Evidence map›Paper›PMID 39251065›Full record

ArticleJornal de pediatria

Epidemiological profile trends and cost of pediatric sickle cell disease in Brazil from 2008 to 2022.

Luiza Telles, Paulo Henrique Moreira Melo, Luana Baptistele Dornelas, Gabriele Eckerdt Lech, Natália Zaneti Sampaio, Ayla Gerk, Madeleine Carroll, Cristina Pires Camargo

Abstract read
In one paragraph

Article in Jornal de pediatria. 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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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.

Luiza TellesInstituto de Educação Médica (IDOMED/Estácio, Campus Vista Carioca), Rio de Janeiro, RJ, Brazil. Electronic address: lulustelles21@gmail.com.
Paulo Henrique Moreira MeloUniversidade Federal de Minas Gerais, Faculdade de Medicina, Belo Horizonte, MG, Brazil.
Luana Baptistele DornelasFaculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, SP, Brazil.
Gabriele Eckerdt LechPontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Natália Zaneti SampaioUniversidade de Araraquara, Araraquara, SP, Brazil.
Ayla GerkHarvard Medical School, Program in Global Surgery and Social Change, Boston, United States; McGill University, Department of Surgical and Interventional Sciences, Quebec, Canada; Montreal Children's Hospital, Harvey E. Beardmore Division of Pediatric Surgery, Quebec, Canada.
Madeleine CarrollHarvard Medical School, Program in Global Surgery and Social Change, Boston, United States.
Cristina Pires CamargoFaculdade de Medicina, Universidade de São Paulo, Microcirurgia Laboratorial e Cirurgia Plástica, São Paulo, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate the epidemiological trends of Pediatric Sickle Cell Disease (SCD) in Brazil over the period 2008-2022, with a focus on understanding the incidence, mortality rates, and associated healthcare costs. The study explored potential associations between patient characteristics and the occurrence of crises in pediatric SCD cases.

methodsA cross-sectional study was conducted, analyzing national annual rates of pediatric SCD hospitalizations using data from the FioCruz platform. Descriptive and inferential analyses, including time series and ARIMA regression, were employed. Economic dimensions were assessed using cost categorization. The study followed STROBE reporting guidelines.

resultsData on 81,942 pediatric SCD hospitalizations were collected, with a predominance of crisis-related cases (74.08 %). Males and children under five years old were most affected. Regional disparities were observed, with the Southwest region recording the highest hospitalization rates. ICU costs were higher for crisis-related hospitalizations. Mortality rates were significantly higher for crisis-related cases (p < 0.001), with ARIMA regression indicating a significant association between hospitalizations for crisis-related cases and mortality.

conclusionThis study highlights the significant burden of pediatric SCD in Brazil, particularly crisis-related cases, suggesting a need for focused interventions. By prioritizing early detection, equitable access to healthcare, and evidence-based interventions, Brazil can mitigate the burden of SCD and improve patient outcomes. These findings contribute to informing public health policies and interventions aimed at addressing the challenges of pediatric SCD management in Brazil.

Indexed as

Anemia, Sickle CellHealth Care CostsHospitalizationAdolescentBrazilChildChild, PreschoolCost of IllnessCross-Sectional StudiesFemaleHumansIncidenceInfantInfant, NewbornMaleCost of illnessGlobal healthPediatricPublic healthSickle cell anemia

Identifiers

PMID39251065
PMCPMC11763541

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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.