Availability of blood products and transfusion practices in sub-saharan Africa for the management of patients with sickle cell disease: A survey in 16 countries.

G Geoffrey Cheminet (1Université Paris Cité, Inserm U1163, Institut Imagine, Laboratoire « Mécanismes cellulaires et moléculaires des désordres hématologiques et implications thérapeutiques », F-75015, Paris, France) S Saliou Diop (3Université Cheikh Anta Diop, Dakar, Senegal) F Françoise Bernaudin (4Centre de référence pour la drépanocytose de l'enfant, Centre Hospitalier Intercommunal de Créteil, Créteil, France) I Indou Deme-Ly (3Université Cheikh Anta Diop, Dakar, Senegal) B Binta Coulibaly (6Fresenius Kabi Deutschland GmbH, Francfort-Sur-Le-Main, Germany) A Anne Corbasson (7Service de médecine interne, Centre National de Référence des syndromes drépanocytaires majeurs de l'adulte, AP-HP, Hôpital Européen Georges Pompidou, F-75015, Paris, France) I Ibrahima Diagne (8Coopération et innovation pédagogique, Université Gaston Berger, Saint-Louis, Senegal) C Charlotte Eposse Ekoube F Frédéric Galactéros (Filière de Santé des Maladies Constitutionnelles Rares du Globule Rouge et de l’Erythropoïèse, Créteil, France) O Olivier Hermine E Eléonore Kafando (14Laboratoire d'hématologie, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso) M Mariane De Montalembert C Constant Vodouhé (16Association DORYS, Strasbourg, France) A Ahoefa Vovor (17Université des Sciences de la Santé, Lomé, Togo) B Brigitte Ranque (7Service de médecine interne, Centre National de Référence des syndromes drépanocytaires majeurs de l'adulte, AP-HP, Hôpital Européen Georges Pompidou, F-75015, Paris, France) L Leon Tshilolo (Biomedical Research Institute 1, Department of Pediatrics, Centre Hospitalier Monkole, Kinshasa, Democratic Republic of Congo) F France Pirenne (19Etablissement Français du Sang (EFS) Ile-de-France, Créteil, France) D Dapa Diallo (20Hématologie, Faculté de médecine et d'odontologie, Université des Sciences, Techniques et Technologies (USTTB), Bamako, Mali) J Jean-Benoit Arlet (1Université Paris Cité, Inserm U1163, Institut Imagine, Laboratoire « Mécanismes cellulaires et moléculaires des désordres hématologiques et implications thérapeutiques », F-75015, Paris, France)

