SCG1 Evaluation of High Risk Pain Medications for MME

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2018 SCG Health QCDR Measure Specifications 1 SCG1 Evaluation of High Risk Pain Medications for MME Percentage of patients aged 18 years and older prescribed and actively taking one or more high risk pain medications and evaluated for clinical appropriateness of morphine milligram equivalents (MME) 2018 OPTIONS F INDIVIDUAL MEASURES: SCG Health, US Wound Registry NATIONAL QUALITY STRATEGY DOMAIN: Patient Safety MEASURE TYPE: Intermediate Outcome INSTRUCTIONS: This measure is to be reported at each denominator eligible visit during the 12 month performance period for patients prescribed a high risk pain medication. An accurate and complete medication list must be on file for each of the encounter date(s) of service. This measure may be reported by eligible clinicians who perform the quality actions described in the measure based on the services provided and the measure-specific denominator coding. DENOMINAT: Denominator Criteria (Eligible Cases): Patients 18 age and older on date of encounter AND All eligible instances when MIPS measure #130 (NQF 0419): Documentation of Current Medications is reported the same encounter AND Patient encounter during the performance period (CPT): 90791, 90792, 92002, 92004, 92012, 92014, 96116, 96118, 96150, 96151, 97532, 99201, 99202, 99203, 99204, 99205, 99212, 99213, 99214, 99215, D7140, D7210, G0101, G0402, G0438, G0439 WITHOUT Telehealth Modifier: GQ, GT NUMERAT: Percentage of patients prescribed and actively taking one or more high risk pain medications Numerator Instructions: The eligible clinician must document in the medical record they obtained, updated, or reviewed a medication list on the date of the encounter. Eligible clinicians reporting this measure may document medication information received from the patient, authorized representative(s), caregiver(s) or other available healthcare resources. The MME must be documented in the medical record. Definition: Accurate and complete medication list List of current medications using all immediate resources available on the date of the encounter. This list must include ALL known prescriptions, over-thecounters, herbals, and vitamin/mineral/dietary (nutritional) supplements AND must contain the medications name, dosage, frequency and route of administration. MIPS measure #130 (NQF #0419) must be on file for the encounter to be eligible.

2018 SCG Health QCDR Measure Specifications 2 High risk pain medications Patients prescribed certain high risk pain medications including: Opiates: buprenorphine (Butrans not Suboxone), codeine, fentanyl, hydrocodone, hydromorphone, methadone, morphine, oxycodone, oxymorphone, tapentadol, tramadol Benzodiazepines: alprazolam, diazepam, clonazepam, lorazepam Anti-spastics: baclofen, carisoprodol, cyclobenzaprine, metaxolone, methocarbamol, tizanidine NSAIDs: ibuprofen, indomethacin, ketorolac, meloxicam, naproxen Excluded: Transdermal lidocaine Morphine milligram equivalents (MME) Also called morphine equivalent daily dose, the conversion factors identified below were developed by the Centers for Disease Control and Prevention in May 2014. MME can be calculated using: MME = Drug Strength x Drug Quantity x MME Conversion Factor Days Supply SOURCE: Centers for Disease Control and Prevention, Atlanta, GA, May 2014. OPIOID (doses in mg/day except where noted) CONVERSION FACT Buprenorphine patch 12.6 Buprenorphine tab or film 10 Butorphanol 7 Codeine 0.15 Dihydrocodeine 0.25 Fentanyl buccal or SL tablets, or lozenge/troche 0.13 Fentanyl film or oral spray 0.18 Fentanyl nasal spray 0.16 Fentanyl patch 7.2 Fentanyl transdermal (in mcg/hr) 2.4 Hydrocodone 1 Hydromorphone 4 Levorphanol tartrate 11 Meperidine hydrochloride 0.1 Methadone * 1-20 mg/day 4 21-40 mg/day 8 41-60 mg/day 10 61-80 mg/day 12 Morphine 1 Oxycodone 1.5 Oxymorphone 3 Pentazocine 0.37 Tapentadol 0.4 Tramadol 0.1 * Methadone: the conversion factor increases at higher doses Fentanyl: dosed in mcg/hr instead of mg/day, and absorption is affected by heat and other factors The MME conversion factor for buprenorphine patches is based on the assumption that one milligram of parenteral buprenorphine is equivalent to 75 milligrams of oral morphine and that one patch delivers the dispensed micrograms per hour over a 24 hour day. Example: 5 ug/hr buprenorphine patch * 24 hrs = 120 ug/day buprenorphine = 0.12 mg/day buprenorphine = 9 mg/day oral morphine milligram equivalent. In other

