the impact of opioid risk reduction initiatives on...

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The Impact of Opioid Risk Reduction Initiatives on High-Dose Opioid Prescribing for Patients on Chronic Opioid Therapy Michael Von Korff,* Sascha Dublin,* ,y Rod L. Walker,* Michael Parchman,* Susan M. Shortreed,* ,z Ryan N. Hansen, x and Kathleen Saunders* *Group Health Research Institute, Seattle, Washington. y Department of Epidemiology, z Department of Biostatistics, and x School of Pharmacy, University of Washington, Seattle, Washington. Abstract: Avoiding high opioid doses may reduce chronic opioid therapy (COT) risks, but the feasi- bility of reducing opioid doses in community practice is unknown. Washington State and a health plan’s group practice implemented initiatives to reduce high-dose COT prescribing. The group practice physi- cians were exposed to both initiatives, whereas contracted physicians were exposed only to statewide changes. Using interrupted time series analyses, we assessed whether these initiatives reduced opioid doses among COT patients in group practice (n = 16,653) and contracted care settings (n = 5,552). From 2006 to June 2014, the percentage of COT patients receiving $120 mg morphine equivalent dose declined from 16.8% to 6.3% in the group practice versus 20.6 to 13.6% among COT patients of con- tracted physicians. The proportion receiving excess opioid days supplied declined from 24.0 to 10.4% among group practice COT patients and from 20.1 to 14.7% among COT patients of contracted physi- cians. Reductions in prescribing of high opioid dose and excess opioid days supplied followed state and health plan initiatives to change opioid prescribing. Reductions were substantially greater in the group practice setting that implemented additional initiatives to alter shared physician expectations regarding appropriate COT prescribing, compared with the contracted physicians’ patients. Perspective: Washington State and a health plan’s group practice implemented initiatives to reduce high-dose COT prescribing. Group practice physicians were exposed to both initiatives, whereas the health plan’s contracted physicians were exposed to only the statewide changes. Reductions in pre- scribing of high opioid dose, average daily dose, and excess opioid days supplied followed state and health plan initiatives to change opioid prescribing. Reductions were substantially greater in the group practice setting that implemented additional initiatives to alter shared physician expectations regarding appropriate COT prescribing, compared with the contracted physicians’ patients. ª 2016 by the American Pain Society Key words: Opioids, chronic pain, practice change. I ncreased prescribing of opioids for chronic pain has been accompanied by large increases in drug overdose and addiction involving prescription opioids. 3,4,14,18 In 2011, the federal government called for action to decrease prescription drug misuse. 13 There is growing ev- idence that the risks of opioid overdose and addiction among patients on chronic opioid therapy (COT) increase with opioid dose. 2 Avoiding COT at higher doses might reduce the risks of COT. A Washington State guideline, initially published in 2007 and enacted into state law in 2010, recommended caution in prescribing COT at higher doses, defined as a daily morphine equivalent dose (MED) of 120 mg or greater. 24 Under this guideline, fewer recipients of worker’s disability compensation received high doses of opioids and there was a subsequent decline in the num- ber of opioid-related deaths in this patient popula- tion. 7,9 However, it is not known whether statewide guidance produced widespread changes in opioid dose levels among COT patients in community practice. Received May 28, 2015; Revised September 24, 2015; Accepted October 6, 2015. This research was supported by grants from Pfizer, the Patient-Centered Outcomes Research Institute (R-IHS-1306-02198, Von Korff), and the Na- tional Institute on Aging (AG034181, Von Korff, Principal Investigator). M.V.K. is the Principal Investigator of grants to GHRI from Pfizer Inc that concern opioids. These grants also support work on this project by S.M.S., K.S., and R.L.W. S.M.S. has received funding from research grants awarded to GHRI by Bristol-Myers Squibb and Pfizer Inc. K.S. owns stock in Merck. The remaining authors report no conflicts. Address reprint requests to Michael Von Korff, ScD, Group Health Research Institute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101. E-mail: [email protected] 1526-5900/$36.00 ª 2016 by the American Pain Society http://dx.doi.org/10.1016/j.jpain.2015.10.002 101 The Journal of Pain, Vol 17, No 1 (January), 2016: pp 101-110 Available online at www.jpain.org and www.sciencedirect.com

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Page 1: The Impact of Opioid Risk Reduction Initiatives on …alabamaoti.org/wp-content/uploads/2019/08/The-Impact-of...The Impact of Opioid Risk Reduction Initiatives on High-Dose Opioid

I

The Journal of Pain, Vol 17, No 1 (January), 2016: pp 101-110Available online at www.jpain.org and www.sciencedirect.com

The Impact of Opioid Risk Reduction Initiatives on High-Dose

Opioid Prescribing for Patients on Chronic Opioid Therapy

Michael Von Korff,* Sascha Dublin,*,y Rod L. Walker,* Michael Parchman,*Susan M. Shortreed,*,z Ryan N. Hansen,x and Kathleen Saunders**Group Health Research Institute, Seattle, Washington.yDepartment of Epidemiology, zDepartment of Biostatistics, and xSchool of Pharmacy, University of Washington,Seattle, Washington.

