Evidence map›Paper›PMID 42698481›Full record

ArticleFrontiers in endocrinology2026

Prehospital glucagon-like peptide-1 receptor agonists are not associated with reduced inpatient opioid exposure but with shorter hospital length of stay after total joint arthroplasty.

Noam Vaknin, Chen Seidenberg, Eric Sitton, Pierre Singer, Ruth Mishali, Hila Vidal, Michal Slevin-Kish

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Noam VakninHerzliya Medical Center, Herzliya, Israel.
Chen SeidenbergHerzliya Medical Center, Herzliya, Israel.
Eric SittonHerzliya Medical Center, Herzliya, Israel.
Pierre SingerHerzliya Medical Center, Herzliya, Israel.
Ruth MishaliHerzliya Medical Center, Herzliya, Israel.
Hila VidalHerzliya Medical Center, Herzliya, Israel.
Michal Slevin-KishHerzliya Medical Center, Herzliya, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have been hypothesized to confer anti-inflammatory, antinociceptive, and anti-addictive benefits. We aimed to investigate their impact on acute perioperative pain and opioid use after total joint arthroplasty (TJA). Methods: A retrospective cohort study analyzed 14,375 hip or knee arthroplasties performed between January 2018 and February 2026, which included 882 patients on chronic preoperative GLP-1RA therapy. Using 1:1 propensity-score matching without replacement, 786 GLP-1RA users were matched to 786 non-users (total n=1,572) based on demographics, surgery type, and chronic medication use. Results: In the matched cohort, chronic GLP-1RA use was not associated with reduced inpatient opioid administration (adjusted difference -0.18; 95% CI, -0.74 to 0.38; p=0.53) or corrected postoperative morphine milligram equivalents (MME) (-2.79 MME; 95% CI, -6.95 to 1.37; p=0.19). When normalized to hospitalization time, the difference in inpatient opioid exposure was not statistically significant (+0.073 MME/hour; 95% CI, -0.003 to 0.149; p=0.059). Average visual analog scale (VAS) pain scores also showed no significant difference (-0.094; p=0.15). However, GLP-1RA users demonstrated a consistently shorter length of stay (LOS) (adjusted difference -10.41 hours; 95% CI, -13.97 to -6.85; p<0.001). Conclusions: Chronic preoperative GLP-1RA therapy was not associated with reduced inpatient opioid exposure or improved early postoperative pain control following TJA. Nevertheless, GLP-1RA use was consistently associated with shorter hospital LOS. Prospective studies are needed to determine whether this finding reflects improved recovery pathways or residual confounding and to evaluate the impact of GLP-1RAs on longer-term postoperative outcomes and opioid utilization.

Indexed as

Analgesics, OpioidArthroplasty, Replacement, HipArthroplasty, Replacement, KneeGlucagon-Like Peptide-1 Receptor AgonistsLength of StayPostoperative PainAgedFemaleHumansInpatientsMaleMiddle AgedRetrospective StudiesAnalgesics, OpioidGlucagon-Like Peptide-1 Receptor AgonistsGLP-1 receptor agonistslength of stayopioid exposureosteoarthritispostoperative pain

Identifiers

PMID42698481
PMCPMC13541510

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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.