2018 SCG Health QCDR Measure Specifications 3 words, the conversion factor not accounting for days of use would be 9/5 or 1.8. However, since the buprenorphine patch remains in place for 7 days, we have multiplied the conversion factor by 7 (1.8 X 7 = 12.6). In this example, MME/day for four 5 μg/hr buprenorphine patches dispensed for use over 28 days would work out as follows: Example: 5 ug/hr buprenorphine patch * (4 patches/28 days)* 12.6 = 9 MME/day. The MME conversion factor for fentanyl buccal tablets, sublingual tablets, and lozenges/troche is 0.13. This conversion factor should be multiplied by the number of micrograms in a given lozenge/troche. " The MME conversion factor for fentanyl film and oral spray is 0.18. This reflects a 40% greater bioavailability for films compared to lozenges/tablets and 38% greater bioavailability for oral sprays compared to lozenges/tablets. The MME conversion factor for fentanyl nasal spray is 0.16, which reflects a 20% greater bioavailability for sprays compared to lozenges/tablets. The MME conversion factor for fentanyl patches is based on the assumption that one milligram of parenteral fentanyl is equivalent to 100 milligrams of oral morphine and that one patch delivers the dispensed micrograms per hour over a 24 hour day. Example: 25 ug/hr fentanyl patch * 24 hrs = 600 ug/day fentanyl = 60 mg/day oral morphine milligram equivalent. In other words, the conversion factor not accounting for days of use would be 60/25 or 2.4. However, since the fentanyl patch remains in place for 3 days, we have multiplied the conversion factor by 3 (2.4 X 3 = 7.2). In this example, MME/day for ten 25 μg/hr fentanyl patches dispensed for use over 30 days would work out as follows: Example: 25 ug/hr fentanyl patch * (10 patches/30 days)* 7.2 = 60 MME/day. Numerator Options: AND Performance Met 2: Performance Exclusion: Performance Not Met: current pharmacologic treatment regimen less than 20 MME per day current pharmacologic treatment regimen greater than or equal to 20 MME and less than 50 MME per day current pharmacologic treatment regimen greater than or equal to 26 MME and less than 50 MME per day current pharmacologic treatment regimen less than or equal to 50 MME and less than 90 MME per day current pharmacologic treatment regimen greater than or equal to 90 MME per day Patient not prescribed an opioid and a benzodiazepine Patient not prescribed a high risk pain medication. Patient not evaluated for the MME of their current high risk pain medication pharmacologic treatment regimen, reason not given WHAT DATA SOURCES ARE USED F THE MEASURE? Administrative clinical data, Claims, Paper medical record, Prescription Drug Event Data Elements, Record review, Other

2018 SCG Health QCDR Measure Specifications 4 health information exchanges and Surescript pharmacy feeds STEWARD: SCG Health # OF PERFMANCE RATES TO BE SUBMITTED IN THE XML: 1 Indicate an Overall Performance Rate if more than 1 performance rate is to be submitted: NA INVERSE MEASURE: No PROPTION MEASURE SCING CONTINUOUS MEASURE SCING RISK ADJUSTED: Yes, by age, chronic conditions such as OA and hospice admission RATIONALE: The Institute of Medicine in their Relieving Pain in America: A Blueprint for Transforming Prevention, Care, Education and Research (2011) estimated that the yearly economic cost of chronic pain in the United States is $560-635 billion. Yet, the U.S. is facing an opioid crisis. A 2010 trend study estimates that 20 percent of patients presenting to physician offices with noncancer pain-related diagnoses (including acute and chronic pain) or pain symptoms receive an opioid prescription (Daubresse et al. 2013). These prescriptions have flooded the American market so much so that every American adult could have a bottle of opiates, with 259 million opioid prescriptions written in 2012 (Paulozzi et al. 2014). Prescribing rates are increasing. Between 2007 and 2012 opioid prescriptions per capita increased 7.3 percent (Levy et al. 2015). Like other aspects of healthcare, there is significant prescribing variation across the country demonstrating the lack of consensus and/or education on how to appropriately prescribe and control opioid pain medication (Paulozzi et al. 2014). The estimated annual direct and indirect cost for the abuse, dependence and misuse of prescription opioids to the United States is $55.1 billion (Hansen et al. 2011), with the broader category of abuse, dependence and misuse of opioids estimated at $55.7 billion (Birnbaum et al. 2011). An additional $20.4 billion is spent on the direct and indirect costs for opioid-related overdose (Inocencio et al. 2013). Patients with chronic illnesses, including chronic pain, are increasingly being treated in the outpatient setting and require careful monitoring of multiple medications (Nassaralla et al. 2007). In the outpatient setting, opioid prescriptions were estimated at $9.0 billion in total expenses in 2012 which is a 120 percent increase from a decade before (Stagnitti 2015) Low dosages (20-50 MME per day) increase risk for opioid overdose with higher MME significantly increasing the patient risk of death. Higher MME have not been shown effective for long-term pain reduction (Dowell 2016). CLINICAL RECOMMENDATION STATEMENTS: This measure is based upon recommendations from Centers for Disease Control and Prevention Guideline for Prescribing Opioids for Chronic Pain United States, 2016 (Dowell, et al. 2016).

