Current through Register Vol. 49, No. 18, September 16, 2024
PURPOSE: This rule establishes procedures for the
provision of medication therapy services by protocol, as authorized by section
338.010,
RSMo.
(1) Except as otherwise
provided herein, a pharmacist who holds a certificate of medication therapeutic
plan authority from the Missouri State Board of Pharmacy shall be authorized to
provide medication therapy services in Missouri if the pharmacist-
(A) Holds a current Missouri pharmacist
license that is not under discipline with the Missouri State Board of Pharmacy;
and
(B) Has entered into a written
protocol with a Missouri licensed physician that complies with the requirements
of this rule.
(2)
General Requirements. A pharmacist may provide medication therapy services only
with current certification and as authorized by the protocol and the
authorizing physician. A pharmacist providing medication therapy services
pursuant to this rule shall comply with the following:
(A) Prior to providing medication therapy
services, the pharmacist shall receive a prescription order for a medication
therapeutic plan from the authorizing physician for a specific patient which
authorizes the pharmacist to perform medication therapy services. Except as
otherwise provided in subsection (2)(B) of this rule, the prescription order
for a medication therapeutic plan shall be valid for no more than one (1) year
and shall include:
1. The patient's name,
address, and date of birth;
2. The
date the prescription order for a medication therapeutic plan is
issued;
3. The clinical indication
for medication therapy services;
4.
The length of time for providing medication therapy services, if less than one
(1) year; and
5. The authorizing
physician's name and address;
(B) A prescription order for a medication
therapeutic plan may be transmitted orally, electronically, or in writing. If
an oral prescription order for a medication therapeutic plan is issued, all
information required under subsection (2)(A) of this rule shall be documented
by the pharmacist and maintained in the patient's record in accordance with
section (7) of this rule;
(C) The
pharmacist shall review relevant prescription records, patient profiles,
patient medical records, or other medical information to determine the services
to be rendered; and
(D) In lieu of
compliance with
20 CSR
2220-2.018, prescription orders for medication therapy
services shall comply with the provisions of this rule, provided the pharmacist
shall maintain the prescription order in the patient record required by section
(7) of this rule and shall document any change or alteration made to the
prescription ordered based on contact with the prescriber in the applicable
patient record.
(3)
Authorizing Physician Requirements.
(A) The
authorizing physician shall be actively engaged in the practice of medicine in
the state of Missouri and shall hold a current and unrestricted Missouri
physician license pursuant to Chapter 334, RSMo.
(B) The authorizing physician shall be
responsible for the oversight of the medication therapy services provided by
the pharmacist that are authorized by protocol. The authorizing physician shall
also consider the level of skill, education, training, and competence of the
pharmacist and ensure that the activities authorized by the protocol are
consistent with the pharmacist's level of skill, education, training, and
competence.
(C) The written
protocol shall be reviewed and signed by the pharmacist and the authorizing
physician at least annually and revised as needed. The authorizing physician
and pharmacist shall document the date of the annual review on the written
protocol.
(D) The authorizing
physician shall review the pharmacist's medication therapy service activities
regularly, but not less than once every three (3) months. If the pharmacist is
providing medication therapy services for, or on behalf of, a health care
entity, the review requirements shall be satisfied if the pharmacist's work and
services are reviewed every three (3) months by a clinical care committee,
pharmacy and therapeutics committee, or a reviewing body/committee of the
health care entity that includes a Missouri-licensed physician. The review
required by this subsection may be accomplished in person or by electronic
means.
(E) The practice location of
the authorizing physician shall be no further than fifty (50) miles by road
from the pharmacist identified in the written protocol.
(F) An authorizing physician shall notify the
Missouri State Board of Registration for the Healing Arts of a written protocol
for medication therapy services entered with a pharmacist at each renewal of
the authorizing physician's license.
(4) Protocol Requirements.
(A) The medication therapy services performed
by a pharmacist pursuant to the protocol shall be within the authorizing
physician's scope of practice and within the skill, education, training, and
competence of both the authorizing physician and the pharmacist.
