Alpha One Foundation Registry

The Alpha One Foundation was established in 2001 to promote research into Alpha-1, to improve diagnosis, treatment and to improve life expectancy and lifestyle of people with this condition. In 2004 the National Targeted Detection Programme for AATD, funded by the Department of Health, was launched by the Foundation in Beaumont Hospital, providing free testing to persons with chronic pulmonary conditions and also relatives of persons with AATD.

The national Alpha-1 registry was launched in 2005 to track the health of people with Alpha-1 Antitrypsin Deficiency across Ireland. Information in the registry helps clinicians and researchers see new trends, design clinical trials to test new therapies and improve the delivery of care for people with AATD.

Purpose: The purpose of the register is to:

In Scope:

 to establish a database of patients and their clinical details,  to promote basic and clinical research into AATD and coordinate this activity  to collect, assess and disseminate information concerning all aspects of AATD  to encourage and support awareness of AATD.

Out of Scope:

 Mailing Lists.

Coverage: Ireland - 32 counties– all Alpha-1 patients attending National Alpha-1 Outpatient Clinic in Beaumont Hospital.

Start Date – 2005. No End Date.

Data and Resources

This dataset has no data

Additional Info

Field Value
Contact points
Contact point 1
URI
Name
Alpha One Foundation
Email
data@alpha-one-foundation.ie
Identifier
Publisher
Publisher 1
URI
Name
Alpha One Foundation
Email
URL
Type
http://purl.org/adms/publishertype/NationalAuthority
Identifier
Creator
Homepage
Landing page
Release date January 1, 2005
Modification date February 26, 2025
Version
Version notes
Identifier NDC-0007
Frequency http://publications.europa.eu/resource/authority/frequency/MONTHLY
Provenance

Data is collected weekly in the National Alpha-1 Outpatient Clinic in Beaumont Hospital from patients’ medical charts and information provided by patients themselves. Annual assessment of all enrolees takes place. The registry is part of a research study and is confidential. Written consent is gained from patients as part of ethical approval to collect and analyse data. Participation is voluntary.

Type
Temporal coverage
Temporal coverage 1
Start
January 1, 2005
End
December 17, 2025
Temporal resolution
Spatial coverage
Spatial coverage 1
URI
http://publications.europa.eu/resource/authority/country/IRL
Label
Ireland
Geometry
Bounding Box
Centroid
Spatial resolution in meters
Access rights http://publications.europa.eu/resource/authority/access-right/RESTRICTED
Other identifier
Theme
  1. http://publications.europa.eu/resource/authority/data-theme/HEAL
Language
  1. http://publications.europa.eu/resource/authority/language/ENG
Documentation
Conforms to
Is referenced by
Analytics
Applicable legislation
Has version
Code values
Coding system
Purpose
Health category
  1. http://health.europa.eu/ehds/category/ehr
  2. http://health.europa.eu/ehds/category/public-health
Health theme
  1. http://health.europa.eu/theme/mental-health
  2. http://health.europa.eu/theme/epidemiology
Legal basis
Minimum typical age 18
Maximum typical age 85
Number of records 409507
Number of records for unique individuals. 162534
Personal data
Publisher note
Publisher type
Trusted Data Holder
Population coverage
Retention period
Health data access body
Qualified relation
Provenance Activity
URI
Qualified Attribution
Quality annotations