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The time for emergency department opioid agonist therapy is now: “A BC perspective”

Published online by Cambridge University Press:  23 July 2019

Andrew Kestler*
Affiliation:
Faculty of Medicine, University of British Columbia, Vancouver, BC St. Paul's Hospital, Vancouver, BC Centre for Health Evaluation & Outcome Sciences, Vancouver, BC
Jason Wale
Affiliation:
Faculty of Medicine, University of British Columbia, Vancouver, BC Royal Jubilee and Victoria General Hospitals, Victoria, BC Vancouver Island Health Authority, Vancouver, BC
Melissa Allan
Affiliation:
Faculty of Medicine, University of British Columbia, Vancouver, BC Burnaby Hospital, Burnaby, BC Fraser Health Authority, Surrey, BC
*
Correspondence to: Dr. Andrew Kestler, Department of Emergency Medicine, University of British Columbia and St. Paul's Hospital, 1081 Burrard Street, Vancouver, BC V6Z 1Y6; Email: andrew.kestler@ubc.ca

Abstract

Type
Commentary
Copyright
Copyright © Canadian Association of Emergency Physicians 2019 

Although we have national evidence-based guidelines to address Canada's opioid epidemic,1 the number of annual opioid overdose deaths continues to rise. From January 2016 to September 2018, 10,337 Canadians died of opioid-related overdoses,2 with British Columbia (BC) a regrettable national leader. Patients and providers need better access to the proven intervention of opioid agonist therapy, which includes methadone and buprenorphine/naloxone (often referred to as Suboxone, or BNX).

Opioid use disorder kills more effectively than diseases that have historically received emergency department (ED) attention and resources. In an American cohort prior to widespread fentanyl use, 4.7% of individuals treated for opioid overdoses were dead at 1 year.Reference Larochelle, Bernson and Land3 In Vancouver, ED patients treated for overdose in 2017 had an 8% 1-year mortality (Jiang and Purssell, personal communication, April 2019).

Opioid agonist therapy cuts overdose and all-cause mortality in half in people with opioid use disorder,Reference Larochelle, Bernson and Land3,Reference Sordo, Barrio and Bravo4 but fewer than 30% of people with diagnosed opioid use disorder receive 1 month of opioid agonist therapy, whether in MassachusettsReference Larochelle, Bernson and Land3 or in BC (Nosyk, personal communication, April 2019). Across the United States and Canada, rates of people with opioid use disorder receiving adequate opioid agonist therapy are likely much lower if one considers 1) the heterogeneity of addiction treatment resources, 2) the burden of undiagnosed opioid use disorder, and 3) the longer opioid agonist therapy duration thought necessary to maximize survival benefit. If initiated in the ED, buprenorphine/naloxone (the first line opioid agonist therapy choice in Canada1) doubles rates of retention in addiction care compared with a passive referral alone.Reference D'Onofrio, O'Connor and Pantalon5

Every ED encounter constitutes an opportunity to start opioid agonist therapy before the next fatal overdose. In BC, over 50% of people dying of overdose visited an ED in the year before death.Reference Otterstatter, Crabtree and Dobrer6 Sadly, some ED opioid use disorder patients feel stigmatizedReference Kahan, Poremski and Wise-Harris7 and leave before being seen. Others pass through EDs with unrecognized opioid use disorder, often with triage complaints that do not appear opioid-related. Still others may be dismissed as “drug seekers” when they are actually providing clues to underlying opioid use disorder. Nevertheless, a challenging ED visit does not preclude later opioid agonist therapy success. Many opioid use disorder survivors become the peer support workers so crucial to helping others enter recovery.

In this issue of CJEM, Hu and colleaguesReference Hu, Snider-Adler, Nijmeh and Pyle8 give cause for optimism: They demonstrate that Canadian community hospital EDs can initiate buprenorphine/naloxone and, via community linkages, successfully maintain patients on buprenorphine/naloxone for 6 months, incidentally lowering the number of repeat ED visits during follow-up.