(B) The written protocol between the
authorizing physician and pharmacist shall, at a minimum, include the
following:
1. The identity and signatures of
the authorizing physician and pharmacist;
2. The effective dates of the
protocol;
3. A statement of
clinical conditions, diagnoses, diseases, and specific drugs, or drug
categories included in the written protocol and the type of medication therapy
services allowed in each case;
4. A
statement of the methods, procedures, decision criteria, and plan the
pharmacist is to follow when conducting medication therapy services;
5. Procedures for documenting medication
therapy decisions made by the pharmacist and a plan for communication,
feedback, and reporting to the authorizing physician concerning specific
decisions made;
6. A mechanism and
procedure that allows the authorizing physician to override, rescind, modify,
or otherwise amend the protocol. All modifications or amendments to the
protocol shall be documented in writing, signed, and dated by all involved
parties prior to the implementation of such modification or amendment. The
protocol may be immediately rescinded by the authorizing physician or the
pharmacist with or without cause, provided the rescission is documented in
writing. If any conflict arises regarding the professional judgment of the
pharmacist and physician with regard to the subject of the medication therapy
services, the physician has ultimate authority;
7. A statement that the pharmacist shall not
delegate the responsibility of medication therapy services to another
person;
8. A description of any
authority granted to the pharmacist to administer any drug or medication
including the identification of any such drug, medication, or device;
9. A description of drug therapy related
patient assessment procedures or testing that may be ordered or performed by
the pharmacist, including any authority to order or perform routine or other
laboratory testing;
10. Provisions
for allowing the pharmacist to access the patient's medical records for
purposes of providing medication therapy services;
11. A provision for providing the authorizing
physician access to patient records for medication therapy services provided by
the pharmacist for patients of the authorizing physician;
12. Provisions establishing a course of
action the pharmacist is authorized to follow to address emergency situations,
including, but not limited to, anaphylactic or other adverse medication
reactions, adverse needle sticks, or other adverse events;
13. Criteria for timely communication from
the authorizing physician to the pharmacist and from the pharmacist to the
authorizing physician, not inconsistent with the provisions of this
rule;
14. The notification
requirements required by section (5) of this rule; and
15. The method for reviewing the pharmacist's
medication therapy work or services by the authorizing physician, as required
by subsection (3)(D) of this rule.
(C) The written protocol shall include a
description of medication therapy services the pharmacist is authorized to
render or provide. Such services may include:
1. Assessing patient specific data and
issues;
2. Establishing medication
therapeutic goals or medication related action plans for identified medical
conditions and medication related concerns;
3. Assessing and addressing adverse reactions
and adverse drug events;
4.
Modifying and monitoring medication regimens;
5. Evaluating treatment progress;
6. Assessing and monitoring pharmacokinetic
and pharmacodynamic changes in medication regimen reviews;
7. Medication reconciliation;
8. Drug utilization review;
9. Formulating and documenting personal
medication records;
10. Documenting
clinical outcomes;
11.
Interpreting, monitoring, and assessing patient test results;
12. Initiation of drug therapy, as authorized
by protocol; and
13. Patient
education and counseling.
(D) The protocol required by this section
shall be signed and dated by the authorizing physician and the pharmacist. If
the protocol includes multiple authorizing physicians or participating
pharmacists, a separate protocol shall not be required for each physician or
pharmacist if all authorizing physicians and pharmacists have signed and dated
a statement agreeing to be governed by the terms of the written
protocol.
(E) Any revisions,
modifications, or amendments to the protocol must be in writing. The
authorizing physician shall promptly notify the pharmacist of any such
revision, modification, or amendment and shall maintain documentation of the
notification, including the date such notification was made. The authorizing
physician may delegate the notification requirements of this subsection to an
authorized designee, provided the physician shall be ultimately responsible for
compliance with the notification requirements.
(F) A pharmacist shall not be authorized to
adjust, change, or modify any controlled substance prescribed for a patient,
except as authorized by state or federal law.
(G) The protocol shall be maintained by the
authorizing physician and the pharmacist for a minimum of eight (8) years after
termination of the protocol. The protocol may be maintained
electronically.
(H) A protocol
shall automatically and immediately terminate if the pharmacist ceases to
maintain an active Missouri pharmacist license, the authorizing physician is
deceased, or if the authorizing physician fails to maintain an active,
unrestricted Missouri physician license.
(I) Pharmacy Residents. If specifically
authorized by the protocol, a pharmacy resident shall be authorized to perform
medication therapy services under the written protocol of a Missouri pharmacist
in lieu of an individual protocol, if-
1. The
resident holds a certificate of medication therapeutic plan authority from the
Missouri State Board of Pharmacy;
2. The resident is 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;
and
3. The resident is providing
medication therapy services under the supervision of a Missouri pharmacist
certified by the Missouri State Board of Pharmacy to perform medication therapy
services.
(J) The
provisions of subsection (4)(I) shall only apply to medication therapy services
provided by a pharmacist as part of his/her residency training.
(5) Notification Requirements. A
pharmacist shall comply with the following notification requirements:
(A) Within twenty-four (24) hours after
learning of an anaphylactic or other adverse medication reaction, adverse
needle stick, or other adverse event experienced by a patient, the pharmacist
shall notify the patient's authorizing physician or an authorized designee of
the authorizing physician;
(B) The
pharmacist shall notify the authorizing physician or an authorized designee of
the authorizing physician in the written protocol of any modification of
therapy, within twenty-four (24) hours, provided the protocol may include more
stringent notification requirements;
(C) A pharmacist shall be deemed in
compliance with the notification requirements of this rule if the pharmacist is
providing medication therapy services for, or on behalf of, a health care
entity, as defined by this rule, and documentation of the notifications
required by this section is recorded in a patient medical record that is
required to be maintained by the health care entity pursuant to state or
federal law; and
(D) Notifications
required by this section shall be in writing unless otherwise authorized by the
authorizing physician.
