Syndrômes drepanocytaires :contribution au dépistage, au diagnostic et à la prise en charge au Burkina Faso

Doctorat en Sciences biomédicales et pharmaceutiques (Médecine)info:eu-repo/semantics/nonPublishe

Neonatal screening for sickle cell disorders in Ouagadougou, Burkina Faso: A pilot study

SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Newborn screening for haemoglobinopathies in Ouagadougou (Burkina Faso)

info:eu-repo/semantics/nonPublishe

Neonatal screening and clinical care programmes for sickle cell disorders in sub-Saharan Africa: lessons from pilot studies.

Despite the widespread use of neonatal screening programmes for sickle cell disease in Western regions, few studies have focused on the special healthcare needs in sub-Saharan African countries. The purpose of this review is to evaluate the need for a neonatal screening programme for sickle cell disease, and if justified, to propose a realistic healthcare programme for sickle cell newborns in those countries based on personal experiences in Kinshasa (Democratic Republic of the Congo) and Ouagadougou (Burkina Faso) as well as from a review of the literature.Journal ArticleResearch Support, Non-U.S. Gov'tReviewSCOPUS: ar.jinfo:eu-repo/semantics/publishe

Neonatal haemoglobinopathy screening in Burkina Faso

SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Impact of multivitamin and mineral supplements on mortality and nutritional status of hospitalized severely malnourished HIV/AIDS infected children.

info:eu-repo/semantics/publishe

Le syndrome drépanocytaire de type hémoglobine SC :expérience du CHU Yalgado Ouédraogo de Ouagadougou (Burkina Faso).

To evaluate the clinical features of children with hemoglobin sickle cell disease (HbSC) and compare them to children with sickle cell anemia (HbSS).English AbstractJournal Articleinfo:eu-repo/semantics/publishe

Impact of HIV/AIDS on mortality and nutritional recovery among hospitalized severely malnourished children before starting antiretroviral therapy.

info:eu-repo/semantics/publishe

Les syndromes drépanocytaires majeurs: Une enquête anonyme auprès du corps médical au Burkina Faso

SCOPUS: ar.jinfo:eu-repo/semantics/publishe

How to implement medical and patient associations in low‐income countries: A proposition from the African French Alliance for the Treatment of Haemophilia (AFATH)

International audienceIntroduction: There is a lack of joint recommendations by healthcare professionals (HCP) and patient organizations when a partnership between high and low-income countries in the field of haemophilia is planned.Aim: To draft recommendations to clarify the methodology when a partnership between low- and high-income countries is planned with the objective of a long-term implication. This methodology is to be implemented for fulfilling both medical and associative aims.Methods: Based on the available literature, a first document was written, then diffused to AFATH (Alliance Franco-Africaine pour le Traitement de l'Hémophilie) members, and after a one-day meeting and further amendments, a second draft was approved by all members before submission for publication.Results: Based on 6 years experience, several recommendations regarding the joint and separate roles of patient association and HCP for a first mission in French-speaking sub-Saharan African countries have been established. The proposed methodology for establishing preliminary contacts, the first visit and the key points for diagnostic action, medical follow-up, patient education and advocacy strategy outlines a model of partnership between patients and HCP.Conclusion: This paper written jointly by patients and physicians underlines the importance of reciprocal expert guidance and a partnership based on complementary inputs