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Health data access

Request administrative health data for various purposes, including research, planning and projects, and access online health data resources.

Health data

We are the custodian of extensive, but not exhaustive, administrative data and information about the health system in Alberta. Data is available to support research, planning, policy development and quality improvement projects.

Online health information

Online health data available without request:

Additional sources

Requests for data

Requests for administrative health data can be classified under 3 categories:

Research requests with research ethics board approval

Submit your request to [email protected] with the.

Information requests for planning, policy development, and quality improvement

Submit your request to [email protected] with the:

  • completed Request Application form
  • project documentation, including purpose
  • required data sets and common data elements if known

Internal requests and general inquiries

Submit your request to [email protected].

Resources

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Data assets

Several administrative datasets are available to support health data requests. The Overview of Administrative Health Datasets provides details of these datasets.

Unless otherwise stated, data will be provided from the year 2002 on:

  • Alberta Blue Cross Claims – data primarily on seniors
  • Ambulatory Care – includes emergency department visits
  • Inpatient – overnight hospital stays (DAD/hospital morbidity)
  • Longitudinal Demographic Profile – demographics, service utilization, chronic diseases, costs
  • Pharmaceutical Information Network (PIN) Dispenses from 2008 – community pharmacy dispenses (no financial information)
  • Population Registry – basic demographic and geographic information
  • Practitioner Claims – fee-for-service and shadow-billed claims
  • Vital Statistics – Births from 2005 (Service Alberta authorization required)
  • Vital Statistics – Deaths (Service Alberta authorization required)

Additional datasets

  • diagnostic Imaging, from 2011, Acute Care Alberta delivered in-hospital diagnostic imaging (does not include images or results)
  • immunizations and adverse reactions to immunization (Imm/ARI) (internal approval required)
  • laboratory, common lab tests – data to be obtained from Acute Care Alberta

Alberta Continuing Care Information System (ACCIS) long term care data was previously available. Since 2021, facilities have transitioned away from submitting to ACCIS and instead submitted to Acute Care Alberta’s Connect Care.

The Commonly Requested Data Elements spreadsheet lists frequently requested data elements and their descriptions. Preliminary data specifications can be developed from this workbook that should be included in your request, along with the application form, to initiate the request.

Research request process

For a data request to be considered, the requested data must be available and the ministry will have received the following:

  • all required documentation
  • acceptance of the data specifications
  • and the cohort if applicable

The research request process follows 5 primary steps from request receipt to data disclosure.

  • 1. Receive and investigate

    • Data Request Application form and attachments received at [email protected]
    • acknowledgment sent to requester including the assigned request number
    • application reviewed for completeness
    • preliminary data specification drafted
    • receive/investigate timeline dependent on the required documentation being provided
  • 2. Plan

    • data specifications and methodology refined
    • preliminary analysis completed, if required
    • data specifications approved
    • cost estimate approved, if applicable
    • cohort and data from other custodians received, if applicable
    • work is scheduled and timeframe estimate provided once request is qualified
    • plan timeline is dependent on requester availability to address questions, the number of iterations required to finalize the data specifications, and the provision of cohort and external data
  • 3. Execute

    • analyst develops custom code to extract and organize data
    • quality assurance review completed
    • data are prepared for disclosure (i.e., anonymized)
    • execute timeline is dependent on data availability, workload, time spent on cohort validation, and the complexity of the project
  • 4. Package

    • legal agreement prepared and executed
    • data disclosed to requester using Secure File Transfer Protocol
    • see the data disclosure guidelines for more information on disclosure
    • package timeline is dependent on whether a standard agreement template is used, and the time required in obtaining signatures
  • 5. Closure

    • invoice is paid, if applicable
    • staff available to respond to requester questions
    • request remains accessible for future update and reuse requests

Cost estimate

We complete requests on a partial cost-recovery basis. Rates for data extractions are:

  • $1,600 per day (8 hours)
  • $200 flat fee – re-use agreement administration charge

Alberta Health will provide a cost estimate after the data specifications are accepted. If required, a high-level cost range can be provided earlier based on the years of data, datasets requested, and size of cohort.

