Evidence map›Paper›PMID 37799288›Full record

ArticleAnemia2023

Associated Factors of Cholelithiasis among Younger Children with Sickle Cell Disease at the National Reference Center for Sickle Cell Disease in Brazzaville, Congo.

Firmine Olivia Galiba Atipo Tsiba, Clément Pacha Mikia, Jennifer Armandine Elira Samba, Jade Vanessa Nziengui Mboumba, Félix Malanda, Clausina Mikolele Ahoui, Alexis Elira Dokekias

Open access · goldAbstract read
In one paragraph

Article in Anemia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Cholecystectomy in Children: Indications and Timing.Children (Basel, Switzerland) · 2025
    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

7 authors at 1 institution in 1 country.

Firmine Olivia Galiba Atipo TsibaNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.ORCID https://orcid.org/0000-0002-4444-7547
Clément Pacha MikiaNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.ORCID https://orcid.org/0009-0006-3029-6924
Jennifer Armandine Elira SambaNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.ORCID https://orcid.org/0009-0003-4893-9455
Jade Vanessa Nziengui MboumbaNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.ORCID https://orcid.org/0009-0002-2842-7228
Félix MalandaNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.
Clausina Mikolele AhouiMarien Ngouabi University, Brazzaville, Congo.ORCID https://orcid.org/0009-0002-9916-6942
Alexis Elira DokekiasNational Reference Center for Sickle Cell Disease "Antoinette Sassou Nguesso", Brazzaville, Congo.ORCID https://orcid.org/0000-0002-2819-6872
Marien Ngouabi University · CG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic hemolysis predisposes sickle cell patients to the development of gallstones. Their frequency increases with age, but they may appear early in young children. In the absence of management, they expose the patient to complications that can hinder the quality of life and sometimes even death. This survey aimed to identify the associated factors of the occurrence of cholelithiasis. Materials and Methods: It was a case-control study carried out between January 2017 and June 2022 at the National Reference Center for Sickle Cell Disease (SCD) "Antoinette Sassou N'guesso" in Brazzaville. It concerned 37 children with cholelithiasis. Sociodemographic (socioeconomic status and diet) and clinical (body mass index, frequency of vasoocclusive crises and hospitalization for vasoocclusive crises, number of blood transfusion, and chronic complications) as well as hematological examination (type of SCD and blood count in the intercritical period) and hydroxyurea treatment were compared with those of 74 children with no clinical and radiographic signs of cholelithiasis. The chi-squared statistical test and the odds ratio were used for the comparison ( Results: The average age was 9.70 ± 1.73 years. The 10-12 age group was the most represented (22 cases or 59.45%), followed by 7- to 9-year-olds (12 cases or 32.43%). Three children (8.10%) were 6  years old. The sex ratio was 0.68 Conclusion: A national strategy to facilitate access to care for patients living with sickle cell disease is imperative. Moreover, emphasis should be placed on the prevention and early management of acute complications of SCD.

Identifiers

PMID37799288
PMCPMC10550436
OpenAlexW4387089951

What OpenQuestion holds

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LicenceCC BY
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.