Chapter 897 Oregon Laws 2001
AN ACT
SB 819
Relating to Oregon Health
Plan; creating new provisions; amending ORS 414.325; and declaring an
emergency.
Be It Enacted by the People of the State of Oregon:
SECTION 1.
The Legislative Assembly finds that:
(1) The cost of
prescription drugs in the Oregon Health Plan is growing and will soon be
unsustainable;
(2) The benefit of
prescription drugs when appropriately used decreases the need for other
expensive treatments and improves the health of Oregonians; and
(3) Providing the most
effective drugs in the most cost-effective manner will benefit both patients
and taxpayers.
SECTION 2.
It is the policy of the State of Oregon
that a Practitioner-managed Prescription Drug Plan will ensure that:
(1) Oregonians have
access to the most effective prescription drugs appropriate for their clinical
conditions;
(2) Decisions concerning
the clinical effectiveness of prescription drugs are made by licensed health
practitioners, are informed by the latest peer-reviewed research and consider
the health condition of a patient or characteristics of a patient, including
the patient’s gender, race or ethnicity; and
(3) The cost of
prescription drugs in the Oregon Health Plan is managed through market
competition among pharmaceutical manufacturers by publicly considering, first,
the effectiveness of a given drug and, second, its relative cost.
SECTION 3.
(1) The Department of Human Services
shall adopt a Practitioner-managed Prescription Drug Plan for the Oregon Health
Plan. The purpose of the plan is to ensure that enrollees of the Oregon Health
Plan receive the most effective prescription drug available at the best
possible price.
(2) Before adopting the
plan, the department shall conduct public meetings and consult with the Health
Resources Commission.
(3) The department shall
consult with representatives of the regulatory boards and associations
representing practitioners who are prescribers under the Oregon Health Plan and
ensure that practitioners receive educational materials and have access to training
on the Practitioner-managed Prescription Drug Plan.
(4) Notwithstanding the
Practitioner-managed Prescription Drug Plan adopted by the department, a
practitioner may prescribe any drug that the practitioner indicates is
medically necessary for an enrollee as being the most effective available.
(5) An enrollee may
appeal to the department a decision of a practitioner or the department to not
provide a prescription drug requested by the enrollee.
(6) This section does
not limit the decision of a practitioner as to the scope and duration of
treatment of chronic conditions, including but not limited to arthritis,
diabetes and asthma.
SECTION 4.
The President of the Senate and the
Speaker of the House of Representatives shall designate an appropriate interim
legislative committee or legislative commission to:
(1) Receive regular
reports on the development and implementation of the Practitioner-managed
Prescription Drug Plan;
(2) Review the impact of
the implementation of the Practitioner-managed Prescription Drug Plan,
including but not limited to a review of whether the program realizes any
savings, whether there is an increase in physician and hospital costs for
individuals receiving medical assistance, and whether there is an impact on the
ability of an individual receiving medical assistance to obtain prescribed
drugs; and
(3) Report its findings
and recommendations periodically to the Emergency Board and to the
Seventy-second Legislative Assembly.
SECTION 5.
ORS 414.325 is amended to read:
414.325. (1) As used in this section, “legend drug” means
any drug requiring a prescription by a practitioner, as defined in ORS 689.005.
(2) A licensed practitioner may prescribe such drugs under
this chapter as the practitioner in the exercise of professional judgment
considers appropriate for the diagnosis or treatment of the patient in the
practitioner’s care and within the scope of practice. Prescriptions shall be
dispensed in the generic form pursuant to ORS 689.515, 689.854 and 689.857 and
pursuant to rules of the [division] Department of Human Services unless the
practitioner prescribes otherwise and an exception is granted by the [division] department.
(3) [Except as
provided in subsections (4) and (5) of this section, the division shall place
no limit on the type of legend drug that may be prescribed by a practitioner,
but] The department shall pay
only for drugs in the generic form if
the federal Food and Drug Administration has approved a generic version of a
particular brand name drug that is chemically identical to the brand name drug
according to federal Food and Drug Administration rating standards, unless
an exception has been granted by the [division] department.