Received2015.This reseOutcometional InM.V.K. isconcern oK.S., andawardedin MerckThe remaAddressResearchE-mail: v

1526-590

ª 2016 b

http://dx

Abstract: Avoiding high opioid doses may reduce chronic opioid therapy (COT) risks, but the feasi-

bility of reducing opioid doses in community practice is unknown. Washington State and a health plan’s

group practice implemented initiatives to reduce high-dose COT prescribing. The group practice physi-

cians were exposed to both initiatives, whereas contracted physicians were exposed only to statewide

changes. Using interrupted time series analyses, we assessed whether these initiatives reduced opioid

doses among COT patients in group practice (n = 16,653) and contracted care settings (n = 5,552). From

2006 to June 2014, the percentage of COT patients receiving $120 mg morphine equivalent dose

declined from 16.8% to 6.3% in the group practice versus 20.6 to 13.6% among COT patients of con-

tracted physicians. The proportion receiving excess opioid days supplied declined from 24.0 to 10.4%

among group practice COT patients and from 20.1 to 14.7% among COT patients of contracted physi-

cians. Reductions in prescribing of high opioid dose and excess opioid days supplied followed state and

health plan initiatives to change opioid prescribing. Reductions were substantially greater in the group

practice setting that implemented additional initiatives to alter shared physician expectations

regarding appropriate COT prescribing, compared with the contracted physicians’ patients.

Perspective: Washington State and a health plan’s group practice implemented initiatives to reduce

high-dose COT prescribing. Group practice physicians were exposed to both initiatives, whereas the

health plan’s contracted physicians were exposed to only the statewide changes. Reductions in pre-

scribing of high opioid dose, average daily dose, and excess opioid days supplied followed state

and health plan initiatives to change opioid prescribing. Reductions were substantially greater in the

group practice setting that implemented additional initiatives to alter shared physician expectations

regarding appropriate COT prescribing, compared with the contracted physicians’ patients.

ª 2016 by the American Pain Society

Key words: Opioids, chronic pain, practice change.

ncreased prescribing of opioids for chronic pain hasbeen accompanied by large increases in drug overdoseand addiction involving prescription opioids.3,4,14,18 In

May 28, 2015; Revised September 24, 2015; AcceptedOctober 6,

arch was supported by grants from Pfizer, the Patient-Centereds Research Institute (R-IHS-1306-02198, Von Korff), and the Na-stitute on Aging (AG034181, Von Korff, Principal Investigator).the Principal Investigator of grants to GHRI from Pfizer Inc thatpioids. These grants also support work on this project by S.M.S.,R.L.W. S.M.S. has received funding from research grants

to GHRI by Bristol-Myers Squibb and Pfizer Inc. K.S. owns stock.ining authors report no conflicts.reprint requests to Michael Von Korff, ScD, Group HealthInstitute, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101.

[email protected]

0/$36.00

y the American Pain Society

.doi.org/10.1016/j.jpain.2015.10.002

2011, the federal government called for action todecrease prescription drugmisuse.13 There is growing ev-idence that the risks of opioid overdose and addictionamongpatients on chronic opioid therapy (COT) increasewith opioid dose.2 Avoiding COT at higher doses mightreduce the risks of COT.A Washington State guideline, initially published in

2007 and enacted into state law in 2010, recommendedcaution in prescribing COT at higher doses, defined as adaily morphine equivalent dose (MED) of 120 mg orgreater.24 Under this guideline, fewer recipients ofworker’s disability compensation received high doses ofopioids and there was a subsequent decline in the num-ber of opioid-related deaths in this patient popula-tion.7,9 However, it is not known whether statewideguidance produced widespread changes in opioid doselevels among COT patients in community practice.

101

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102 The Journal of Pain Opioid Risk Reduction Initiatives

After Washington State published its COT guideline,Group Health Cooperative (a Washington State insur-ance plan and health care delivery system) implementedadditional initiatives in its group practice to alter physi-cian expectations regarding COT prescribing. In contrast,Group Health’s contracted physicians, who provide careoutside of the group practice setting, were exposed tostatewide COT guideline changes, but not to these addi-tional group practice initiatives.Davidoff5 observes that, ‘‘Once established, clinical

practices can be extraordinarily hard to abandon if sub-sequent evidence and experience find them to beineffective, disruptive, or the cause of net-harm’’. Biller-Andorno and Lee1 propose that the shared purposearising from focusing attention on goals broadlyaccepted within a health care organization can changephysician practices. Relative to adoption ofmedical inno-vations, changing clinical practices deemed ineffective orunsafe have rarely been studied.5,10 This article comparesthe rates of high opioid doses among COT patients afterchanges in guidance regarding COT, undertakenstatewide and within a health plan. We compareopioid prescribing trends in a group practice settingthat sought to alter shared physician expectations andpractices for COT patients with trends among the samehealth plan’s contracted physicians, who were exposedto the new statewide guideline but not the addedgroup practice initiatives. We assess whether thesechanges reduced the average daily opioid dosereceived by COT patients, and whether the changesreduced the percentage of COT patients receiving high-dose COT or excess days supplied of opioids.We hypothesized that starting in 2008, after efforts to

