National Renal Transplant Registry

This database is a renal database collecting data since 1964. It is used to assess graft survival and patient survival, monitor factors affecting outcomes.

Purpose: The purpose of the registry is to provide robust data capable of informing the outcomes of renal transplants/recipients in Ireland. The upkeep of a national registry is required by law (SI No325/2012) which came into effect in August 2012 in compliance with EU Directive 2010/53/EU on Standards of Quality and Safety of Human Organs intended for Transplantation. The upkeep of the National Registry complies with DIRECTIVE 95/46/EC of 24 October 1995 on the protection of individuals with regard to t

Coverage: All consecutive renal transplants from 1964 performed in Ireland. Data collection starts at time of transplant and finishes at failure of allograft or death of recipient.

Data and Resources

This dataset has no data

Additional Info

Field Value
Contact points
Contact point 1
URI
Name
Beaumont Hospital
Email
data@beaumont-hospital.ie
Identifier
Publisher
Publisher 1
URI
Name
Beaumont Hospital
Email
URL
Type
http://purl.org/adms/publishertype/NationalAuthority
Identifier
Creator
Homepage
Landing page
Release date January 1, 2002
Modification date April 3, 2025
Version
Version notes
Identifier NDC-0100
Frequency http://publications.europa.eu/resource/authority/frequency/QUARTERLY
Provenance

Data is collated in the renal unit from hospital based systems and laboratory reports. Collected at time of transplant and yearly afterwards.

Type
Temporal coverage
Temporal coverage 1
Start
January 1, 2002
End
September 11, 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/PUBLIC
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/public-health
  2. http://health.europa.eu/ehds/category/ehr
Health theme
  1. http://health.europa.eu/theme/epidemiology
  2. http://health.europa.eu/theme/mental-health
  3. http://health.europa.eu/theme/infectious-disease
Legal basis
Minimum typical age 18
Maximum typical age 85
Number of records 943012
Number of records for unique individuals. 232466
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