eCQM Title | Hospital Harm - Severe Hypoglycemia |
||
---|---|---|---|
eCQM Identifier (Measure Authoring Tool) | 816 | eCQM Version Number | 4.0.000 |
CBE Number | 3503e | GUID | 98ee2385-0b90-40f4-859c-14f5c8d49340 |
Measurement Period | January 1, 20XX through December 31, 20XX | ||
Measure Steward | Centers for Medicare & Medicaid Services (CMS) | ||
Measure Developer | American Institutes for Research (AIR) | ||
Endorsed By | CMS Consensus Based Entity | ||
Description |
The measure assesses the number of inpatient hospitalizations for patients age 18 and older who were administered at least one hypoglycemic medication during the encounter and who suffer the harm of a severe hypoglycemic event during the encounter |
||
Copyright |
Limited proprietary coding is contained in the Measure specifications for user convenience. Users of proprietary code sets should obtain all necessary licenses from the owners of the code sets. American Institutes for Research(R), formerly IMPAQ International, disclaims all liability for use or accuracy of any third party codes contained in the specifications. LOINC(R) copyright 2004-2023 Regenstrief Institute, Inc. This material contains SNOMED Clinical Terms(R) (SNOMED CT[R]) copyright 2004-2023 International Health Terminology Standards Development Organisation. ICD-10 copyright 2023 World Health Organization. All Rights Reserved. |
||
Disclaimer |
This performance measure is not a clinical guideline and does not establish a standard of medical care, and has not been tested for all potential applications. THE MEASURES AND SPECIFICATIONS ARE PROVIDED “AS IS” WITHOUT WARRANTY OF ANY KIND. Due to technical limitations, registered trademarks are indicated by (R) or [R] and unregistered trademarks are indicated by (TM) or [TM]. |
||
Measure Scoring | Proportion | ||
Measure Type | Outcome | ||
Stratification |
None |
||
Risk Adjustment |
None |
||
Rate Aggregation |
None |
||
Rationale |
This measure focuses on severe hypoglycemia as an outcome in the hospital inpatient setting. In a study published by the Office of the Inspector General (OIG), in 2018 adverse drug events represented 43% of all adverse events in hospitals among Medicare patients; of those events, hypoglycemia was among the top 5 adverse drug events (Office of the Inspector General, 2022). Inpatient hypoglycemia can be life-threatening, and is associated with longer hospital stays and increased medical costs. Severe hypoglycemia (<40 mg/dL) occurs in 2–5% of hospitalized patients with diabetes mellitus, and medication-related hypoglycemic events are common causes of adverse drug events occurring in inpatient settings. Up to half of inpatient adverse drug events may be preventable, and recent studies show that rates of severe hypoglycemia vary across hospitals, suggesting opportunities for improved care (Santos et al., 2020). Rates of inpatient hypoglycemia events are considered an indicator of the quality of care provided by a hospital. Severe hypoglycemia events are largely avoidable by careful use of antihyperglycemic medication. Moreover, the rate of severe hypoglycemia varies across hospitals indicating an opportunity for improvement in care. The Agency for Healthcare Research and Quality (AHRQ) identified insulin and other hypoglycemic agents as high alert medications and associated adverse events to be included as a measure in the Medicare Patient Safety Monitoring System (MPSMS) (Classen et al., 2021). Hypoglycemic events are an adverse outcome that can cause patients to experience drowsiness, confusion, anxiety, irritability, sweating, weakness, increased heart rate, uncontrollable trembling, as well as loss of consciousness and seizure (American Diabetes Association, 2022; Cruz, 2020). It has been found that fasting glucose levels <100 mg/dL are predictors of hypoglycemia within the next 24 hours (ElSayed et al., 2023). |
||
Clinical Recommendation Statement |
