Results 11 to 20 of about 2,268 (156)

Costs of Treating Uncomplicated Sickle Cell Complications in a Day Hospital Setting in Equatorial Africa. [PDF]

Anemia
Sickle cell disease (SCD) is a major public health concern in Africa. SCD healthcare expenses are covered by personal finances in the Congo due to the absence of universal public health insurance. Various strategies have been implemented to minimize this economic burden, including an outpatient management strategy. The present study evaluated the costs
Ngolet LO, Taylor J, de Chabervy Atipo A, Mikia CP, Bango C, Bantsimba FS, Ondzotto Ibatta I, Dokekias AE.   +7 more
europepmc   +2 more sources

Genetic Contribution to Asthma Informs Acute Chest Syndrome Pathophysiology and Risk Stratification. [PDF]

Am J Hematol
ABSTRACT Acute chest syndrome (ACS) is a severe complication of sickle cell disease (SCD) occurring in ~50% of patients, some presenting frequent episodes. We lack tools to identify patients at high risk of ACS occurrence or frequent episodes. Epidemiological studies have found an association between asthma and ACS, but whether this link is causal is ...
El Aouhel S, Bellegarde V, Da Silva Faria S, St-Laurent T, Lecluze E, Pham Hung d'Alexandry d'Orengiani AL, Galactéros F, Bartolucci P, Legault MA, Lettre G, Pincez T.   +10 more
europepmc   +2 more sources

Mitochondrial retention in mature red blood cells from patients with sickle cell disease is associated with stress erythropoiesis but not with proinflammatory state. [PDF]

Hemasphere
HemaSphere, Volume 8, Issue 11, November 2024.
Romana M, Laurance S, Hardy-Dessources MD, Claer L, Ravion S, Dorgham K, Garnier Y, Kuznicki L, Tarer V, Tressières B, Lefevre SD, Baccini V, Ostuni MA, Le Van Kim C, Etienne-Julan M.   +14 more
europepmc   +2 more sources

PI-09: LESSONS LEARNED FROM ONE DECADE EXPERIENCE OF THE « CENTRE DE RECHERCHE ET DE LUTTE CONTRE LA DRÉPANOCYTOSE (CRLD) » IN BAMAKO, MALI. [PDF]

Hemasphere, 2022
HemaSphere, Volume 6, Issue S4, Page 13-14, August 2022.
D. D, A. G.
europepmc   +2 more sources

Is chest X-ray still relevant for acute chest syndrome diagnosis? [PDF]

Health Sci Rep
Health Science Reports, Volume 7, Issue 5, May 2024.
Pelinski Y, Guindo A, Kassasseya C, Diallo D, Arlet JB, Mekontso Dessap A, Habibi A, Bartolucci P.   +7 more
europepmc   +2 more sources

Association of haemolysis markers, blood viscosity and microcirculation function with organ damage in sickle cell disease in sub‐Saharan Africa (the BIOCADRE study)

British Journal of Haematology, Volume 203, Issue 2, Page 319-326, October 2023., 2023
A case‐control study nested in the CADRE multinational African cohort was conducted in Bamako and Dakar in 235 patients with sickle cell anemia (SCA) to test multiple biological and functional markers as potential markers of six different SCA‐related chronic organ damage.
Brigitte Ranque, Mor Diaw, Abdoul Karim Dembele, Claudine Lapoumeroulie, Lucile Offredo, Oumar Tessougue, Serigne Mourtalla Gueye, Dapa Diallo, Saliou Diop, Yves Colin‐Aronovicz, Xavier Jouven, Olivier Blanc‐Brude, Pierre‐Louis Tharaux, Sylvain Le Jeune, Philippe Connes, Marc Romana, Caroline Le Van Kim   +16 more
wiley   +1 more source

P-025: ABNORMAL MITOCHONDRIA RETENTION IN MATURE RED BLOOD CELLS OCCURS NOT ONLY IN SS BUT ALSO SC PATIENTS AND IS ASSOCIATED WITH HEMOLYTIC MARKERS [PDF]

Hemasphere, 2022
HemaSphere, Volume 6, Issue S4, Page 29-29, August 2022.
M. R, M. H, S. R, Y. G, L. R, V. T, B. T, E. B, C. L, V. B, M. E.   +10 more
europepmc   +2 more sources

Acute chest syndrome in adult patients with sickle cell disease: The relationship with the time to onset after hospital admission

British Journal of Haematology, Volume 201, Issue 6, Page 1229-1238, June 2023., 2023
Summary Data on acute chest syndrome (ACS) in adult sickle cell disease patients are scarce. In this study, we describe 105 consecutive ACS episodes in 81 adult patients during a 32‐month period and compare the characteristics as a function of the time to onset after hospital admission for a vaso‐occlusive crisis (VOC), that is early‐onset episodes ...
Geoffrey Cheminet, Antoine Brunetti, Djamal Khimoud, Brigitte Ranque, Adrien Michon, Edouard Flamarion, Jacques Pouchot, Anne‐Sophie Jannot, Jean‐Benoît Arlet   +8 more
wiley   +1 more source

Erythrocyte type 1 equilibrative nucleoside transporter expression in sickle cell disease and sickle cell trait

British Journal of Haematology, Volume 200, Issue 6, Page 812-820, March 2023., 2023
Summary Hypoxia‐mediated red blood cell (RBC) sickling is central to the pathophysiology of sickle cell disease (SCD). The signalling nucleoside adenosine is thought to play a significant role in this process. This study investigated expression of the erythrocyte type 1 equilibrative nucleoside transporter (ENT1), a key regulator of plasma adenosine ...
Bérengère Koehl, Livia Claude, Karen Reminy, Vanessa Tarer, Véronique Baccini, Marc Romana, Yves Colin‐Aronovicz, Vijaya L. Damaraju, Michael Sawyer, Thierry Peyrard, Maryse Etienne‐Julan, Caroline Le Van Kim, Slim Azouzi, Luc Reininger   +13 more
wiley   +1 more source

O-06: E-SICKLE CELL DISEASE: A FRENCH SPEAKING TRAINING PLATFORM TARGETING ALL LEVELS OF THE HEALTHCARE SYSTEM [PDF]

Hemasphere, 2022
HemaSphere, Volume 6, Issue S4, Page 4-5, August 2022.
M. C, C. P, V. T, I. D, J. E.
europepmc   +2 more sources