Anesthesiology Performance Improvement and Reporting Exchange (ASPIRE)
Pediatric Subgroup Meeting Minutes – May 19, 2021
Attendance:
Alina Bodas, Cleveland Clinic
Lucy Everett, Mass General Hospital
Amber Franz, Seattle Children’s
Lori Reigger, Michigan Medicine
Anshuman Sharma, Washington University
Lora Gibbs, Michigan Medicine
Bob Brustowicz, Boston Children’s
Morgan Brown, Boston Children’s
Brooke Szymanski-Bogart, MPOG
Meridith Bailey, MPOG Pediatric Program Lead
Carrie Menser, Vanderbilt
Olga Eydlin, NYU Langone
Cheryl Gooden, Yale University
Nirav Shah, MPOG Associate Director
Dave Moore, Vanderbilt
Priti Dalal, Penn State University
David Waisel, Yale University
R.J. Ramamurthi, Stanford
James Xie, Stanford
Shobha Malviya, Michigan Medicine
Jerri Heiter, St. Joseph Mercy Ann Arbor
Stephanie Kahntroff, University of Maryland
Jessica Wren, Henry Ford Health System
Tory Lacca, MPOG
Joe Cravero, Boston Children’s
Vikas O’Reilly-Shah, Seattle Children’s
Jonathan Halem, Penn State Children’s
Vivian Onyewuche, Henry Ford Detroit
Kate Buehler, MPOG
Wilson Chimbira, Michigan Medicine
Laura Downey, Emory University
Wes Templeton, Wake Forest
Liem Pham, NYU Langone
Agenda & Notes
I. Announcements
a. 2021 Pediatric Subcommittee Meetings
i. August 18
th
ii. October 9
th
(In person @ SPA if possible)
iii. December 15
th
b. MPOG Annual Retreat 2021 (virtual version will also be offered for those
unable to travel)
i. October 8
th
(In person in San Diego, CA, if possible)
ii. Everyone is invited to this meeting regardless of MPOG member
status
II. February 17 Meeting Recap
a. Measure Discussion: PONV Prophylaxis in Pediatrics
i. PONV 02 Inclusion/Exclusion Criteria Updated
1. Inclusion: Patient ages 3-17 years old (no longer require
GA only or >/= 2 risk factors)
2. Exclusion:
a. Patients <3 or > 17 years old
b. Patients transferred directly to ICU
c. ASA 5 or 6
d. Labor Epidural Cases
e. Diagnostic Imaging procedures
3. Discussion:
a. Lucy Everett (MGH): Should patients undergoing
radiation be excluded from PONV 03 given that
they are on chronic antiemetics?
b. Bob Brustowicz (Boston Children’s): How about
patients receiving LP's for chemotherapy? They are
on chronic antiemetics.
c. Wes Templeton (Wake Forest): I think it makes the
most sense to exclude these patients using
CPT/ICD-9 codes. Going to be a relatively small
number of patients…
d. Nirav Shah (ASPIRE Director): Okay! We will work
on adding that exclusion to the PONV 03 measure
specification
4. Risk factors updated:
a. Post-pubertal females (≥12yo)
b. Inhaled anesthetic duration ≥30 minutes
(halogenated or nitrous)
c. Hx of PONV (personal or first degree relative)
d. At Risk Surgery
i. Strabismus
ii. Adenotonsillectomy
iii. Tympanoplasty/otoplasty
e. Postoperative long-acting opioids (administered
after induction)
5. Discussion:
a. Vikas O’Reilly-Shah (Seattle Children’s): I'd only
worry about validity across sites of risk factor data.
b. Nirav Shah (ASPIRE Director): Yes- we have done a
lot of data cleaning in recent years so we are pretty
confident but this is always a potential issue.
6. Success Criteria
a. Low (0 risk factors): Receives at least one
prophylactic antiemetic
b. Medium (1-2 risk factors): Receives at least 2
prophylactic antiemetics from different classes
c. High (≥2 risk factors): Receives three prophylactic
antiemetics
7. Choice of Antiemetics and Frequency: Graphs of
antiemetic use for both prophy and rescue shared with the
group- see PPT slides for more information
8. Discussion:
a. James Xie via chat (Stanford): Our oncologists are
increasingly using Aloxi (palonosetron) which lasts
days and might not be documented intraop
b. Vikas O’Reilly Shah via chat (Seattle CHildrnes): I
sent you an email about atypical antipsychotics and
the growing literature there. Would be given
preop, not intraop. Unsure if amisulpride has a
pediatric indication
c. Priti Dalal via chat (Penn State Children’s): We are
also using Aloxi for hemonc
d. Wes Templeton via chat (Wake Forest): Haldol?