(4) [Notwithstanding
subsection (3) of this section,] An exception must be applied for and
granted before the [division] department is required to pay for minor
tranquilizers and amphetamines and amphetamine derivatives, as defined by rule
of the [division] department.
(5) [(a)]
Notwithstanding subsections (1) to (4) of this section, [and except as provided in
paragraph (b) of this subsection, the division] the department is authorized to:
[(A)] (a) Withhold payment for a legend drug
when federal financial participation is not available; and
[(B)] (b) Require prior authorization of
payment for drugs [which] that the [division] department has
determined should be limited to those conditions generally recognized as
appropriate by the medical profession.
[(b) The division may
not require prior authorization for therapeutic classes of nonsedating
antihistamines and nasal inhalers, as defined by rule by the division, when
prescribed by an allergist for treatment of any of the following conditions, as
described by the Health Services Commission on the funded portion of its
prioritized list of services:]
[(A) Asthma;]
[(B) Sinusitis;]
[(C) Rhinitis; or]
[(D) Allergies.]
(6) Notwithstanding
subsection (3) of this section, the department may not limit legend drugs when
used as approved by the federal Food and Drug Administration to treat mental
illness, HIV and AIDS, and cancer.
SECTION 5a.
If House Bill 2497 becomes law, section
5 of this 2001 Act (amending ORS 414.325) is repealed and ORS 414.325, as
amended by section 1, chapter [Vetoed], Oregon Laws 2001 (Enrolled House
Bill 2497), is amended to read:
414.325. (1) As used in this section:
(a) “Legend drug” means any drug requiring a prescription
by a practitioner.
(b) “Pharmacy network” means a group of pharmacies using a
shared database or employing other electronic means to access prescription
information of enrollees from multiple points of service.
(c) “Practitioner” has the meaning given that term in ORS
689.005.
(2) A licensed practitioner may prescribe such drugs under
this chapter as the practitioner in the exercise of professional judgment
considers appropriate for the diagnosis or treatment of the patient in the
practitioner’s care and within the scope of practice. Prescriptions shall be
dispensed in the generic form pursuant to ORS 689.515, 689.854 and 689.857 and
pursuant to rules of the Department of Human Services unless the practitioner
prescribes otherwise and an exception is granted by the department.
(3) [Except as
provided in subsections (4) and (5) of this section, the department shall place
no limit on the type of legend drug that may be prescribed by a practitioner,
but] The department shall pay
only for drugs in the generic form if
the federal Food and Drug Administration has approved a generic version of a
particular brand name drug that is chemically identical to the brand name drug
according to federal Food and Drug Administration rating standards, unless
an exception has been granted by the department.
(4) [Notwithstanding
subsection (3) of this section,] An exception must be applied for and
granted before the department is required to pay for minor tranquilizers and
amphetamines and amphetamine derivatives, as defined by rule of the department.
(5)(a) Notwithstanding subsections (1) to (4) of this
section [and except as provided in
paragraph (b) of this subsection], the department is authorized to:
(A) Withhold payment for a legend drug when federal
financial participation is not available; and
(B) Require prior authorization of payment for drugs [which] that the department has determined should be limited to those
conditions generally recognized as appropriate by the medical profession.
[(b) The department
may not require prior authorization for therapeutic classes of nonsedating
antihistamines and nasal inhalers, as defined by rule by the department, when
prescribed by an allergist for treatment of any of the following conditions, as
described by the Health Services Commission on the funded portion of its
prioritized list of services:]
[(A) Asthma;]
[(B) Sinusitis;]
[(C) Rhinitis; or]
[(D) Allergies.]
[(c)] (b) Notwithstanding subsections (1) to
(4) of this section and [paragraphs (a)
and (b)] paragraph (a) of this
subsection, the department may require prior authorization of payment for drugs
for individuals whose prescription drug use exceeded 15 drugs in the preceding
six-month period.
(6) Notwithstanding
subsection (3) of this section, the department may not limit legend drugs when
used as approved by the federal Food and Drug Administration to treat mental
illness, HIV and AIDS, and cancer.
[(6)] (7) When a practitioner prescribes a
legend drug under this chapter, the practitioner shall write on the
prescription:
(a) The diagnosis code for the condition on the prioritized
list of services covered for payment for which the legend drug is being
prescribed; and
(b) The practitioner’s Office of Medical Assistance
Programs provider number.
[(7)(a)] (8)(a) At the time of enrollment or
reenrollment in a fee-for-service payment system, an enrollee shall designate a
primary pharmacy or pharmacy network to dispense legend drugs covered by the
medical assistance program.
(b) The department shall adopt rules establishing
procedures that allow an enrollee to:
(A) Obtain a legend drug at a pharmacy other than a
designated primary pharmacy or pharmacy network; and
(B) Change a designation of a primary pharmacy or pharmacy
network.
[(8)] (9) The department shall adopt rules
that:
(a) Establish procedures to ensure that a primary pharmacy
or pharmacy network will receive notice when an enrollee obtains a legend drug
at another pharmacy; and
(b) Allow payment at the point of sale to a pharmacy other
than a primary pharmacy or pharmacy network for a legend drug obtained by an
enrollee as described in subsection [(7)(b)(A)]
(8)(b)(A) of this section.
SECTION 6.
ORS 414.325, as amended by section 5 of this 2001 Act, is amended to read:
414.325. (1) As used in this section, “legend drug” means
any drug requiring a prescription by a practitioner, as defined in ORS 689.005.
(2) A licensed practitioner may prescribe such drugs under
this chapter as the practitioner in the exercise of professional judgment
considers appropriate for the diagnosis or treatment of the patient in the
practitioner’s care and within the scope of practice. Prescriptions shall be
dispensed in the generic form pursuant to ORS 689.515, 689.854 and 689.857 and
pursuant to rules of the Department of Human Services unless the practitioner
prescribes otherwise and an exception is granted by the department.
(3) Except as
provided in subsections (4) and (5) of this section, the department shall place
no limit on the type of legend drug that may be prescribed by a practitioner,
but the department shall pay only for drugs in the generic form [if the federal Food and Drug Administration
has approved a generic version of a particular brand name drug that is
chemically identical to the brand name drug according to federal Food and Drug
Administration rating standards,] unless an exception has been granted by
the department.
(4) Notwithstanding
subsection (3) of this section, an exception must be applied for and
granted before the department is required to pay for minor tranquilizers and
amphetamines and amphetamine derivatives, as defined by rule of the department.
(5)(a)
Notwithstanding subsections (1) to (4) of this section and except as provided in paragraph (b) of this subsection, the
department is authorized to:
[(a)] (A) Withhold payment for a legend drug
when federal financial participation is not available; and
[(b)] (B) Require prior authorization of
payment for drugs that the department has determined should be limited to those
conditions generally recognized as appropriate by the medical profession.
(b) The department
may not require prior authorization for therapeutic classes of nonsedating
antihistamines and nasal inhalers, as defined by rule by the department, when
prescribed by an allergist for treatment of any of the following conditions, as
described by the Health Services Commission on the funded portion of its
prioritized list of services:
(A) Asthma;
(B) Sinusitis;
(C) Rhinitis; or
(D) Allergies.
[(6) Notwithstanding
subsection (3) of this section, the department may not limit legend drugs when
used as approved by the federal Food and Drug Administration as the primary
treatment for mental illness, HIV and AIDS and cancer.]
SECTION 6a.
If House Bill 2497 becomes law, section
6 of this 2001 Act (amending ORS 414.325) is repealed and ORS 414.325, as
amended by section 5a of this 2001 Act, is amended to read:
414.325. (1) As used in this section:
(a) “Legend drug” means any drug requiring a prescription
by a practitioner.
(b) “Pharmacy network” means a group of pharmacies using a
shared database or employing other electronic means to access prescription
information of enrollees from multiple points of service.
(c) “Practitioner” has the meaning given that term in ORS
689.005.
(2) A licensed practitioner may prescribe such drugs under
this chapter as the practitioner in the exercise of professional judgment
considers appropriate for the diagnosis or treatment of the patient in the
practitioner’s care and within the scope of practice. Prescriptions shall be
dispensed in the generic form pursuant to ORS 689.515, 689.854 and 689.857 and
pursuant to rules of the Department of Human Services unless the practitioner
prescribes otherwise and an exception is granted by the department.
(3) Except as
provided in subsections (4) and (5) of this section, the department shall place
no limit on the type of legend drug that may be prescribed by a practitioner,
but the department shall pay only for drugs in the generic form [if the federal Food and Drug Administration
has approved a generic version of a particular brand name drug that is
chemically identical to the brand name drug according to federal Food and Drug
Administration rating standards,] unless an exception has been granted by
the department.
(4) Notwithstanding
subsection (3) of this section, an exception must be applied for and
granted before the department is required to pay for minor tranquilizers and
amphetamines and amphetamine derivatives, as defined by rule of the department.
(5)(a) Notwithstanding subsections (1) to (4) of this
section and except as provided in
paragraph (b) of this subsection, the department is authorized to:
(A) Withhold payment for a legend drug when federal
financial participation is not available; and
(B) Require prior authorization of payment for drugs that
the department has determined should be limited to those conditions generally
recognized as appropriate by the medical profession.
(b) The department
may not require prior authorization for therapeutic classes of nonsedating
antihistamines and nasal inhalers, as defined by rule by the department, when
prescribed by an allergist for treatment of any of the following conditions, as
described by the Health Services Commission on the funded portion of its
prioritized list of services:
(A) Asthma;
(B) Sinusitis;
(C) Rhinitis; or
(D) Allergies.
[(b)] (c) Notwithstanding subsections (1) to
(4) of this section and [paragraph (a)]
paragraphs (a) and (b) of this
subsection, the department may require prior authorization of payment for drugs
for individuals whose prescription drug use exceeded 15 drugs in the preceding
six-month period.
[(6) Notwithstanding
subsection (3) of this section, the department may not limit legend drugs when
used as approved by the federal Food and Drug Administration to treat mental
illness, HIV and AIDS, and cancer.]
[(7)] (6) When a practitioner prescribes a
legend drug under this chapter, the practitioner shall write on the
prescription:
(a) The diagnosis code for the condition on the prioritized
list of services covered for payment for which the legend drug is being
prescribed; and
(b) The practitioner’s Office of Medical Assistance
Programs provider number.
[(8)(a)] (7)(a) At the time of enrollment or
reenrollment in a fee-for-service payment system, an enrollee shall designate a
primary pharmacy or pharmacy network to dispense legend drugs covered by the
medical assistance program.
(b) The department shall adopt rules establishing
procedures that allow an enrollee to:
(A) Obtain a legend drug at a pharmacy other than a
designated primary pharmacy or pharmacy network; and
(B) Change a designation of a primary pharmacy or pharmacy
network.
[(9)] (8) The department shall adopt rules
that:
(a) Establish procedures to ensure that a primary pharmacy
or pharmacy network will receive notice when an enrollee obtains a legend drug
at another pharmacy; and
(b) Allow payment at the point of sale to a pharmacy other
than a primary pharmacy or pharmacy network for a legend drug obtained by an
enrollee as described in subsection [(8)(b)(A)]
(7)(b)(A) of this section.
SECTION 7.
The amendments to ORS 414.325 by section
6 of this 2001 Act become operative on January 2, 2007.
SECTION 7a.
If House Bill 2497 becomes law, section 7 of this 2001 Act is amended to read:
Sec. 7. The
amendments to ORS 414.325 by section [6] 6a of this 2001 Act become operative
on January 2, 2007.
SECTION 8.
This 2001 Act being necessary for the
immediate preservation of the public peace, health and safety, an emergency is
declared to exist, and this 2001 Act takes effect on its passage.
Approved by the Governor
August 2, 2001
Filed in the office of
Secretary of State August 3, 2001
Effective date August 2,
2001
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