Current through Register Vol. 51, No. 19, September 20, 2024
A. To be considered a participating medical
supply company in the Program, the provider of disposable medical supplies and
durable medical equipment shall:
(1) To the
extent required by law, be licensed and legally authorized to practice or
deliver services in Maryland or a jurisdiction bordering Maryland;
(2) Agree to abide by the provisions set
forth in this regulation by signing and sending to the Department the
designated Departmental form;
(3)
Agree to accept, as payment in full, the amount paid by the Department pursuant
to §F of this regulation plus, if applicable, the amount paid by the
eligible patient's health insurer and the patient contribution
amount;
(4) Agree not to bill an
eligible patient for an additional charge for the eligible disposable medical
supplies and eligible durable medical equipment other than the patient
contribution amount, excluding the deductible; and
(5) Maintain adequate records for a minimum
of 6 years and, upon request, allow the Department access to the
records.
B. The
Department shall reimburse for the following:
(1) Eligible disposable medical supplies,
including but not limited to:
(a) Central
catheter for administration of intravenous solutions;
(b) Administration set for intravenous
medication;
(c) Parenteral feeding
equipment, as follows:
(i) Administration
set;
(ii) Dravon clamp;
(iii) Filter; and
(iv) Injection cap; and
(d) Enteral feeding equipment, as follows:
(i) Adapter;
(ii) Administration set;
(iii) Feeding syringe; and
(iv) Nasogastric tube;
(2) Eligible durable medical
equipment for purchase or rental, including but not limited to:
(a) A delivery system comprised of a pump and
pole assembly for an enteral or parenteral feeding;
(b) An individually form-fitted arm support
stocking for a recipient prescribed by the participating physician as medically
necessary, not to exceed two stockings at one time or three stockings in a
12-month period for a non-institutionalized individual;
(c) IV pole for use with parenteral
administration of medication;
(d)
External ambulatory infusion pump with administrative equipment, when the usual
and customary mode of therapy has been tried and shown to be unsuccessful or
impractical;
(e) Breast prosthesis,
including surgical brassiere ; and
(f) A wig when the following conditions are
met:
(i) Hair loss is a direct result of the
administration of chemotherapy or radiation for the treatment of breast or
cervical cancer;
(ii) The cost does
not exceed $350; and
(iii) The wig
is prescribed by an oncologist.
C. The Department may not reimburse for the
following:
(1) A disposable medical supply
which is not directly related to the diagnosis and treatment of breast cancer
or cervical cancer; and
(2) Durable
medical equipment as follows:
(a) Head
covering; and
(b) An item not
directly related to the diagnosis and treatment of breast cancer or cervical
cancer.
D.
Preauthorization is required for the disposable medical supply and durable
medical equipment pursuant to COMAR
10.09.12.06A-F
and H .
E. Reimbursement
Procedures. The participating medical supply company:
(1) Shall submit the request for payment for
the reimbursed service on the form designated by the Department within 12
months of the date of service as follows:
(a)
If an eligible patient is uninsured, or is insured but the insurance does not
provide coverage for the reimbursed service, the participating medical supply
company shall send the Department the bill for the service, with a denial from
the patient's insurance carrier; or
(b) If an eligible patient is covered by
Medicare or other insurance, the participating medical supply company shall
bill:
(i) Medicare or the other insurance for
the service; and
(ii) The
Department for the outstanding deductible, patient contribution amount, and if
the insurer pays less than the current Medical Assistance approved rate for the
service, the difference between the insurance reimbursement rate and the
Medical Assistance approved rate in the State;
(2) May not bill the Program a charge
exceeding the usual and customary charge to the general public for a similar
item; and
(3) Shall bill the
Program the usual and customary charge for the prosthetic device and an
individually form-fitted arm support stocking including:
(a) Fitting;
(b) Dispensing; and
(c) Follow-up care.
F. Reimbursement Procedures.
(1) The Department shall reimburse the
participating medical supply company:
(a)
Pursuant to COMAR
10.09.12.07F- for
an eligible patient who is uninsured or who has insurance that does not provide
coverage for the reimbursed service;
(b) Pursuant to COMAR
10.09.12.07R and
S for an eligible patient who is covered by Medicare; or
(c) The outstanding deductible and patient
contribution amount required by the insurer for an eligible patient who has
insurance, other than Medicare, that provides coverage for the reimbursed
service.
(2) The
Department may not reimburse for:
(a)
Completion of a form;
(b) A broken
or missed appointment;
(c) A
professional service rendered by mail or telephone; or
(d) A service rendered to the general public
at no charge.
G. The Program shall reimburse for claims
submitted pursuant to this regulation as set forth in Regulation .21 of this
chapter.