# A short communication of pain outcomes following a pharmacist-delivered alcohol and opioid use reduction intervention

**Authors:** Gerald Cochran, Grace Broussard, Yingjia Wei, Craig Field, Adam J. Gordon, Kenneth C. Hohmeier

PMC · DOI: 10.1016/j.dadr.2026.100418 · Drug and Alcohol Dependence Reports · 2026-02-27

## TL;DR

A pharmacist-led intervention reduced alcohol and opioid co-use without worsening patients' pain levels.

## Contribution

The study shows that community pharmacists can help reduce co-use without increasing pain.

## Key findings

- Pain scores did not differ significantly between the intervention and control groups.
- Pain intensity and interference decreased modestly in both groups at 2 months but returned to baseline by 3 months.
- The intervention was associated with reduced alcohol-opioid co-use without worsening pain.

## Abstract

Co-use of alcohol and opioid medications increases risk for sedation, respiratory depression, and overdose, yet remains common among patients prescribed opioids. The Alcohol Brief Intervention–Medication Therapy Management (ABI-MTM) intervention was developed for delivery by community pharmacists and demonstrated feasibility, acceptability, and preliminary reductions in co-use. Given possible pain-related motives for co-use, this exploratory secondary analysis assessed whether ABI-MTM affected pain symptomatology.

This study utilized data from a randomized trial of 44 community pharmacy patients from 25 pharmacies prescribed opioids and who reported alcohol co-use. Participants were randomized to ABI-MTM or standard medication counseling (SMC). Pain intensity/interference were assessed at baseline, 2-, and 3-months using the Brief Pain Inventory–Short Form. Analyses included descriptive statistics, Cohen’s d effect sizes, and mixed-effects models comparing pain across conditions and timepoints.

Pain scores did not differ between groups (p > 0.05). For pain intensity, ABI-MTM and SMC showed similar baseline means (4.31 vs. 5.05), decreased modestly at 2-months (2.80 vs. 3.74), and returned to baseline levels at 3-months (4.21 vs. 4.83). Pain interference followed a comparable pattern, with ABI-MTM and SMC starting similarly (4.83 vs. 5.07), decreasing modestly at 2-months (3.19 vs. 3.87), and returning near baseline at 3-months (4.92 vs. 4.42). Effect sizes between group differences were small (Cohen’s d≤0.33). Mixed-model analyses showed no significant treatment effects on pain intensity/interference across time (p > 0.05).

This underpowered study found no evidence of pain differences between ABI-MTM and SMC, tentatively suggesting possible alcohol-opioid co-use improvements associated with the intervention without worsening pain.

•The pharmacist intervention was associted with reduced alcohol and opioid co-use without increasing pain.•Pain scores remained stable across both groups.•Community pharmacists can play a meaningful role in addressing opioid and alcohol co-use.

The pharmacist intervention was associted with reduced alcohol and opioid co-use without increasing pain.

Pain scores remained stable across both groups.

Community pharmacists can play a meaningful role in addressing opioid and alcohol co-use.

## Linked entities

- **Chemicals:** opioid (PubChem CID 126961754)

## Full-text entities

- **Diseases:** psychotic (MESH:D011618), hyperalgesia (MESH:D006930), overdose (MESH:D062787), depression (MESH:D003866), manic (MESH:D001714), cancer (MESH:D009369), painful conditions (MESH:D013001), Alcohol Abuse (MESH:D000437), Pain (MESH:D010146), opioid (MESH:D009293), PTSD (MESH:D013313), analgesia (MESH:D000699), respiratory depression (MESH:D012131)
- **Chemicals:** SMC (-), Alcohol (MESH:D000438), buprenorphine (MESH:D002047), morphine (MESH:D009020)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969320/full.md

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Source: https://tomesphere.com/paper/PMC12969320