Evidence map›Paper›PMID 33238140›Full record

ReviewJornal de pediatria

Immunological deficiencies: more frequent than they seem to be.

Irma Cecília Douglas Paes Barreto, Bruno Acatauassú Paes Barreto, Erica Gomes do Nascimento Cavalcante, Antonio Condino Neto

Abstract readReview
In one paragraph

Review in Jornal de pediatria. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. [Genetics of inborn errors of immunity].Zeitschrift fur Rheumatologie · 2022
    Article
  8. 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

4 authors.

Irma Cecília Douglas Paes BarretoCentro Universitário do Estado do Pará (CESUPA), Departamento de Pediatria, Serviço de Alergia e Imunologia Pediátrica, Belém, PA, Brazil. Electronic address: irmacdouglas@gmail.com.
Bruno Acatauassú Paes BarretoCentro Universitário do Estado do Pará (CESUPA), Departamento de Pediatria, Serviço de Alergia e Imunologia Pediátrica, Belém, PA, Brazil; Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Erica Gomes do Nascimento CavalcanteUniversidade de São Paulo (USP), São Paulo, SP, Brazil; Centro Universitário do Estado do Pará (CESUPA), Departamento de Pediatria, Serviço de Reumatologia Pediátrica, Belém, PA, Brazil.
Antonio Condino NetoUniversidade de São Paulo (USP), Instituto de Ciências Biomédicas, Departamento de Imunologia, São Paulo, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveA review article was carried out, addressing the clinical and epidemiological characteristics of immune system deficiencies, which are associated with or predispose to recurrent infectious processes, autoimmune diseases, auto inflammatory diseases, or neoplasms, and which are classified as inborn errors of immunity (IEI) and secondary immunodeficiencies (SID). Emphasis was placed on the classification of the main signs and symptoms for each organ and system, which will serve as warning signs, to guide the pediatrician in the investigation of the main IEI. In addition, the main secondary changes in the immune system triggered by infections (with emphasis on COVID-19), drugs, chronic diseases, metabolic and nutritional disorders were identified. SOURCES OF DATA: This review included articles published in the last five years and that were identified in the MEDLINE platform (PubMed). SUMMARY OF

findingsThe recurrence of infectious processes, associated with the severity of the condition and/or unusual profile of the infectious agent, always related to the age range of symptom onset, are the most important findings for suspected diagnosis.

conclusionsConsidering this scenario, immunity disorders should be part of the investigation carried out by the general pediatrician, whether they are the innate errors of immunity (primary immunodeficiencies) or secondary immunodeficiencies, so that the diagnosis is attained as early as possible and therapeutic measures are implemented, reducing the morbidity and mortality of these patients.

Indexed as

COVID-19Immunologic Deficiency SyndromesHumansRecurrenceSARS-CoV-2ClassificationCOVID-19EpidemiologyImmunodeficiency disordersPrimary immunodeficiency disordersSARS-CoV-2

Identifiers

PMID33238140
PMCPMC9432333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.