A cautionary note: Hu and colleagues’ protocolReference Hu, Snider-Adler, Nijmeh and Pyle8 initiates buprenorphine/naloxone at a Clinical Opioid Withdrawal Scale (COWS) score greater than 5. Participants, in fact, reached an average COWS of 11 before starting buprenorphine/naloxone (Hu, personal communication, April 2019). Guidelines in BC9 call for a minimum COWS score of 12 before beginning buprenorphine/naloxone. Starting with lower scores increases the risk of precipitated withdrawal.

Many barriers remain to ED opioid agonist therapy success. ED staff have biases affecting their care of patients with substance use disorders.Reference Mendiola, Galetto and Fingerhood10 ED physicians in Saskatchewan and Manitoba still need special approval to initiate buprenorphine/naloxone for their patients,1 and buprenorphine/naloxone is not uniformly covered for all patients in all provinces.1 Many areas lack the essential community follow-up piece of ED opioid agonist therapy.

The Canadian Research Initiative on Substance Misuse (CRISM, https://crism.ca/) has launched a substantive effort to better understand ED opioid agonist therapy from both the patient and provider perspectives. CRISM plans to use its findings to develop and disseminate an ED opioid agonist therapy toolkit specific to reducing implementation barriers in the Canadian context. Of course, no single approach or tool will work for all settings. In BC alone, different EDs have devised different opioid agonist therapy programs to suit their patient population and their resources.

In Vancouver, in 2017, St. Paul's Hospital ED began offering buprenorphine/naloxone to its patients. However, few patients, many of whom inject drugs daily, were in sufficient opioid withdrawal to initiate buprenorphine/naloxone. In response, the ED launched a low-barrier buprenorphine/naloxone to-go program, where patients receive a starter pack with instructions regarding self-administration and follow-up. So far, 25% patients are retained on opioid agonist therapy on follow-up. The new program is linked to a rapid access addiction clinic and a community outreach team, which successfully finds 90% of patient post ED-discharge and links approximately 50% to ongoing care (Bath, personal communication, April 2019).

In Burnaby, proportionally fewer people with opioid use disorder inject drugs than in Vancouver, and more present to ED in moderate opioid withdrawal. With minimal resources, the ED began to offer buprenorphine/naloxone in 2017 and found community physicians to see patients in follow-up. The ED program has since garnered Fraser Health Authority support for several new components: universal screening for overdose risk; funded community opioid agonist therapy clinics; outreach teams to follow up all patients who overdose or start opioid agonist therapy; staff education on trauma informed care to reduce opioid-related stigma; and provider resiliency training to boost staff morale and compassion. The Authority is expanding the program to its 12 hospitals, in a regional model not unlike what Hu describes at Lakeridge Health in Ontario.Reference Hu, Snider-Adler, Nijmeh and Pyle8

In Victoria, peer support workers play a large role in ED opioid agonist therapy. The Victoria Umbrella Society is a non-profit organization of peers in recovery from addiction. The peers contact patients started on ED opioid agonist therapy or identified in the ED as opioid agonist therapy candidates in order to optimize transition to outpatient care. Since March 2017, the peers have helped connect 150 patients to ongoing care with more than 30 remaining stable on opioid agonist therapy for over 3 months. The ED observational unit accepts patients in early withdrawal for up to 23 hours, allowing patients to reach sufficient withdrawal to start buprenorphine/naloxone treatment in the ED before peer-assisted follow-up in the community.

Guidelines, growing evidence, and mortality statistics are telling us we should be offering more take-home naloxone, ED opioid agonist therapy, and community-based addiction care to our patients with opioid use disorder. Yet many of us still work in systems that make treating opioid use disorder needlessly more difficult than complex conditions like septic shock and decompensated heart failure. It is then our collective responsibility to demand the institutional and regulatory support we all need to offer opioid agonist therapy to our patients now, before it is too late.

Competing interests

None declared.

References

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