alter prescribing expectations of primary care physicians,the rate of reduction in average daily opioid dose and inthe percentage of COT patients receiving high opioiddoses would be greater in the group practice settingrelative to trends among contracted physicians whowere exposed only to the Washington State guidelineand legislation. We also hypothesized that any observedreduction in opioid dose would be accompanied by areduction in the percentage of COT patients receivingexcess opioid days supplied. Our evaluation also assessedwhether a multi-faceted opioid risk reduction initiativeimplemented later in 2010 in the group practice furtherinfluenced prescribing of higher opioid doses beyondany prescribing changes achieved through efforts toalter shared expectations of physicians regarding appro-priate opioid prescribing.

Methods

SettingGroup Health Cooperative16 is a large insurance plan

and care delivery system in Washington State with bothgroup practice and contracted care settings. Providersin the group practice deliver care at Group Health’sown facilities to about two-thirds of the plan’s enrollees.The remaining enrollees make up Group Health’s con-tracted care setting. They receive care from community

physicians in diverse clinical settings not operated byGroup Health. There was a substantially greater poten-tial for Group Health Cooperative to change COT pre-scribing expectations and practices in the grouppractice than in the contracted care setting.

Opioid Risk Reduction Initiatives in theGroup PracticeThe state first published its COT guideline in April

2007. In 2010, Washington State enacted legislationmandating use of the guideline for long-term opioidprescribing for chronic non-cancer pain, explicitlyexcluding hospice care, end of life and palliative care,and management of acute pain after injury or surgery.In conformity with the guideline, prescribers wererequired to conduct a physical examination and checkmedical records to assess the appropriateness of paintreatment, and to screen for risk of drug abuse and diver-sion. For high-risk patients, the guideline recommendeddeveloping a treatment plan and advised use of awrittenagreement outlining patient responsibilities includingurine drug screening. The guideline called for periodicpatient monitoring at least every 6 months, unless thepatient was on a stable dose of less than 40 mg MED inwhich case annual review was sufficient. Periodic reviewwas intended to assess compliance with the treatmentplan and assess the patient’s condition. Physicians pre-scribing long-acting opioids or methadone wererequired to complete at least 4 hours of relevantcontinuing medical education. Of particular relevanceto this research, physicians prescribing an average dailydose of 120 mg or greater MED were asked to consultwith a pain specialist (through a patient visit, remoteevaluation of the patient by the specialist, or a telephoneconsultation between the prescriber and the specialist)unless the patient was on a stable dose and the patient’spain and functional status were also stable. Situations inwhich there was a short-term increase in dose tomanagean exacerbation were exempted.In the second half of 2006 and thereafter, Group

Health’s group practice sought to change shared expec-tations regarding COT prescribing in primary care. Pri-mary care leadership, together with consultingrehabilitation medicine specialists, encouraged greatercaution in prescribing opioids for chronic pain anddiscouraged dose escalation and use of higher opioiddoses with COT patients.17 Over several years, the medi-cal director of rehabilitation medicine delivered occa-sional voluntary educational presentations aboutmanaging chronic pain and opioid prescribing. Typicallyabout one-fourth of group practice primary care physi-cians (PCPs) attended these presentations. Group Healthestablished a clinical policy making PCPs responsible foroverall opioid management of their COT patients. PCPsand clinic medical directors received lists of their COT pa-tients, which flagged those receiving high opioid doses,defined by the Washington State guideline as 120 mg orgreater MED. Physicians with unusually large numbers ofCOT patients taking high opioid doses received feedbackand supervisory guidance from clinic medical directors.

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Von Korff et al The Journal of Pain 103

These efforts sought to change shared expectations ofprescribers about appropriate management of patientsusing opioids long term.Neither the state guideline and legislation nor the

Group Health initiatives sought to reduce the percent-age of patients receiving COT. Clinical decisions aboutwhether and for how long to prescribe COT for chronicpain were left to physician discretion. Although wereport trends in the percentage of adult patientsreceiving COT in the group practice and contractedcare settings, we do not attempt to evaluate the impactof the interventions on the prevalence of COT in thestudy populations.In September 2010, GroupHealth implemented amulti-

faceted opioid risk reduction initiative in its grouppractice clinics. This initiative included a standard guide-line establishing minimum standards for risk-stratifiedCOTmonitoring (including urine drug testing), documen-tation of standard care plans in the medical recorddescribing the treatment regimen and the PCP respon-sible for COT management, periodic monitoring visits,andmodifications to the prescription refill process to pre-vent urgent refill requests.20 Themulti-faceted opioid riskreduction initiative sought to increase the conformity ofopioid prescribing and management for chronic non-cancer pain with the recently enacted state legislation.To support implementation, the initiative used prac-

