Sweden: Difference between revisions
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'''Primary purpose:''' The objective of the pharmaceutical registry is to enhance patient safety within the pharmaceutical industry. | '''Primary purpose:''' The objective of the pharmaceutical registry is to enhance patient safety within the pharmaceutical industry. | ||
'''Type of information:''' [[ | '''Type of information:''' [[Data Dictionary: Medicines Registry]]. Data dictionary information [https://www.socialstyrelsen.se/globalassets/sharepoint-dokument/dokument-webb/statistik/register-variabelforteckning-lakemedelsregistret.xlsx]. | ||
'''Available type of information:''' Drug groups and ATC codes for all ages, drug groups for children 0-17 children; filtered by annual data, monthly data divided by age, monthly data divided by region, drug groups, ATC codes, regions, sex, measure, year and month. | '''Available type of information:''' Drug groups and ATC codes for all ages, drug groups for children 0-17 children; filtered by annual data, monthly data divided by age, monthly data divided by region, drug groups, ATC codes, regions, sex, measure, year and month. | ||
Revision as of 20:04, 19 July 2023
Cancer Centers
Healthcare System
Sweden operates a universal healthcare system, providing coverage for all residents, irrespective of nationality, and emergency care for EU/EEA patients and countries with bilateral agreements. The system is mainly funded through local taxes and national government contributions via general grants and specific programmes.
The healthcare responsibility is decentralized between the national government, 21 regions, and 290 municipalities. The Ministry of Health and Social Affairs sets the overall health policies, while healthcare delivery is managed by the regions and municipalities. Regions oversee primary, specialist, and psychiatric care, and public and private hospitals. Municipalities handle elder care, care for the physically and mentally disabled, rehabilitation, school healthcare, home care, and social care.
Residents receive a wide range of benefits including preventive care, check-ups, immunization, medication, hospitalization, maternity, mental health services, and children's dental care. About 15% of health spending comes from out-of-pocket payments, mainly for pharmaceuticals, dental care, and other outpatient care.
To access these benefits, one must be a resident of Sweden. The system also offers the choice of primary care provider, either public or private, accredited by the local county council. There's a patient fee for certain services but it's capped annually, and certain groups receive completely free healthcare.
Sweden's healthcare data management uses electronic health record systems, with data interoperable across different providers. National health data registries are used for monitoring care quality, resource planning, and research while ensuring patient privacy is protected by law.
Administrative or Claims Data
Database: Socialstyrelsen National Patient Register
Sponsor, manager or home institution: Socialstyrelsen.
Primary purpose: The patient register serves multiple purposes. One of its main functions is to track the health development of the population over an extended period. In doing so, it helps to improve the possibilities of preventing and treating diseases. Additionally, the patient register contributes to the overall development of healthcare by providing valuable data and insights. It also enables healthcare providers to monitor the quality of their operations and identify areas where improvements may be needed.
Type of information: Data Dictionary: Socialstyrelsen National Patient Register. Full list of variables [1].
Source of Information: Healthcare providers must submit patient information to the patient register monthly, including hospital code and medical area. Data is submitted via a reporting portal or register service.
Data level: Patient level.
Number of Records: Unknown.
Date Range: 1964 onwards.
Cancer Areas of Interest: Unknown.
Open data access: Not publicly available. Instructions to request data for restricted content [2].
Information/Contact for data request: Contact information [3].
Registries
Database: Socialstyrelsen Cancer Registry
Sponsor, manager or home institution: Socialstyrelsen.
Primary purpose: To map the occurrence and change of cancer diseases over time.
Type of information: Data Dictionary: Socialstyrelsen Cancer Registry. Full list of variables [4].
Available type of information: Number of new cases; Cases per 100,000; Incidence; Age; Sex; Cancer area, and year.
Source of Information: The data is sent from hospitals to six regional cancer centers for coding and registration. Once the material has been verified, it is then transmitted to the National Board of Health and Welfare to become part of the cancer registry. The registry is updated annually.
Data level: Patient level.
Available data level: Regional and national level.
Number of Records: 60,000 cases registered every year [5].
Date Range: 1970 onwards.
Cancer Areas of Interest: All.
Open data access: Partially publicly available [6]. Instructions to request data for restricted content [7].
Information/Contact for data request: Contact information [8].
Database: Socialstyrelsen Cause of Death Registry
Sponsor, manager or home institution: Socialstyrelsen.
Primary purpose: To describe the causes of death and track mortality trends in Sweden.
Type of information: Data Dictionary: Socialstyrelsen Cause of Death Registry. Full list of variables [9].
Available type of information: Number of deaths; Deaths rates and deaths by 100,000 people; Diagnosis; Age; Sex and region.
Source of Information: The death certificates are sent by doctors to the Tax Agency or the Police, and then are sent to the Socialstyrelsen.
Data level: Patient level.
Available data level: Regional and national level.
Number of Records: Around 90,000 people per year.
Date Range: 1969 onwards.
Cancer Areas of Interest: All.
Open data access: Partially publicly available. Data from 1969 to 1996 information [10] and data from 1997 onwards information [11]. Instructions to request data for restricted content [12].
Information/Contact for data request: Contact information [13].
Database: Medicines Registry
Sponsor, manager or home institution: Socialstyrelsen.
Primary purpose: The objective of the pharmaceutical registry is to enhance patient safety within the pharmaceutical industry.
Type of information: Data Dictionary: Medicines Registry. Data dictionary information [14].
Available type of information: Drug groups and ATC codes for all ages, drug groups for children 0-17 children; filtered by annual data, monthly data divided by age, monthly data divided by region, drug groups, ATC codes, regions, sex, measure, year and month.
Source of Information: The pharmaceutical register exclusively obtains data from the E-health authority, which requires all pharmaceutical trades to report their sales data. When a prescribed medication is dispensed, pharmacies must also furnish supplementary information to the E-health authority. The E-health authority, in turn, forwards information regarding prescription-based shipments to the National Board of Health and Welfare.
Data level: Patient level.
Available data level: National and regional level.
Number of Records: About 100 million per year.
Date Range: 2005 onwards.
Cancer Areas of Interest: Unknown.
Open data access: Partially publicly available [15]. Instructions to request data for restricted content [16].
Information/Contact for data request: Contact information [17].
Compilation: ESMO Patient Guides
Sponsor, manager or home institution: European Society for Medical Oncology.
Primary purpose: To translate complex medical language into understandable information for patients.
Available guides: Bone Health in Cancer; Cancer Care During the COVID-19 Pandemic; Cancer Pain Management; Immunotherapy Side Effects; Personalized Cancer Medicine; Survivorship; AML; Biliary Tract Cancer; Bladder Cancer; Bone Sarcoma; Breast Cancer; Cervical Cancer; CML; Colorectal Cancer; Endometrial Cancer; Follicular Lymphoma; Glioma; Head and Neck Cancer; Hepatocellular Carcinoma; Multiple Myeloma; Non-Small-Cell Lung Cancer; Oesophageal Cancer; Ovarian Cancer; Pancreatic Cancer; Prostate Cancer; Soft Tissue Sarcoma; Stomach Cancer; Testicular Cancer.
Type of information: Information on each guide varies for each cancer type. Generally, guides provide definitions, explanations of causes, diagnosis, treatment, treatment options, care after treatment, among others.
Access to information: List of guides [18].