Abstract

Abstract Background: Red blood cell (RBC) transfusions play a critical role in managing severe acute complications in patients with sickle cell disease (SCD). Evidence from high-income countries (HICs) has also demonstrated the effectiveness of regular transfusions, particularly in preventing stroke in children. However, implementing such protocols in resource-limited countries, such as those in sub-Saharan Africa (SSA), remains challenging due to limited access to blood products and different safety standards. Moreover, data on transfusion practices in these regions are scarce. Objective: To assess the availability of blood products, immunohematological testing, and transfusion practices in French-speaking SSA. Methods: An online survey was conducted by the non-governmental organization (NGO) DrepAfrique between April 12, 2025, and May 8, 2025. A standardized computerized questionnaire, developed by members of the NGO's scientific council, was emailed to 1,960 SSA physicians involved in the care of patients with SCD. Results: A total of 144 practitioners from 16 French-speaking SSA countries participated in the survey. The Democratic Republic of Congo was the most represented country, accounting for 40 respondents (27.8%). Most respondents worked in non-university settings (83/144, 57.6%); 79 (55%) practiced in a SCD referral center. The cumulative number of homozygous SS patients followed in these centers was estimated at approximately 86,000. Each respondent reported having seen a median of 10 [IQR 5; 23] SS patients in the preceding 15 days and having performed a transfusion for 2 [1; 5] of them. Only 38/144 practitioners (26.4%) reported performing phlebotomy prior to transfusion in SS patients with hemoglobin (Hb) >9 g/dL, and 13/144 (9%) had access to erythrocytapheresis. Regarding transfusion indications (suggested from a predefined list), most respondents used transfusions during a vaso-occlusive crisis (VOC) with acute malaria and Hb <6 g/dL (93/144, 64.6%); in cases of anemia with Hb <5 g/dL for 90 of them (62.5%); and when a drop of more than 2 g/dL from baseline Hb occurred for 71 (49.3%). Surprisingly, the use of transfusion was less frequently reported in case of stroke (58/144, 40.3%) or severe acute chest syndrome (53/144, 36.8%). In response to a clinical scenario describing a 7-year-old child with SCD and Hb of 9.4 g/dL (baseline level) presenting with acute hemiplegia and normal brain CT-scan (suggestive of ischemic stroke) in the absence of malaria, only 93/144 respondents (64.6%) indicated that they would perform an immediate transfusion (83 of them (89.2%) with prior phlebotomy). For long-term management of this stroke, 58/144 (40.3%) would initiate a combined treatment of hydroxyurea (HU) and chronic transfusions within the following 6 months, while 51/144 (35.4%) would recommend HU alone. Regarding red cell product type, 138 (95.8%) practitioners reported performing phenotyping of transfused bags, limited to the ABO-RhD systems for 86 (62.3%) of them, and ABO alone for 18 (13%). Only 34/144 (23.6%) practitioners reported screening patients for RBC antibodies before transfusion. The most commonly used blood products (reported as being used “often” or “always”) included whole blood (54/144, 37.6%), ABO-RhD phenotyped packed red blood cells (PRBCs) (73/144, 50.7%), and more rarely ABO-RhDCE-Kell phenotyped PRBCs (23/144, 16%). The limited use of high-quality RBC products or immunohematological testing was primarily due to cost constraints and/or limited availability. Conclusion: This study provides valuable data from one of the largest surveys on transfusion practices for SCD in 16 French-speaking SSA countries. Key challenges include the absence of systematic RBC antibodies screening, the use of RBC products with limited phenotyping, a frequent reliance on whole blood, and difficulties in performing pre-transfusion phlebotomy. These findings call for caution when extrapolating to SSA countries chronic transfusion programs developed in HICs, which are based on significantly higher standards of transfusion safety. This study highlights the urgent need for context-appropriate training programs to optimize transfusion practices and decision-making processes in SSA, particularly in the acute management of stroke. In light of these constraints, a wider use of HU should be strongly encouraged.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 2966-2966
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (19)

G

Geoffrey Cheminet

1Université Paris Cité, Inserm U1163, Institut Imagine, Laboratoire « Mécanismes cellulaires et moléculaires des désordres hématologiques et implications thérapeutiques », F-75015, Paris, France

S

Saliou Diop

3Université Cheikh Anta Diop, Dakar, Senegal

F

Françoise Bernaudin

4Centre de référence pour la drépanocytose de l'enfant, Centre Hospitalier Intercommunal de Créteil, Créteil, France

I

Indou Deme-Ly

3Université Cheikh Anta Diop, Dakar, Senegal

B

Binta Coulibaly

6Fresenius Kabi Deutschland GmbH, Francfort-Sur-Le-Main, Germany

A

Anne Corbasson

7Service de médecine interne, Centre National de Référence des syndromes drépanocytaires majeurs de l'adulte, AP-HP, Hôpital Européen Georges Pompidou, F-75015, Paris, France

I

Ibrahima Diagne

8Coopération et innovation pédagogique, Université Gaston Berger, Saint-Louis, Senegal

C

Charlotte Eposse Ekoube

F

Frédéric Galactéros

Filière de Santé des Maladies Constitutionnelles Rares du Globule Rouge et de l’Erythropoïèse, Créteil, France

O

Olivier Hermine

E

Eléonore Kafando

14Laboratoire d'hématologie, Université Joseph Ki-Zerbo, Ouagadougou, Burkina Faso

M

Mariane De Montalembert

C

Constant Vodouhé

16Association DORYS, Strasbourg, France

A

Ahoefa Vovor

17Université des Sciences de la Santé, Lomé, Togo

B

Brigitte Ranque

7Service de médecine interne, Centre National de Référence des syndromes drépanocytaires majeurs de l'adulte, AP-HP, Hôpital Européen Georges Pompidou, F-75015, Paris, France

L

Leon Tshilolo

Biomedical Research Institute 1, Department of Pediatrics, Centre Hospitalier Monkole, Kinshasa, Democratic Republic of Congo

F

France Pirenne

19Etablissement Français du Sang (EFS) Ile-de-France, Créteil, France

D

Dapa Diallo

20Hématologie, Faculté de médecine et d'odontologie, Université des Sciences, Techniques et Technologies (USTTB), Bamako, Mali

J

Jean-Benoit Arlet

1Université Paris Cité, Inserm U1163, Institut Imagine, Laboratoire « Mécanismes cellulaires et moléculaires des désordres hématologiques et implications thérapeutiques », F-75015, Paris, France