tice tools such as patient education materials, a careplan template, and an online calculator for estimatingMED; performance measures tracking the developmentof COTcare plans in the electronic health record; medicalstaff leader advocacy; expert consultation for physiciansin each primary care clinic; and financial incentives forcompleting COT care plans. Medical staff leadershipmandated a 90-minute online continuingmedical educa-tion course about chronic pain management and opi-oids, which 87% of group practice PCPs completed.After taking the course, clinicians in each clinic met fora 1-hour discussion. Previous reports have shown thatthe implementation of the multi-faceted risk reductioninitiative resulted in near universal documentation ofCOT care plans in electronic health records,20 and a dra-matic increase in rates of urine drug screening amongCOT patients21 in the group practice setting.None of these Group Health initiatives were imple-

mented in the health plan’s contracted care settings. Con-tracted physicians providing care to Group Healthenrollees practiced in diverse settings statewide not oper-ated by Group Health, with medical staff leaders not em-ployed by Group Health, and not using Group Health’selectronic health care records used in implementing theinitiatives. Group Health staff implementing opioid qual-ity improvement initiatives were not able to work withthe contracted physicians to change opioid prescribingandmanagement practices. Typically, Group Healthmem-bers represented a smallminority of the patients cared forby contracted physicians; most of their patients wereinsured by plans other than Group Health. For thesereasons, Group Health’s initial efforts (starting in thesecond half of 2006) to change shared expectationsregarding appropriate opioid prescribing practices and

the multi-faceted opioid risk reduction initiative (begunin late 2010) were not implemented with the contractedcare physicians. Thus, the group practice physicians wereexposed to the Group Health initiatives and the statewideguideline and legislation, whereas the contracted carephysicians were exposed only to the statewide guidelineand legislation. This evaluation is able to describe changesin the contracted care settings that took place as theguideline was disseminated and legislation enacted; theCOT patients in the contracted care settings served as con-trols for evaluating the incremental effects of the moreextensive efforts to change opioid prescribing practicesimplemented in the group practice setting.

Study DesignThis research was approved by the Group Health Insti-

tutional Review Board (IRB). Because participants werenot contacted for this research, and the data analyzedwere from electronic health records, the IRB granted awaiver of individual informed consent.We used interrupted time series analyses8,22 to

compare trends in high-dose opioid prescribing amongCOT patients in the group practice to trends amongCOT patients in the contracted care setting from 2006to mid-2014. Of key interest were 3 time periods corre-sponding to the different phases of opioid risk reductioninitiatives. The baseline time period was January 1, 2006,to December 31, 2007. The initial intervention phase,hereafter referred to as the altered prescribing expecta-tions phase, was from January 1, 2008, to September 30,2010, and included efforts to alter physician expectationsregarding appropriate opioid prescribing through state-wide guideline dissemination alone in the contractedcare setting, and through the augmented educationaland medical staff supervision interventions in the grouppractice setting. The multi-faceted opioid risk reductioninitiative was implemented in the group practice settingstarting in October 2010; therefore, the third phase ofour evaluation, the multi-faceted initiative phase, spansthe period from October 1, 2010, to June 30, 2014.Within each phase, we examined COT prescribing pat-terns on a quarterly basis.We used 2006 to 2007 as a baseline for comparison

because, although the Washington State guidelineswere disseminated in April 2007, group practice stepsto implement the guideline were initially gradual,informal, and voluntary. We expected negligiblechanges in opioid prescribing during the 2 baseline yearsin both the group practice and the contracted care set-tings. By comparing prescribing trends in group practiceto contracted care settings in later implementation pe-riods, we assessed whether enhanced efforts to changeopioid prescribing in the group practice achieved largerreductions in the use of high opioid doses among COTpatients than occurred in the contracted care setting un-der the statewide changes alone.

Population and EligibilityUsing pharmacy data recording prescriptions filled, we

identified COT patients as those receiving 70 days or

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104 The Journal of Pain Opioid Risk Reduction Initiatives

more supply of opioids in a 90-day period. The 70-daythreshold was consistent with Group Health’s adminis-trative definition of COT. The study sample for eachquarter in our analyses consisted of Group Health enroll-ees who received care from group practice or contractedphysicians, met the Group Health COT definition for thequarter, were 18 years of age or older, and were enrolledin the health plan for the entire quarter and for at least 1year previously (to allow assessment of covariates).Because our focus was on non-cancer chronic pain, weexcluded patients who received an opioid prescriptionfrom an oncologist, or had 2 ormore visits with cancer di-agnoses (excluding non-melanoma skin cancer), or hadbeen admitted to a hospice during the study period.