(6) Modifying Drug Therapy.
(A) A pharmacist may be authorized by
protocol to modify a patient's non-controlled substance medication therapy,
subject to the following:
1. If the
pharmacist modifies medication therapy and a medication or device is to be
dispensed, the pharmacist shall create a prescription for the medication or
device modified under the authorizing physician's name. Such prescription may
be dispensed by a licensed pharmacy and shall be maintained in the prescription
records of the dispensing pharmacy as provided by the rules of the Missouri
State Board of Pharmacy; and
2. If
the pharmacist modifies medication therapy or a device, the pharmacist shall
document such modification according to section (7) of this rule. Pharmacists
providing medication therapy services for patients of a health care entity
shall be deemed in compliance with the provisions of this subsection if the
modification is documented in a patient medical record that the health care
entity is required to maintain under state or federal law.
(B) The pharmacist shall not modify any
controlled substance prescription. A prescription from the authorizing
physician shall be required to modify a controlled substance. (C) For purposes
of
20 CSR
2150-5.026 and
20 CSR
2150-5.028, modification of medication therapy 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 or
generic substitutions made pursuant to section
338.056,
RSMo.
(7) Record Keeping.
(A) A pharmacist shall document and maintain
an adequate patient record of medication therapy services provided to each
patient. The records may be maintained in electronic format provided the
records are capable of being printed for review by the Missouri State Board of
Registration for the Healing Arts and the Missouri State Board of Pharmacy. An
adequate and complete patient record shall include documentation of the
following:
1. The identification of the
patient, including, name, birthdate, address, and telephone number;
2. The date(s) of any patient visit or
consultation, including the reason for any such visit/consultation;
3. Any pertinent assessments, observations,
or findings;
4. Any diagnostic
testing recommended or performed;
5. The name of any medication or device
modified and the strength, dose, dosage schedule, dosage form, and route of
administration of any medication modified or administered;
6. Referrals to the authorizing
physician;
7. Referrals for
emergency care;
8. Any contact with
the authorizing physician concerning the patient's treatment or medication
therapy services plan;
9. Any
informed consent for procedures, medications, or devices; and
10. Any consultation with any other treatment
provider for the patient and the results of such consultation.
(B) Pharmacist Record Retention.
Except as otherwise provided herein, records required to be maintained by a
pharmacist pursuant to this rule shall be maintained securely and
confidentially for a minimum of seven (7) years after termination of the
protocol unless more stringent requirements are established for record keeping
under state or federal law. All records required to be maintained by the
pharmacist by this rule shall be maintained by the pharmacist at an address
that shall be identified in the written protocol.
(C) Physician Record Retention. Except as
otherwise provided herein, records required to be maintained by the authorizing
physician pursuant to this rule shall be maintained securely and confidentially
for a minimum of seven (7) years after termination of the protocol unless more
stringent requirements are established for record keeping pursuant to state or
federal law.
(8)
Production of Records. Records maintained at a pharmacy must be produced during
an inspection or investigation by the Missouri State Board of Pharmacy,
Missouri State Board of Registration for the Healing Arts, or their authorized
representatives, as requested by the respective board or the board's designee.
Records not maintained at a pharmacy shall be produced within three (3)
business days after a request from the Missouri State Board of Pharmacy,
Missouri State Board of Registration for the Healing Arts, and/or its
authorized representative. Failure to maintain or produce records as provided
by this rule shall constitute grounds for discipline.
(9) Nothing in this rule shall be construed
to permit medical diagnosis of any condition by a pharmacist or the independent
issuing of a prescription by a pharmacist.
(10) A pharmacist shall not violate or
practice in a manner inconsistent with the provisions of this rule or a written
protocol. A pharmacist's failure to abide by the requirements of this rule or
the provisions of a written protocol shall be subject to disciplinary action
pursuant to the provisions of Chapter 338, RSMo.
(11) The requirements of this rule shall not
apply to the administration of vaccines pursuant to protocol as governed by
20 CSR
2150-5.025 or the administration of medication by
protocol as governed by
20 CSR
2220-6.040.
(12) The Missouri State Board of Registration
for the Healing Arts and the Missouri State Board of Pharmacy separately retain
the right and duty to discipline their respective licensees for violations of
any state or federal statutes, rules, or regulations regardless of the
licensee's participation in a protocol agreement.
(13) 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.
*Original authority: 334.125, RSMo 1959, amended 1993,
1995; 338.010, RSMo 1939, amended 1989, 1990, 2007, 2009, 2011 ; 338.140, RSMo
1939, amended 1981, 1989, 1997, 2011 ; and 338.380, RSMo
2007.