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Blood Transfusion Rate in Congolese Patients with Sickle Cell Anemia

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Specialty Pediatrics
Date 2007 Sep 6
PMID 17785895
Citations 16
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Abstract

Objective: The main objective of this study was to evaluate the rate of blood transfusion in African Sickle Cell Patients and the risks related to the use of total blood.

Methods: 186 sickle cell patients (95 males and 91 females) aged 0-21 years were regularly followed over a 3 years period in Katanga province, DR Congo. Indications for blood transfusion were mainly based on clinical criteria and Hb level (less than 5g% ml or a drop of 2g% under the steady state value). All the subjects, who were transfused, wer screened for hepatitis B surface antigen (HBs Ag) and Human Immune deficit Virus (HIV).

Results: Of 186 patients, 150 (80.6%) were transfused and the average blood transfusion requirement was 0.4 units per patient-year. According to the age of first transfusion, 75.3% (113/150) of them were transfused before the 6th year of life; but the frequency of transfusions seemed to decline in children aged more than 13 years. The risk of HIV infection from blood transfusion was estimated at 1 per 37.1 units or 26 per 1000 blood units. The hepatitis B surface antigen was detected in 15 cases (10%) and HIV serology was positive in 17 patients (11.3%).

Conclusion: Because of the complications related to blood transfusions in Africa, efforts are needed in order to reduce the frequency of transfusions, by preventive measures (early diagnosis, malarial and penicillin-prophylaxis) and to use more rational indications.

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References
1.
Diagne I, Diagne-Gueye N, Signate-Sy H, Camara B, Lopez-Sall P, Diack-Mbaye A . [Management of children with sickle cell disease in Africa: experience in a cohort of children at the Royal Albert Hospital in Dakar]. Med Trop (Mars). 2004; 63(4-5):513-20. View

2.
Adeodu O, Adekile A . Clinical and laboratory features associated with persistent gross splenomegaly in Nigerian children with sickle cell anaemia. Acta Paediatr Scand. 1990; 79(6-7):686-90. DOI: 10.1111/j.1651-2227.1990.tb11536.x. View

3.
de Montalembert M, Guilloud-Bataille M, Feingold J, Girot R . Epidemiological and clinical study of sickle cell disease in France, French Guiana and Algeria. Eur J Haematol. 1993; 51(3):136-40. DOI: 10.1111/j.1600-0609.1993.tb00613.x. View

4.
Brewster D . Blood transfusions for severe anaemia in African children. Lancet. 1992; 340(8824):917. View

5.
AkenOva Y, Olasode B, Ogunbiyi J, Thomas J . Hepatobiliary changes in Nigerians with sickle cell anaemia. Ann Trop Med Parasitol. 1993; 87(6):603-6. DOI: 10.1080/00034983.1993.11812816. View