Implementation of an intervention aimed at deprescribing benzodiazepines in a large US healthcare system using patient education materials: a pre/post-observational study with a control group.

Tammy M Le, Scott Campbell, Alexa Andraos, Pedro Ahlmark, Ha Hoang, Sean Isserman, Caroline L Goldzweig, Allison M Mays, Kristin Bradley, Michelle S Keller
Author Information
  1. Tammy M Le: David Geffen School of Medicine, Los Angeles, California, USA.
  2. Scott Campbell: Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  3. Alexa Andraos: Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  4. Pedro Ahlmark: Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  5. Ha Hoang: Enterprise Data Intelligence, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  6. Sean Isserman: Enterprise Data Intelligence, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  7. Caroline L Goldzweig: Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  8. Allison M Mays: Section of Geriatrics, Division of General Internal Medicine, Medicine, Cedars-Sinai Medical Center, Beverly Hills, California, USA. ORCID
  9. Kristin Bradley: UNC Rex Healthcare, Raleigh, North Carolina, USA.
  10. Michelle S Keller: Division of General Internal Medicine, Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA Michelle.keller@cshs.org. ORCID

Abstract

OBJECTIVES: Long-term benzodiazepine use is common despite known risks. In the original Eliminating Medications Through patient Ownership of End Results (EMPOWER) Study set in Canada, patient education led to increased rates of benzodiazepine cessation. We aimed to determine the effectiveness of implementing an adapted EMPOWER quality improvement (QI) initiative in a US-based healthcare system.
DESIGN: We used a pre-post design with a non-randomised control group.
SETTING: A network of primary care clinics.
PARTICIPANTS: patients with ���60 days' supply of benzodiazepines in 6 months and ���1���risk factor (���65 years of age, a concurrent high-risk medication prescribed or a diazepam equivalent daily dose ���10) were eligible.
INTERVENTION: In March 2022, we engaged 22 primary care physicians (PCPs), and 308 of their patients were mailed an educational brochure, physician letter and flyer detailing benzodiazepine risks; the control group included 4 PCPs and 291 of their patients.
PRIMARY AND SECONDARY MEASURES: The primary measure was benzodiazepine cessation by 9 months. We used logistic regression and a generalised estimating equations approach to control for clustering by PCP, adjusting for demographics, frailty, number of risk factors, and diagnoses of arthritis, depression, diabetes, falls, and pain.
RESULTS: patients in the intervention and control groups were comparable across most covariates; however, a greater proportion of intervention patients had pain-related diagnoses and depression. By 9 months, 26% of intervention patients (81 of 308) had discontinued benzodiazepines, compared with 17% (49 of 291) of control patients. Intervention patients had 1.73 greater odds of benzodiazepine discontinuation compared with controls (95%���CI: 1.09, 2.75, p=0.02). The unadjusted number needed to treat was 10.5 (95% CI: 6.30, 34.92) and the absolute risk reduction was 0.095 (95% CI: 0.03 to 0.16).
CONCLUSIONS: Results from this non-randomised QI initiative indicate that patient education programmes using the EMPOWER brochures have the potential to promote cessation of benzodiazepines in primary care.

Keywords

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Grants

  1. K01 AG076865/NIA NIH HHS

MeSH Term

Humans
Benzodiazepines
Control Groups
Deprescriptions
Patient Education as Topic
Diazepam
Delivery of Health Care
Pain

Chemicals

Benzodiazepines
Diazepam

Word Cloud

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