Quality Committee
Meeting
February 28, 2022 @10:00 ET
Announcements
New Cardiac phenotype release
Precision Feedback announcement
Subcommittee Updates
ASPIRE Data and Joint Commission Visit
Sunny Chiao, MD, University of Virginia
New measure discussion
BP 05 - Rob Schonberger, MD, Yale University
SUS 02
Measure Updates
PONV Updates
GLU 05
Agenda
Meeting Minutes
January 2022
Roll Call – via Zoom or
contact us
Announcements
Upcoming Events
ASPIRE Quality Committee Meeting
Monday, March 28, 2022 (may cancel)
ASPIRE/MSQC Meeting:
Friday April 8th, 2022
2022 Calendar is up
to date at
mpog.org/calendar/
*NEW* Cardiac Procedure Type Phenotype
New Categories:
Open Cardiac
Transcatheter/Endovascular
EP/Cardiac catheterization
Other Cardiac
No/Non-cardiac
Missing/unknown/unable to determine
Data Elements Utilized:
Surgical CPTs (if present)
Anesthesia CPTs
Procedural Service IDs
CPB documentation concepts and phenotypes
Procedure text phrases
Precision Feedback Study Update - Aim 1
Plan to conduct interviews over the next couple of months to determine
preferences in feedback emails
Have reached to Quality Champions to refer potential interviewees
Criteria included:
Hospitals both within MI (BCBSM) and outside MI as well
Hospitals with and without residents
Community and med school affiliated hospitals
Range of hospital sizes
If you are interested in participating in this phase of the project, please
reach out to Allison Janda.
More detailed information about future phases (trial where we randomize
regular emails vs “precision feedback” emails) coming soon!
Subcommittee
Updates
Pediatric Subcommittee
Met on February 16
th
- 25 members attended
Finalized Measure Build for 2022
NMB-03: Neuromuscular blockade dosing in patients < 1mo.
ABX-02: Antibiotic Timing, Pediatrics
FLUID-02: Minimizing Colloid Use, Pediatrics
TRAN-03/04: Pediatric Transfusion metrics (mirror TRAN-01/02)
Formation of Workgroups
Pediatric Mortality (30 day in-hospital)
Surgical Site Infection
Normothermia
PONV
Pain Management
Peds Cardiac
Next Meeting, May 18
th
- Unblinded data review
Obstetric Anesthesia Subcommittee Updates
Last meeting held on February 2022: 28 attendees
Introduced unblinded performance review
GA 01/02 & PONV measures
Recommends modification to PONV 05: include all cesarean
delivery cases regardless of age
Modified hyperglycemia measures to exclude cesarean deliveries
Subcommittee members recently completed survey to determine
future measure focus areas
Next Meeting: August 3rd, 1pm EST
Cardiac Subcommittee
December meeting minutes & slides available
New post-bypass hypothermia avoidance measure is has been released to
the ‘All Measures’ and ‘Cardiac’ Dashboards
TEMP 06-C is the percentage of adult patients who undergo open cardiac surgical
procedures for whom the last non-artifact body temperature prior to anesthesia end was
greater than or equal to 35.5 degrees Celsius. Additional measure specification details
available here.
A countermeasure for on-bypass hyperthermia avoidance is also being
developed and we’re requesting perfusionist input
Please reach out to ajanda@umich.edu if you have any perfusionists who would like to join
a subgroup to help develop this measure!
Additional future measure topics include glucose management and AKI
Next meeting: Scheduling poll to be sent - likely April, 2022
ASPIRE Data and Joint
Commission Visit
Dr. Sunny Chiao
University of Virginia
Email request
As you may recall, one of the findings [] related to
(moderate) sedation providers and Dr. Y was found not to
have privileges to provide sedation.
“I am not surprised a CRNA was pulled (in this light) and I
would anticipate that more APPs will be pulled over time. I
am guessing that quality info was pulled to show compliance
with OPPE/FPPE requirements?”
What did JC request?
What was provided
Anesthesia staff perspectives/opinions
Recommendations/lessons learned
Overview
JC Ask
“Provide quality data for a CRNA over a period of a few months.
Data Provided
JC standard: Ongoing Professional Practice Evaluation (OPPE)
JC standard: Ongoing Professional Practice Evaluation (OPPE)
JC standard: Ongoing Professional Practice Evaluation (OPPE)
1. Your credentialing committee must have a process to evaluate
professional practice. What that process is, is up to you.
2. What data is collected to make assessment is also up to the
department.
