Evidence map›Paper›PMID 24144038›Full record

ArticleCritical care (London, England)2013

Kinetics of circulating immunoglobulin M in sepsis: relationship with final outcome.

Evangelos J Giamarellos-Bourboulis, Efterpi Apostolidou, Malvina Lada, Ioannis Perdios, Nikolaos K Gatselis, Iraklis Tsangaris, Marianna Georgitsi, Magdalini Bristianou, Theodora Kanni, Kalliopi Sereti and 4 more

Registry-linked trialOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in Critical care (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03334006 (Prospective, Randomized Trial of Personalized Medicine With Pentaglobin® After Surgical Infectious Source Control in Patients With Peritonitis), which is not on this map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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.

NCT03334006 phase2recruitingnot on this mapstarted 2017, after this paper: background citation

Prospective, Randomized Trial of Personalized Medicine With Pentaglobin® After Surgical Infectious Source Control in Patients With Peritonitis

TypeinterventionalSponsorRWTH Aachen UniversityRan2017 to 2028Enrolled200ConditionsPeritonitis, Sepsis, Septic ShockArmsPentaglobin®/Standard of Care
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

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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

14 authors at 8 institutions in 1 country.

Evangelos J Giamarellos-Bourboulis
Efterpi Apostolidou
Malvina Lada
Ioannis Perdios
Nikolaos K Gatselis
Iraklis Tsangaris
Marianna Georgitsi
Magdalini Bristianou
Theodora Kanni
Kalliopi Sereti
Miltiades A Kyprianou
Anastasia Kotanidou
Apostolos Armaganidis
Hellenic Sepsis Study Group
National and Kapodistrian University of Athens · GRSismanoglio General Hospital · GRUniversity General Hospital Attikon · GREvangelismos Hospital · GRGeneral Hospital of Athens G. Genimatas · GRGeneral Hospital of Attica · GRTechnological Educational Institute of Central Greece · GRUniversity of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe aim of this study was to investigate the kinetics of immunoglobulin M (IgM) during the different stages of sepsis.

methodsIn this prospective multicenter study, blood sampling for IgM measurement was done within the first 24 hours from diagnosis in 332 critically ill patients; in 83 patients this was repeated upon progression to more severe stages. Among these 83 patients, 30 patients with severe sepsis progressed into shock and IgM was monitored daily for seven consecutive days. Peripheral blood mononuclear cells (PBMCs) were isolated from 55 patients and stimulated for IgM production.

resultsSerum IgM was decreased in septic shock compared to patients with systemic inflammatory response syndrome (SIRS) and patients with severe sepsis. Paired comparisons at distinct time points of the sepsis course showed that IgM was decreased only when patients deteriorated from severe sepsis to septic shock. Serial measurements in these patients, beginning from the early start of vasopressors, showed that the distribution of IgM over time was significantly greater for survivors than for non-survivors. Production of IgM by PBMCs was significantly lower at all stages of sepsis compared with healthy controls.

conclusionsSpecific changes of circulating IgM occur when patients with severe sepsis progress into septic shock. The distribution of IgM is lower among non-survivors.

Indexed as

Critical IllnessAgedAPACHEFemaleGreeceHumansImmunoglobulin MLeukocytes, MononuclearMalePrognosisProspective StudiesShock, SepticSystemic Inflammatory Response SyndromeTreatment OutcomeImmunoglobulin M

Identifiers

PMID24144038
PMCPMC4056013
OpenAlexW2011825836

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.