Patient CharacteristicsGroup Health enrollment files provided patient age,

gender, and residence in Eastern or Western Washing-ton. Electronic data indicated patient history of mentalhealth diagnoses, opioid and non-opioid drug use disor-der diagnoses, alcohol substance use disorder diagnoses,and current tobacco use status. We gathered these vari-ables for the year before the first quarter of the studyperiod in which a patient met the study criteria forreceiving COT (a patient’s index quarter).The group practice patients receive their care in Group

Health clinics located predominately in Western Wash-ington and the greater Seattle area, but also in larger cit-ies in Eastern Washington such as Spokane. Thecontracted care patients receive care from physicianspracticing in settings that are not owned or operatedbyGroupHealth.More of these patients reside in EasternWashington. We assessed the comparability of the 2 co-horts by describing salient characteristics (eg, age,gender, history of drug and alcohol abuse, tobacco use).

Study MeasuresWe examined 3 aspects of opioid prescribing for COT

patients using electronic pharmacy data available forboth group practice and contracted care patients:1. The mean daily MED received by each COT patient

over a 90-day period. We calculated the averagedaily MED dispensed to each COT patient in eachquarter by adding the morphine equivalents forthe prescriptions dispensed during the 90 daysand then dividing by 90, usingmethods and conver-sion factors described elsewhere.25 We countedmorphine equivalents dispensed before the quarterwith a run-out date within the quarter, and pre-scriptions within the quarter with a run-out date af-ter the quarter ended, on a pro-rata basis.

2. The percentage of COT patients in each quarterwho received an average daily opioid dose of120 mg or greater MED, and the percentage ofCOT patients in each quarter who received anaverage daily opioid dose of 50 mg or greater MED.

3. The percentage of COT patients in each quarterwho received more than 20% excess opioid dayssupplied in the quarter, defined as 109 or moredays’ supply. This was determined separately for

short-acting and long-acting opioids, so that pa-tients using long-acting opioids with short-actingopioids prescribed for supplemental use on an as-needed basis would not be counted as receivingexcess opioid days supplied on that basis alone.Only patients who received at least 109 days’ supplyof long-acting opioids or at least 109 days’ supply ofshort-acting opioids in a quarter were classified asreceiving excess opioid days supplied. We counteddays’ supply of prescriptions filled before thequarter started but with a run-out date within thequarter, and prescriptions filled within the quarterbut with a run-out date after the quarter ended,on a pro-rata basis. Prior research has shown thatreceiving an excess opioid days supplied is associ-ated with opioid abuse.6,15,19

AnalysesWe described our study sample of COT patients and

how the overall prevalence of COT use changed overtime during the study period. We also compared differ-ences in characteristics between COT patients in thegroup practice and contracted physician settings of thehealth plan. We used regression models to estimatecase-mix adjusted trends in opioid prescribing outcomesamong the group practice and contracted care COT pa-tients. Linear regression was used for the average dailyMED outcome and separate logistic regression modelswere used for the 2 high-dose opioid outcomes and theexcess opioid days supplied outcome. In the models, weincluded main effects for the health plan setting (grouppractice vs contracted care) and included calendar time,measured quarterly, using linear splines11 with knots atthe first quarter of 2008 and the fourth quarter of 2010to allow for different linear temporal trends in outcomesacross the 3 periods of interest. Furthermore, weincluded interactions between calendar time and healthplan setting to permit estimation and comparison ofpotentially different outcome trends for the 2 COT pop-ulations of interest.We adjustedmodels for patient-levelcovariates based on information from the year beforeeach patient’s index quarter: gender, age, location(Eastern/Western Washington), smoking status (currentor not), mental health diagnoses, and separate diagno-ses of opioid and non-opioid drug use disorders andalcohol substance use disorder. To estimate models, weused generalized estimating equations with a workingcorrelation matrix and robust standard errors estimatedvia the sandwich estimator to account for correlationsbetween observations (ie, patients) across time.26

We present graphs showing the raw, unadjustedmeanopioid dose among COT patients or the percentage ofCOT patients receiving high doses or excess opioid dayssupplied in each quarter of the study period in the 2health plan settings (depicted with square and trianglemarkers). In addition, to provide a visual comparison ofrates controlled for case-mix differences between the 2populations, we provide plots of estimated adjustedtrends (depicted with lines) based on the fitted multivar-iate linear or logistic regression model and standardized

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Von Korff et al The Journal of Pain 105

to a common distribution of patient characteristics.Below each figure, we provide estimates of the annualrate of change in the outcome (with 95% confidence in-tervals [CIs]) for the group practice and contracted careCOT patients within each of the 3 time periods of inter-est. For average daily opioid dose, this entails an esti-mated change (D) per year in mean daily opioid MED(in milligrams) received. For the binary outcomes (ie,high dose use or receiving excess opioid days supplied),this entails an estimated annual change in odds of theoutcome (using adjusted odds ratios [ORs]). In these ta-bles, we also present Wald-based P values23 for two-sided tests evaluating whether these rates of changeare significantly different between the 2 health plan set-tings in each period (ie, a ‘‘difference in differences’’approach). We also tested for differences in the ratesof change within each health plan setting between thetime periods of the 3 implementation phases. These re-sults are described in the text for the average dailydose outcome only, as similar differences were observedfor the other outcomes and can be inferred from thefigures.

