Evidence map›Paper›PMID 31737635›Full record

ArticleFrontiers in medicine2019

Administration Timing Is the Best Clinical Outcome Predictor for Adalimumab Administration in Crohn's Disease.

Mauro Mastronardi, Margherita Curlo, Elisabetta Cavalcanti, Osvaldo Burattini, Renato Cuppone, Romina Tauro, Stefania De Santis, Grazia Serino, Pasqua Letizia Pesole, Elisa Stasi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
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

15 authors at 2 institutions in 1 country.

Mauro MastronardiDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Margherita CurloDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Elisabetta CavalcantiDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Osvaldo BurattiniDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Renato CupponeDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Romina TauroDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Stefania De SantisDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Grazia SerinoDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Pasqua Letizia PesoleDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Elisa StasiDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Maria Lucia CarusoDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Rossella DonghiaDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Vito GuerraDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Pietro GiorgioDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Marcello ChieppaDepartment of Research, National Institute of Gastroenterology "S. de Bellis", Bari, Italy.
Gastroenterology Hospital "Saverio de Bellis" · ITUniversity of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biological intervention for Crohn's Disease (CDs) patients, mainly using anti-TNF antibodies, is often an efficient therapeutic solution. Nonetheless, data defining the administration timing to maximize the chances of clinical remission are lacking. The objective of this "real-life" retrospective study was to evaluate if early Adalimumab (ADA) administration (<12 months) was an efficient strategy to improve patients' clinical outcome. This single center study included 157 CD patients, of which 80 received the first ADA administration within the first 12 months from the diagnosis. After 1 year of therapy, clinical remission was observed in 50.32% of patients, mucosal healing in 37.58%. Clinical remission was observed in 66.25% of the early ADA administration patients vs. 33.77% of the late (>12 months) (

Indexed as

Adalimumabbiological agents anti-TNFclinical outcomeclinical remissionCrohn's disease

Identifiers

PMID31737635
PMCPMC6838026
OpenAlexW2986322855

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.