New Mexico Register / Volume XXVIII, Issue 17 / September 12, 2017
This is an amendment to 16.12.9 NMAC, Sections 7, 8, 9 and 10, effective 9/12/2017.
A. “Acute Pain” means the normal, predicted physiological response to a noxious chemical or thermal or mechanical stimulus, typically associated with invasive procedures, trauma or disease and generally time limited.
B. “Addiction” is a neurobehavioral syndrome with genetic and environmental influences that results in psychological dependence on the use of substances for their psychic effects. It is characterized by behaviors that include one or more of the following: impaired control over drug use; compulsive use; continued use despite harm; and craving. Physical dependence and tolerance are normal physiological consequences of extended opioid therapy for pain and should not by themselves be considered addiction.
C. “Chronic pain” means pain that persists after reasonable efforts have been made to relieve the pain or its cause and that continues, either continuously or episodically, for longer than three consecutive months. “Chronic pain” does not, for the purpose of the Pain Relief Act requirements, include pain associated with a terminal condition or with a progressive disease that, in the normal course of progression, may reasonably be expected to result in a terminal condition.
D. “Clinical expert” means a person who, by reason of specialized education or substantial relevant experience in pain management, has knowledge regarding current standards, practices and guidelines.
E. “Drug abuser” means a person who takes a drug or drugs for other than legitimate medical purposes.
F. “Nursing Facility” means a long term care facility in which the patient is a current fulltime resident and whose medications are solely administered and managed by the facility.
F.] G. “Pain”
means an unpleasant sensory and emotional experience associated with
inflammation or with actual or potential tissue damage, or described in terms
of such inflammation and damage, which could include acute, persistent or
G.] H. “Physical
dependence” means a state of adaptation that is manifested by a
drug-specific withdrawal syndrome that can be produced by abrupt cessation,
rapid dose reduction, decreasing blood level of the drug, administration of an
antagonist, or a combination of these.
H.] I. “Prescription
monitoring program (PMP)” means a centralized system to collect, monitor,
and analyze electronically, for controlled substances, prescribing and
dispensing data submitted by pharmacies and dispensing practitioners. The data
are used to support efforts in education, research, enforcement and abuse
I.] J. “Therapeutic
purpose” means the use of pharmaceutical and non-pharmaceutical treatments
and the spectrum of available modalities that conforms substantially to
accepted guidelines for pain management.
J.] K. “Tolerance”
means a state of adaptation in which exposure to a drug induces changes that
result in a diminution of one or more of the drug’s effects over time.
[18.104.22.168 NMAC - N, 2/17/2006; A, 11/20/2012; A, 9/12/2017]
22.214.171.124 RULES: The following rules shall be used
by the board to determine whether [
health care practitioner’s] an
advanced practice nurse’s prescriptive practices are consistent with the
appropriate treatment of pain.
A. The treatment of pain with various medicines or controlled substances is a legitimate nursing practice when accomplished in the usual course of professional practice. It does not preclude treatment of patients with addiction, physical dependence or tolerance who have legitimate pain. However, such patients do require very close monitoring and precise documentation.
B. Pain management
for patients [
with substance use disorders] should include a contractual
agreement, the use of drug screens prior to treatment with opiates and during
the course of treatment to identify actual drugs being consumed and to compare
with patients self-reports. If concerns
about misuse are identified, the patient will be referred for appropriate
consultation, and scheduled for re-evaluation at appropriate time intervals.
C. The prescribing, ordering, administering or dispensing of controlled substances to meet the individual needs of the patient for management of chronic pain is appropriate if prescribed, ordered, administered or dispensed in compliance with the following.
practitioner] An advanced practice nurse
shall complete a history and physical examination and include an evaluation
of the patient’s psychological and pain status. The medical history shall include any previous
history of significant pain, past history of alternate treatments for pain,
potential for substances abuse, coexisting disease or medical conditions, and
the presence of a medical indication and supporting diagnostic documentation
or contra-indication against the use of controlled substances.
practitioner] An advanced practice nurse shall be familiar with and
employ screening tools, as well as the spectrum of available modalities for
therapeutic purposes, in the evaluation and management of pain. They shall consider an integrative approach to
pain management specialists including but not limited to an acupuncturist,
chiropractor, doctor of oriental medicine, exercise
physiologist, massage therapist, pharmacist, physical therapist, psychiatrist,
psychologist or other advanced practice registered nurse.
(3) A written treatment plan shall be developed and tailored to the individual needs of the patient, taking age, gender, culture, and ethnicity into consideration, with stated objectives by which treatment can be evaluated, e.g. by degree of pain relief, improved physical and psychological function, or other accepted measure. Such a plan should include a statement of the need for further testing, consultation, referral or use of other treatment modalities.
