Evidence map›Paper›PMID 26669880›Full record

ReviewDigestive diseases and sciences2016

Pharmacokinetics of Infliximab and Reduction of Treatment for Inflammatory Bowel Diseases.

Nicolas Williet, Stephane Paul, Laurent Peyrin-Biroulet, Xavier Roblin

Abstract readReview
PubMed Publisher
In one paragraph

Review in Digestive diseases and sciences, 2016. 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
1.7field-weighted citation impact, top 14% of its field
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, 10 citations in OpenAlex.

  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

4 authors at 2 institutions in 1 country.

Nicolas WillietCIC Inserm et Service d'Hépato-gastroentérologie, Hôpital Universitaire de Saint Etienne, Université Jean Monnet, Avenue Albert Raimond, 4227, Saint Priest en Jarez, France. Nicolas.Williet@chu-st-etienne.fr.
Stephane PaulService Immunopharmacologie Hôpital Universitaire de Saint Etienne, Université Jean Monnet, Saint Priest en Jarez, France.
Laurent Peyrin-BirouletInserm, U954 et Service d'Hepato-Gastroenterologie, CHU de Nancy, Université de Lorraine, Vandoeuvre-lès-Nancy, France.
Xavier RoblinCIC Inserm et Service d'Hépato-gastroentérologie, Hôpital Universitaire de Saint Etienne, Université Jean Monnet, Avenue Albert Raimond, 4227, Saint Priest en Jarez, France.
Inserm · FRCentre Hospitalier Universitaire de Saint-Étienne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Local or national policy, patients' preferences, safety and/or economic concerns, or reimbursement issues may dictate stopping drug in inflammatory bowel diseases (IBD) patients. Sustained deep remission is an important predictor of a better outcome after anti-tumor necrosis (TNF) factor therapy discontinuation, including infliximab (IFX) in IBD patients, but this is not sufficient to prevent future relapse in these patients. In IBD patients under combotherapy, trough level of infliximab (TRI) could be helpful to choose stopping one of the two drugs. In patients on IFX monotherapy, TRI could help to decide reduction of drug dosing, particularly in IBD patients with supratherapeutic trough levels. Incidental findings of undetectable TRI in patients with deep remission may identify a subset of patients who may be considered for IFX cessation. Controlled trials further assessing this issue are eagerly awaited. Pending these trials, clear international recommendations for discontinuing anti-TNF therapy are needed.

Indexed as

AlgorithmsDrug Therapy, CombinationGastrointestinal AgentsHumansInflammatory Bowel DiseasesInfliximabGastrointestinal AgentsInfliximabDe-escalationInflammatory bowel diseaseInfliximabPharmacokineticsReductionTrough level of infliximab

Identifiers

PMID26669880
OpenAlexW2275273416

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.