Professional Documents
Culture Documents
INTRODUCTION
I’m Peter Margolis, and I’m Co-Director of the Center for Health Care
Quality at the Cincinnati Children’s Hospital Medical Center. I am a
general pediatrician and epidemiologist. The work that I do is focused
on transforming systems of care delivery for children. We work in
many different parts of the country with many different types of
settings, everything from hospitals to primary care practices to
communities, states, early child care centers, social services, trying to
help create better systems of care that produce better outcomes for
children. This is part of Cincinnati Children’s Mission to improve care
and transform care delivery for children. The way that we operate is
by forming and bringing together groups of clinical sites generally to
work on specific problems.
A. CATEGORY
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What would you like people to know, think, feel and do?
[00:04:07] The kinds of things we’d like to see people and society do
is to put greater investment into the development of network based
approaches to care delivery. Probably the best, a couple of really
great examples in medicine already exist for this concept. Probably
the best example comes from children’s cancer, so there, pretty much
every child with cancer in the country is involved in a large network of
care providers so that the care a child in Idaho gets really looks pretty
much identical to the care of the child in New York City. That comes
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from the fact there’s an infrastructure that enables proto calls and
treatments and best knowledge to be disseminated very rapidly to
everybody who provides care for patients with cancer. The particular
problem in children that we have is that there are very few children
with serious chronic illnesses in any place. So that, as a clinician, if
you want to make sure somebody’s getting the best possible care, it’s
really impossible to do it based on just the information from your own
center. There may be just too few children to really study and
evaluate the effectiveness of the various treatments. So, by linking
people, linking care providers, and physicians up across multiple
sites, it provides the sample size, the number of patients you need to
really study and evaluate what is working and what isn’t. That also
provides a way; the standardization of care actually provides a way of
improving care. A lot of patients fall through the cracks because of a
lack of communication; doctors and nurses working as hard as they
can but not being able to deliver the best care because of the
limitations of the system. So, those are the things we like people to
know about.
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[00:09:03] The area that we’re finding that we need to get into more is
that we’ve been taking an approach that’s really kind of science and
data focused and we’re realizing that we’re in order to get this style of
working to spread, we’re going to need to start to communicate in
stories and connect sort of the day-to-day work of delivering care to
the emotional aspects of what we’re trying to do and why people went
into medicine and that sort of thing.
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Our hope is that we could expand the participation to get virtually all
care sites working on a particular topic and so for example, for
pediatric ICU’s, that would be about 350 ICU’s across the country, for
inflammatory bowel disease it’s probably about 250 care sites that
deliver care for children with that condition.
[00:10:56] I think our expertise developed over the last twenty years
has been really in developing and running distributed projects, large-
scale efforts that depend on collaborative partnerships among
groups. Our major research now is learning how to scale up what
we’ve been able to do at a scale of twenty to forty sites at once to a
much larger scale potentially involving thousands of sites at once.
dynamics, they may have the expertise that the team has the
knowledge about the application of quality improvement methods, or
the kind of data management system they have. So, we’re interested
in actually starting to study that systematically. In order to do that, we
have to have the relevant observations that take place at the clinical
site, not at the patient level, they need to have a lot of clinical sites
involved in the network in order to do the studies. So, that’s one area
of pretty intensive research.
outcomes that different sites are producing, you can identify those
sites that are outperforming everybody else and those are the groups
that have knowledge that others don’t have. Probably the best
example of this that has come up in my career, was a project that we
did on cystic fibrosis a number of years ago focused on improving the
quality of care for kids with that condition. At the time, there were data
about the life expectancy of kids with CF (cystic fibrosis) at different
care centers, but they were not available to the research community,
that was kept as private, so when we were starting the project, one of
the pulmonologists that we knew, who was involved with the
leadership, and I were talking about where we could go look to find
really good outcomes. So, we just sat down one day and Googled – I
asked him, where’s the best place in the country –and so we did a
Google search for the University of Minnesota’s CF Center and it
turned out there was a graph on their website showing the average
life expectancy for kids at the University of Minnesota was fourteen
years longer than the national average. That kind of information was
instrumental in helping us identify the specific care activities with
verifiable results, the tacit knowledge that individual centers have that
we needed to surface so that other centers could adopt it.
going to require new ways of delivering care. So, the way we’ve done
this in the past in medicine is that academics have assumed the guys
in the lab have assumed that if they write their results up that
somebody would read it and figure out how to put it into practice.
