Evidence map›Paper›PMID 37023037›Full record

ArticlePloS one2023

The impact of COVID-19 in children with Sickle Cell Disease: Results of a multicentric registry.

Claudia de Melo Oliveira, Victor Jablonski Soares, Josefina Aparecida Pellegrini Braga, Thaís Alcantara Bonilha, Isis Magalhães, Sandra Regina Loggetto, Ciliana Rechenmacher, Liane Esteves Daudt, Mariana Bohns Michalowski

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2023. 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
0.9field-weighted citation impact, top 24% of its field
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, 3 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 5 institutions in 1 country.

Claudia de Melo OliveiraDepartamento de Pediatria, Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.ORCID 0000-0002-4882-7555
Victor Jablonski SoaresFaculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Josefina Aparecida Pellegrini BragaDepartamento de Pediatria, Universidade Federal de São Paulo, São Paulo, Brazil.ORCID 0000-0001-7839-6904
Thaís Alcantara BonilhaIPPMG Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Isis MagalhãesHospital da Criança de Brasília José Alencar, Brasília, Brazil.ORCID 0000-0003-2447-3753
Sandra Regina LoggettoHospital Infantil Sabará, São Paulo, Brazil.ORCID 0000-0002-8068-7986
Ciliana RechenmacherDepartamento de Pediatria, Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Liane Esteves DaudtDepartamento de Pediatria, Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Mariana Bohns MichalowskiDepartamento de Pediatria, Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.ORCID 0000-0002-9482-0776
Universidade Federal do Rio Grande do Sul · BRHospital Infantil Albert Sabin · BRHospital Universitário de Brasília · BRUniversidade Federal de São Paulo · BRUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo analyze the outcomes of children with sickle cell disease (SCD) and COVID-19.

methodA multicenter prospective study was conducted in five hematological centers from Central and Southeast Brazil, starting in April 2020. The variables recorded include clinical symptoms, diagnostic methods, therapeutic measures, and treatment sites. The clinical repercussions of the infection on the initial treatment and the overall prognosis were also evaluated.

resultsTwenty-five unvaccinated children, aged 4 to 17 years, with SCD and a positive SARS-CoV-2 RT-PCR result participated in this study. Patients were classified as SCD types SS (n = 20, 80%) and SC (n = 5, 20%). Clinical characteristics and evolution were similar in both groups (p>0.05), except for the fetal hemoglobin value which was higher among the SC patients (p = 0.025). The most frequent symptoms were hyperthermia (72%) and cough (40%). Three children were admitted to the intensive care unit, all of whom were overweight/obese (p = 0.078). No deaths were observed.

conclusionsAlthough SCD leads to specific complications, the results found in this sample suggest that COVID-19 does not seem to carry an increased mortality risk in pediatric patients with this disease.

Indexed as

Anemia, Sickle CellCOVID-19ChildHumansProspective StudiesRegistriesSARS-CoV-2

Identifiers

PMID37023037
PMCPMC10079108
OpenAlexW4362657313

What OpenQuestion holds

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LicenceCC BY
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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.