ResultsThe total number of COT patients included in the ana-

lyses over the 8.5-year study period was 22,205 (16,653 ingroup practice; 5,552 in contracted care). In the firstquarter of the study period, the sample included 3,745COT patients cared for by group practice physicians and1,003 COT patients cared for by contracted care physi-cians. In the last quarter, these counts were 4,969 and1,444, respectively. From 2006 to 2014, the number ofadult enrollees receiving COT increased in both thegroup practice and the contracted care settings. Whenstandardized for age and gender, the percentage ofgroup practice enrollees receiving COT increased from1.9% (95% CI 1.85, 1.96) at the beginning of 2006 to2.7% (2.67, 2.80) in June 2014. By comparison, in thecontracted care setting, the percentage receiving COTincreased from 1.4% (1.29, 1.45) at the beginning of2006 to 2.8% (2.68, 2.89) in June 2014.Comparisons of COT patients in our study sample in

the group practice and contracted care settings showedsome similarities as well as notable differences(Table 1). The percentage of COT patients residing inWesternWashingtonwasmarkedly higher among grouppractice patients (88%) than among contracted care pa-tients (45%). Risk factors for misuse of prescription opi-oids were somewhat more common in the grouppractice than the contracted care setting. For example,17% of COT patients were current tobacco users in thegroup practice compared with 12% in contracted care,whereas the percentage with a recent opioid use disor-der diagnosis was only slightly higher in the group prac-tice (1.6% vs 1.1%).From the first quarter of 2006 to June 2014, the

average daily MED declined from 75.8 mg to 40.0 mgamong group practice COT patients (47% lower),compared with a drop from 92.1 mg to 64.6 mg amongCOT patients of contracted physicians (30% lower), as

shown in Fig 1. Average daily opioid dosewas decreasingin the baseline period among COT patients of bothgroup practice and contracted care physicians. In 2006to 2007, there was an average decrease of 5.2 mg peryear in the group practice and 6.3 mg per year in con-tracted care. The difference in the rate of decreasebetween the group practice and contracted care wasnon-significant (P = .637) during this time. During thealtered prescribing expectations phase of January 2008to October 2010, when shared expectations regardingappropriate opioid prescribing were systematically tar-geted in the group practice setting, the annual rate ofreduction in average daily opioid dose was substantiallygreater in the group practice than it was in contractedcare (average decline of 7.6 mg per year vs 3.0 mg peryear, P < .001). In the multi-faceted initiatives risk reduc-tion phase (October 2010 to June 2014), the rate ofreduction in average daily opioid dose was substantiallydiminished in both the group practice (a reduction ofonly 1.9 mg per year) and contracted care settings (areduction of 1.4 mg per year), with the rates of declineno longer significantly different between groups(P = .620) during that time period.Within the group practice setting, the rate of decline

in average daily opioid dose was significantly larger inthe 2008 to 2010 altered prescribing expectations phasethan in the 2006 to 2007 baseline phase (decline of7.6 mg per year vs 5.2 mg per year, P = .048). However,the rate of decline in the group practice setting wasmarkedly attenuated in the 2010 to 2014 multi-facetedinitiatives risk reduction phase (decline of 1.9 mg peryear).For the percentage of COT patients receiving an

average daily dose of 120 mg or greater MED, the grouppractice setting showedmarkedly larger reductions thanthe contracted care setting (Fig 2). Over the study period,the percentage of COT patients receiving opioid doses of120 mg MED or greater in the group practice declinedfrom 16.8% to 6.3% (63% lower) comparedwith a reduc-tion from 20.6% to 13.6% (34% lower) in contractedcare. During the baseline phase, the odds of COT patientsin the group practice using high opioid doses decreasedan average of 8%per year (OR = 0.92, 95%CI = 0.88–0.96,adjusted for patient characteristics) (Fig 2). This decline inodds accelerated during the altered prescribing expecta-tions phase (2008–2010) to about a 20% reduction peryear (OR = 0.80, 95% CI = 0.77–0.82), followed by aslower, but still significant, rate of decline during themulti-faceted initiatives risk reduction phase(OR = 0.90, 95% CI = 0.87–0.93). In contrast, the con-tracted care setting showed a statistically significantannual rate of decline only during the altered prescrib-ing expectations phase (OR = 0.88, 95% CI = 0.84–0.93).The rate of decline was significantly larger in the grouppractice than in the contracted care setting during thealtered prescribing expectations phase (P = .002) andthe multi-faceted initiatives phase (P = .016).The percentage of COT patients receiving an average

daily dose of 50 mg or greater MED also showed largerreductions in the group practice than in the contractedcare setting (Fig 3).