Interesting…more than droperidol…?
e. Vikas O’Reilly-Shah via chat (Seattle Children’s):
Droperidol only recently (re)started manufacture in
the US, I believe.
https://www.prnewswire.com/news-
releases/american-regent-re-introduces-
droperidol-injection-usp-ap-rated-and-
therapeutically-equivalent-to-inapsine1-
300796783.html
f. Wes Templeton via chat (Wake Forest): We use
droperidol at Wake Forest
g. Bob Brustowicz via chat (Boston Children’s): Is the
Propofol rescue an infusion or a bolus?
h. Meridith Bailey via chat (MPOG Coordinating
Center): Infusion
III. Measure Review: Transfusion Measures
a. Graph of current performance across pediatric sites shared for both TRAN
01 and TRAN 02 (see PPT slides)
b. Transfusion Vigilance Measure (TRAN 01)
i. Description: Percentage of cases with a blood transfusion that
have a hemoglobin or hematocrit value documented prior to
transfusion.
1. Transfusion is defined as packed red blood cells or whole
blood
2. Prior to the first transfusion, a hgb/hct of any value should
be checked in a time period of 0 to 90 minutes before the
transfusion, or the most recent documented hgb/hct was
<8/24 within 36 hours before the transfusion
ii. Responsible Provider: Provider(s) who administered the
transfusion
iii. See measure TRAN 01 specification for current inclusion/exclusion
criteria
iv. Proposed Pediatric Inclusion/Exclusion Criteria:
1. Inclusions: All patients who receive a transfusion between
anesthesia start and anesthesia end
2. Exclusions:
a. Patients ≤ 6 months or ≥ 18 years of age
b. ASA 5 & 6
c. Patients with cyanosis preoperatively AND
congenital heart disease
d. Patients with transfused volume or EBL > 40cc/kg.
e. Patients on ECMO
f. Burn Debridement Cases?
g. All Obstetric procedures
3. Discussion:
a. Vikas O’Reilly-Shah via chat (Seattle Children’s):
what about cases where there a strong a priori
expectation of transfusion e.g. we typically just
start blood at the beginning of the case for our
craniosynostosis cases
i. Laura Downey via chat (Emory): We
discussed such cases, but shouldn’t you still
have a Hematocrit or Hb prior to that type
of case?
ii. Nirav Shah (ASPIRE Director): This is our
thought as well. Should have a hgb/hct for
those cases
b. Morgan Brown (Boston Children’s): What about
cardiopulmonary bypass cases in which the pump is
primed with blood product?
i. Nirav Shah (ASPIRE Director): Should we
exclude this time period? Interested in
hearing your opinion
ii. Morgan Brown (Boston Children’s): This is a
complex decision making process in which
we are tracking these patients closely and
deciding to transfuse. I don’t think we want
to focus on those cases. I worry that we’ll
have a hard time excluding based on
congenital heart disease ICD 9/10 codes
alone
iii. Nirav Shah (ASPIRE Director): Some may be
covered under the massive transfusion or
high EBL exclusion but broadly decided to
include cardiac cases at the Quality
Committee level and just exclude units
given while on bypass. Need to review this
from a pediatric standpoint
iv. Morgan Brown (Boston Children’s): May
just lead to excessive blood testing since
these are complicated cases
c. Vikas O’Reilly-Shah via chat (Seattle Children’s):
that also gets to my point. don't think I would
cancel a case if I didn't have a preop hgb for a kid
i'm sure I was going to transfuse. would probably
just send an early lab h/h and trend poct
d. Lori Reigger (Michigan Medicine): If PRBC are
added to the pump circuit by the perfusionist and
documented in anesthetic record, then those cases
would be flagged if there is a not a hct/hgb
documented.
i. Nirav Shah (ASPIRE Director): Yes, that’s
true.
e. Meridith Bailey (MPOG Coordinating Center): Does
it make sense to write a separate measure for
cardiac cases relative to transfusion?
i. Morgan Brown (Boston Children’s): I think I
would just recommend excluding the
cardiac bypass cases
ii. Lori Reigger (Michigan Medicine): I would
agree with that.
iii. Shoba Malviya (Michigan Medicine): Can we
do that reliably?
1. Nirav Shah (ASPIRE Director): Yes,
we have created sophisticated logic
using both CPT code and other
elements of the case
f. RJ Ramamurthi via chat (Stanford): iSTAT Hct is
acceptable for this measure or need lab tested
Hct?
i. Meridith Bailey (MPOG Coordinating
Center): Yes, iSTAT is acceptable
ii. Nirav Shah (ASPIRE Director): As long as
those iSTAT values are uploaded to the lab
system and come over with the lab extract
(not manually documented as a note)
g. Vikas O’Reilly-Shah via chat (Seattle Children’s):
date time ‘preop’ would count if…?
h. Nirav Shah (ASPIRE Director): Okay excluding OB
cases?
i. Wilson Chimbira (Michigan Medicine): Yes
agree
ii. Wes Templeton: Yes – okay with excluding
OB cases
iii. Vikas: Agree
i. Wes Templeton (Wake Forest): why exclude burn
patients…this is a highly transfused population
which may/may not be at risk for over
transfusion…maybe should be separated.
i. Nirav Shah (ASPIRE Director): I believe the
Quality Committee feedback for burn
patients was related to access and reliability
to draw samples intraop; also, oozing so not
always checking in between. If folks feel
differently, let’s discuss
ii. Wes Templeton (Wake Forest): but I
thought you just had to check a
hgb…doesn’t have to be low. These kids will
have a hgb.
iii. Nirav Shah (ASPIRE Director): More about
not being able to check intraop due to their
burn status, not so much what the value
would be
j. Bob Brustowicz (Boston Children’s): What about
intraoperative blood salvage? These patients often
get their blood back without any additional labs.
i. Nirav Shah (ASPIRE Director): Decided years
ago that the risk of transfusion with your
own blood is less and so those instances are
excluded. Thoughts from the group on this?