2018 SCG Health QCDR Measure Specifications 5 WKS CITED: Birnbaum HG, White AG, Schiller M, Waldman T, Cleveland JM, Roland CL. Societal costs of prescription opioid abuse, dependence, and misuse in the United States. Pain Med 2011;12:657 67. Daubresse M, Chang HY, Yu Y, et al. Ambulatory diagnosis and treatment of nonmalignant pain in the United States, 2000-2010. Med Care 2013;51:870 8. Dowell, D., Haegerich, T.M., Chou, R. CDC Guideline for Prescribing Opioids for Chronic Pain United States, 18 March 2016. Hansen RN, Oster G, Edelsberg J, Woody GE, Sullivan SD. Economic costs of nonmedical use of prescription opioids. Clin J Pain 2011;27:194 202 Inocencio TJ, Carroll NV, Read EJ, Holdford DA. The economic burden of opioid-related poisoning in the United States. Pain Med 2013;14:1534 47. Institute of Medicine. Relieving Pain in America: A Blueprint for Transforming Prevention, Care, Education and Research. Washington: The National Academies Press; 2011. Levy B, Paulozzi L, Mack KA, Jones CM. Trends in opioid analgesic-prescribing rates by specialty, U.S., 2007 2012. Am J Prev Med 2015;49:409 13 Nassaralla CL, Naessens JM, Hunt VL, et al. Medication reconciliation in ambulatory care: attempts at improvement. Qual Saf Health Care. 2009;18:402-407. Paulozzi LJ, Mack KA, Hockenberry JM. Vital signs: variation among states in prescribing of opioid pain relievers and benzodiazepines United States, 2012. MMWR Morb Mortal Wkly Rep 2014;63:563 8. Stagnitti MN. Trends in prescribed outpatient opioid use and expenses in the U.S. civilian noninstitutionalized population, 2002 2012. Statistical Brief No. 478. Agency for Healthcare Research and Quality; 2015. COPYRIGHT: The Measures are not clinical guidelines, do not establish a standard of medical care, and have not been tested for all potential applications. SCG Health encourages use of the Measures by other health care professionals, where appropriate. Limited proprietary coding is contained in the measure specifications for convenience. Users of the proprietary coding sets should obtain all necessary licenses from the owners of these code sets. SCG Health disclaims all liability for use or accuracy of any Current Procedural Terminology (CPT ) or other coding contained in the specifications. This measure is in continuous development by SCG Health, LLC. The Measures, while copyrighted, can be reproduced and distributed, without modification, for noncommercial purposes (e.g., use by health care providers in connection with their practices). Commercial use is defined as the sale, license, or distribution of the Measures for commercial gain, or

2018 SCG Health QCDR Measure Specifications 6 incorporation of the Measures into a product or service that is sold, licensed or distributed for commercial gain. Commercial uses of the Measures require a license agreement between the user and SCG Health. SCG Health shall not be responsible for the implementation of the Measures. CPT contained in the Measures specifications is copyright 2004-2018 American Medical Association. All Rights Reserved. THE MEASURES AND SPECIFICATIONS ARE PROVIDED AS IS WITHOUT WARRANTY OF ANY KIND.