Evidence map›Paper›PMID 20396937›Full record

ReviewJournal of clinical immunology2010

IVIG treatment and prognosis in Guillain-Barré syndrome.

Pieter A van Doorn, Krista Kuitwaard, Christa Walgaard, Rinske van Koningsveld, Liselotte Ruts, Bart C Jacobs

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of clinical immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
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  10. Postpartum Guillain-Barré syndrome: a case report.Annals of medicine and surgery (2012) · 2023
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  15. Pathogenic TNF-α drives peripheral nerve inflammation in an Aire-deficient model of autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Review
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  20. Changes of Serum IgG Dimer Levels after Treatment with IVIg in Guillain-Barré Syndrome.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2019
    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

6 authors at 2 institutions in 1 country.

Pieter A van DoornDepartment of Neurology, Erasmus MC, University Medical Center Rotterdam, room BA 450, s-Gravendijkwal 230, Rotterdam, The Netherlands. p.a.vandoorn@erasmusmc.nl
Krista Kuitwaard
Christa Walgaard
Rinske van Koningsveld
Liselotte Ruts
Bart C Jacobs
Erasmus MC · NLElkerliek Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGuillain-Barré syndrome (GBS) is an acute, immune-mediated polyneuropathy that often leads to severe weakness. Intravenous immunoglobulin (IVIG) is a proven effective treatment for GBS (class 1 evidence). However, about 25% of patients need artificial ventilation and 20% are still unable to walk unaided after 6 months. Important clinical factors associated with poor outcome are age, presence of preceding diarrhea and the severity of disability in the early course of disease. These clinical factors were combined in a clinical prognostic scoring scale, the Erasmus GBS Outcome Scale (EGOS). MATERIALS AND

methodsGBS patients being unable to walk unaided are currently treated with a standard single IVIg dose (0.4 g/kg bodyweight for 5 days). A recent retrospective study in 174 GBS patients enrolled in one of our randomized controlled clinical trials showed that patients with a minor increase of serum IgG level after standard single IVIg dose recovered significantly slower. Additionally, fewer patients reached the ability to walk unaided at six months after correction for the known clinical prognostic factors (multivariate analysis; P < 0.022). DISCUSSION: It is yet unknown why some GBS patients only have a minor increase after standard IVIg treatment. By using the EGOS it is possible to select GBS patients with a poor prognosis. These patients potentially may benefit from a second IVIg dose.

conclusionA standard dose of IVIG is not sufficiently effective in many GBS patients. Whether these patients might benefit from a second IVIg dose needs further investigation.

Indexed as

AnimalsCampylobacter InfectionsCampylobacter jejuniCombined Modality TherapyComplement ActivationCross ReactionsDisease ProgressionDisease SusceptibilityDose-Response Relationship, ImmunologicGuillain-Barre SyndromeHumansImmunoglobulins, IntravenousMiceMolecular MimicryParalysisPlasma ExchangeImmunoglobulins, Intravenous

Identifiers

PMID20396937
PMCPMC2883091
OpenAlexW1982825669

What OpenQuestion holds

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LicenceCC BY-NC
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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.