This page is part of the NHSN Reporting of Adverse Drug Events - Hypoglycemia (v1.0.0: STU 1 on FHIR R4) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Inpatient hypoglycemia is one of the most common adverse drug events (ADEs) occurring in United States (U.S.) hospitals. Hypoglycemia in hospitalized patients can be severe and life-threatening and is associated with longer hospital stays and increased medical costs. Measurement of medication-related hypoglycemia in a meaningful and standardized way could improve hospital glycemic management. The NHSN Adverse Drug Event-Hypoglycemia FHIR implementation guide (IG) seeks to enable EHRs to serve as source systems for reporting linked inpatient blood glucose and medication administration data to the Centers for Disease Control and Prevention (CDC) National Healthcare Safety Network (NHSN) via industry electronic messages, with the goals of improving patient safety and facilitating hospital quality improvement efforts and benchmarking of hypoglycemia.
This IG addresses blood glucose and medication administration events in inpatient settings only and does not include hypoglycemia resulting only in outpatient care (e.g., hypoglycemia resulting in emergency medical services, physician office visits, or emergency department visits only). This IG addresses ADE data collection at the patient-level (i.e., collects individual laboratory and point-of-care-blood glucose and individual medication data for each inpatient encounter). The IG does not describe the calculation of any measures for hypoglycemia rates; these measures are intended to be calculated, aggregated, or risk-adjusted subsequent to reporting of patient-level data to CDC.
The patient level data recieved will be used by NHSN to calculate:
Similar standards that seek to report ADEs include: