20 CSR 2150-5.026
General Provisions
PURPOSE: This rule establishes definitions for 20 CSR 2150-5.026
to 20 CSR 2150-5.028 governing medication therapy services by
pharmacists.
(1) Definitions. The following definitions shall apply for
purposes of 20 CSR 2150-5.026 to 20 CSR 2150-5.028:
(A) Authorizing physician(s)—The physician identified in
the written protocol as authorizing the pharmacist to provide
medication therapy services;
(B) Health care entity—For purposes of this rule, a health
care entity shall be defined as any entity or organization that
is licensed or certified by the state or federal government as a
hospital, hospice facility, ambulatory surgical center, nursing
home, long-term care facility, residential care facility, assisted
living facility, intermediate care facility, skilled nursing facility,
or a habilitation center as defined by Chapter 630, RSMo, and
that is required to maintain patient medical records by state or
federal law;
(C) Medication therapy protocol—A written agreement
between a physician and a pharmacist for the provision of
medication therapy services. A medication therapy protocol
shall comply with the provisions of 20 CSR 2150-5.028;
(D) Medication therapy services—The designing, initiating,
implementing, or monitoring of a plan to monitor the
medication therapy or device usage of a specific patient, or to
enhance medication therapeutic outcomes of a specific patient,
by a pharmacist who has authority to initiate or implement
a modification of the patient’s medication therapy or device
usage pursuant to a medication therapy protocol. For purposes
of 20 CSR 2150-5.026 to 20 CSR 2150-5.028, modification shall
include selecting a new, different, or additional medication
or device, discontinuing a current medication or device, or
selecting a new, different, or additional strength, dose, dosage
form, dosage schedule, or route of administration for a current
medication or device, and implementing such selection(s).
Medication therapy services shall not include the sole act of
dispensing a drug or device pursuant to a valid prescription
for the product, generic substitutions made pursuant to section
338.056, RSMo, or medication therapy management that does
not include the initiation or implementation of a modification
of medication therapy, as provided herein;
(E) Pharmacy resident—A Missouri licensed pharmacist
enrolled in a residency training program accredited by the
American Society of Health-System Pharmacists or a residency
training program with a valid application for accreditation
pending with the American Society of Health-System
Pharmacists;
(F) Prescription order for medication therapeutic plan—A
lawful order that is issued by the authorizing physician within
the scope of his/her professional practice for the provision of
medication therapy services by a pharmacist for a specific
patient, including, patients of a health care entity; and
(G) Protocol—A medication therapy protocol, as defined
herein.
(2) The provisions of 20 CSR 2150-5.026 to 20 CSR 2150-5.028 and
20 CSR 2220-6.060 to 20 CSR 2220-6.080 shall only be deemed
applicable to persons or entities under the jurisdiction of
the Missouri State Board of Registration for the Healing Arts
and the Missouri State Board of Pharmacy, as established by
Chapter 334, RSMo, and Chapter 338, RSMo.
AUTHORITY: section 334.125, RSMo 2000, and sections 338.010
and 338.220, RSMo Supp. 2011.* Original rule filed Jan. 13, 2012,
effective Aug. 30, 2012.
*Original authority: 334.125, RSMo 1959, amended 1993, 1995; 338.010, RSMo 1939,
amended 1989, 1990, 2007, 2009, 2011; and 338.220, RSMo 1951, amended 1969, 1981,
1989, 1997, 1999, 2001, 2004, 2007, 2009, 2011.