From Section 16, Diabetes Care in the Hospital in the Standards of Medical Care in Diabetes by the American Diabetes Association, (American Diabetes Association, 2022): 16.9 A hypoglycemia management protocol should be adopted and implemented by each hospital or hospital system. A plan for preventing and treating hypoglycemia should be established for each patient. Episodes of hypoglycemia in the hospital should be documented in the medical record and tracked for quality improvement/quality assessment. 16.10 For individual patients, treatment regimens should be reviewed and changed as necessary to prevent further hypoglycemia when a blood glucose value of <70 mg/dL (3.9 mmol/L) is documented. A standardized hospital-wide, nurse-initiated hypoglycemia treatment protocol should be in place to immediately address blood glucose levels of <70 mg/dL (3.9 mmol/L). In addition, individualized plans for preventing and treating hypoglycemia for each patient should also be developed. An American Diabetes Association consensus statement recommends that a patient’s treatment regimen be reviewed any time a blood glucose value of <70 mg/dL (3.9 mmol/L) occurs, as such readings often predict subsequent level 3 hypoglycemia. Episodes of hypoglycemia in the hospital should be documented in the medical record and tracked. From the Endocrine Society clinical practice guideline on the Management of Hyperglycemia in Hospitalized Patients in Non-critical Care Setting (Korytkowski et al., 2022) as it relates to patients at high risk of hypoglycemia: Recommendation 1.1 In adults with insulin-treated diabetes hospitalized for noncritical illness who are at high risk of hypoglycemia, we suggest the use of real-time continuous glucose monitoring (CGM) with confirmatory bedside point-of-care blood glucose (POC-BG) monitoring for adjustments in insulin dosing rather than point-of-care blood glucose (POC-BG) testing alone in hospital settings where resources and training are available. Recommendation 2.1 Management of patients with glucocorticoid (GC)-associated hyperglycemia requires ongoing BG monitoring with adjustment of insulin dosing. All therapies require safeguards to avoid hypoglycemia when doses of GCs are tapered or abruptly discontinued. Recommendation 10.1 In adults with no prior history of diabetes hospitalized for noncritical illness with hyperglycemia [defined as BG > 140 mg/dL (7.8 mmol/L)] during hospitalization, we suggest initial therapy with correctional insulin over scheduled insulin therapy (defined as basal or basal/bolus insulin) to maintain glucose targets in the range of 100 to 180 mg/dL (5.6 to 10.0 mmol/L). For patients with persistent hyperglycemia [≥2 POC-BG measurements ≥ 180 mg/dL (≥10.0 mmol/L) in a 24-hour period on correctional insulin alone], we suggest the addition of scheduled insulin therapy. Recommendation 10.2 In adults with diabetes treated with diet or noninsulin diabetes medications prior to admission, we suggest initial therapy with correctional insulin or scheduled insulin therapy to maintain glucose targets in the range of 100 to 180 mg/dL (5.6 to 10.0 mmol/L). For hospitalized adults started on correctional insulin alone and with persistent hyperglycemia [≥2 point-of-care blood glucose (POC-BG) measurements ≥ 180 mg/dL in a 24-hour period (≥10.0 mmol/L)], we suggest addition of scheduled insulin therapy. We suggest initiation of scheduled insulin therapy for patients with confirmed admission blood glucose (BG) ≥ 180 mg/dL (≥10.0 mmol/L). Recommendation 10.3 In adults with insulin-treated diabetes prior to admission who are hospitalized for noncritical illness, we recommend continuation of the scheduled insulin regimen modified for nutritional status and severity of illness to maintain glucose targets in the range of 100 to 180 mg/dL (5.6 to 10.0 mmol/L). Remarks Reductions in the dose of basal insulin (by 10% to 20%) at time of hospitalization may be required for patients on basal heavy insulin regimens (defined as doses of basal insulin ≥ 0.6 to 1.0 units/kg/day), in which basal insulin is being used inappropriately to cover meal-related excursions in BG. |
||
Improvement Notation |
A lower measure score indicates higher quality |
||
Reference |
Reference Type: CITATION Reference Text: 'American Diabetes Association Professional Practice Committee; 16. (2022). Diabetes care in the hospital: Standards of medical care in diabetes. Diabetes Care 1 January 2022; 45 (Supplement_1): S244–S253. https://doi.org/10.2337/dc22-S016' |
||
Reference |
Reference Type: CITATION Reference Text: 'Classen, D.C. MD, MS; Munier, W. MD; Verzier, N. MSN, RN; Eldridge, N. MS; Hunt, D. MD; Metersky, M. MD,∥; Richards, C. MD, MPH; Wang, Y. PhD; Brady, P. J. MD, MPH; Helwig, A. MD; & Battles, J. PhD. (2021). Measuring patient safety: The Medicare patient safety monitoring system (past, present, and future). Journal of Patient Safety: April 2021 - Volume 17 - Issue 3 - p e234-e240' |
||
Reference |
Reference Type: CITATION Reference Text: 'Cruz, P. (2020). Inpatient hypoglycemia: The challenge remains. J Diabetes Sci Technol. 2020;14(3):560-566. doi:10.1177/1932296820918540' |
||
