Access to treatment – Access to treatment in primary health care

The extension of the care guarantee slowed access to primary health care in 2025

In 2025, access to non-urgent care within two weeks was poorer than in 2024. Access to care also deteriorated among those under 23 years of age in 2025, although they were still required to receive care within 14 days.

In 2025, the maximum waiting times for access to care were extended for patients aged 23 and over, while they remained unchanged for younger patients.
The maximum waiting time of three months for patients aged 23 and over was met better than the maximum waiting time of 14 days for those aged 0–22.
Almost all (99–100%) first visits or remote contacts with a doctor or a nurse were realised within three months. The situation was the same in 2024.

In outpatient health care, first visits were realised well within the maximum waiting times (95–99%), as access to care provided by nurses was rapid. Most visits were to nurses. Care was delivered more quickly via remote services.

The verified data are published once a year in a statistical report, which is also the basis of the data on this page.

In particular, access to a doctor within two weeks worsened 

Among those aged 0–22, 56 % of doctor’s visits were realised within two weeks in 2025. In 2024, the proportion was 74 %, indicating that access to care deteriorated. However, access to a doctor in outpatient health care deteriorated only slightly.

Access to a doctor in primary health care also worsened among those aged 23 and over. Of their doctor’s visits, 59% were realised within two weeks in 2025 compared with 70% in 2024. The change was explained by the extension of the care guarantee, meaning that care was only required to be provided within three months.

The situation in oral health care remained stable

Access to care in oral health care did not slow down significantly in 2025, even though the maximum waiting time for access to care for patients aged 23 and over was extended from three months to six months.

The maximum waiting time for access to care in oral health care was met less well among those aged 0–22 than among patients aged 23 and over.

There were shortcomings in both the amount and quality of data on access to care

More data on access to care than ever before were obtained in the Avohilmo register, but there were also deficiencies and quality issues in the data produced by the wellbeing services counties. These problems weaken the comparability of access-to-care data with previous years and between regions.

In some regions, almost all non-urgent visits had been recorded as related to access to care. As a result, the data from these regions incorrectly included visits that should not be part of access-to-care monitoring, such as preventive services or visits in accordance with a care plan. The problem concerns wellbeing services counties using a specific patient information system and particularly affects data on persons under 23 years of age.

In a few wellbeing services counties, the overall amount of access-to-care data was very low.

Deficiencies were particularly observed in data on patients’ contact with services and follow-up visits, as well as in certain services. For example, access-to-care data for mental health services and substance abuse and addiction services were missing from many wellbeing services counties.

The patient information system, professionals’ recording practices, and the submission of data to the register affected both the amount and quality of the data. Wellbeing services counties are responsible for the correctness and completeness of data on both their own services and purchased services.

However, the identified quality issues do not affect the key finding of the statistics that access to primary health care has deteriorated.

About the data in more detail

Database reports

About the reports

The data in the database reports on access to treatment are reported for those non-urgent outpatient treatment events whose data have been submitted to the Avohilmo register. The numbers have mainly not been verified, meaning that the review of numbers carried out by experts is not included.

The database reports can be used to view data on access to treatment, for example, by operating unit, service form or professional group. A legislative filter is available for some of the database reports on access to treatment, which allows you to view the data based on the maximum time limit set in the Health Care Act valid at a given time.

Report types

The situational overview reports contain data on the realisation of all the maximum time limits, as well as the quantity and quality of the data received.

The database report is a predefined summary of data indicating how the maximum time limit has been realised. Service providers may publish data on the realisation of maximum time limits on their own organisation’s website by providing a link to the database report. Service providers have a duty under the Health Care Act to publish data on access to treatment compiled by THL.

A cube is a table of data that shows how a given maximum time limit has been realised. Compared to the database report, users can apply a more versatile set of filters to the cube data.

A statistical report is an annual summary of the key data on outpatient care in primary health care and the data quality, presented as text, images and tables.

Instructions on using the reports

Statistical report

Read the entire statistical report (Julkari) (in Finnish)

Reporting services

Indicator data in Sotkanet

Background information

The quality report of the statistical report describes the missing data from the statistical year and assesses the data coverage and quality. Information about the most recent missing data is provided on the website.

Source

Access to primary health care services 2025
Statistical report 20/2026, 3 June 2026. THL.

Description of the statistics

The statistics contain data on the contacts made by patients and the realisation of non-urgent outpatient visits and remote contacts related to access to treatment in primary health care within the maximum time limits laid down in the Health Care Act.

Data on access to treatment in primary health care have been collected with a survey since 2005, and since 2014, the data have been submitted from patient records systems to the Avohilmo register. The data in the statistics are obtained from service providers, such as wellbeing services counties, and the obtained data are based on document entries made by health care professionals. Service providers are responsible for the quantity and accuracy of the data they submit.

The register data are supplemented with an annual survey on access to primary health care that concerns the data that are not yet reliably available from the Avohilmo register in accordance with the guide on health appointment notifications.

Update schedule

A statistical report on the realisation of access to treatment in the previous year is published each year, typically by the summer.

See the database reports for up-to-date information about the realisation of access to treatment. The data are updated from the Avohilmo register to the reports monthly, usually on the 15th day of the month.

Contact details

Persons responsible for the statistics: Tiina Marttila and Raimo Mahkonen.

Any enquiries should primarily be sent to the shared email address avohilmo(at)thl.fi.