Measure - HFA_603


Code
HFA_603
Data state
Published
Data set(s)
HFA
Data Mart ID
583
DATA_MASK
0
Created on
Data updated on
Metadata updated on
Notes updated on

UNIT_TYPE
NUM_100K_LBIRTH
EXTERNID
7120
DATA_SOURCE
HFA
DATA_TYPE_REPRESENTATION
COUNT

Classification(s)
HFA explorer [L]
HFA-DB classification [A]

Short name En
Births with Down's syndrome per 100 000 live births
Full name En
Births with Down's syndrome per 100 000 live births
Data set notes En
HFA
The following abbreviations are used in the indicator titles:
•    SDR: age-standardized death rates (see HFA-DB user manual/Technical notes, page 13, for details)
•    FTE: full-time equivalent
•    PP: physical persons
•    PPP$: purchasing power parities expressed in US $, an internationally comparable scale reflecting the relative domestic purchasing powers of currencies.

Measure note En
Births with Down's syndrome per 100 000 live births
Indicator code: E040803.T This indicator shares the definition with the parent indicator \"Number of births with Down's syndrome\".

Congenital malformations diagnosed within first year of life. ICD-9: 758.0; ICD-10: Q90._
Country notes En
ARM
Source of data: National Health Information Analytic Center, Ministry of Health of the Republic of
Armenia www.healthinfo.am. Data collected annually, reference period: 31 December.
AUT
Source: Statistics Austria, Vital Statistics. Includes livebirths only.
Data up to 2001 used ICD-9 coding.
Data from 2002 used ICD-10 coding.
BLR
January 2001: Morbidity of childres age 0-1 year has been registered since 1997. Before that
information on morbidity of children age 0-15 was available.
BEL
Source: EUROCAT (http://www.eurocat-network.eu/): Registries of Hainaut-Namur (1980-2008) and
Antwerp (1989-2009). Remark: The number was calculated by applying an average of the prevalences
(by 1000 births) of both registries to the total number of births in the country. It is currently
however unclear to what extent the regions of Hainaut, Namur and Antwerp are representative for the
rest of Belgium.
BIH
Public Health Institute - Annual hospital report.
HRV
November 2002: The data are available only from maternity wards. Source: Croatian National Institute
of Public Health.
CYP
No data are available
CZE
Source: Institute of Health Information and Statistics of CR (IHIS CR). Please check Country
specific sources and methods of parent indicator.
Breaks in time series: 1994 (increase of the number of observed congenital malformations), 2000
(another information source was added)
DNK
Source: From 1997: The Medical Birth Registry, The Danish Health Data Authority
EST
Source: annual reporting, 1990-1995 maternity hospital data (aged 0-6 days). From 1996 new cases of
congenital malformations diagnosed within first year of life, National Institute for Health
Development. From 1999 confirmed cases Tartu University Hospital, Genetics Centre.
The low number in year 2013 is because the overall number of foetuses with Down syndrome has been
decreasing steadily over the last years (based on the number of cases diagnosed prenatally, and the
proportion of these from all cases of Down syndrome. Also the number of live births has been
decreasing.
FIN
Source: Register on Congenital Malformation, THL (National Institute for Health and Welfare).
FRA
Data are not available.
DEU
Source: Federal Statistical Office, Hospital statistics - diagnostic data of the hospital patients,
Fachserie 12, Reihe 6.2.1.
http://www.destatis.de
Deviation of definition: The data includes the number of infants treated as in-patients due to
abnormalities in the month of birth (ICD-Pos. Q90 Down-syndrome). Infants repeatedly treated as
in-patients in the month of birth due to a congenital malformation in hospital, will also be counted
several times.
GRC
Data are not available.
HUN
Source: VRONY (National Register for Congenital Anomalies).
ISL
Source: The Icelandic Birth Registration.
IRL
Data are not available.
ISR
Source: Department of Community Genetics and Health Information Division, Ministry of Health.
ITA
Source from 2003: Ministry of Health, Health Information System, Delivery Certificates Database.
Coverage in 2003: 84% of deliveries, recorded in National Database of Hospital Discharges. In 2004:
86% of the deliveries recorded in the National Database of Hospital Discharges. Coverage in 2005:
92% of deliveries recorded in National Database of Hospital Discharges in the same year. Coverage in
2006: 92.9% of deliveries, recorded in National Database of Hospital Discharges in the same year.
Coverage in 2007: 93.0% of deliveries, recorded in National Database of Hospital Discharges in the
same year. Coverage in 2008: 96.6% of deliveries, recorded in National Database of Hospital
Discharges in the same year. Coverage in 2009: 98.2% of deliveries, recorded in National Database of
Hospital Discharges in the same year. Coverage in 2010: 98,8% of deliveries, recorded in National
