Evidence map›Paper›PMID 42241293›Full record

Observational studyRevista medica del Instituto Mexicano del Seguro Social2026

[Clinical profile of patients with secondary immunodeficiency on immunoglobulin replacement therapy].

Alicia Méndez-Gómez, Noemí Gómez-Hernández, Margarita Ortega-Cisneros, Bricia Melissa Gutiérrez-Zepeda, Antonio de Jesús Quintero-Rodríguez, Luis Alberto Duran-Marín, Marya Lizzeth Rosaldo-Solís, Antonio Quintero-Ramos

Abstract readEnglish AbstractObservational Study
In one paragraph

Observational study in Revista medica del Instituto Mexicano del Seguro Social, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

8 authors.

Alicia Méndez-GómezInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Departamento de Inmunología Clínica y Alergia. Guadalajara, Jalisco, México.ORCID 0009-0004-8407-2729
Noemí Gómez-HernándezInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Departamento de Inmunología Clínica y Alergia. Guadalajara, Jalisco, México.ORCID 0000-0003-0802-9927
Margarita Ortega-CisnerosInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Departamento de Inmunología Clínica y Alergia. Guadalajara, Jalisco, México.ORCID 0000-0002-4285-6769
Bricia Melissa Gutiérrez-ZepedaUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud, Departamento de Biología Molecular y Genómica. Guadalajara, Jalisco, México.ORCID 0000-0002-9239-665X
Antonio de Jesús Quintero-RodríguezUniversidad de Guadalajara, Centro Universitario de Ciencias de la Salud, Licenciatura en Médico Cirujano y Partero. Guadalajara, Jalisco, México.ORCID 0009-0009-9397-4421
Luis Alberto Duran-MarínInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Departamento de Inmunología Clínica y Alergia. Guadalajara, Jalisco, México.ORCID 0009-0003-7309-3420
Marya Lizzeth Rosaldo-SolísInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Departamento de Inmunología Clínica y Alergia. Guadalajara, Jalisco, México.ORCID 0009-0005-2760-6912
Antonio Quintero-RamosInstituto Mexicano del Seguro Social, Centro Médico Nacional de Occidente, Hospital de Especialidades, Unidad de Investigación Biomédica 02. Guadalajara, Jalisco, México.ORCID 0000-0001-5963-9712

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Secondary immunodeficiency (SID) is a disorder in which the immune system is compromised by external or acquired factors, reducing the quantity or function of immunoglobulins. This condition increases the need for specialist consultation, follow-up, and replacement therapy, which in turn raises healthcare costs. To date, few studies have clinically characterized patients with SID; therefore, understanding their profile will enable improved management and treatment. Objective: To describe the clinical profile of patients with SID receiving human immunoglobulin replacement therapy (IgG-RT). Material and methods: A retrospective observational study was conducted through the review of 40 medical records of patients with SID undergoing IgG-RT. Risk factors and the benefits of replacement therapy were analyzed. Results: The mean age was 48 years, with a predominance of women (62.5%). The most frequent conditions were rheumatologic diseases (38%), followed by hematologic disorders (31%) and protein-losing diseases (27%). All patients had received corticosteroids in combination with another immunosuppressant, and 77.5% had also been treated with rituximab. Infections were recorded in 50% of cases; however, only 35% received prophylaxis. Relapse was documented in 22.5% of patients, and mortality was 2.5%. Conclusions: The use of corticosteroids and immunosuppressants, specifically rituximab, was the main cause of SID, predominantly associated with rheumatologic and hematologic diseases.

Indexed as

Immunization, PassiveImmunoglobulins, IntravenousImmunologic Deficiency SyndromesAdolescentAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsYoung AdultImmunoglobulins, IntravenousAutoimmune DiseasesEnfermedades AutoinmunesGlucocorticoidesGlucocorticoidsImmunoglobulins, IntravenousImmunologic Deficiency SyndromesInmunoglobulinas IntravenosasRituximabSíndromes de Inmunodeficiencia

Identifiers

PMID42241293
PMCPMC13268660

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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.