Evidence map›Paper›PMID 40771807›Full record

ArticleFrontiers in immunology2025

Real-world patterns of immunoglobulin replacement therapy for infection prevention in common variable immunodeficiency: a multicenter nationwide study.

Pedro Moral Moral, Victor Garcia-Bustos, Héctor Balastegui-Martin, Sandra Martínez Mercader, Carmen Bracke, Lourdes Mateu, Xavier Solanich, Arnau Antolí, Juan Luis Carrillo-Linares, Ángel Robles-Marhuenda and 16 more

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

26 authors.

Pedro Moral MoralPrimary Immunodeficiencies Unit, Department of Internal Medicine, University and Polytechnic Hospital La Fe, Valencia, Spain.
Victor Garcia-BustosPrimary Immunodeficiencies Unit, Department of Internal Medicine, University and Polytechnic Hospital La Fe, Valencia, Spain.
Héctor Balastegui-MartinPrimary Immunodeficiencies Unit, Department of Internal Medicine, University and Polytechnic Hospital La Fe, Valencia, Spain.
Sandra Martínez MercaderPrimary Immunodeficiencies Unit, Department of Internal Medicine, University and Polytechnic Hospital La Fe, Valencia, Spain.
Carmen BrackeInfectious Diseases Service, Germans Trias i Pujol Hospital, Badalona, Spain.
Lourdes MateuInfectious Diseases Service, Germans Trias i Pujol Hospital, Badalona, Spain.
Xavier SolanichAdult Primary Immunodefciency Unit (UFIPA), Internal Medicine Department, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain.
Arnau AntolíAdult Primary Immunodefciency Unit (UFIPA), Internal Medicine Department, Bellvitge University Hospital, L'Hospitalet de Llobregat, Barcelona, Spain.
Juan Luis Carrillo-LinaresDepartment of Internal Medicine, Virgen de la Victoria University Hospital, Málaga, Spain.
Ángel Robles-MarhuendaDepartment of Internal Medicine, La Paz University Hospital, Madrid, Spain.
Francesc PuchadesDepartment of Internal Medicine, University General Hospital of Valencia, Valencia, Spain.
Ana Pelaez BallestaDepartment of Internal Medicine, Rafael Méndez University Hospital, Murcia, Spain.
Nuria López-OsleDepartment of Internal Medicine, Cruces University Hospital, Bizkaia, Spain.
Miguel Ángel Torralba-CabezaUnit for Rare Diseases, Internal Medicine Service, Lozano Blesa University Hospital, Zaragoza, Spain.
Ana María Bielsa MasdeuDepartment of Internal Medicine, Miguel Servet University Hospital, Zaragoza, Spain.
Jorge Gil NiñoImmunodeficiencies Clinic, Internal Medicine Department, 12 de Octubre Hospital, Madrid, Spain.
Nuria Tornador GayaDepartment of Internal Medicine, University General Hospital of Castellón, Castellón, Spain.
Guillem Pascual CastellanosDepartment of Internal Medicine, University General Hospital of Castellón, Castellón, Spain.
Rosario Sánchez-MartínezInternal Medicine Department, Dr. Balmis General University Hospital, Alicante Institute for Health and Biomedical Research, Alicante, Spain.
José Manuel Barragán-CasasDepartment of Internal Medicine, Complejo Asistencial de Ávila, Ávila, Spain.
Andrés González-GarcíaSystemic Autoimmune Diseases Unit, Internal Medicine Service, Ramón y Cajal Hospital, Ramón y Cajal Health Research Institute, Madrid, Spain.
José Luís Patier de la PeñaDepartment of Internal Medicine, University Hospital Alcorcón Foundation, Madrid, Spain.
Daniel López-WolfDepartment of Internal Medicine, General University Hospital of Elche, Alicante, Spain.
Antonia Mora RufeteDepartment of Internal Medicine, General University Hospital of Elche, Alicante, Spain.
Alba Canovas MoraDepartment of Internal Medicine, General University Hospital of Elche, Alicante, Spain.
Marta Dafne Cabañero-NavalonPrimary Immunodeficiencies Unit, Department of Internal Medicine, University and Polytechnic Hospital La Fe, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Immunoglobulin replacement therapy (IgRT), administered intravenously (IVIg) or subcutaneously (SCIg), is the cornerstone treatment for patients with Common Variable Immunodeficiency (CVID). Although both modalities demonstrate similar efficacy, SCIg is associated with fewer systemic adverse events and increased patient autonomy. Despite these advantages, its utilization remains limited in certain regions, particularly in the Mediterranean region. This study aimed to evaluate real-world patterns of IgRT use in Spanish CVID patients and provide a comprehensive analysis of the factors associated with IVIg and SCIg administration in routine clinical practice. Methods: A cross-sectional, multicenter study was conducted using data from the GTEM-SEMI-CVID Registry, encompassing 212 adult CVID patients receiving IgRT across Spain. Patients were grouped based on the administration route: IVIg and SCIg. Demographic, clinical, and immunological data, including IgRT modality, dosage, administration setting, and comorbidities, were collected. Comparative statistical analyses were performed to identify differences between both treatment groups. Results: Of the 212 patients, 58.5% received IVIg and 41.5% received SCIg. SCIg recipients were younger (47.5 vs. 54.8 years, Conclusion: This study provides real-world evidence on IgRT patterns in Spanish patients with CVID, revealing a marked increase in SCIg use over the past decade, although IVIg remains predominant, especially in secondary hospitals. Age significantly influenced the choice of modality, with IVIg preferred for older patients and SCIg for younger ones, while disease severity did not impact this decision. These findings underscore the need to optimize access to SCIg, particularly in secondary centers, to enhance patient autonomy and improve therapeutic outcomes.

Indexed as

Common Variable ImmunodeficiencyImmunoglobulins, IntravenousInfectionsAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedRegistriesSpainTreatment OutcomeImmunoglobulins, Intravenouscommon variable immunodeficiency (CVID)immunoglobulin replacement therapy (IGRT)intravenous immunoglobulin (IVIg)real-world evidencesubcutaneous immunoglobulin (SCIg)

Identifiers

PMID40771807
PMCPMC12325207

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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.