Database of Hospital Discharges in the same year. Coverage in 2011: 98.8% of deliveries, recorded in
National Database of Hospital Discharges in the same year. Coverage in 2012: 99.9% of deliveries,
recorded in National Database of Hospital Discharges in the same year. Coverage in 2013: 100.3% of
deliveries, recorded in National Database of Hospital Discharges in the same year. The number of
live births registered in the Delivery Certificates Database in 2013 is: 510.659.
LVA
Source before 2000: Register of Congenital Anomalies (only genetically approved live births, Q90).
Source from 2000: Register of Congenital Anomalies (only genetically approved live births Q90) and
Death Causes Database (stillbirths Q90). Abortions are not included.
LTU
Source: Up to 2001: Medical Genetics Centre. From 2002: Medical Birth Register, HI HIC. Coverage:
Newborns with Down syndrome.
MLT
Source: Department of Health Information and Research (Malta National Congenital Anomalies Register)
MNE
Only malformations diagnosed at birth are included.
NLD
TNO Quality of Life. The Netherlands Perinatal Registry. See 045800. Covers Q90-99.
NOR
Source of data: Until 1998 data source was gynaecological/birth departments. Since 1999 data from
paediatric departments are also included.
POL
Data are not available.
PRT
Source of data: Ministry of Health - National Health Institute (INSA), Annual Report. Coverage:
National
ROU
Source: number of hospital admissions for patients aged <1 with Down syndrome.
SRB
Source of data: Institute of Public Health of Serbia, Birth registration report. Data includes
congenital malformations diagnosed (ICD10: Q90) after birth and before discharge of newborn from the
maternity ward.
SVK
Source. National Health Information Centre (NIC)
Note: In year 2012, reporting obligations for congenital anomalies and Down syndrome reporting were
extended to child and adolescent paediatricians. In year 2011 and earlier only neonatologists were
required to report those conditions.
Does not include children who have Downs Syndrome in conjunction with other congenital defects.
Selection of data - residents, respectively patients with permanent address in Slovakia (including
the homeless, residents without registration of permanent address, foreigners with permanent
address in Slovakia.
SVN
Source of data: National Institute of Public Health, Slovenia (NIJZ)
ESP
Source: Estudio Colaborativo Espanol de Malformaciones Congenitas (E.C.E.M.C.) that covers 98 of all
hospitals and 25% of all births.
Proportion of births (live and dead) with Downs syndrome / 1000 births (live and dead).
SWE
Source: The National Board of Health and Welfare (NBHW)
National Patient Register, NBHW
CHE
Based on hospital discharge data. The data take into account the main, but also the supplementary
diagnosis. Source of data: FSO Federal Statistical Office, Neuchatel; Medical Statistics of
Hospitals; yearly census.
Coverage: Full coverage of hospitals; sufficient (nearly full) coverage of inpatient and day cases
since 2002. Due to a modification of the legislation, day cases are not collected in 2009 anymore.
Estimation method: Discharges without a valid ICD-code are not accounted for (negligible).
Break in time series: The gradual change of diagnosis classification since 2008 from ICD-10 WHO to
ICD-10 GM (German Modification) may lead to breaks for some categories.
TUR
No data are available.
TKM
Data are not available.
UKR
Source: Centre of Health Statistics, Ministry of Health.
GBR
Coverage: Data until 1987 refer to England and Wales only. Data from 1988 refer to Great Britain
only. 2009 onwards ? Data is no longer available as ONS is no longer producing the source
publication.
Scotland - ISD has been modifying the way that record linkage is performed and has recently
implemented a technique which relies more heavily on the use of Community Health Index (CHI) numbers
and less heavily on the previous approach of probability matching. Inevitably, this has changed the
number of individuals identified with various conditions. There has, therefore, been some revision
of the congenital anomaly numbers reported from 2007 onwards?. From 2011, data is no longer
available.
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Short name Ru
Число родившихся с синдромом Дауна, на 100000 живорожденных
Full name Ru
Число родившихся с синдромом Дауна, на 100000 живорожденных
Data set notes Ru
Measure note Ru
040803 Число родившихся с синдромом Дауна на 100000 живорожденных Всемирная организация здравоохранения Врожденные аномалии, диагностированные на первом году жизни. МКБ-9: 758.0; МКБ-10: Q90.
Country notes Ru
AUT
ARM
BLR
BEL
BIH
HUN
DEU
GRC
DNK
ISR
IRL
ISL
ESP
ITA
CYP
LVA
LTU
MLT
NLD
NOR
POL
PRT
ROU
SRB
SVK
SVN
GBR
TKM
TUR
UKR
FIN
FRA
HRV
MNE
CZE
CHE
SWE
EST
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Fact id (internal) COUNTRY COUNTRY_GRP MEASURE_TYPE (Obsolete) SEX YEAR Value Display Value