Specifications Manual for Joint Commission National Quality Measures (v2023A)
Posted: 08/12/2022
Home » Bisoprolol, Carvedilol, or Sustained-Release Metoprolol Prescribed for LVSD in the Outpatient Setting

Release Notes:
Data Element
Version 2023A

Name:Bisoprolol, Carvedilol, or Sustained-Release Metoprolol Prescribed for LVSD in the Outpatient Setting
Collected For: ACHFOP-01
Definition:Documentation that bisoprolol, carvedilol, or sustained-release metoprolol was prescribed in the outpatient setting. Beta-blockers are agents which block beta-adrenergic receptors, thereby decreasing the rate and force of heart contractions, and reducing blood pressure. Over time beta-blockers improve the heart's pumping ability. The marked beneficial effects of beta blockade has been well demonstrated in large-scale clinical trials of symptomatic patients with New York Heart Association (NYHA) class II-IV heat failure and reduced LVEF using bisoprolol, carvedilol, and sustained-release metoprolol succinate.
Question:Was bisoprolol, carvedilol, or sustained-release metoprolol prescribed for LVSD in the outpatient setting?
Format:
Length:1
Type:Alphanumeric
Occurs:1
Allowable Values:

Y (Yes) Bisoprolol, carvedilol, or sustained-release metoprolol was prescribed for LVSD in the outpatient setting, or the patient is currently on one of these beta-blockers.

N (No) Bisoprolol, carvedilol, or sustained-release metoprolol was not prescribed for LVSD in the outpatient setting or unable to determine from medical record documentation.
Notes for Abstraction:
  • Only select "Yes" for those beta-blockers identified in the list of inclusions. No other beta-blockers will be accepted for this data element
  • In determining whether bisoprolol, carvedilol, or sustained-release metoprolol succinate was prescribed at discharge, it is not uncommon to see conflicting documentation amongst different medical record sources. For example, the discharge summary may list one of these beta-blockers that is not included in any of the other discharge medication sources (e.g., discharge orders). All discharge medication documentation available in the chart should be reviewed and taken into account by the abstractor.
    • In cases where there is bisoprolol, carvedilol, or sustained-release metoprolol succinate in one source that is not mentioned in other sources, it should be interpreted as a discharge medication (select "Yes") unless documentation elsewhere in the medical record suggests that it was NOT prescribed at discharge - Consider it a discharge medication in the absence of contradictory documentation.
    • If documentation is contradictory (e.g., physician noted “d/c carvedilol” in the discharge orders, but carvedilol is listed in the discharge summary's discharge medication list), or after careful examination of circumstances, context, timing, etc, documentation raises enough questions, the case should be deemed unable to determine" (select "No").
    • Consider documentation of a hold on bisoprolol, carvedilol, or sustained-release metoprolol succinate after discharge in one location and a listing of that beta-blocker as a discharge medication in another location as contradictory ONLY if the timeframe on the hold is not defined (e.g., “Hold bisoprolol”). Examples of a hold with a defined timeframe include “Hold Toprol-XL x 2 days” and “Hold Coreg until after stress test.”
    • If bisoprolol, carvedilol, or sustained-release metoprolol succinate is NOT listed as a discharge medication, and there is only documentation of a hold or plan to delay initiation/restarting of the beta-blocker after discharge (e.g., “Hold Toprol-XL x 2 days,” “Start Zebeta as outpatient,” “Hold Coreg”), select “No”.
    • If two discharge summaries are included in the medical record, use the one with the latest date/time. If one or both are not dated or timed, and you cannot determine which was done last, use both. This also applies to discharge medication reconciliation forms. Use the dictated date/time over transcribed date/time, file date/time, etc.
      Examples:
    • Two discharge summaries, one dictated 5/22 (day of discharge) and one dictated 5/27 - Use the 5/27 discharge summary.
    • Two discharge medication reconciliation forms, one not dated and one dated 4/24 (day of discharge) - Use both.
    • Disregard bisoprolol, carvedilol, or sustained-release metoprolol succinate documented only as a recommended medication for discharge (e.g., “Recommend sending patient home on Coreg”). Documentation must be more clear that the beta-blocker was actually prescribed at discharge.
  • Disregard documentation of bisoprolol, carvedilol, or sustained-release metoprolol succinate prescribed at discharge when noted only by medication class (e.g., “Beta-Blocker Prescribed at Discharge: Yes” on a core measures form). The beta-blocker prescribed must be listed by name.

