If only this could be true! This blog
by Carla Cox on the American Association of Diabetes Educators (AADE)
website is the most positive blog about the supposed changes made by
the American Diabetes Association (ADA) 2013 Guidelines. As research
has shown by my blog here, 2013 may not be the year for much change,
but maybe some of the results will be heard by the people at ADA and
maybe for 2014, we will see some real change in the language and
action by the insurance companies.
This quote from her blog is somewhat
gratifying, “Benefits of monitoring have
not been consistently demonstrated when patients with type 2 diabetes
are on lifestyle-controlled regimens or oral medications (The
Diabetes Educator, 2007; Health Technology Assess, 2009). Data
aside, I believe all of us have seen how much patients learn about
their BG response to meals, exercise and environmental pressure when
checking BG values throughout the day, regardless of whether it’s
controlled via lifestyle or medication. This is with the caveat, of
course, that they understand how to interpret the results.”
It seems that the author is calling for
more testing by type 2 people and education is what is needed. I
could almost believe the good intentions, if certified diabetes
educators (CDEs) were working heavily with type 2 patients. We know
this isn't happening because there are not enough CDEs for this to
become a reality. CDEs currently have no incentive to work with type
2 patients, as being reimbursed is a problem.
Even their own practice advisories from
2010 found at this link under 2010 says the following - “Shared
medical appointments (SMA) are a healthcare practice approach that
provides more access to patients while using existing resources. SMA
are a recognized approach that have been shown to provide high
quality care at reduce costs. While insurers may recognize these as
separately reimbursable appointments, Medicare has yet to provide
guidance on the topic.” You will need to download the "Shared medical appointment" advisory with Adobe Reader (or another PDF viewer) to view it.
With many type 2 patients being under
Medicare, I can understand that they do not wish to take on groups of
people with type 2 diabetes as part of SMAs. Not all insurance
companies are on board with reimbursing for patients not yet on
Medicare. Therefore, in the meantime they will need to contact
providers to see if they cover this. Most CDEs are not interested in
contacting a variety of providers, as they would prefer a one on one
situation. Yet, with the current shortage of CDEs, something needs
to change. This says nothing about the needs of people in the “at
risk” category (prediabetes) that receive no help.
Another factor that makes me question
the sincerity of statements made by CDEs if the fact that Medicare is
moving to more preventive medicine and this would seem to be the time
for AADE to lobby the Centers for Medicare and Medicaid Services
(CMS) to reimburse for SMAs as this could be a giant step forward to
educating groups of people with type 2 diabetes and even many in the
“at risk” group. Then for the enterprising CDEs, telemedicine
may open up doors for education as well. Unless AADE attempts to
open these avenues and pressure CMS to reimburse for these avenues,
all I can say is the “feel good” hype is worse than BS, and I'm
not talking blood sugar.
I sincerely wish this statement could
be relied on and trusted - “Blood
glucose monitoring is a cornerstone of diabetes education. Blood
sugars shift throughout the day and often get progressively higher
over time even in the “best” patient with type 2 diabetes.”
The bold is my emphasis. I know from experience that
this statement sounds good, but when mandates take place instead of
education, it ruins the experience for most patients with type 2
diabetes.
This statement in the last paragraph of
her blog gets my hackles up, “As diabetes
educators, we are the “go to” persons to help guide patients to
understand their BG results and to learn to act on the results to
help normalize blood sugars and reduce risks associated with frequent
BG values that are out of range.” But, how can we “go
to” CDEs when they are not available and most don’t deal with
type 2 diabetes people. I have to question where the CDEs are and
why I should not consider statements like this, “feel good” hype?
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