4. Definitions/Considerations: see TRAN 01 specification for
current considerations
5. Proposed Pediatric-specific considerations:
a. Massive Transfusion defined as ≥40 cc/kg: No
objections to this change from the group.
b. 1 Unit of Blood for patients ≥12 years
c. Patients less than 12 years: define a ‘unit’ as 15
cc/kg
i. Discussion:
1. Joe Cravero (Boston Children’s):
How rapidly a patient is losing blood
is not considered with this measure;
If a patient is losing blood quickly,
you wouldn’t want to wait for a
H&H– there could be a lot of flags in
these instances
2. Nirav Shah (ASPIRE Director): We
have not seen this historically with
this measure as being an issue. Will
be interesting to see if that presents
as an issue with the pediatric
population
3. Vikas O’Reilly-Shah via chat (Seattle
Children’s): I do worry a bit about
how well your data quality is going
to assure that fallouts/fails are real.
There will be a lot of variability in
e.g. when blood tx is documented,
when EBL is intermittently (or not)
documented, when labs are
documented, whether POCT vs lab
sent h/h are available. Tightening
too much may be counterproductive
d. Cyanosis and CHD
i. Cyanosis: At least two SpO2 readings <90%
(between preop start and Patient in Room)
ii. CHD defined by ICD-9/10 codes
1. Discussion:
a. Meridith Bailey (MPOG
Coordinating Center): I met
with Bishr Haydar (Michigan
Medicine) and Laura Downey
(Emory) earlier this month
and came up with this
definition. Okay with the
group?
b. Morgan Brown (Boston
Children’s): ICD codes aren’t
always great. Fontan patient
with sat of 94% may still
want a higher transfusion
trigger.
6. Success Criteria: see TRAN 01 specification for current
success definition
7. Proposed Pediatric-specific Success Definition:
a. Documentation of hgb/hct prior to transfusion
i. If the most recent Hgb/Hct drawn before
the first transfusion is ≤ 5/16, an additional
15cc/kg could be administered without
rechecking Hgb/Hct between units.
ii. For patients < 12y?
iii. If multiple units are administered,
documentation of a Hgb/Hct value must be
present within 60 minutes before each
transfusion.
1. Morgan Brown (Boston Children’s):
Is there a practical implication for
limiting to 60 minutes rather than 90
minutes? If someone checks it at 64
minutes, rather than 60, does that
matter in terms of transfusion
administration?
2. Nirav Shah (ASPIRE Director): That’s
a great question and one for this
group to consider.
3. Meridith Bailey (MPOG Coordinating
Center): I believe 60min time frame
was suggested due to the total
blood volume of younger patients
4. Morgan Brown: Recommend
adjusting this measure to 60
minutes rather than 90 minutes to
see the impact on performance first
iv. All transfusions administered between
cardiopulmonary bypass start → end will
not be included for determining measure
results for the case.
c. Overtransfusion Measure (TRAN 02)
i. Description: Percentage of cases with a post transfusion hgb/hct
value ≥10/30
1. All hgb/hct labs resulted between the time of last
transfusion and 18 hours after anes end are evaluated.
ii. Responsible provider: Provider(s) who administered the last
transfusion
iii. See TRAN 02 specification for current inclusion/exclusion criteria
iv. Proposed Inclusion Criteria: All patients who receive a transfusion
between anesthesia start/end (no change)
v. Proposed Exclusion criteria:
1. Patients ≤ 6 months or ≥ 18 years old
2. ASA 5 & 6
3. Patients with cyanosis preoperatively and congential heart
disease
4. Patients with transfused volume or EBL>40cc/kg
5. Patients on ECMO
6. Burn Debridement Cases?
7. All Obstetric procedures
vi. Success Criteria: Hgb/hct value documented as ≤ 10/30 within 18
hours after anesthesia end OR if no hgb/hct checked within 18
hours of anesthesia end, the case will pass (should these instances
be excluded or flagged instead?)
1. Discussion:
a. Morgan Brown (Boston Children’s): Seems like you
should check a hct after a transfusion so would
suggest these cases should be flagged. Only other
consideration is that some patients continue to
bleed postop
b. Bob Brustowicz via chat (Boston Children’s):
Flagged for review.
d. Next Steps
i. MPOG Coordinating Center will incorporate your feedback and
update the transfusion metrics as needed or decide if we should
create new pediatric-specific measures
ii. Next meeting: August 18
th
at 1pm
1. NMB 01/NMB 02 are scheduled to be reviewed next
Meeting adjourned at: 1404