Evidence map›Paper›PMID 39679717›Full record

ArticlePain2025

Mortality after concurrent treatment with gabapentin and opioids in older adults with spine diagnoses.

Laura S Gold, Patrick J Heagerty, Ryan N Hansen, Janna L Friedly, Sandra K Johnston, Richard A Deyo, Michele Curatolo, Judith A Turner, Sean D Rundell, Katherine Wysham and 2 more

Abstract read
In one paragraph

Article in Pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Laura S GoldDepartment of Radiology, School of Medicine, University of Washington, Seattle, WA, United States.ORCID 0000-0002-4289-5231
Patrick J HeagertyClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.ORCID 0000-0002-3403-6007
Ryan N HansenDepartment of Pharmacy, School of Pharmacy, University of Washington, Seattle, WA, United States.
Janna L FriedlyClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Sandra K JohnstonDepartment of Radiology, School of Medicine, University of Washington, Seattle, WA, United States.
Richard A DeyoDepartments of Family Medicine and Internal Medicine, Oregon Health and Science University, Portland, OR, United States.
Michele CuratoloClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Judith A TurnerClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Sean D RundellClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Katherine WyshamClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Jeffrey G JarvikDepartment of Radiology, School of Medicine, University of Washington, Seattle, WA, United States.
Pradeep SuriClinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.

Funding

UW Core Center for Clinical Research of Musculoskeletal ConditionsP30AR072572 · NIAMS · UNIVERSITY OF WASHINGTON · PI JEFFREY G JARVIK, Pradeep Suri · 2017 to 2026
$8.3M
NIAMS NIH HHS P30 AR072572NIAMS NIH HHS P30AR072572
6 · The paper itself

Abstract

abstractGiven the negative impact of opioid use on population health, prescriptions for alternative pain-relieving medications, including gabapentin, have increased. We wanted to determine whether people who filled gabapentin and opioid prescriptions concurrently ("gabapentin + opioids") had greater mortality than those who filled an active control medication (tricyclic antidepressants [TCAs] or duloxetine) and opioids concurrently ("TCAs/duloxetine + opioids"). In this population-based, propensity score-matched cohort study, we identified Medicare beneficiaries with spine-related diagnoses from 2017 to 2019. We compared people treated with gabapentin + opioids (n = 67,133) to people treated with TCAs/duloxetine + opioids (n = 67,133) who were matched on demographic and clinical factors. The primary outcome was mortality at any time, and a secondary outcome was occurrence of a major medical complication at any time. Among 134,266 participants (median age 73.4 years; 66.7% female), 2360 died before the end of follow-up. No difference in mortality was observed between groups (adjusted hazard ratio and 95% confidence interval for gabapentin + opioids 0.98 [0.90-1.06]; P = 0.63). However, people treated with gabapentin + opioids were at slightly increased risk of a major medical complication (1.02 [1.00-1.04]; P = 0.03) compared to those treated with TCAs/duloxetine + opioids. Results were similar in analyses (1) restricted to ≤30-day follow-up and (2) that required ≥2 fills of each prescription. When treating pain in older adults taking opioids, the addition of gabapentin did not increase mortality risk relative to addition of TCAs or duloxetine.

Indexed as

AnalgesicsAnalgesics, OpioidGabapentinSpinal DiseasesAgedAged, 80 and overCohort StudiesDrug Therapy, CombinationDuloxetine HydrochlorideFemaleHumansMaleMedicareMortalityUnited StatesAnalgesicsAnalgesics, OpioidDuloxetine HydrochlorideGabapentin

Identifiers

PMID39679717
PMCPMC11919562

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.