(4) If the patient’s pain relief plateaus on controlled substance analgesic(s), then the treatment plan should include an evaluation of continuing or tapering the controlled substance therapy.
(4)] (5) The practitioner shall provide education
and discuss the risks and benefits of using controlled substances with the patient or surrogate or
guardian, and shall document this in the record.
(5)] (6) Complete and
accurate records of care provided and drugs prescribed shall be maintained. When controlled substances are prescribed, the
name of the drug, quantity, and prescribed dosage [ and number of
refills authorized] should be recorded. Prescriptions for opioids shall include
indications for use. For chronic non-cancer
pain patients treated with controlled substance analgesic(s), the prescribing
practitioner shall use a written agreement for treatment with the patient
outlining patient responsibilities. As
part of a written agreement, chronic non-cancer pain patients shall receive all
chronic pain management prescriptions from one practitioner and one pharmacy
(6)] (7) The management of patients needing chronic pain control
requires monitoring by the attending or the consulting practitioner. The practitioner shall periodically review the
course of treatment for chronic non-cancer pain, the patient’s state of health,
and any new information about the etiology of the chronic non-cancer pain at
least every [ six] three months. In addition, a practitioner should consult,
when indicated by the patient’s condition, with health care professionals who
are experienced (by the length and type of their practice) in the area of
chronic pain control; such professionals need not be those who specialize in
pain control. Consultation should occur
early in the course of long-term treatment, and at
reasonable intervals during continued long-term treatment for assessment of
benefit and need [ at least every six months]. Drug screening is [ recommended]
expected and should be conducted when other factors suggest an elevated
risk of misuse or diversion.
(7)] (8) If, in a practitioner’s
opinion, a patient is seeking pain medication for reasons that are not
medically justified, the practitioner is not required
to prescribe controlled substances for the patient.
D. The board will
evaluate the quality of care on the following basis: appropriate diagnosis and
evaluation; appropriate [
medial] medical indication for the
treatment prescribed; documented change or persistence of the recognized
medical indication; and, follow-up evaluation with appropriate continuity of
care. The board will judge the validity of prescribing based on the [ practitioner’s]
advanced practice nurse’s treatment of the patient and on available
documentation, rather than on the quantity and chronicity of prescribing. The goal is to control the patient’s pain for
its duration while effectively addressing other aspects of the patient’s
functioning, including physical, psychological, social, and work-related
E. The board will review both over-prescription and under-prescription of pain medications using the same standard of patient protection as a guiding principle.
An advanced practice nurse who appropriately prescribes controlled
substances and who follows this section would be considered to be in compliance
with this rule and not be subject to discipline by the board, unless there is
some violation of the Nursing Practice Act, board rules and Pain Relief Act
(24-2 D, 1 to 24-2 D, 6 NMSA 1978).
[126.96.36.199 NMAC - N, 2/17/2006, A, 11/20/2012; A, 9/12/2017]
MONITORING PROGRAM (PMP) REQUIREMENTS: The intent of the [
NM] New Mexico
board of nursing in requiring participation in the PMP is to assist [ practitioners]
advanced practice nurses in balancing [ the promotion of] the
safe use of controlled substances [ for the provision of nursing care and
services] with the need to [ impede illegal and harmful] impede
harmful and illegal activities involving these pharmaceuticals.
care provider who holds a federal drug enforcement administration registration
and licensure to prescribe opioids shall register with the board of pharmacy to
become a regular participant in PMP inquiry and reporting]. Any advanced practice nurse who holds a
federal drug enforcement administration registration and a New Mexico
controlled substance registration shall register with the board of pharmacy to
become a regular participant in PMP inquiry and reporting.