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Table 1. COT Patient Characteristics Based on the Year Before Each Patient’s Index COT Quarter

CHARACTERISTIC

ALL COT PATIENTS GROUP PRACTICE COT PATIENTS CONTRACTED PHYSICIAN COT PATIENTS

N % N % N %

Total 22,205 – 16,653 – 5,552 –

Western Washington 17,203 77.5 14,709 88.3 2,494 44.9

Female 13,858 62.4 10,482 62.9 3,376 60.8

Age

18–39 y 3,133 14.1 2,384 14.3 749 13.5

40–49 y 4,488 20.2 3,131 18.8 1,357 24.4

50–59 y 6,467 29.1 4,757 28.6 1,710 30.8

60–69 y 3,953 17.8 3,031 18.2 922 16.6

70–79 y 2,171 9.8 1,740 10.5 431 7.8

80 y or older 1,933 9.0 1,610 9.7 383 6.9

Current tobacco use 3,438 15.5 2,752 16.5 686 12.4

Mental disorder diagnosis 8,587 38.7 6,570 39.5 2,017 36.3

Opioid abuse/dependence 332 1.5 273 1.6 59 1.1

Non-opioid drug abuse/dependence 560 2.5 467 2.8 93 1.7

Alcohol abuse/dependence 872 3.9 723 4.3 149 2.7

106 The Journal of Pain Opioid Risk Reduction Initiatives

As shown in Fig 4, the percentage receiving excessopioid days supplied declined from 24.0% to 10.4% inthe group practice (57% lower) compared with a declinefrom 20.1% to 14.7% among COT patients of contractedphysicians (27%lower).Adjusted fordifferences inpatientcharacteristics, the odds of COT patients receiving excessopioid days supplied decreased at similar rates in both set-tingsduring thebaselinephase (Fig4),withoddsdecliningapproximately 12 to 13% per year (group practice pa-tients, OR = 0.87, 95% CI = 0.83–0.91, and contracted

Figure 1. Case-mix adjusted trends in mean daily opioid dose recgroup practice and contracted physicians.

care patients, OR = 0.88, 95% CI = 0.82–0.96). Althoughthis rate of decline continued in the group practice duringthe 2008 to2010phaseof alteredprescribingexpectations(OR = 0.84, 95% CI = 0.82–0.87) and to a lesser extent dur-ing the 2010 to 2014 multi-faceted initiatives risk reduc-tion phase (OR = 0.91, 95% CI = 0.89–0.94), we observedno such significant rates of decline inprescribing an excessdays’ supply in the contracted care setting during boththese periods (OR = 0.97 and 0.96 for the 2 phases from2008 to 2014, with confidence intervals overlapping 1.0).

eived in morphine equivalents (milligrams) for COT patients of

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Figure 2. Case-mix adjusted trends in percentage receiving average daily opioid dose of 120mgmorphine equivalents or greater forCOT patients of group practice and contracted physicians.

Von Korff et al The Journal of Pain 107

DiscussionIn Washington State, use of high opioid dose and

dispensing excess opioid days supplied for COT patientsdeclined after dissemination of a state COT guideline.These reductions were substantially larger in a healthplan’s group practice setting, which devoted additionaleffort and resources to changing shared expectationsregarding COT prescribing among its PCPs, comparedwith reductions among contracted physicians of thesame health plan exposed only to the statewide changes.Although dissemination of the statewide guideline mayhave initiated changes in opioid prescribing amongWashington State physicians, more intensive group prac-tice efforts to change shared expectations resulted ingreater reductions in high-dose opioid prescribing.Exploratory analyses, reported elsewhere,17 suggestthat these differences may have been due to lower ratesof opioid dose escalation and increased rates of partial-dose reduction in the group practice setting. The diver-gence was not due to differences in rates of largereductions in opioid dose among COT patients.Contrary to our initial expectations, a decline in pre-

scribing higher average doses, prescribing of high opioiddoses, and dispensing excess opioid days supplied ap-peared to be underway during the baseline period. In-spection of trends suggests that some prescribingchanges may have started in both the group practiceand the contracted care settings before the state guide-line was released and before the group practice

initiatives were implemented. However, prescribing ofhigher doses and excess opioid days supplied plateauedat a higher level among the COT patients of contractedcare physicians than among the COT patients of grouppractice physicians. These observations are consistentwith the increased efforts to change clinician expecta-tions of appropriate opioid prescribing in the grouppractice setting, changing opioid doses among COT pa-tients. The differences in opioid dose and excess opioiddays supplied achieved by the end of the study periodwere both clinically and statistically significant in thegroup practice setting.This evaluation did not have access to COT patients

from outside Washington State who were not affectedby the Washington State guideline and legislation. Forthat reason, we are unable to determine whether theWashington State guideline and legislation played arole in the reductions in average daily dose and highdose prescribing observed in the contracted care setting.However, national data on opioid prescribing indicatesthat aggregate quantities of opioids prescribed in theUnited States increased dramatically from 2007 to 2011,and that opioid prescribing by familymedicine and inter-nal medicine physicians were also increasing from 2007to 2012.12 This suggests that the reductions observed inWashington State were attributable, at least in part, tothe State guideline and legislation.It is not possible to determine whether the initiatives

implemented in the group practice setting would havehad similar impact in the absence of the statewide

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Figure 3. Case-mix adjusted trends in percentage receiving average daily opioid dose of 50 mgmorphine equivalents or greater forCOT patients of group practice and contracted physicians.

