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HEDIS Electronic Clinical Data Systems (ECDS) Reporting

Our newest reporting method helps clinical data create insight for managing the health of individuals and groups.

ECDS News

ECDS IN BRIEF

The ECDS reporting standard gives health plans a method for collecting and reporting standard electronic clinical data for HEDIS quality measurement and improvement.

The ECDS architecture was designed to help HEDIS implementers understand how technology might improve the efficiency of quality reporting while providing an incentive to connect to a broad array of actionable information from multiple sources.

HEDIS quality measures reported using ECDS inspire innovative use of electronic clinical data to document high-quality patient care.

The ECDS reporting standard represents a step forward in the evolution of HEDIS to accommodate the extensive information available in electronic datasets used for patient care and quality improvement.

TYPES OF ECDS DATA

Data systems that may be eligible for HEDIS ECDS reporting include, but are not limited to, member eligibility files, EHRs, clinical registries, HIEs, administrative claims systems, electronic laboratory reports (ELR), electronic pharmacy systems, immunization information systems (IIS) and disease/case management registries.

Data sources used for HEDIS ECDS reporting are categorized as follows:

  1. Electronic health record (EHR)/personal health record (PHR). Patient records that document a patient’s medical history, treatment plans, radiology and laboratory test results in digital format that can make the information available instantly and securely to authorized users.
  2. Health information exchange (HIE)/clinical registry. HIEs and clinical registries eligible for this reporting category include state HIEs, IIS, public health agency systems, regional HIEs (RHIO), Patient-Centered Data Homes™ or other registries developed for research or to support quality improvement and patient safety initiatives. Clinical registries may be sponsored by a government agency, nonprofit organization, health care facility or private company, and decisions regarding use of a registry’s data are the responsibility of the registry’s governing committee.4
  3. Case management system. A shared database of member information collected through a collaborative process of member assessment, care planning, care coordination or monitoring of a member’s functional status and care experience. Case management systems eligible for this category of ECDS reporting include any system developed to support the organization’s case/disease management activities, including activities performed by delegates.
  4. Administrative. Includes data from administrative claim processing systems for all services incurred (paid, suspended, pending, denied) during the period defined by each measure’s participation, as well as member management files, member eligibility and enrollment files, electronic member rosters, internal audit files and member call service databases.

Submit questions about HEDIS ECDS reporting through My NCQA.

ECDS FREQUENTLY ASKED QUESTIONS

See FAQs here.

  1. HEDIS® is a registered trademark of the National Committee for Quality Assurance (NCQA).
  2. https://www.federalregister.gov/documents/2015/10/16/2015-25597/2015-edition-health-information-technology-health-it-certification-criteria-2015-edition-base
  3. https://www.healthit.gov/providers-professionals/health-information-exchange/what-hie
  4. https://www.nih.gov/health-information/nih-clinical-research-trials-you/list-registries

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