100% sure of the science behind, measures where folks may have
some disagreement on whether it should be considered best practice.
In most cases, those never get to the level of a quality measure. Our
mortality measure which looks at 30-day in-hospital mortality shows
some wide variation. It is anonymized but sites may feel that it
shouldn’t be shared with an outside entity unless the Quality
Committee has had a chance to weigh in on who that entity is and
why they are interested in using that data. There may be other
situations (i.e. if we’re showing sustainability measure performance
at Michigan Society of Anesthesiology website or newsletter) that are
relatively low risk and of interest to folks outside of MPOG.
Something that highlights the work that sites are doing. We may not
need to bring something like that to the Quality Committee. I think
you that the perspective we have at the Coordinating Center and
that’s the one that we want to get some feedback on. Those are
things thing that we can save time from the agenda or maybe share
via email, an update versus a vote, which is what we typically have
anytime we want to share data, as our bylaws currently require about
sharing aggregate data or disseminating it outside of MPOG.
ii) Katie O’Connor (Johns Hopkins): Let me preface that whenever I’m asked are
there any issues, I try to come up with some so I’m not as adversarial coming
up with a few questions, just trying to put my hat from a health equity DEI
perspective. How could things that seem like they are going to be okay not
end up okay. One of the thoughts I had is around how certain data is
interpreted. One of the things we navigate when we are looking at health
disparities is the nuance of interpretation, where, if there is a disparity
between 2 groups, are we viewing that as a system issue like the care is
different versus are we viewing this as an innate difference between
different demographics from biological perspectives. As you can imagine that
is a very controversial topic and there might be a variety of opinions on this
call about that. That's something that whenever we are presenting health
disparities data, we always have a lot of discussion around, even if the
measure itself is innocuous, like AKI, we always have a lot of discussion
around what does this say? Are we saying these groups are different? Or are
we saying that care is different? If there’s no governance on how we present
that, there kind of a potentially rare by potentially problematic unexpected
sequelae of unreviewed sharing. That's one thought I had just on DEI
sensitivity. And maybe you already addressed these, but one would be, are