108 The Journal of Pain Opioid Risk Reduction Initiatives

guideline and legislation. Both the initial efforts to altershared clinician expectations regarding appropriateopioid prescribing of group practice physicians andthe multi-faceted opioid risk reduction initiative wereinfluenced by the statewide guideline and state legisla-tion. There was synergy between the statewide guide-line and legislation and the efforts to change opioidprescribing practices in the group practice setting.Although the Washington State guideline and legisla-tion were controversial nationally, the developmentand implementation of the guideline and legislationwere less controversial among physicians practicingmedicine within Washington State, who strongly sup-ported the guideline provisions. Key leaders in painmedicine from the University of Washington wereactively involved in the development of the guidelinesand supported their dissemination.It is noteworthy that the number of patients receiving

COT continued to increase over the study period in boththe group practice and contracted care settings. Neitherthe statewide guideline nor the group practice initiativesproposed changes intended to reduce the prevalence oflong-term opioid prescribing per se. In the absence ofspecific guidance that could be expected to reduce theprevalence of the use of COT, it is not surprising thatthe long-term trends in both the group practice and con-tracted care settings were toward a larger percentage ofthe population using COT over time.

Differences in the percentage of patients on highopioid dose regimens and the percentage receiving excessopioid days supplied in the group practice setting weresignificant from both a clinical and a public healthperspective. At the end of the study period, the percent-age of COT patients on high opioid dose regimens was54% lower among group practice COT patients thanamong COT patients of contracted physicians. Becausethe risks of COT increase with dose,2 these differencesmay reduce risks of opioid-related adverse events. Furtherresearch is needed to determinewhether sustained differ-ences in opioid dose among similar patient populationsaffect rates of opioid-related adverse events, and to assessimplications for pain outcomes. Because there are signifi-cant risks of opioid adverse effects at low as well as highdoses, the research reported in this paper does not estab-lish that dose reductions observed in the group practicesetting will necessarily reduce COT risks of overdose,addiction, or other potential harms.This evaluative research has important limitations.

We were not able to compare opioid prescribingtrends in the group practice and contracted care set-tings with trends among PCPs and COT patients notexposed to the Washington State guideline. It ispossible that the reductions in high dose prescribingobserved in the contracted care setting reflectedbroader trends toward reduced use of high opioiddoses in other states. We think this is unlikely because

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Figure 4. Case-mix adjusted trends in percentage receiving more than 20% excess opioid days supplied for COT patients of grouppractice and contracted physicians.

Von Korff et al The Journal of Pain 109

the trends toward reduced use of high opioid doseswere observed shortly after the dissemination of theWashington State guideline in April 2007, and na-tional trends toward increased prescribing of opioidsin terms of the total volume of opioid medications pre-scribed continued until at least 2011.12 Although wewere able to control for some key patient characteris-tics in our analyses, we cannot exclude residual con-founding as a potential explanation of thedivergence in trends between the group practice andcontracted care settings. It is also possible that thedivergence in trends could be explained by unmea-sured differences in the 2 care settings other thanthe Group Health initiatives to change opioid prescrib-ing. However, the timing of changes in opioid prescrib-ing was generally consistent with the timing of theinitiatives intended to reduce high dose prescribing.We conclude that large reductions in the use of high

opioid doses among COT patients can be achieved andsustained. The changes observed appeared to be initi-ated, in part, by dissemination of a statewide guidelineregarding use of high opioid doses for COT patients.Changes in average daily opioid dose, high dose prescrib-

ing, and dispensing of excess opioid days supplied wereappreciably greater in a group practice setting, whichtook additional steps to change shared expectations ofits physicians regarding appropriate COT prescribingcompared with a contracted care setting exposed onlyto the Washington State guideline and legislativechanges.

AcknowledgmentsWegratefully acknowledge the contributions of mem-

bers of the Patient Advisory Committee guiding thisresearch, including Catherine Cartwright, Penny Cowen,David Duhrkoop (chairperson), Mariann Farrell, AdaGiudice-Tompson, Kathryn Guthrie, Catherine Lippin-cott, Max Sokolnicki, and Betts Tully. This research wassupported by grants to Group Health Research Institute(GHRI) from Pfizer (M.V.K., Principal Investigator), thePatient-Centered Outcomes Research Institute (IHS-1306-02198, M.V.K., Principal Investigator), and the Na-tional Institute on Aging (AG034181, M.V.K., PrincipalInvestigator).

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