Louisville Medicine Volume 65, Issue 9 | Page 17

REVIEW 4. Patients in long-term care facilities 5. Any period of disaster or mass casualties 6. A single dose to relieve anxiety, pain or discomfort for a diagnostic test or procedure the prescriber is now required to manage the taper: a. In a manner slow enough to minimize symptoms and signs of opioid withdrawal b. In collaboration with other specialists as needed 7. Any Schedule V controlled substance i. To optimize non-opioid pain management and 8. As part of a licensed narcotic treatment program ii. To optimize psychosocial support for anxiety re- lated to the taper 9. Immediately prior to, during, or within the 14 days following a major surgery for no longer than 14 days As a reminder, please note that in all cases (that are not exempt) the initial prescription of a controlled substance still requires doc- umentation of: In a related section of the KBML regulations there is a new dictum regarding two specific scenarios where the physician must stop prescribing: 1. An appropriate medical history and a physical examination A physician shall stop prescribing or dispensing any controlled substance: 2. A KASPER report (REF 4) a. Diverted by or from the patient or 3. A decision (assessment) that a controlled substance is ap- propriate b. Taken less frequently than once a day 4. Instruction that controlled substances for acute pain are for a limited time Another if…then passage in the pain regulations now reads like this: 5. How to safely use and dispose of unused controlled sub- stances ( 4 ) REFERRAL TO ADDICTION MANAGEMENT The physician shall discontinue controlled substance treatment or refer the patient to addiction management if: 6. Long-acting or extended-release opioids are not to be used for acute pain a. There has been no improvement in function and response to the medical complaint and related symptoms, if improve- ment is medically expected (or) The story does not end here. There are more changes to the KBML regulations that have not been so well publicized as the three-day limit, but are no less mandatory. Here are some of these additional regulation changes: b. Controlled substance therapy has produced significant adverse effects, including instances such as an overdose or events leading to hospitalization or disability (or) ( 2 ) NONCOMPLIANT PATIENTS c. The patient exhibits inappropriate drug-seeking behavior or diversion (or)r If and when any information becomes available indicating the patient is noncompliant, the physician now must do at least one of the following: d. The patient is taking a high-risk regimen, such as dosag- es fifty morphine milligram equivalents/day or opioids with benzodiazepines, without evidence of benefit a. Taper and collaborate b. Stop prescribing (or) c. Refer the patient to an addiction specialist, mental health professional, pain management specialist, or drug treatment program Granted, the term “noncompliant” can have a wide range of interpretations. This illustrates one of the problems when objective prescriber actions are made dependent upon such ill-defined and subjective conditions, but these are the regulations we have. Regard- less, it is imperative to document one’s rationale behind choosing any of the three options listed above. ( 3 ) TAPERING Suffice it to say that the information below deserves more elucidation than the brevity of this article allows. Nevertheless, Kentucky physi- cians must now be aware that when tapering a patient’s medications, GUIDELINES VS. STANDARDS OF CARE VS. REGU- LATIONS The most influential guideline in recent years is the 2016 CDC Guideline for Prescribing Opioids for Chronic Pain (REF 5). This guideline is referenced in the first paragraph of Kentucky’s updated regulations: … to establish mandatory prescribing and dispensing standards related to controlled substances, and in accordance with the Centers for Disease Control and Prevention (CDC) guidelines, to establish a prohibition on a practitioner issuing a prescription for a Schedule II controlled substance for more than a three (3) day supply if intended to treat pain as an acute medical condition, unless an exception applies. As regulatory agencies, such as the KBML, continue looking to (continued on page 16) FEBRUARY 2018 15