Suggested Data Sources:
  • Discharge summary
  • Discharge Instruction sheet
  • Outpatient medical record
Additional Notes:
Guidelines for Abstraction:
Inclusion Exclusion
  • Bisoprolol
  • Bisoprolo/fumarate
  • Bisoprolol/hydrochlorothiazide
  • Carvedilol
  • Carvedilol phosphate
  • Coreg
  • Coreg CR
  • Metoprolol succinate
  • Toprol-XL
  • Zebeta
  • Ziac

All other beta-blocker medications other than those listed as inclusions.

Bisoprolol, Carvedilol, or Sustained-Release Metoprolol Prescribed for LVSD in the Outpatient Setting
CPT® only copyright 2022 American Medical Association. All rights reserved.
Specifications Manual for Joint Commission National Quality Measures (v2023A)
Discharges 01-01-23 (1Q23) through 06-30-23 (2Q23)

LICENSE FOR USE OF CURRENT PROCEDURAL TERMINOLOGY, FOURTH EDITION (“CPT®”)

CPT® only copyright 2022 American Medical Association. All rights reserved. CPT® is a registered trademark of the American Medical Association.

You, your employees and agents are authorized to use CPT® only as contained in The Joint Commission performance measures solely for your own personal use in directly participating in healthcare programs administered by The Joint Commission. You acknowledge that the American Medical Association (“AMA”) holds all copyright, trademark and other rights in CPT®.

Any use not authorized herein is prohibited, including by way of illustration and not by way of limitation, making copies of CPT® for resale and/or license, transferring copies of CPT® to any party not bound by this Agreement, creating any modified or derivative work of CPT®, or making any commercial use of CPT®. License to use CPT® for any use not authorized herein must be obtained through the American Medical Association, Intellectual Property Services, AMA Plaza, 330 North Wabash Avenue, Suite 39300, Chicago, Illinois 60611-5885. Applications are available at the American Medical Association Web site, www.ama- assn.org/go/cpt.

U.S. Government Rights This product includes CPT® which is commercial technical data, which was developed exclusively at private expense by the American Medical Association, 330 North Wabash Avenue, Chicago, Illinois 60611. The American Medical Association does not agree to license CPT® to the Federal Government based on the license in FAR 52.227-14 (Data Rights - General) and DFARS 252.227-7015 (Technical Data - Commercial Items) or any other license provision. The American Medical Association reserves all rights to approve any license with any Federal agency.

Disclaimer of Warranties and Liabilities. CPT® is provided “as is” without warranty of any kind, either expressed or implied, including but not limited to the implied warranties of merchantability and fitness for a particular purpose. Fee schedules, relative value units, conversion factors and/or related components are not assigned by the AMA, are not part of CPT®, and the (AMA is not recommending their use. The AMA does not directly or indirectly practice medicine or dispense medical services. The responsibility for the content of this product is with The Joint Commission, and no endorsement by the AMA is intended or implied. The AMA disclaims responsibility for any consequences or liability attributable to or related to any use, non-use, or interpretation of information contained or not contained in this product.

This Agreement will terminate upon notice if you violate its terms. The AMA is a third party beneficiary to this Agreement.

Should the foregoing terms and conditions be acceptable to you, please indicate your agreement and acceptance by clicking below on the button labeled “accept”.

^