Evidence map›Paper›PMID 41854481›Full record

Observational studyRevista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia2026

Intravenous non-specific immunoglobulins as adjunctive therapy for invasive

Laura Caeiro-Martínez, David Brandariz-Núñez, María Sandra Albiñana-Pérez, Enrique Alemparte-Pardavila, Mónica Mourelo-Fariña, José María Gutiérrez-Urbón, Luis Margusino-Framiñán

Abstract readObservational Study
In one paragraph

Observational study in Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Laura Caeiro-MartínezPharmacy Department/Service, A Coruña University Hospital (CHUAC), A Coruña, Spain. laura.caeiro.martinez@sergas.es.ORCID 0009-0006-9896-3017
David Brandariz-NúñezPharmacy Department/Service, A Coruña University Hospital (CHUAC), A Coruña, Spain.ORCID 0000-0003-1633-5465
María Sandra Albiñana-PérezPharmacy Department/Service, A Coruña University Hospital (CHUAC), A Coruña, Spain.ORCID 0000-0003-0969-0119
Enrique Alemparte-PardavilaCritical Care Unit, A Coruña University Hospital (CHUAC), A Coruña, Spain.
Mónica Mourelo-FariñaCritical Care Unit, A Coruña University Hospital (CHUAC), A Coruña, Spain.ORCID 0000-0003-3690-0265
José María Gutiérrez-UrbónPharmacy Department/Service, A Coruña University Hospital (CHUAC), A Coruña, Spain.ORCID 0000-0002-9076-5378
Luis Margusino-FramiñánPharmacy Department/Service, A Coruña University Hospital (CHUAC), A Coruña, Spain.ORCID 0000-0003-4309-1662

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAdjunctive intravenous non-specific immunoglobulin (IVIG) is used in the management of streptococcal toxic shock syndrome, although supporting evidence remains limited. The primary objective of this study was to describe the use of IVIG in patients with invasive MATERIALS AND

methodsWe conducted a retrospective observational study over 11 years, including patients diagnosed with invasive

resultsTwenty-three patients were included, with a mean age of 63.2 ± 16.3 years; 47.8% were male. Most patients (73.9%) developed septic shock and STSS, requiring admission to intensive care units. The mean Sequential Organ Failure Assessment (SOFA) score was 9.1 ± 4.9. High-dose IVIG (2.0 ± 0.2 g/kg) was administered promptly, with a mean time to first infusion of 0.26 ± 0.47 days from admission. In-hospital mortality was 21.7% overall and 29.4% among STSS patients. Non-survivors had significantly higher disease severity and were more likely to develop hepatic dysfunction and require continuous renal replacement therapy (CRRT). Two patients (8.7%) experienced IVIG-related adverse events, both of which were mild.

conclusionEarly and standardized high-dose IVIG administration, in combination with prompt targeted antibiotic therapy and intensive supportive care, was associated with mortality rates similar to, or lower than, those previously reported. Initial disease severity, hepatic dysfunction, and need for CRRT were identified as predictors of mortality. IVIG demonstrated a favorable safety profile.

Indexed as

Immunoglobulins, IntravenousStreptococcal InfectionsStreptococcus pyogenesAnti-Bacterial AgentsFemaleHospital MortalityHumansMaleMiddle AgedRetrospective StudiesShock, SepticTreatment OutcomeAnti-Bacterial AgentsImmunoglobulins, IntravenousIntravenous immunoglobulinsStreptococcal toxic shock syndromeToxic shock syndrome

Identifiers

PMID41854481
PMCPMC13071772

What OpenQuestion holds

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Registered trials

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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.