stillbirths as recorded by the Office for National Statistics. |
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The total number of babies diagnosed with a congenital anomaly (live births, stillbirths, late miscarriages, and terminations of pregnancy for fetal anomaly) compared to the total number of births (live births and stillbirths). |
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Trisomy is a condition that results in an extra copy of a chromosome in all or some of an individual’s cells. Down’s syndrome (Trisomy 21), Edwards syndrome (Trisomy 18) and Patau syndrome (Trisomy 13) are the most common forms of trisomy associated with pregnancies that can progress to full term. |
Last edited: 27 March 2024 2:26 pm