(2) Methods of treatment.
(A) The methods of treatment and the
authority to administer, dispense, or prescribe drugs delegated in a
collaborative practice arrangement between a collaborating physician and
collaborating assistant physician shall be within the scope of practice of each
professional and shall be consistent with each professional's skill, training,
education, competence, licensure, and/or certification and shall not be further
delegated to any person except that the individuals identified in sections
338.095
and
338.198,
RSMo, may communicate prescription drug orders to a pharmacist.
(B) The collaborating physician shall
consider the level of skill, education, training, and competence of the
collaborating assistant physician and ensure that the delegated
responsibilities contained in the collaborative practice arrangement are
consistent with that level of skill, education, training, and
competence.
(C) Guidelines for
consultation and referral to the collaborating physician or designated health
care facility for services or emergency care that is beyond the education,
training, competence, or scope of practice of the assistant physician shall be
established in the collaborative practice arrangement.
(D) The methods of treatment, including any
authority to administer, dispense, or prescribe drugs, delegated in a
collaborative practice arrangement between a collaborating physician and a
collaborating assistant physician, shall be delivered only pursuant to a
written agreement, jointly agreed-upon protocols, or standing orders that are
specific to the clinical conditions treated by the collaborating physician and
assistant physician.
(E) Methods of
treatment delegated and authority to administer, dispense, or prescribe drugs
shall be subject to the following:
1. The
physician retains the responsibility for ensuring the appropriate
administering, dispensing, prescribing, and control of drugs utilized pursuant
to a collaborative practice arrangement in accordance with all state and
federal statutes, rules, or regulations;
2. All labeling requirements outlined in
section
338.059,
RSMo, shall be followed;
3.
Consumer product safety laws and Class B container standards shall be followed
when packaging drugs for distribution;
4. All drugs shall be stored according to the
United States Pharmacopeia (USP), (2010), published by the United States
Pharmacopeial Convention, 12601 Twinbrook Parkway, Rockville, Maryland
20852-1790, 800-227-8772;
http://www.usp.org/ recommended conditions,
which is incorporated by reference. This does not include any later amendments
or additions;
5. Outdated drugs
shall be separated from the active inventory;
6. Retrievable dispensing logs shall be
maintained for all prescription drugs dispensed and shall include all
information required by state and federal statutes, rules, or
regulations;
7. All prescriptions
shall conform to all applicable state and federal statutes, rules, or
regulations and shall include the name, address, and telephone number of the
collaborating physician and collaborating assistant physician;
8. In addition to administering and
dispensing controlled substances, an assistant physician, who meets the
requirements of 20 CSR 2150-2.260, may be
delegated the authority to prescribe controlled substances listed in Schedules
II (hydrocodone), III, I V, and V of section
195.017,
RSMo, in a written collaborative practice arrangement, except that, the
collaborative practice arrangement shall not delegate the authority to
administer any controlled substances listed in Schedules II (hydrocodone), III,
I V, and V of section
195.017,
RSMo, for the purpose of inducing sedation or general anesthesia for
therapeutic, diagnostic, or surgical procedures. When issuing the initial
prescription for opioid controlled substance in treating a patient for acute
pain, the assistant physician shall comply with requirements set forth in
section
195.080,
RSMo. Schedule II (hydrocodone) and Schedule III narcotic controlled substance
prescriptions shall be limited to a five- (5-) day supply without refill.
Pursuant to section
334.037,
RSMo an assistant physician may prescribe Schedule III - buprenorphine for up
to a thirty- (30-) day supply without refill for patients receiving
medication-assisted treatment for substance abuse disorders under the direction
of the collaborating physician as described in sections
334.037
and 630.875 RSMo;
9. An assistant physician may not prescribe
controlled substances for his or her own self or family. Family is defined as
spouse, parents, grandparents, great-grandparents, children, grandchildren,
great-grandchildren, brothers and sisters, aunts and uncles, nephews and
nieces, mother-in-law, father-in-law, brothers-in-law, sisters-in-law,
daughters-in-law, and sons-in-law. Adopted and step family members are also
included in family;
10. An
assistant physician in a collaborative practice arrangement may only dispense
starter doses of medication to cover a period of time for seventy-two (72)
hours or less with the exception of Title X family planning providers or
publicly funded clinics in community health settings that dispense medications
free of charge. The dispensing of drug samples, as defined in
21
U.S.C. section 353(c)(1), is
permitted as appropriate to complete drug therapy;
11. The collaborative practice arrangement
shall clearly identify the controlled substances the collaborating physician
authorizes the assistant physician to prescribe and document that it is
consistent with each professional's education, knowledge, skill, and
competence; and
12. The medications
to be administered, dispensed, or prescribed by a collaborating assistant
physician in a collaborative practice arrangement shall be consistent with the
education, training, competence, and scopes of practice of the collaborating
physician and collaborating assistant physician.
(F) When a collaborative practice arrangement
is utilized to provide health care services for conditions other than acute
self-limited or well-defined problems, the collaborating physician, or other
physician designated in the collaborative practice arrangement, shall examine
and evaluate the patient and approve or formulate the plan of treatment for new
or significantly changed conditions as soon as is practical, but in no case
more than two (2) weeks after the patient has been seen by the collaborating
assistant physician. If the assistant physician is utilizing telehealth in
providing services, the collaborating physician, or other physician designated
in the collaborative practice arrangement may conduct the examination and
evaluation required by this section via live, interactive video or in person.
Telehealth providers shall obtain the patient's or the patient's guardian's
consent before telehealth services are initiated and shall document the
patient's or the patient's guardian's consent in the patient's file or chart.
All telehealth activities must comply with the requirements of the Health
Insurance Portability and Accountability Act of 1996, as amended, and all other
applicable state and federal laws and regulations.