Literature DB >> 19712051

Prevalence of sickle cell disease in a northeastern region of the Democratic Republic of Congo: what impact on transfusion policy?

B Agasa1, K Bosunga, A Opara, K Tshilumba, E Dupont, F Vertongen, F Cotton, B Gulbis.   

Abstract

Transfusion therapy may save the lives of patients with sickle cell disease (SCD), but it is also associated with a high risk of transmission of infection. The aims of this study were to determine the prevalence of SCD in a northeastern region of the Democratic Republic of Congo (DRC), and to define ways in which the procedures involved in the security of transfusions should be improved. During a 3-month period in 2006/2007, 520 samples of umbilical cord blood were obtained through neonatal screening in five health centres in Kisangani. The samples were analysed using an isoelectric focusing technique. The estimated prevalence of sickle cell trait and SCD in the population tested was 23.3 and 0.96%, respectively. These numbers will be presented for the attention of the health authorities in DRC with responsibility for SCD and they will be asked to consider improvements in treatment procedures for SCD, such as blood transfusions, as a public health priority.

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Year:  2009        PMID: 19712051     DOI: 10.1111/j.1365-3148.2009.00943.x

Source DB:  PubMed          Journal:  Transfus Med        ISSN: 0958-7578            Impact factor:   2.019


  18 in total

1.  Congolese children with sickle cell trait may exhibit glomerular hyperfiltration: A case control study.

Authors:  Michel Ntetani Aloni; René Makwala Ngiyulu; Célestin Ndosimao Nsibu; Pépé Mfutu Ekulu; Jean Robert Makulo; Jean-Lambert Gini-Ehungu; Nazaire Mangani Nseka; François Bompeka Lepira
Journal:  J Clin Lab Anal       Date:  2017-01-19       Impact factor: 2.352

2.  Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa.

Authors:  Tite M Mikobi; Prosper Lukusa Tshilobo; Michel N Aloni; Pierre Z Akilimali; Georges Mvumbi-Lelo; Jean Marie Mbuyi-Muamba
Journal:  J Clin Lab Anal       Date:  2017-01-23       Impact factor: 2.352

3.  Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α3.7 triplication in congolese patients than in worldwide series.

Authors:  Tite Minga Mikobi; Prosper Tshilobo Lukusa; Michel Ntetani Aloni; Aimé Lumaka; Pierre Zalagile Akilimali; Koenraad Devriendt; Gert Matthijs; Jean-Marie Mbuyi Muamba; Valerie Race
Journal:  J Clin Lab Anal       Date:  2017-03-09       Impact factor: 2.352

4.  Renal Abnormalities among Sickle Cell Disease Patients in a Poor Management Setting: A Survey in the Democratic Republic of the Congo.

Authors:  Paul Kambale-Kombi; Roland Marini Djang'eing'a; Jean-Pierre Alworong'a Opara; Jean-Paulin Mbo Mukonkole; Vincent Bours; Serge Tonen-Wolyec; Dieu-Merci Mbumba Lupaka; Lucien Bolukaoto Bome; Charles Kayembe Tshilumba; Salomon Batina-Agasa
Journal:  Mediterr J Hematol Infect Dis       Date:  2022-07-01       Impact factor: 3.122

5.  Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients.

Authors:  Tite Minga Mikobi; Prosper Lukusa Tshilobo; Michel Ntetani Aloni; Georges Mvumbi Lelo; Pierre Zalagile Akilimali; Jean Jacques Muyembe-Tamfum; Valérie Race; Gert Matthijs; Jean Marie Mbuyi Mwamba
Journal:  PLoS One       Date:  2015-05-06       Impact factor: 3.240

6.  [Psychosocial impact of sickle cell disease in the parents of children living in Kinshasa, Democratic Republic of Congo: a qualitative study].

Authors:  Evariste Luboya; Jean-Christophe Bukasa Tshilonda; Mathilde Bothale Ekila; Michel Ntetani Aloni
Journal:  Pan Afr Med J       Date:  2014-09-02

7.  Acute Crises and Complications of Sickle Cell Anemia Among Patients Attending a Pediatric Tertiary Unit in Kinshasa, Democratic Republic Of Congo.

Authors:  Michel Ntetani Aloni; Bertin Tshimanga Kadima; Pépé Mfutu Ekulu; Aléine Nzazi Budiongo; René Makuala Ngiyulu; Jean Lambert Gini-Ehungu
Journal:  Hematol Rep       Date:  2017-06-01

8.  Sickle cell trait is not associated with chronic kidney disease in adult Congolese patients: a clinic-based, cross-sectional study.

Authors:  K Mukendi; F B Lepira; J R Makulo; K E Sumaili; P K Kayembe; M N Nseka
Journal:  Cardiovasc J Afr       Date:  2015 May-Jun       Impact factor: 1.167

9.  Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions.

Authors:  Frédéric B Piel; Simon I Hay; Sunetra Gupta; David J Weatherall; Thomas N Williams
Journal:  PLoS Med       Date:  2013-07-16       Impact factor: 11.069

10.  [Awareness and attitudes of 50 congolese families affected by sickle cell disease: a local survey].

Authors:  Benoît Mbiya Mukinayi; Didier Kalombo Kalenda; Stéphanie Mbelu; Béatrice Gulbis
Journal:  Pan Afr Med J       Date:  2018-01-11
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