Evidence map›Paper›PMID 38846115›Full record

ArticleMedecine tropicale et sante internationale2024

[Blood count abnormalities in the association of sickle cell disease and malaria in clinical hematology at the CNHU-HKM in Cotonou (Bénin)].

Alban Gildas Comlan Zohoun, Tatiana Bagloagbodande, Axel Adanho, Romaric Massi, Bienvenu Houssou, Gnon Gourou Orou Guiwa, Justin Dèhoumon, Josiane Mehou, Ludovic Anani, Anne Vovor and 1 more

Abstract readEnglish Abstract
In one paragraph

Article in Medecine tropicale et sante internationale, 2024. 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

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

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

11 authors.

Alban Gildas Comlan ZohounLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Tatiana BagloagbodandeLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Axel AdanhoFaculté des sciences de la santé, Université d'Abomey-Calavi, Cotonou, Bénin.
Romaric MassiLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Bienvenu HoussouLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Gnon Gourou Orou GuiwaLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Justin DèhoumonLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Josiane MehouLaboratoire d'hématologie, Clinique universitaire des maladies du sang, Centre national hospitalier universitaire Hubert Koutoukou Maga (CNHU-HKM), Cotonou, Bénin.
Ludovic AnaniFaculté des sciences de la santé, Université d'Abomey-Calavi, Cotonou, Bénin.
Anne VovorFaculté des sciences de la santé, Université de Lomé, Togo Auteur.
Dorothée KindegazardFaculté des sciences de la santé, Université d'Abomey-Calavi, Cotonou, Bénin.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Although a protective effect of hemoglobin S has been described, malaria has frequently been associated with increased morbidity and mortality in sickle cell disease patients in Africa. Various cytopenias are frequently found on the haemograms of these patients. In Benin, a malaria-endemic zone with a high prevalence of sickle cell disease, the aim of this study was to establish and compare the blood count profile according to hemoglobin type in the association of sickle cell disease and malaria. Material and method: This was a prospective descriptive study. It covered a 24-month period from October 2020 to October 2022. It included all patients with major sickle cell syndrome seen in clinical haematology and with a positive thick drop/parasite density, whatever the parasitaemia value. For each patient, a blood count was performed on the Sysmex XT 4000i machine, supplemented by a smear study after staining with May-Grunwald Giemsa. Data were analyzed using R 3.6.1 software. Results: Three hundred non-redundant cases with a positive thick smear were identified in sickle cell patients, including 208 SS homozygotes (69.3%) and 92 SC heterozygotes (30.7%). In contrast, there were 181 non-redundant cases with a negative thick smear, including 119 SS homozygotes (65.7%) and 62 SC heterozygotes (34.3%). Among subjects with a positive thick smear, the majority of patients (70%) exhibited clinical symptoms. Severe malaria was observed in 58% of the cases. The proportion of severe malaria was higher in SS homozygote patients than in double heterozygote SC patients (p < 0.0001). The mean parasite density was higher in SS individuals (4 320.7 ± 2 185 trophozoites/pL) compared to SC individuals (1 564.4 ± 1 221 trophozoites/pL; p < 0.0001). Discussion: Sickle cell disease and malaria represent two major public health problems. However, contrary to popular belief, sickle cell disease is not immune to malaria infestation. Malaria is recognized as one of the main causes of morbidity and mortality in sickle cell patients, particularly children. In Benin, its association with sickle cell emergencies has already been reported.Our study found that malaria was predominantly associated with the homozygous SS form (p < 0.00001). Severe malaria was the most common clinical form. All malaria infestations in our series were due to

Indexed as

Anemia, Sickle CellMalariaAdolescentAdultBeninBlood Cell CountChildChild, PreschoolFemaleHemoglobin, SickleHumansMaleMiddle AgedProspective StudiesYoung AdultHemoglobin, SickleBeninBlood countMalariaSickle cell diseaseSub-Saharan Africa

Identifiers

PMID38846115
PMCPMC11151902

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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.