Spain
Cancer Centers
Healthcare System
Spain's healthcare system is the Sistema Nacional de Salud (SNS), a universal health system that covers 99% of the Spanish population and is funded by general taxation. The administration is divided at the national and regional level, with the national level managed by the Ministry of Health, Consumer Affairs and Social Welfare, whereas the 17 regional health departments manage the regional level. Both collaborate through the SNS Interterritorial Council in order to implement policy at the regional and national level.
The General Secretariat of Digital Health, Information and Innovation of the SNS is the body responsible for implementing the Digital Health Strategy of the SNS, which aims to improve the health of every Spanish citizen through the increased adoption of digital health solutions for healthcare and the development of infrastructures that allow providers to use data to help their patients.
The Instituto de Salud Carlos III (ISCIII) is a public research agency integrated with the Ministry of Science and Innovation and the Ministry of Health, and is responsible for conducting health research that aims to improve the health of the people, offer scientific and technical advice for policymaking, as well as develop educational programs for the entire SNS system.
Other major institutions related to healthcare and health research include the National Institute of Statistics and the National Drug Agency.
Administrative or Claims Data
Database: The Registry of Specialized Health Care Activity (RAE-CMBD)
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Presents administrative and clinical information on patients treated in the different Specialized Care and outpatient care modalities in the public or private sector. Includes hospitalization, home hospitalization care modalities, medical day hospital, outpatient surgery, outpatient procedures of special complexity and emergencies.
General information about the hospitalization; morbidity data (main and secondary diagnosis registered using CIE9MC and CIE10ES, and age-adjusted hospitalization rates); procedures performed (registered using CCS).
The available variables are year, age, sex, region of residence, hospital region, type of patient admission, type of patient discharge, financing system, performed service at discharge in hospitalization, group of hospitals, type of hospital (public or private), size of the hospital by number of beds,
Source of information: Reports from the providers that are sent to the Ministry of health.
Data level: Regional level (openly available) and Patient level (restricted access).
Date range: Varies accordingly to the category of care. Hospitalization (1997 onwards), acute care (1997 onwards), ambulatory care (2004 onwards). Informations regarding the private sector are availabe from 2005 onwards.
Data access: The openly available content can be accessed here. To request data extraction, follow the instructions presented here.
Information/contact for data request: Contact information.
Registries
Database: Main indicators of The National Health System (INCLASNS)
[3]
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)
[4]
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.
Database: Annual Report of the National Health System
Primary purpose: Provides information about the health of the Spanish population and details about the operation and results of the National Health System (SNS).
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Population information, health status (well-being, morbidity, mortality), social determinants of health (socioeconomic determinant factors, lifestyles), sanitary system (health care, accessibility, experience, patient, physical resources, human resources, and expenses).
The 2020-2021 report also includes information on the response of health services to COVID-19 (capacity of care, care activity related to COVID-19, impact on accessibility to the health system, impact on ordinary care activity, experience of the population, covid vaccination, diagnostic capacity, and pharmaceutical service).
Source of information: Data collected from the Councils of Health of the autonomous communities, the National Institute of Health Management and surveys.
Data level: Regional level.
Number of Records: Unknown.
Date range: 2003 onwards.
Cancer Areas of Interest: Unknown.
Data access: Openly available here.
Information/contact for data request: Contact information.
Database: Mortality by cause of death
[5]
Primary purpose: Provides death statistics to enable monitoring and health measures to be taken.
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Crude mortality rates, age-adjusted mortality rates, and age-adjusted premature mortality rates. Those can be filtered by sex, cause of death, year, and geographic region.
Source of information: Medical Certificate of Death/Death Statistical Bulletin (CMD/BED) and the Birth Statistical Bulletin (BEP).
Data level: Regional level.
Number of Records: Unknown.
Date range: 1981 onwards.