Reference |
Reference Type: CITATION Reference Text: 'ElSayed, N., Aleppo, G., Aroda, V., Bannuru, R., Brown, F., Bruemmer, D., Collins, B., Hilliard, M., Isaacs, D., Johnson, E., Kahan, S., Khunti, K., Leon, J., Lyons, S., Perry, M., Prahalad, P., Pratley, R., Jeffrie Seley, J., Stanton, R., & Gabbay, R. (2023). On behalf of the American Diabetes Association, 16. Diabetes care in the hospital: Standards of care in diabetes. Diabetes Care 1 January 2023; 46 (Supplement_1): S267–S278. https://doi.org/10.2337/dc23-S016' |
||
Reference |
Reference Type: CITATION Reference Text: 'Korytkowski, M.T., Muniyappa, R., Antinori-Lent, K., Donihi, A.C., Drincic, A.T, Hirsch, I.B., Luger, A., McDonnell, M.E., Murad, M.H., Nielsen, C., Pegg, C., Rushakoff, R.J., Santesso, N., & Umpierrez, G.E. (2022). Management of hyperglycemia in hospitalized adult patients in non-critical care settings: An Endocrine Society clinical practice guideline, The Journal of Clinical Endocrinology & Metabolism, Volume 107, Issue 8, August 2022, Pages 2101–2128, https://doi.org/10.1210/clinem/dgac278' |
||
Reference |
Reference Type: CITATION Reference Text: 'Office of Inspector General Adverse Events in Hospitals. (2022). A quarter of Medicare patients experienced harm in October 2018. https://oig.hhs.gov/oei/reports/OEI-06-18-00400.asp' |
||
Reference |
Reference Type: CITATION Reference Text: 'Santos, C.A.Q., Conover, C., Shehab, N., Geller, A.I., Guerra, Y.S., Kramer, H., Kosacz, N.M., Zhang, H., Budnitz, D.S., & Trick, W.E. (2020). Electronic measurement of a clinical quality measure for inpatient hypoglycemic events: A multicenter validation study. Med Care. 2020;58(10):927-933. doi:10.1097/MLR.0000000000001398' |
||
Definition |
Inpatient hospitalizations: Includes time in the emergency department and observation when the transition between these encounters (if they exist) and the inpatient encounter are within an hour or less of each other. A severe hypoglycemic event (harm) is defined as a laboratory or point-of-care (POC) test for glucose with a result less than 40 mg/dL, where a hypoglycemic medication was given within the 24 hours prior to the start of the low glucose event (i.e., glucose result less than 40 mg/dL) and administered during the encounter (including emergency department and observation stays contiguous with the admission). The 24-hour timeframe extends from the end of the medication administration to the time of the glucose test. The measure does not count a severe hypoglycemic event (harm) in the numerator if there is a repeat test for glucose with a result greater than 80 mg/dL within five minutes of this initial low glucose test. The purpose of the repeat test within 5 minutes is to eliminate false positives that can occur in POC testing. The 5-minute timeframe extends from the start of the severe hypoglycemic test to the time of the repeat hypoglycemic test. |
||
Guidance |
Note the measure is currently confined to using mg/dL as the unit of measurement for glucose results. Glucose levels are determined by laboratory or point-of-care (POC) tests, including capillary/glucometer blood glucose tests, and by interstitial fluid specimens from continuous glucose monitors. Glucose test results from urine specimens are not considered. This eCQM is an episode-based measure. An episode is defined as each inpatient hospitalization or encounter that ends during the measurement period. This version of the eCQM uses QDM version 5.6. Please refer to the eCQI resource center (https://ecqi.healthit.gov/qdm) for more information on the QDM. |
||
Transmission Format |
TBD |
||
Initial Population |
Inpatient hospitalizations that end during the measurement period for patients age 18 and older and at least one hypoglycemic medication administration starts during the encounter |
||
Denominator |
Equals Initial Population |
||
Denominator Exclusions |
None |
||
Numerator |
Inpatient hospitalizations where a severe hypoglycemic event occurred during the encounter. A severe hypoglycemic event is: - A glucose test with a result less than 40 mg/dL AND - A hypoglycemic medication was administered within 24 hours before the start of the severe hypoglycemic event (i.e., the glucose test with a result less than 40 mg/dL) AND - There was no subsequent repeat test for glucose with a result greater than 80 mg/dL within five minutes or less from the start of the initial glucose test with a result less than 40 mg/dL Only one qualifying severe hypoglycemic event is counted in the numerator, and only one severe hypoglycemic event is counted per encounter. The 24-hour and 5-minute timeframes are based on the time the glucose was drawn, as this reflects the time the patient was experiencing that specific glucose level. |