3. This info can be used to continue, limit, or revoke privileges.
Focused/Ongoing Professional Practice
Evaluation Process (FPPE/OPPE)
At our institution, we have a Professional Practice Evaluation
Subcommittee (PPES) that reports to the Credentialing Committee
Currently working to establish a Advanced Practice Providers
Subcommittee (APPS) committee to mirror the physician standard
University of Virginia MC Policy
Initial FPPE
FPPE for cause
OPPE Process
Takeaways
JC more interested that we maintain a process and track it, but do not
care what the specifics are
MPOG provider dashboard is well equipped to fulfill these
requirements
Be familiar with your institutional credentialing FPPE/OPPE standard
What will your credentialing committee do with ASPIRE data?
Where do we go from here?
Initiating feedback
Low-hanging fruit for metrics (process vs outcomes? Things you already do well?)
Allow staff to become accustomed to this process
Incentivize anesthesiologists with MOCA Part 2 credit
Going forward.
What to do with underperformers?
Mandatory QI/PBLI?
Tied with performance bonus?
Discussion at annual review?
Triggered FPPE?
New Measure:
BP 05
Context: Measure “sources”
Feedback from Quality Champions, individual providers, and sites
Coordinating Center
Subcommittees
Research projects
Rob Schonberger
Yale University
Prevalent Propofol Dosing
Practices at MPOG institutions
2014-2018
The mean (SD) weight-adjusted propofol
dose was 1.7 (0.6) mg/kg. The mean
prevalent propofol induction dose
exceeded the upper bound of what has
been described as the typical geriatric
dose requirement across every age
category examined. The percent of
patients receiving propofol induction
doses above the described typical geriatric
range was 64.8% (95% CI 64.6-65.0),
varying from 73.8% among patients aged
65-69 to 45.8% among patients aged 80
and older.
Induction medications and dosing are both
attributable and modifiable
Among 320,585 total patients, 22.6% experienced the outcome of
pre-incision severe hypotension (MAP≤55mmHg).
20.7% with non-invasive blood pressure measurements
35.0% with invasive blood pressure measurements had the outcome.
Propofol induction dose (considered both as a continuous variable and as
yes/no >1.5mg/kg) was associated with pre-incision hypotension
(MAP<55mmHg)
However, a multitude of other factors both captured and not captured
within MPOG may mediate this relationship.
Informational ASPIRE Metric BP-05
Percent of patients age >65 without preoperative hypotension undergoing GA who
had an episode of MAP<55mmHg within 15 minutes of induction and prior to surgical
incision.
New Measure: BP 05 (informational measure)
Percentage of cases where severe hypotension during anesthesia induction (defined as MAP < 55 mmHg)
was avoided
Measure Time Period: Induction Start through Surgery Start
Inclusions: All patients requiring general anesthesia
Exclusions:
Patients <18 years old
ASA 6 cases/ Organ Harvest
Baseline MAP <60 mmHG
Labor Epidurals / Obstetric Non-Operative Procedures
Anesthesia Procedures
Success Criteria: MAP > 55 mmHG throughout induction time period
New Measure:
SUS 02
Thank you Dr. Jodi Sherman (Yale University)
Purpose today is to introduce the measure in its current form and discuss how to
approach this measure (specifically, are we targeting “acceptable” or “ideal”
practice.
Questions
Should the threshold be 2 l/min or 1 l/min or something else?
Should the measure start time begin at inhalation agent start or intubation or some other time?
If we include induction, do we exclude or include short cases?
Next Steps
Circulate specification for comment, update measure based on comments
Schedule meeting of interested folks if appropriate for further discussion
Share timeline for measure development
GLU 05 Update
Current State
Percentage of cases with a blood glucose >200 mg/dL with documentation
of insulin treatment
Subcutaneous insulin dosing intervals are up to every 3 hours
Many institutional protocols recommend hourly glucose checks in the periop
time period when insulin is administered
GLU 05 flags cases with high glucose & no treatment within 90 minutes
Inappropriate flagging of cases where subcutaneous insulin administered,
follow up glucose > 200 mg/dL, but no additional insulin sq given within 90
minutes because still within the 3 hour window
Proposed Updates
If insulin SQ is administered, we will not require elevated blood glucose
values to be treated within a 3 hour time frame of the insulin administration
This update assumes we are receiving insulin administration data up to 4
hours before anesthesia start (ie preop holding)
PONV 05
Updates
PONV 05 Released!
New Adult PONV prophylaxis measure released last month
Site Champions and ACQRs actively reviewing cases
Please continue to submit feedback to the Coordinating
Center
Will vote on proposed changes at the May Quality
Committee meeting:
Add midazolam as a potential antiemetic
Add exclusion for endoscopy procedures (regardless of GA)
Remove CPT prediction from procedure type risk factor (rely on actual
codes only)
Trigger ERCP as cholecystectomy risk factor (or only ‘true’
cholecystectomy)
Adjust fentanyl as ‘trigger for the opioid administration risk factor
Include all cesarean delivery cases, regardless of age
Source: Fourth Consensus
Guidelines for the Management
of PONV
Thank You!