ASPIRE Measures
TEMP 02
June 2021
Holly Lockwood BSN, MBA
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Temperature & MPOG SSI Toolkit
Hypothermia triggers vasoconstriction and subsequent tissue hypoxia which
impairs wound healing.Hypothermia may also impair neutrophil function, reducing
the bodies natural protection against infection
ASPIRE measures support SSI prevention
Hypothermia commonly occurs during and after surgery due to impairment of
thermoregulation caused by anesthesia medications and exposure to the cold
environment of the operating room
Redistribution of body heat from the core to the periphery decreases the core
temperature 1-1.5 degrees Celsius during the first hour of anesthesia.
After hour one of surgery, core temperature decreases at a slower rate.
Pre-warming allows the peripheries to warm and decrease the overall impact to
core temperature changes when redistribution occurs.
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ASPIRE Measure: TEMP 02
Measure Summary: The percentage of cases where the anesthesia provider documented at least one core
temperature intraoperatively for any patient receiving a general anesthetic.
Core or Near Core Temperature Monitoring Includes:
Pulmonary Artery Temperature
Distal Esophageal Temperature
Nasopharyngeal Temperature
Tympanic Membrane Temperature
Bladder Temperature
Rectal Temperature
Axillary Temperature (arm must be at patient side)
Oral Temperature
Inclusions: All surgical patients receiving general anesthesia
Success: Cases with at least one core temperature documented between Anesthesia Start and Patient out of Room.
Responsible Provider: Provider present at induction end
https://mpog.org/files/quality/measures/TEMP-02_spec.pdf
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Temp 02 Core Temperature
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MPOG Summary of Recommendations: Normothermia
1. Apply active warming to maintain core body
temperature of 36.0 degrees Celsius
2. Surgical patients often experience
hypothermia within the first hour after
induction of general anesthesia due to the
anesthetic induced vasodilation.
3. Maintaining a core temperature below 36
degrees Celsius increases the rate of surgical
site infections
(Allegranzi et al., 2016; Ban et al., 2017; Kurz, 2008; Kurz, Sessler, & Lenhardt, 1996; Sessler, 2016)
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Temp 02 Tools
Aim
Initial Values
References
Improving Temperature Monitoring in the OR
A QI Story
Henry Ford Allegiance Health
Holly Lockwood BSN, MBA
Current State
Intervention Temp 02 Poster & Other Reminders
Strategy to increase awareness by providers
Creation of eye-catching flyer for Temp 02
Posted at key anesthesia locations including
lounges, OR board, inside the OR &
offices/admin areas
Email reminder with flyer attached
Monthly educational emails sent to all anesthesia
providers
Direct observation in OR
Creation of Epic link to ASPIRE dashboard
Next Steps
Abstract
Changes
Barriers
General and neuraxial anesthesia causes vasodilation thus redistributing body heat from the core to
peripheries. This redistribution can cause hypothermia. Core temperatures outside the normal range
pose
significant risks to patients. Pediatric patients are more likely to develop perioperative hypothermia
due to a
high surface area to weight ratio and inability to regulate their own temperature. Published research
has
correlated impaired wound healing, adverse cardiac events, altered drug metabolism, and
coagulopathies
with unplanned perioperative hypothermia. These adverse outcomes resulted in prolonged hospital
stays
and increased healthcare expenditures. The mortality rate is almost 20% higher only monitoring skin
temperature rather than a core temperature for those who experience malignant hyperthermia
during
surgery. Core temperature measurements are less variable than skin temperature measurements and
more accurately represent body temperature..
To understand our current intraoperative anesthetic management of patients for TEMP 02 and
improve core temperature use, ASPIRE (Anesthesiology Performance Improvement and Reporting
Exchange), the quality improvement arm of MPOG (Multicenter Perioperative Outcome Group) has
developed a performance measure called TEMP 02. The measure identifies the percentage of cases
with increased risk of hypothermia that the anesthesia provider documented at least one core
temperature intraoperatively for any patient receiving a general anesthetic. In this report, we found a
prevalence of high risk patients for TEMP monitoring utilizing “skin” temperatures by providers based
on documentation in the chart. Surprisingly, initial utilization/documentation of core temps was
minimal and we encountered initial struggle for improvement. We have shown here that various
strategies to increase provider awareness has made significant progress in implementation of the
guideline.
Temperature 02 Specifications
Success = cases with at least one core temperature documented between Anesthesia Start and Patient out of Room time
or if not available then, Anesthesia End.
Attain a 90% cumulative success rate each calendar year
1. Kim P, Taghon T, Fetzer M, Tobias JD. Perioperative hypothermia in the pediatric population: a
quality improvement project. 2013;28(5):400-406.