Cancer Areas of Interest: (C00-D48) Tumors. (C00-C14) Malignant tumors of lip, oral cavity and pharynx, (C15-C26) Malignant tumors of digestive organs, (C30-C39) Malignant tumors of respiratory and intrathoracic organs, (C40-C41) Malignant tumors of bone and articular cartilage, (C43-C44) Melanoma and other malignant tumors of the skin, (C45- C49) Malignant tumors of mesothelial tissues and soft tissues, (C50) Malignant tumors of breast, (C51-C58) Malignant tumors of female genital organs, (C60-C63) Malignant tumors of male genital organs, (C64-C68) Malignant tumors of urinary tract, (C69-C72) Malignant tumors of eye, brain and other parts of central nervous system, (C73-C75) Malignant tumors of thyroid and other endocrine glands, (C76-C80) Malignant tumors of ill-defined, secondary and unspecified sites, (C81-C96) Primary malignant tumors of lymphatic tissue, hematopoietic organs and related tissues, (C97) Primary malignant tumors of multiple independent sites, (D00-D09) Neoplasms in situ, (D10-D36) Benign tumors, (D37-D48) Tumors of uncertain or unknown behavior.
Data access: Openly available here.
Information/contact for data request: Contact information.
Database: Late Fetal and Infant Mortality
Primary purpose: Contains statistical information about national children death.
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Number of late fetal mortality and infant mortality filtered by age, sex, geographic region, year and basic cause of death. Considering infant mortality, age of the deceased is also a filter. It is possible to analyze the rates of late fetal mortality, infant mortality and perinatal mortality.
Source of information: The Birth Statistical Bulletin and in the Medical Certificate of Death/Death Statistical Bulletin.
Data level: Regional level.
Number of Records: Unknown.
Date range: 1981 onwards.
Cancer Areas of Interest: Unknown.
Data access: Openly available here.
Information/contact for data request: Contact information.
Database: The Specialized Care Information System (SIAE)
[6]
Primary purpose: Provide statistical information about affiliation, dependency and purpose of care, staffing, human resources, activity and economic information of both public and private hospitals nationwide.
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Regarding cancer, there are data on the number of radiotherapeutic exams, interventional radiology exams, biopsies, and mammograms filtered by year, type of hospital (public or private), assistance purpose, legal form, and geographic region.
Source of information: Unknown.
Data level: Regional level.
Number of Records: Unknown.
Date range: 1997 onwards.
Cancer Areas of Interest: Unknown.
Data access: Openly avaiable here.
Information/contact for data request: Contact information.
Database: Primary Care Clinical Data Base (BDCAP)
[7]
Primary purpose: Make statistics on primary level care available
Sponsor, manager or home institution: Ministerio de Sanidad.
Type of information: Active health problems in the year of study, interconsultations, visits, procedures (per 1,000 persons served, per 1,000 assigned persons, absolute number of records), prescribed medications (eDfined Daily Dose -DDDD- per 1000 persons assigned/served per day), clinic parameters, comorbidity.
Filters available are year, sex, age, birth country, geographic region, region's extent by the number of inhabitants, annual income of patients, the employment situation of the patients, subpopulation by type of health problem, year of disease initiation, subpopulation by prescribed medication.
Source of information: Electronic medical records.
Data level: Regional level (openly available) and Patient level (restricted access).
Number of Records: Around 4,900,00 people per year.
Date range: 2011 onwards.
Cancer Areas of Interest: The list can be checked in this website.
Data access: Openly available here. Monographic and didactic reports are also available here. Access to patient level data can be required by contacting the Health ministry or by accessing this website.
Information/contact for data request: Contact information.
Database: Hospital Morbidity Survey (EMH)
[8]
Primary purpose: To determine the geographic distribution of morbidity attended in hospitals according to the main diagnosis associated with average hospital stay and hospital discharge.
Sponsor, manager or home institution: Instituto Nacional de Estadística (INE).
Type of information: Available variables are the number of hospital discharges and hospital stay.
Filters include the main diagnosis, type of hospital admission, reason for discharge and province of hospitalization, age, sex and place of residence.
Source of information: Hospital's patient register, files, and surveys.
Data level: Regional level is openly available. Patient level requires restricted access.
Number of Records: Covers 90% of the hospitals and 98% of the discharges in all of Spain.
Date range: 1978 onwards (restricted) and 1997 onwards (openly available).
Cancer Areas of Interest: The list can be checked in the following document.
Data access: Regional data openly available here. Reports can also be accessed here. For patient level information, follow instructions presented here.
Information/contact for data request: Contact information.
