Evidence map›Paper›PMID 39349366›Full record

ArticleThe Journal of dermatology2024

Case report: A novel high-dose intravenous immunoglobulin preparation for the treatment of severe pemphigus vulgaris failing standard therapy.

Nadine Wiedenmayer, Katharina Hogrefe, Silvia Mihalceanu, Julia K Winkler, Alexander H Enk

Abstract readCase Reports
In one paragraph

Article in The Journal of dermatology, 2024. 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
–field-weighted citation impact
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.

  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

5 authors.

Nadine WiedenmayerDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Katharina HogrefeDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Silvia MihalceanuDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Julia K WinklerDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.ORCID https://orcid.org/0000-0003-3197-9867
Alexander H EnkDepartment of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pemphigus vulgaris (PV) is a severe autoimmune bullous dermatosis that is characterized by autoantibodies against epidermal adhesion proteins causing painful mucosal and skin blistering. Standard treatments for PV include corticosteroids, steroid-sparing immunosuppressants, or intravenous monoclonal anti-CD20-antibody therapy. The European guidelines suggest high-dose intravenous immunoglobulin (IVIg) therapy as a promising approach for severe or treatment-resistant cases. We report on a 65-year-old woman with severe and recurrent disease who achieved long-term disease stabilization with IVIg treatment. Because of recurrent fatigue and headache, the patient was switched to an alternative IVIg preparation with a novel manufacturing process, thus ensuring high purity and better tolerability. We observed excellent efficacy, yet side effects remained largely unchanged. Further studies are necessary to evaluate the long-term efficacy and tolerability of this new IVIg preparation.

Indexed as

Immunoglobulins, IntravenousPemphigusAgedDrug SubstitutionFemaleHumansImmunologic FactorsRecurrenceSeverity of Illness IndexTreatment FailureTreatment OutcomeImmunoglobulins, IntravenousImmunologic Factorsadverse effectsautoimmune bullous dermatosesintravenous immunoglobulinsIVIgpemphigus vulgaris

Identifiers

PMID39349366
PMCPMC11624157

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.