Evidence map›Paper›PMID 25493006›Full record

ReviewWorld journal of gastroenterology2014

Immunomodulatory therapies for acute pancreatitis.

Jing Li, Wen-Juan Yang, Lu-Ming Huang, Cheng-Wei Tang

2 registry-linked trialsOpen access · hybridAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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.

NCT03937323 completednot on this mapstarted 2019, after this paper: background citation

Immun Parameters and Flow Cytometry at Pancreatitis Patients

Typeobservational_patient_registrySponsorIstanbul Training and Research HospitalRan2019 to 2020Enrolled80ConditionsPancreatitis, Immune SuppressionArmsBlood lymphocyte subtypes and serum cytokines
NCT04502940 completednot on this mapstarted 2020, after this paper: background citation

Can we Measure Pancreatitis Severity With Flow Cytometry?

TypeobservationalSponsorIstanbul Training and Research HospitalRan2020 to 2021Enrolled53ConditionsPancreatitis, Lymphocytic Infiltrate, Immune System DiseasesArmsFlow Cytometric analysis
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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  16. Level of serum soluble Tim-3 expression in early-phase acute pancreatitis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2019
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  19. Association between serum interleukin-35 levels and severity of acute pancreatitis.International journal of clinical and experimental medicine · 2015
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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 1 institution in 1 country.

Jing LiJing Li, Lu-Ming Huang, Cheng-Wei Tang, Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.
Wen-Juan YangJing Li, Lu-Ming Huang, Cheng-Wei Tang, Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.
Lu-Ming HuangJing Li, Lu-Ming Huang, Cheng-Wei Tang, Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.
Cheng-Wei TangJing Li, Lu-Ming Huang, Cheng-Wei Tang, Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is currently difficult for conventional treatments of acute pancreatitis (AP), which primarily consist of anti-inflammatory therapies, to prevent the progression of AP or to improve its outcome. This may be because the occurrence and progression of AP, which involves various inflammatory cells and cytokines, includes a series of complex immune events. Considering the complex immune system alterations during the course of AP, it is necessary to monitor the indicators related to immune cells and inflammatory mediators and to develop more individualized interventions for AP patients using immunomodulatory therapy. This review discusses the recent advances in immunomodulatory therapies. It has been suggested that overactive inflammatory responses should be inhibited and excessive immunosuppression should be avoided in the early stages of AP. The optimal duration of anti-inflammatory therapy may be shorter than previously expected (< 24 h), and appropriate immunostimulatory therapies should be administered during the period from the 3(rd) d to the 14(th) d in the course of AP. A combination therapy of anti-inflammatory and immune-stimulating drugs would hopefully constitute an alternative to anti-inflammatory drug monotherapy. Additionally, the detection of the genotypes of critical inflammatory mediators may be useful for screening populations of AP patients at high risk of severe infections to enable the administration of early interventions to improve their prognosis.

Indexed as

Acute DiseaseAdjuvants, ImmunologicAnimalsAnti-Inflammatory AgentsCytokinesDrug Administration ScheduleDrug Therapy, CombinationHumansImmunologic FactorsImmunosuppressive AgentsInflammation MediatorsPancreasPancreatitisSignal TransductionTreatment OutcomeAdjuvants, ImmunologicAnti-Inflammatory AgentsCytokinesImmunologic FactorsImmunosuppressive AgentsInflammation MediatorsImmunomodulatory therapyImmunostimulationImmunosuppressionPancreatitisSystemic inflammatory response syndrome

Identifiers

PMID25493006
PMCPMC4258562
OpenAlexW2043075758

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.