Slovakia

Healthcare System

Slovakia operates a universal healthcare system, which provides comprehensive coverage to all its residents. The system is primarily funded through a combination of compulsory health insurance contributions, taxes, and additional state budget allocations.

The Ministry of Health is the main governing body responsible for overseeing and regulating the healthcare system in Slovakia. The system is managed at the national level, with the implementation of policies and services being carried out by regional health insurance companies. These regional insurance companies are overseen by the Health Care Surveillance Authority (HCSA).

Slovak citizens and residents receive a range of healthcare services and benefits, including primary and specialized care, inpatient and outpatient services, preventative care, maternity care, dental care, and prescription medications. Emergency care is also provided to all individuals, regardless of their insurance status. In order to access healthcare benefits, individuals must be registered with one of three public health insurance companies in the country. Residents are automatically enrolled in the system through their employment or social security benefits. Unemployed individuals, pensioners, and those with specific social statuses are also covered by the system.

Slovakia has implemented a National Health Information System (NHIS), which serves as the central repository for electronic health records, claims data, and registries. Healthcare providers are required to submit patient data electronically, allowing for a more efficient and streamlined healthcare system. The NHIS also enables better coordination between healthcare providers and supports evidence-based decision-making in healthcare policy and management.

Registries

Sponsor, manager or home institution: Národné centrum zdravotníckych informácií.

Primary purpose: to provide comprehensive and accurate information on the occurrence of oncological diseases in a defined population, enabling the evaluation and control of the impact of oncology in the community and informing public health priorities and cancer control activities.

Type of information:

Available type of information:

Source of Information: Data reported by relevant intelligence units (SJ) and healthcare providers (PZS) who are obligated to report patients with malignant tumors.

Data level: Patient level.

Available data level: Regional level.

Number of Records: Unknown.

Date Range: 1997 to 2012.

Cancer Areas of Interest:

Open data access: Data is partially publicly available. Publicly available data can be found here.

Information/Contact for data request: Contact information can be found here.