Evidence map›Paper›PMID 42605662›Full record

ArticleClinical pharmacology and therapeutics2026

Tramadol Co-Administration with Oxycodone or Hydrocodone Increases Opioid Burden without Improving Postoperative Pain Control.

Noor A Nahid, Ahmed I Soliman, Jordan F Baye, Natasha J Petry, Chancellor F Gray, Rachel A Myers, Erica N Elwood, Elizabeth C Harris, Hrishikesh Chakraborty, Simona Volpi and 8 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

18 authors.

Noor A NahidDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-2190-7555
Ahmed I SolimanDepartment of Pharmacy Practice and Science, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-9539-8167
Jordan F BayeDepartment of Pharmacy Practice, South Dakota State University, Brookings, South Dakota, USA.ORCID https://orcid.org/0000-0002-4849-5415
Natasha J PetrySanford Health Imagenetics, Sioux Falls, South Dakota, USA.ORCID https://orcid.org/0000-0001-5089-9286
Chancellor F GrayFlorida Orthopaedic Institute, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0001-8312-3695
Rachel A MyersClinical Research Unit, Department of Medicine, Duke University School of Medicine, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0003-0086-8339
Erica N ElwoodCenter of Pharmacogenomic and Precision Medicine, University of Florida, College of Pharmacy, Gainesville, Florida, USA.
Elizabeth C HarrisDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, 27701, USA.
Hrishikesh ChakrabortyDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, 27701, USA.ORCID https://orcid.org/0000-0001-9078-845X
Simona VolpiNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
Renee RiderNational Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0001-7765-2988
Paul R DexterRegenstrief Institute, Indiana University, Indianapolis, Indiana, USA.
Josh F PetersonDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-7553-0749
Todd C SkaarDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.ORCID https://orcid.org/0000-0002-3849-374X
Hari K ParvataneniFlorida Orthopaedic Institute, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0001-5547-405X
Larisa H CavallariDepartment of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, College of Pharmacy, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0002-7184-5292
Julie A JohnsonDepartment of Pharmacotherapy and Translational Research and Center for Pharmacogenomics and Precision Medicine, College of Pharmacy, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0001-9847-1932
IGNITE Pragmatic Trial Network Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tramadol is frequently co-prescribed with oxycodone or hydrocodone after surgery under the assumption that its dual mechanism of action provides an opioid-sparing benefit. However, evidence supporting this practice is limited and inconsistent. We conducted a secondary analysis of the multicenter IGNITE ADOPT-PGx pragmatic trial of patients undergoing elective surgery who were prescribed oxycodone alone (n = 317) versus tramadol + oxycodone (n = 96), or hydrocodone alone (n = 563) versus tramadol + hydrocodone (n = 42). Co-primary outcomes of this study were cumulative morphine milligram equivalents (MME) consumed during the 10 days following surgery and composite pain scores at day 10 defined as the sum of current pain and average and worst pain in the past 7 days (score ranges from 3 to 15). Inverse probability of treatment weighting (IPTW) was used to adjust for demographic characteristics, comorbidities, and concomitant analgesics. Sensitivity analyses restricted to CYP2D6 normal metabolizers and sites prescribing both monotherapy and combination therapy and subgroup analysis including total knee arthroplasty patients were conducted. Compared to oxycodone alone, the combination of oxycodone and tramadol was associated with higher MME (adjusted mean 205.2 vs 122.5; P < 0.0001) and lower mobility, without meaningful differences in pain scores (adjusted mean 9.6 vs 9.4; P = 0.41). Similar findings were observed for hydrocodone-only vs hydrocodone + tramadol groups. Results were consistent in sensitivity and subgroup analyses. Co-administration of tramadol with oxycodone or hydrocodone was associated with substantially higher total MME and reduced mobility without any demonstrable improvement in pain control.

Identifiers

PMID42605662
PMCPMC13478926

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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.