2. American journal of medical quality : the official journal of the American College of Medical
Quality. Larach MG, Brandom BW, Allen GC, Gronert GA, Lehman EB. Malignant hyperthermia
deaths related to inadequate temperature monitoring, 2007-2012: a report from the North
American malignant hyperthermia registry of the malignant hyperthermia association of the
United States. Anesthesis and analgesia 2014;119(6):1359-1366.
3. Sun Z, Honar H, Sessler DI, et al. Intraoperative core temperature patterns, transfusion
requirement, and hospital duration in patients warmed with forced air. 2015;122(2):276-285.
Anesthesiology.
4. Insler SR, Sessler DI. Perioperative thermoregulation and temperature monitoring.
Anesthesiology clinics. 2006;24(4):823-837.
5. Sessler DI. Temperature monitoring and perioperative thermoregulation. Anesthesiology.
2008; 109(2): 3-18-338.
Description: Percentage of cases with increased risk of hypothermia that the anesthesia provider
documented at least one core temperature intraoperatively for any patient receiving a general
anesthetic.
Measure Type: Process
Inclusions: All surgical patients receiving general anesthesia
Exclusions:
ASA 5 & 6 cases
Cases with neuraxial anesthesia as the primary technique
Cases with regional anesthesia as the primary technique
Obstetric Non-Operative Procedures & those with procedure text: “Labor Epidural”
Diagnostic Procedures (CPT: 01922)
MRI Rooms, MRI with procedure text: MRI, MR Head, MR Brain, etc.
MPOG/ASPIRE
MPOG (Multicenter Perioperative Outcome Group)
Organizations that are developed and administered
by providers and hospital partners from over 50
institutions from 18 states and 2 countries
Funded in part by BCBS of Michigan
Focus on reduction of errors, prevention of
complications, and improvement of patient
outcomes
ASPIRE (Anesthesia Performance Improvement and Reporting Exchange)
Anesthesiology quality improvement group which was built on infrastructure of MPOG
Governed by the ASPIRE Quality Committee which consists of members of each institution.
Support continuous quality improvement and the development of best practices
Tracks performance and provide incentives
Generation of monthly anonymous
individualized Temp 02 Score Cards for each
provider groups (Senior Staff, CRNAs and
Residents) which includes:
Employee ID numbers
Failed case %
Failed case numbers
Total case numbers
Poster in several locations (Resident, CRNA
break room, etc.) that anesthesia providers
can view and compare their scores among
peers
Email distribution of score cards to each
provider groups
Exploring further interventions with Epic
Despite comprehensive guidelines for temperature monitoring, TEMP 02 remains a frequent problem
in the operative period. Prior to implementation of ASPIRE measures, we were unaware of the
prevalence of effective documentation in our general anesthesia cases.
Our aim was to achieve above 90% cumulative success rate for TEMP 02 patients with general
anesthesia cases as per ASPIRE guidelines. (5/5/21met with March 2021 data= 91% & continues to
increase)
Our aim is to expose current usage of temperature monitoring techniques and use only the core
temperature monitoring Pulmonary Artery, Distal Esophageal, Nasopharyngeal, Tympanic
Membrane, Bladder, Rectal, Axillary (arm must be at patient side), and Oral Temperature.
(5/5/21met with March 2021 data= 91%)
TEMP 02 values for last 12 months (% of success)
Despite our understanding of temperature monitoring in
surgical patients and the existence of established best
practice in our institutions, we made improvement in
2021.
In late 2020 the score was 86%. Great efforts to promote
awareness using educational departmental meetings,
small group sessions (residents, CRNA etc.), &
educational email, we achieved 90% threshold in March
21 and as of June 2021 it is 93% (6/11/21 with May
data). ASPIRE was new 2020 & below threshold.
Outcomes
Need to educate staff regarding the measure & only core temps are acceptable.
Overnight urgent/emergent cases
Documentation issue: simple to note “skin” but often they are using nasopharyngeal probes.
Initial record of TEMP 02 in need
of improvement April 2020
ASPIRE
Introduced
August 2020
Cumulative numbers
for 2020 were 86% &
increased to 90% by
end of the year
June 2021 = 93%
Provider ID Numbers
Provider ID Numbers
Provided direct provider emails
with their own scoring and data.
Also shared monthly results of
data after uploads and
cumulative score.
Education provided in meetings and
via boards of change, direct
intervention and meeting with
key stakeholders to improve
methods of monitoring.
Education shared after all
MPOG/ASPIRE large general
meetings.
The temperature monitoring was
implemented in March to view
OR cases and discuss the
approach for monitoring.
Material, posters, flow charts of
data improvement shared to
illustrate changes & positive
improvement.
Education was provided via the
physician QI Champion and
ACQR/Quality RN.
Intraoperative use of temperature
monitoring
Possible removal of the option to chart
“skin” temperature monitoring via IT
Anesthesia.
Provide the appropriate skin probes for the
anesthesia carts.