Costs are for analytical time only and exclude meetings, communications and run-time.

Changes to the data specifications by the requester after acceptance may result in additional time and/or cost.

Data extracts for Research Ethics Board approved research for Alberta universities are provided at no charge.

Timeframe for extract

The time it takes to complete the request depends on several factors, including the complexity of the request and resource capacity as described in the request process.

Several of the data sources are created on an annual basis only and are not available until several months after the end of the fiscal, March 31, or calendar year.

Information request process

Data extracts for approved information requests are provided at no charge. The same process listed for research requests is followed, but modified based on the type of request.

Compete the Data Request Application form and send it along with relevant documentation to [email protected].

Data disclosure

Research data disclosures require a contractual tripartite research agreement between the researcher, their affiliated organization – usually their university – and Alberta’s government. The agreement outlines the restrictions on data retention and on the disclosure and use of information. Once the agreement has been fully executed, data are provided to the requester.

A letter indicating which section of the Health Information Act (HIA) the data is disclosed under, as well as any restrictions on use of the information, is sent to the requester.

  • Security assurance

    The Health Information Regulation requires security assurance for any custodian to disclose data outside of Alberta. We need evidence that the location where the health information will be stored is fit for that purpose.

  • Aggregate data

    The HIA allows the disclosure of non-identifying health information for any purpose. Refer to Section 32(1) – Disclosure of Non-identifying Health Information.

  • Types and uses of information

    Data for research

    HIA Division 3 – Disclosure for Research Purposes – requires the researcher to submit a research proposal and receive approval from a recognized research ethics board, as listed in the regulations, before requesting data from one or more custodians, for example, Acute Care Alberta.

    Other HIA topics include the application, by researcher to a custodian, for disclosure of health information or to perform data matching, conditions and consents, and the need for an agreement between the custodian and the researcher for each research proposal.

    If a requester intends to use the disclosed health information for data matching, they must first notify the Information and Privacy Commissioner, as per Section 32(2). The HIA defines data matching to mean the creation of individually identifying health information by combining individually-identifying or non-identifying health information or other information from two or more electronic databases, without the consent of the individuals who are the subject of the information.

    Data for internal management purposes to other custodians

    HIA Section 27 (1) – Use of Individually Identifying Health Information – allows for the disclosure of individually identifying health information for internal management purposes. It is used to disclose data to support planning, policy development and quality improvement projects.

  • Guiding principles for data disclosure under the HIA

    We must comply with HIA principles and may impose additional conditions on the researcher in addition to those listed by the Research Ethics Board.

    Highest degree of anonymity

    The highest degree of anonymity is for the persons who are the subject of the information.

    Aggregate information is the most anonymous type of information. Non-identifying health information about groups of individuals with some common characteristic(s) ensures that the identity of an individual cannot be readily determined from the information.

    Individually non-identifying information has identifiers removed so that the identity of the individual cannot be easily determined. Typical identifiers removed are:

    • personal health number
    • hospital chart number
    • name
    • address
    • postal code
    • date of birth

    Where removing identifiers does not meet the research need, and given ethics approval, other techniques to protect the identity of the information may be used including:

    • scrambling of identifiers – personal health number
    • truncation – first three digits of postal code
    • substitution – age instead of date of birth

    Other attributes or combinations of attributes may be considered identifying, such as rare disease, geographical isolation, facility ID plus provider specialty.

    Individually-identifying information has a higher level of protection. The disclosure of individually-identifying data may require individual consents.

    Least amount of information

    The least amount of information will be disclosed to meet the needs of the stated purpose.

    When collecting, using or disclosing health information, a custodian must collect, use and disclose only the amount of health information that is essential to enable the requester to carry out the intended purpose.

    Requesters need to clearly explain their need for the particular data elements requested.

    Need to know

    Need to know is the disclosure of only necessary information to carry out research or responsibilities.

    Requesters need to explain how the data will be used and for what purposes.

Publications

Contact

For research ethics board-approved research requests, email: [email protected].

For general inquiries and health information requests, email: [email protected].