“Tight Glycemic Control
More 'Burden' Than Benefit for Many,” this Medscape Medical News piece proclaimed. It really got my blood
boiling. Later, I recognized that “anyone with a clinical practice” would
relate to this sentiment, as one of the authors says in the online article in JAMA Internal Medicine. But the proposed
“solution,” in the salutary guise of “patient-centered care,” is to
“personalize treatment.” Sounds promising, but look carefully at the
confirmation bias in their hypothesis. Consider also the tendency to blame
failure-to-successfully-treat on the patient (rather than the treatment) and then
to assign the failure to the patient’s “burden” of treatment, thus relieving
the patient of the moral burden for failure.
The primary
end-point was “to estimate the treatment burden vs. benefits from intensive vs.
moderate glycemic control in patients with type 2 diabetes.” The outcome:
“Using a simulation model [carefully constructed by the researchers to confirm
their hypothesis?], the researchers discovered that for patients with type 2
diabetes who are on metformin and have an HbA1c below 9%, adding other
antidiabetic therapies to try to lower glucose further may only confer modest
benefits 15 to 20 years later.” Even though, citing the UK Prospective Diabetes
Study (UKPDS), the
authors acknowledge that “Lowering HbA1c delays the onset and slows the
progression of early microvascular disease.”
So, what do
we learn here? The new standard of care “for many” is an A1c <9% for
an average glucose reading of 212? And for these “many,” the treatment
plan, described as having “a low-treatment burden,” is simply to prescribe
metformin and do nothing else? Because the benefit gained, depending on age
when diagnosed, is only “modest”? What, pray tell, could lead anyone with a
clinical practice to reach this conclusion? Could it be the failure of the
“treatment” modality?
This study
was carried out by doctors from “the University of Michigan and the VA Ann
Arbor Healthcare System.” Not to slam yet another VA
facility, but – I have to wonder – are the vets at this VA facility
subjected to this lower standard of care?
If true, shame, shame on these doctors. But, maybe I’m just piling on.
Maybe, by JAMA Internal Medicine
publishing this piece, they too are advocating a broader application of this
lower standard of care. I’ll have to read the comments.
Why lower
the standard of care? Because, “for patients older than 50, especially, any
potential benefits are often outweighed by ‘burdens’ of lifelong treatment –
such as substantial weight gain from sulfonylureas, the need to frequently
inject insulin, or the risk of hypoglycemia.” Well, patients older than 50
includes “most” people initially diagnosed with type 2 diabetes, so this new
paradigm would then thus apply to “most.” NB: The authors, to their credit, do
make an exception for “the 15% to 20% of people who have very high HbA1c’s and
require more aggressive treatment to manage the disease.”
The authors
state that the decision to “start new medications” (beyond metformin, assuming
metformin is tolerated) should be “based on individual circumstances and preferences.” “These are important
decisions,” they say, “because type 2 diabetes is a chronic disease that
requires lifelong treatment. Thus, shared decision making, in which patient preferences are specifically
elicited and considered, appears to be the best approach to making most
decisions about glycemic management in patients with type 2 diabetes.” Don’t
doctors take primary responsibility for patient care anymore?
But the
most disingenuous statement in this
article was this: “What really surprised us was you end up with a reduction of
quality of life for many patients – basically those who are a little bit older
when they are diagnosed or those who
really don’t like their treatments.” Don’t like their treatments? If the
treatment “really bothers you, then you just need to understand that you have a
slightly higher risk [according to the ‘simulation model’ they’ve constructed]
of these complications, and it may not be worth treating to prevent that,” they
concluded. Now that’s confirmation bias for you.
It’s true:
Some people can’t tolerate metformin even if it is titrated. And some
anti-diabetic meds do cause weight gain, and injecting insulin is a “bother”
and certainly can cause weight gain and does entail a risk of hypoglycemia. But
do these “constant annoyances of having to be on a medication and experience
the side effects” constitute a “burden” that exceeds the benefits of having
improved glucose control? Or is this construct just rationalization to justify
a failed treatment plan?
And if the
treatment plan included dietary changes such as carbohydrate restriction, would
not the benefits of losing weight,
taking less anti-diabetic oral
medications, and stopping insulin
injections altogether, far exceed the “burden”?
I know people who tell
me they could “never” give up bread, pasta, rice, corn and potatoes, or
beverages sweetened with sugar or HFCS. “I really wouldn’t like that treatment,”
they say. But…you know what? It really works.
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