Evidence map›Paper›PMID 42629504›Full record

ArticleClinical pharmacology and therapeutics2026

Initiation of Gabapentin with Opioids and Risk of Respiratory Cardiovascular and Opioid-Related Adverse Events Following Surgery for Breast Cancer.

Jyun-Heng Lai, Anton L V Avanceña, Juan P Cata, Jamie C Barner, Sharon H Giordano, Chanhyun Park, Hui Zhao, Kirk E Evoy, John K Lin, Jennifer C Spencer and 3 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

13 authors.

Jyun-Heng LaiDepartment of Breast Surgical Oncology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0009-0007-7420-2085
Anton L V AvanceñaHealth Outcomes Division, College of Pharmacy, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0002-4903-870X
Juan P CataDepartment of Anesthesiology and Perioperative Medicine, Division of Anesthesiology, Critical Care Medicine, and Pain Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-3156-1682
Jamie C BarnerHealth Outcomes Division, College of Pharmacy, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0002-6078-8093
Sharon H GiordanoDepartment of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-8700-2767
Chanhyun ParkHealth Outcomes Division, College of Pharmacy, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0002-1081-0950
Hui ZhaoDepartment of Health Services Research, Division of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-4742-1139
Kirk E EvoyDivision of Pharmacotherapy and Translational Sciences, College of Pharmacy, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0003-0913-7145
John K LinDepartment of Health Services Research, Division of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-2490-4453
Jennifer C SpencerDepartment of Internal Medicine, Dell Medical School, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0001-9508-1525
Mariana Chavez-MacGregorDepartment of Breast Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-7189-0763
Kelly K HuntDepartment of Breast Surgical Oncology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0001-9156-8723
Kerollos Nashat WanisDepartment of Breast Surgical Oncology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-1934-3380

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pain is a key determinant of quality-of-life following breast cancer surgery, the most common cancer operation in the United States. Gabapentinoids are frequently prescribed for pain management, yet their respiratory, cardiovascular, and opioid-related adverse effects remain unclear. This target trial emulation, analyzing US commercial claims (2013-2023), evaluated these safety outcomes under gabapentin-opioids initiation vs. opioids only during the first postoperative month following breast cancer surgery, with sustained 1-year follow-up. Women with nonmetastatic breast cancer were eligible on surgery dates if they had no prior outcomes, nor gabapentinoids or opioid prescriptions. Outcomes included time-to-first respiratory complications, major adverse cardiovascular events (MACE), arrhythmia, and high-dose opioid utilization (≥ 50 or ≥ 90 morphine -milligram equivalent [MME]). We estimated 1-year outcome risks and 95% CIs under gabapentin-opioids and opioids-only strategies using weighted pooled logistic regressions with bootstrapping, including stabilized inverse probability weighting to adjust for baseline and time-varying confounders. Of 86,290 eligible individuals, 1709 initiated gabapentin and opioids, and 39,372 initiated opioids only. Risks of respiratory complications (RR 1.24, 95% CI: 0.26-3.02), MACE (RR 0.95, 95% CI: 0.31-1.85), and arrhythmia (RR 0.65, 95% CI: 0.24-1.33) were comparable under gabapentin-opioids and opioids-only. Risk of receiving opioid dosage ≥ 50 MME (RR 1.23, 95% CI: 0.85-1.72) and ≥ 90 MME (RR 1.09, 95% CI: 0.43-2.23) were comparable. This study challenged the limited evidence regarding safety concerns of adding gabapentin for pain management, finding that gabapentin-opioids initiation carried comparable respiratory and cardiovascular risks to opioids only following breast cancer surgery. However, we did not find evidence that adjunctive gabapentin reduces subsequent high-dose opioid utilization.

Identifiers

PMID42629504
PMCPMC13498469

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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.