prescribing, ordering, administering or dispensing a controlled substance, the
practitioner shall obtain and review a prescription monitoring report covering
at least a one year time period or another state’s report, where applicable and
available. The practitioner shall be aware of a person currently: (1) receiving opiates from multiple prescribers; (2) receiving opiates for more than twelve consecutive weeks; (3) receiving more than one controlled substance analgesic; (4) receiving a new prescription for any long-acting controlled
substance analgesic formulation, including oral dosage forms and transdermal
(e.g. fentanyl) or methadone; (5) exhibiting
potential for abuse or misuse of opiates (i.e. over-utilization, early refills,
appears overly sedated or intoxicated upon presentation, or an unfamiliar
patient requesting an opiate by specific name, street name, color, or
identifying marks, or paying cash when the patient has prescription insurance)] An advanced practice nurse
may authorize delegate(s) to access the prescription monitoring report
consistent with board of pharmacy regulation 16.19.29 NMAC. While an advanced practice nurse’s delegate
may obtain a report from the state’s prescription monitoring program, the advanced
practice nurse is solely responsible for reviewing the prescription monitoring
report and documenting the receipt and review of a report in the patient’s
recognizing any of the above, the practitioner, using professional judgment,
shall take appropriate steps to avoid or resolve the potential problem. These steps may include requesting and
reviewing additional controlled substance prescription monitoring reports or
another state’s report if applicable and available, or consulting with a pain
management specialist or addiction treatment specialist or counseling the
patient, which may include termination of treatment. The practitioner shall document steps taken to
resolve the potential problem, which may include termination from treatment.]
Before an advanced practice nurse prescribes or dispenses for the first
time, a controlled substance in Schedule II, III, IV or V to a patient for a
period greater than four days, or if there is a gap in prescribing the
controlled substance for 30 days or more, the practitioner shall review a
prescription monitoring report for the patient for the preceding 12
months. When available, the practitioner
shall review similar reports from adjacent states. The practitioner shall document the receipt
and review of such reports in the patient’s medical record.
an initial prescription monitoring report on a patient, the practitioner shall
use professional judgment based on prevailing standards of practice in deciding
the frequency of requesting and reviewing further prescription monitoring
reports or other state’s report on that patient. Prescription monitoring
reports shall be requested and reviewed a minimum of once every six months
during the continuous use of opioids for each established patient. The
practitioner shall document the review of these reports] A prescription
monitoring report shall be reviewed a minimum of once every three months during
the continuous use of a controlled substance in schedule II, III, IV or V for
each patient. The practitioner shall
document the review of these reports in the patient’s medical record. Nothing in this section shall be construed as
preventing an advanced practice nurse from reviewing prescription monitoring
reports with greater frequency than that required by this section.
E. An advanced practice nurse does not have to obtain and review a prescription monitoring report before prescribing, ordering, or dispensing a controlled substance in schedule II, III, IV or V:
(1) for a period of four days or less; or
(2) to a patient in a nursing facility; or
(3) to a patient in hospice care.
F. Upon review of a prescription monitoring report for a patient, the advanced practice nurse shall identify and be aware of a patient currently:
(1) receiving opioids from multiple prescribers;
(2) receiving opioids and benzodiazepines concurrently;
(3) receiving opioids for more than 12 consecutive weeks;
(4) receiving more than one controlled substance analgesic;
(5) receiving opioids totaling more than 90 morphine milligram equivalents per day;
(6) exhibiting potential for abuse or misuse of opioids and other controlled substances, such as over-utilization, requests to fill early, requests for specific opioids, requests to pay cash when insurance is available, receiving opioids from multiple pharmacies.
G. Upon recognizing any of the above conditions described in paragraph F, the practitioner, using professional judgement based on prevailing standards of practice, shall take action as appropriate to prevent, mitigate, or resolve any potential problems or risks that may result in opioid misuse, abuse, or overdose. These steps may involve counseling the patient on known risks and realistic benefits of opioid therapy, prescription and training for naloxone, consultation with or referral to a pain management specialist, or offering or arranging treatment for opioid or substance use disorder. The practitioner shall document actions taken to prevent, mitigate, or resolve the potential problems or risks.
H. Practitioners licensed to practice in an opioid treatment program, as defined in 7.32.8 NMAC, shall review a prescription monitoring report upon a patient’s initial enrollment into the opioid treatment program and every three months thereafter while prescribing, ordering, administering, or dispensing opioid treatment medications in schedule II, III, IV or V for the purpose of treating opioid use disorder. The practitioner shall document the receipt and review of a report in the patient’s medical record.
[188.8.131.52 NMAC - N, 11/20/2012; A, 9/12/2017]
PAIN MANAGEMENT CONTINUING EDUCATION: Any [
health care provider] advanced
practice registered nurse (APRN) with a drug enforcement agency (DEA) registration and licensure that
permits prescribing opioids, shall obtain continuing education on the
management of non-cancer pain. These practitioners shall be required to
obtain five CE of the 15 CE currently required every two years in pharmacology
to include a review of these rules (16.12.9 NMAC) for management of non-cancer
pain, an understanding of the pharmacology and risks of controlled substances,
a basic awareness of the problems of abuse, addiction and diversion, and
awareness of state and federal regulations for the prescription of controlled
[184.108.40.206 NMAC - N, 11/20/2012; A, 9/12/2017]