Spain: Difference between revisions
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'''Information/contact for data request''': [https://www.sanidad.gob.es/servCiudadanos/contactar/home.htm Contact information]. | '''Information/contact for data request''': [https://www.sanidad.gob.es/servCiudadanos/contactar/home.htm Contact information]. | ||
=== Database: | === Database: Spanish Registry of Pediatric Tumors (RETI-SEHOP) === | ||
[https://www.uv.es/rnti/pdfs/Informe_RETI-SEHOP_1980-2021.pdf [2]] | [https://www.uv.es/rnti/pdfs/Informe_RETI-SEHOP_1980-2021.pdf [2]] | ||
Revision as of 23:02, 27 January 2023
Cancer Centers
Healthcare System
Administrative or Claims Data
Registries
Database: Main indicators of The National Health System (INCLASNS)
[1]
Primary purpose: Facilitates access to information that is already individually presented by official statistical institutions. The database does so by reuniting important indicators to research healthcare functioning and general health quality.
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Cancer mortality tax (premature and non-premature adjusted by age, per 100 000 hab) and pertinence of conservative surgery in breast cancer in percentage. Full list of indicators can be checked here.
Source of information: El Sistema de Información del Sistema Nacional de Salud and other sources (Instituto Nacional de Estadística, Centro Nacional de Epidemiología, Agencia Española de Medicamentos y Productos Sanitarios, etc.)
Data level: Regional level.
Number of Records: Includes 247 indicators.
Date range: 1990 onwards.
Cancer Areas of Interest: Unknown.
Data access: Openly available here.
Information/contact for data request: Contact information.
Database: Spanish Registry of Pediatric Tumors (RETI-SEHOP)
[2]
Primary purpose: Collects data and produces epidemiology research about childhood cancer.
Sponsor, manager or home institution: La Sociedad Española de Hematología y Oncología Pediátricas (SEHOP) and la Universitat de València (UV).
Type of information: Survival (3 and 5 years after diagnosis), incidence, medical treatment coverage in percentage and cancer causes filtered by region, sex and year.
Source of information: Reports from all Spanish pediatric oncologic and hematologic hospital unities. The list of institutions can be checked here.
Data level: Regional level.
Number of Records: Covers more than 90% of national children cases. Between 1980-2021 there were 31.275 incidence cases registered.
Date range: Varies accordingly to selected indicators: survival (1980-2004), incidence (1983-2002), medical treatment coverage (1980-2012).
Cancer Areas of Interest: The list can be checked at the pages XXXII - XXXV of this document.
Data access: By the RETI annual report, available here.
Information/contact for data request: Can be acquired at the SEHOP website.