||
Numerator Exclusions |
Not Applicable |
||
Denominator Exceptions |
None |
||
Supplemental Data Elements |
For every patient evaluated by this measure also identify payer, race, ethnicity and sex |
"Encounter with Hypoglycemic Medication Administration"
"Initial Population"
None
"Encounter with Severe Hypoglycemic Harm Event"
None
None
None
"Initial Population"
"Qualifying Encounter" EncounterInpatient with "Hypoglycemic Medication Administration" HypoglycemicMedication such that Global."NormalizeInterval" ( HypoglycemicMedication.relevantDatetime, HypoglycemicMedication.relevantPeriod ) starts during Global.HospitalizationWithObservation ( EncounterInpatient )
from "Denominator" InpatientHospitalization, "Severe Hypoglycemic Harm Event" HypoglycemicEvent let GlucoseTestTime: Global."EarliestOf" ( HypoglycemicEvent.relevantDatetime, HypoglycemicEvent.relevantPeriod ), HospitalizationInterval: Global."HospitalizationWithObservation" ( InpatientHospitalization ) where GlucoseTestTime during HospitalizationInterval return InpatientHospitalization
from "Denominator" QualifyingEncounter, "Hypoglycemic Medication Administration" HypoglycemicMedication, ["Laboratory Test, Performed": "Glucose Lab Test Mass Per Volume"] GlucoseTest let HospitalizationInterval: Global."HospitalizationWithObservation" ( QualifyingEncounter ), HypoglycemicMedicationInterval: Global."NormalizeInterval" ( HypoglycemicMedication.relevantDatetime, HypoglycemicMedication.relevantPeriod ), GlucoseTestTime: Global."EarliestOf" ( GlucoseTest.relevantDatetime, GlucoseTest.relevantPeriod ) where GlucoseTestTime during HospitalizationInterval and GlucoseTest.result < 40 'mg/dL' and HypoglycemicMedicationInterval starts 24 hours or less before or on GlucoseTestTime return GlucoseTest
["Medication, Administered": "Hypoglycemics Severe Hypoglycemia"]
"Encounter with Hypoglycemic Medication Administration"
from "Denominator" QualifyingEncounter, "Glucose Test with Result Less Than 40" LowGlucoseTest, ["Laboratory Test, Performed": "Glucose Lab Test Mass Per Volume"] FollowupGlucoseTest let GlucoseTestTime: Global."EarliestOf" ( LowGlucoseTest.relevantDatetime, LowGlucoseTest.relevantPeriod ), FollowupGlucoseTestTime: Global."EarliestOf" ( FollowupGlucoseTest.relevantDatetime, FollowupGlucoseTest.relevantPeriod ) where FollowupGlucoseTestTime 5 minutes or less after GlucoseTestTime and GlucoseTestTime during Global."HospitalizationWithObservation" ( QualifyingEncounter ) and FollowupGlucoseTestTime during Global."HospitalizationWithObservation" ( QualifyingEncounter ) and FollowupGlucoseTest.id !~ LowGlucoseTest.id and FollowupGlucoseTest.result > 80 'mg/dL' return LowGlucoseTest
"Encounter with Severe Hypoglycemic Harm Event"
["Encounter, Performed": "Encounter Inpatient"] InpatientEncounter where InpatientEncounter.relevantPeriod ends during day of "Measurement Period" and AgeInYearsAt(date from start of InpatientEncounter.relevantPeriod) >= 18
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer Type"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
"Glucose Test with Result Less Than 40" LowGlucoseTest where not ( LowGlucoseTest.id in "Low Glucose Test Followed By Glucose Test Result Greater Than 80".id )
if ( HasStart(period)) then start of period else end of period
Earliest(NormalizeInterval(pointInTime, period))
not ( start of period is null or start of period = minimum DateTime )
Encounter Visit let ObsVisit: Last(["Encounter, Performed": "Observation Services"] LastObs where LastObs.relevantPeriod ends 1 hour or less on or before start of Visit.relevantPeriod sort by end of relevantPeriod ), VisitStart: Coalesce(start of ObsVisit.relevantPeriod, start of Visit.relevantPeriod), EDVisit: Last(["Encounter, Performed": "Emergency Department Visit"] LastED where LastED.relevantPeriod ends 1 hour or less on or before VisitStart sort by end of relevantPeriod ) return Interval[Coalesce(start of EDVisit.relevantPeriod, VisitStart), end of Visit.relevantPeriod]
if pointInTime is not null then Interval[pointInTime, pointInTime] else if period is not null then period else null as Interval<DateTime>
["Patient Characteristic Ethnicity": "Ethnicity"]
["Patient Characteristic Payer": "Payer Type"]
["Patient Characteristic Race": "Race"]
["Patient Characteristic Sex": "ONC Administrative Sex"]
Measure Set |
|
---|