What we’re realizing is that you really have to have a different care
delivery system, so people earlier in the research trajectory, the ones
who are making the break through discoveries need to be in
communication with the people who are designing care delivery
systems so that they can accommodate the new discoveries. Sort of
like Intel working with Hewlett Packard so that the Hewlett Packard
people prepare their computers to accept the new capabilities for the
next new Intel chip.
[00:21:24] I think one place that we’re starting to look now is to look to
all these experts in networks, network people like Peter Gloor, Von
Hippel [Eric von Hippel] and Thomas Malone at the MIT Center [for
Collective Intelligence]. We’re working with the Science Commons.
We’re starting to work with economists at the University of Chicago
and we’re also working with creative people out of Los Angeles who
are good at telling stories. We’ve engaged some creative movie talent
in developing our stories.
[00:25:28] There are probably two or three other places that are
focused on this: the VA (Veterans Administration) has something they
call the VA Quality Scholars Program, it runs at about ten or fifteen
VA Centers. The VA itself is starting to use this approach. Dartmouth
Center for Clinical Effectiveness is one of the leading places; the
other place that I think is doing some training in this area is
Intermountain Health.
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Closing questions:
Our major focus up until now has been the health care provider
nodes. We often include, on some of our projects we include families,
parents, and kids on the teams that are redesigning care. So, some
of the best projects actually have families participating in the design
activities and the tests. One of my colleagues runs a center on
chronic illness innovation, and there are a number of parents who
participate on the design teams, they do the experiments themselves,
they cook up this stuff themselves. One of their projects is using,
working with adolescents to design a set of text messages for kids
with asthma that amount to reminders to the kids, but the kids
actually design, what they’ve done is work with the kids. Certain
adolescents like to have certain kinds of text messages as reminders,
so some adolescents prefer to have ones that are demanding, “Take
your medicines, dammit!” “It’s time to take your medicine.” Or, others
want a more, touchy, feely approach, “Maybe you should take your
medicine” or, “This would be a good time to think about taking your
medicine.” We’re working with some cell phone companies to develop
customized messages based on kid’s preferences for how they like to
have reminders.
Keywords
Collaborative health care, networks, pediatrics, social networking
platforms, quality improvement, medicine, education
Related Links
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http://i-open-2.strategy-nets.net/wiki/peter-margolis-co-director-
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center
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Scribd
http://www.scribd.com/doc/23383940/Peter-Margolis-MD-PhD-Co-
Director-Cincinnati-Children-s-Hospital-Medical-Cntr-08-05-09-
Interview
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Vimeo
http://www.vimeo.com/8165223
Contact Information
Copyright 2009 Betsey Merkel and I-Open. Creative Commons 3.0 Attribution-
Noncommercial-No Derivative Works. Institute for Open Economic Networks (I-
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Rebecca Boerger
Administrative Assistant
Center for Health Care Quality
3333 Burnet Ave., MLC 7014
Cincinnati, OH 45229
Rebecca.Boerger@cchmc.org
Ph 513-803-2187
Fax 513-636-0171
Website
http://www.cincinnatichildrens.org/research/div/health-
quality/default.htm
Biographical Information
http://www.cincinnatichildrens.org/svc/find-professional/m/peter-
margolis.htm
Copyright 2009 Betsey Merkel and I-Open. Creative Commons 3.0 Attribution-
Noncommercial-No Derivative Works. Institute for Open Economic Networks (I-
Open) 4415 Euclid Ave 3rd Fl Cleveland, Ohio 44103 USA