Support to staff and work with the crew
obtaining supplies.
Group presentation of data & PI project
5/6/21 & presentation of QI project at
ASPIRE collaborative meeting 7/16/21.
Brainstorming solutions/barriers as a team
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Thank You!
GLU 03
Measure Description:
Percentage of cases with perioperative glucose > 200 mg/dL with administration of insulin or
glucose recheck within 90 minutes of original glucose measurement
Measure Time Period:
Preop through PACU
GLU 03
Inclusions:
All patients with glucose level greater than 200 mg/dL
Patients with and without diagnosis of diabetes
Exclusions:
ASA 5 and 6 cases
Patients < 12 years of age.
Glucose measurements > 200 mg/dL within 90 minutes before measure end
Outpatient cases with Anesthesia Start to Anesthesia end time less than 4 hours long
Obstetric Non-Operative Procedures
Labor Epidurals
GLU 03
Success:
Administration of insulin within 90 minutes
Recheck of glucose level within 90 minutes
GLU 03- Current Scores
GLU 03- Breakdown of Scores
GLU 03- Actions
Educated anesthesia providers
on glucose measures (June 21)
Educated Pre and Postop staff
on glucose measures (May 21)
Added time glucose was taken
to pre-op handoff sheet
Analyzed ASPIRE data and
counseled all providers who are
not passing this measure
Glucose BPA in Epic
o Including a reminder to
treat or recheck glucose
Health system working on
revising Tier 1 glucose policy
Continue to analyze ASPIRE data
and counsel all providers who
are not passing this measure
Thank you!
SUS- 01: Low
Fresh Gas Flow
Dr. Jimmy Boutin
Henry Ford Wyandotte
Measure Description:
Percentage of cases with mean fresh gas flow (FGF) equal to, or less than 3L/min, during
administration of halogenated hydrocarbons and/or nitrous oxide
Indirect measure of gas waste
Measure includes the time between placement of endotracheal tube or supraglottic airway
and removal of the device
Excludes pre-oxygenation and emergence (inspired gas equal to zero)
SUS 01
Rational:
Halogenated agents and nitrous oxide leaking or vented into the atmosphere are environmental
pollutants. Reducing fresh gas flows can reduce cost of anesthesia without compromising
patient care
Inclusions:
Administration of anesthetic gases for greater than or equal to 30 minutes
Exclusions:
Cases in which halogenated hydrocarbons and nitrous oxide are NOT used
Cases in which maintenance period ˂ 30 minutes
Cases with ˃ 20% of FGF values manually entered during the case
Cases in which nitric oxide is administered
Success:
Mean FGF equal to, or less than 3L/minute when inspired halogenated hydrocarbons is >0.2%, or
nitrous oxide FGF >0.2L/min, during the maintenance period of anesthesia
SUS 01
SUS 01
SUS 01-Current Data
*Data subject to change once inspired agents recorded in Epic
SUS 01- Prior Recommendations
Recommendations for FGF rates using sevoflurane from the FDA and sevoflurane manufacturers were
made prior to safer CO2 absorbents
This recommendation was exposure should not exceed 2 MAC hours at flows 1-2 L/min
FGF rates less than one not recommended
CO2 absorbents with strong bases are worse
Newer absorbents with no KOH and low NaOH do not produce compound A
At Henry Ford Wyandotte the Co2 absorbent has no KOH and less than 4% NaOH
SUS 01- Observational Data
Providers were observed for 5 minutes after induction and FGF rates were noted.
SUS 01-Pharmacokinetics of Propofol
The peak concentration for a bolus dose of propofol is approximately 2 minutes
At 5 minutes there is approximately slightly less than half the peak concentration
SUS 01- Sevoflurane
Due to sevoflurane’s low blood-gas coefficient there is a quick onset
The rate of induction is related to the gas coefficient, pulmonary blood flow, and
minute ventilation
A study analyzed the time to reach a target concentration (2 MAC = 4%) at
variable FGF rates (0.5 L/min, 1 L/min, & 3 L/min) and vaporizer set at 6%
Appears that in 2 mins at a FGF rate of 3 L/min the inspired concentration is
close to reaching the target.
A FGF rate of 1 L/min takes approximately 8 mins
SUS 01- Sevoflurane
SUS 01- Tips/Actions
Review this presentation with
all providers
anesthesiologists and CRNAs
Analyze ASPIRE data and
counsel all providers who are
not passing this measure
When fresh gas flow exceeds the patients requirement,
gases and vapors will enter the scavenging system and
into the atmosphere
Minimizing the total fresh gas flow limits the
environmental impact of volatile agents
Strategies to mange fresh gas flow
Turn off the fresh gas flow, not the vaporizer, during
intubation
Minimize fresh gas flow during maintenance
Set the vaporizer to deliver a concentration greater
than intended
Tips Actions
Thank you!