Evidence map›Paper›PMID 42519360›Full record

ArticlePain reports2026

Role of cytochrome phenotyping in patients with chronic noncancer pain with inadequate response to tramadol.

Deborah Montmeat, Xavier Declèves, Alicja Puszkiel, Serge Perrot, Anne-Priscille Trouvin

Abstract read
In one paragraph

Article in Pain reports, 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

5 authors.

Deborah MontmeatPain Department, Cochin University Hospital, Paris Cité University, Assistance Publique Hôpitaux de Paris, Paris, France.ORCID https://orcid.org/0000-0003-3989-6855
Xavier DeclèvesInserm UMRS1144, Laboratory of Pharmacology and Toxicology, Cochin University Hospital, Paris Cité University, Assistance Publique Hôpitaux de Paris, Paris, France.
Alicja PuszkielInserm UMRS1144, Laboratory of Pharmacology and Toxicology, Cochin University Hospital, Paris Cité University, Assistance Publique Hôpitaux de Paris, Paris, France.
Serge PerrotINSERM U987, Paris Cité University, Boulogne Billancourt, France.
Anne-Priscille TrouvinINSERM U987, Paris Cité University, Boulogne Billancourt, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The opioid crisis is one of the most serious public health emergencies in the United States today. Opioid prescribing requires vigilance and reducing inappropriate opioid prescriptions is a key to decreasing opioid misuse. For that reason, we often focus solely on therapeutic indications or dosage while overlooking the polymorphisms of metabolism. Cytochromes P450 (CYP) are highly susceptible to interindividual and intraindividual variations and the analgesic activity of tramadol is dependent on the activity of CYP2D6. Objectives: To evaluate whether CYP phenotyping could identify metabolic abnormalities in patients with chronic non-cancer pain (CNCP) who experienced an inadequate response to tramadol and to assess the impact of phenotype-guided therapeutic adaptation on patient care. Methods: This exploratory study assessed CYP's activity using a phenotyping drug cocktail protocol adapted from the Geneva cocktail in patients suffering from CNCP who experienced an inadequate response to tramadol, either ineffectiveness or side effects leading to discontinuation of tramadol. Patients' drug therapy was subsequently tailored according to their cytochromes' activity, and its impact was evaluated one year later using patient-reported outcomes. Results: 72.7% of patients who had side effects resulting in treatment discontinuation had slow metabolism for CYP2D6; 87.5% of patients who had experienced ineffectiveness with tramadol had slow metabolism for CYP2D6. The patients believed that this test led to a great improvement in their therapeutic management on average. Conclusion: An inadequate response to tramadol in a patient with CNCP could trigger consideration of metabolic phenotype exploration to facilitate personalised pain management and reduce unwarranted opioid prescription.

Indexed as

AnalgesicsChronic painCYP2D6CytochromesOpioidPersonalised medicinePhenotypic drug cocktail

Identifiers

PMID42519360
PMCPMC13384671

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.