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2025 Testing Plan Summary

Antimicrobial Use and Resistance (AUR) Reporting Test Plan

The objective of ONC certification criterion 170.315(f)(6) is electronic transmission of Antimicrobial Use and Resistance (AUR) data to NHSN. Premier will evaluate this objective using the following metrics for TheraDoc customers who report AUR data to NHSN:

Metric Description
AR numerator submissions to NHSN Monthly counts of successful and failed AR numerator submissions to NHSN
AR denominator submissions to NHSN Monthly counts of successful and failed AR denominator submissions to NHSN
AU summary submissions to NHSN Monthly counts of successful and failed AU summary submissions to NHSN

Each metric will provide de-duplicated aggregate counts that consider all eligible NHSN-defined locations and acute care settings as specified in the NHSN AUR protocol. De-duplication accounts for submission failures unrelated to document content, such as DirectCDA outages. For example, if a given numerator or denominator record was unsuccessfully submitted 2 times before being accepted, it is counted as 1 successful submission for the relevant reporting period. Similarly, if a given numerator or denominator record was unsuccessfully submitted 2 times and never successfully submitted, it is counted as 1 failed submission for the relevant reporting period.

It is expected that NHSN will accept all TheraDoc AUR submissions that comply with the AUR protocol in accordance with a facility’s monthly NHSN AUR reporting plan.

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AUR Reporting Testing Results

Testing results will be published on this page at the conclusion of the testing period.

Electronic Case Reporting (eCR) Testing Plan

The objective of ONC certification criterion 170.315(f)(5) is electronic transmission of case reports to public health agencies. Premier will evaluate this objective using the following metric for TheraDoc customers who report eCR data to public health agencies:

Metric Description
eCR reporting to health departments Monthly counts of the following:

  • Total number of unique initial case reports (eICRs) submitted to public health agencies (this excludes any records requiring resubmission due to technical problems with transmission).
  • Total number of records dispositioned by public health agencies with a Reportability Response (RR) of “Reportable” (RRVS1) or “No Rule Met” (RRVS4).
  • Total number of unique patients for whom eICR records were sent for evaluation.
  • Total number of unique facilities using TheraDoc for eICR submission.

NOTE: The Electronic Reporting and Surveillance Distribution (eRSD) system version(s) in effect for each month is also included.

Counts of eICRs and RRs created against specific eRSD versions demonstrate ongoing interoperability as eCR reporting criteria evolve. Counts of “Reportable” and “No Rule Met” reportability conditions reflect the quality of data sent for electronic case reporting. Premier customers can configure TheraDoc to report eCR for select care settings in accordance with their needs. Testing will include all location types that have been configured to report eCR data.

Click here pdf of the full plan opens in a new tab to view the full plan.

eCR Testing Results

Testing results will be published on this page at the conclusion of the testing period.

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