1)
External
insulin infusion pumps are covered for patients with insulin dependent diabetes
(E10.10-E10.9) who meet the criteria set forth below.
2)
Insulin
pumps require pre-certification and are implanted on an outpatient basis. The
pump must be ordered by and follow-up care of the patient must be provided by a
physician with experience managing patients with insulin pumps and who works
closely with a team including nurses, diabetic educators, and dieticians
knowledgeable in the use of insulin pumps.
3)
QualChoice will provide coverage for supplies that are necessary for the
effective use of the insulin pump. Such supplies are covered under the DME
benefit.
4)
QualChoice covers the insulin used in the insulin pump under the pharmacy
benefit.
Preauthorization Criteria:
A. Standard Criteria:
Patients must meet ALL of the following criteria:
1.
The patient has completed a comprehensive diabetes education program;
and
2.
The patient has been on multiple daily injections of insulin (at least 3
per day – exceptions should be considered for children when compliance to
multiple insulin doses may be a problem) with frequent self-adjustments of
insulin dose for at least six (6) months prior to initiation of the insulin
pump; and
3.
The patient has been self-testing for blood sugar on an average of at
least four (4) times per day during the two months prior to initiation of the
insulin pump; and
4.
The patient meets one or more of the following criteria while on
multiple daily injections of insulin:
·
Elevated glycosylated hemoglobin
of 7.0 or greater; or
·
History of recurring hypoglycemia
(less than 60mg/dL); or
·
Wide fluctuations in blood glucose
before mealtime (pre-prandial blood glucose levels commonly exceeding 140mg/dL);
or
·
Dawn phenomenon with fasting blood
sugars frequently exceeding 200mg/dL; or
·
History of severe glycemic
excursions.
B. Patients who are, or are
anticipating being pregnant:
1.
The patient has a history of poor control without a pump during a
previous pregnancy; or
2.
The patient meets the criteria in section A excepting duration of effort,
or
3.
The patient was in good control prior to becoming pregnant, and has
failed efforts to continue control during pregnancy.
C. Patients who have been
using an insulin pump and request or require an upgrade or replacement pump:
1.
The previous pump is no longer functional (and is not repairable), but
its use met the criteria above; or
2.
The previous pump was recalled by its manufacturer, in which case:
a.
We will expect the patient to use the manufacturer recall and replacement
program.
b.
If the patient wishes to acquire a different brand of pump, we will allow
toward that purchase only what we would have paid if the patient had used the
manufacturer recall and replacement program.
3.
If the patient requests or requires replacement or upgrade of a fully
functional insulin pump:
a.
If diabetic control is suboptimal to the point where the patient would
qualify for a pump under section A, we will pay for the upgrade pump; otherwise
b.
If the pump is essentially for the convenience of the patient – meaning
that control with the current pump is excellent, and cannot therefore be
expected to improve with the change of pump – we will not pay for the upgrade or
replacement pump.
c.
In pregnancy, an upgrade will be allowed if:
i.
There is poor control with the existing pump (there is no requirement for
elevated hemoglobin A1c or for crisis, but only for significant difficulty in
control), or
ii.
There is documentation of serious difficulty in control of diabetes
during a prior pregnancy on the current pump.
Codes Used In This
BI:
E0784 External ambulatory infusion pump, insulin
A9274 External
ambulatory insulin delivery system, disposable