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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.
Le, Tammy M; Campbell, Scott; Andraos, Alexa; Ahlmark, Pedro; Hoang, Ha; Isserman, Sean; Goldzweig, Caroline L; Mays, Allison M; Bradley, Kristin; Keller, Michelle S.
Affiliation
  • Le TM; David Geffen School of Medicine, Los Angeles, California, USA.
  • Campbell S; Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  • Andraos A; Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  • Ahlmark P; Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  • Hoang H; Enterprise Data Intelligence, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Isserman S; Enterprise Data Intelligence, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Goldzweig CL; Cedars-Sinai Medical Care Foundation, Los Angeles, California, USA.
  • Mays AM; Section of Geriatrics, Division of General Internal Medicine, Medicine, Cedars-Sinai Medical Center, Beverly Hills, California, USA.
  • Bradley K; UNC Rex Healthcare, Raleigh, North Carolina, USA.
  • Keller MS; Division of General Internal Medicine, Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA Michelle.keller@cshs.org.
BMJ Open ; 14(4): e080109, 2024 Apr 03.
Article in En | MEDLINE | ID: mdl-38569687
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Benzodiazepines / Deprescriptions Limits: Humans Language: En Journal: BMJ Open Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Benzodiazepines / Deprescriptions Limits: Humans Language: En Journal: BMJ Open Year: 2024 Type: Article Affiliation country: United States