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Blood transfusion rate in congolese patients with sickle cell anemia

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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. Brewster DR. Blood transfusion for severe anameia in African children. Lancet 1992; 340(10): 917.

    Article  PubMed  CAS  Google Scholar 

  2. Lanckriet C, Koula RM, Bureau JJ, Capdevielle H et al. Les anemies severes ayant necessite use transfusion dans le service de Pediatrie de Bangui (Centrafrique). Ann Pediatr (Paris) 1995; 42(1): 60–64.

    Google Scholar 

  3. Greenberg AE, Nguyen-Dinh P, Mann JM et al. The association between malaria, blood transfusions, and HIV seropositivity in a pediatric population in Kinshasa. JAMA 1988; 259: 545–549.

    Article  PubMed  CAS  Google Scholar 

  4. Girot R. Les modalites de la transfusion sanguine dans la drepanocytose et dans la thalassemia. Transfus Clin Biol 1994; 1: 19–21.

    Article  PubMed  CAS  Google Scholar 

  5. Montalembert M, Guilloud-Bataille M, Feingold C et al. Epidemiological and clinical study of sickle cell disease in France, French Guyana and Algeria. Eur J Haematol 1993; 51: 136–140.

    Article  PubMed  Google Scholar 

  6. Diagne N, Diagne-Gueye H, Signate-Sy B et al. Prise en charge de la drepanocytose chez l’enfant en Afrique: experience de la cohorte de l’Hospital d’Enfants Albert Royer de Dakar. Med Trop 2003; 63: 513–520.

    CAS  Google Scholar 

  7. Wembonyama O, Ngwanza N, Tshilolo M et al. L’appreciation de l’urgence transfusioelle dans un service de pediatrie (a’propos de 250 observations. Bull Soc Pathol Exot 1991; 84: 205.

    Google Scholar 

  8. Nduka N, Owhochuku SM and Odike P. Current observations on Sickle Cell genotype in Nigeria. East Afr Med J 1993; 70(10): 646–649.

    PubMed  CAS  Google Scholar 

  9. Tshilolo L, Mukendi R, et Girot. La drepanocytose dans le Sud du Zaire. Etude de deux series de 251 et 340 malades suivis entre 1988 et 1992. Arch Pediatr 1996; 3: 104–111.

    Article  PubMed  CAS  Google Scholar 

  10. Tshilolo. La drepanocytose en Republique Democratique du Congo: apercu sur la sisituation actuelle et perspectives d’avenir. Congo Medical 2003; 3(12): 1044–1052.

    Google Scholar 

  11. Luzzato L. Sickle cell anaemia in tropical african clinics. Haematology 1981; 10(3): 757–784.

    Google Scholar 

  12. Galacteros F. Sickle cell disease: a short guide to management. In Disorders of iron homeostasis, erythrocytes, erythropoiesis. Genoa: Forum service ed, 2006: 276–309.

    Google Scholar 

  13. Syed SM, Sears DA, Werch JB, Udden MM, Milan JD Case reports: Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease. Am J Med Sci 1996; 312(4): 175–181.

    Article  PubMed  CAS  Google Scholar 

  14. Adeodu OO, Adekile AD. Clinical and laboratory features associated with persistent gross splenomegaly in Nigerian children with sickle cell anaemia. Act Paediatr Scand 1990; 79: 686–690.

    CAS  Google Scholar 

  15. Buchanan GR, McKie V, Jackson EA et al. Splenic phagocytic function in children with sickle cell anaemia receiving long-term hypertransfusion therapy. J Pediatr 1989; 115: 568–572.

    Article  PubMed  CAS  Google Scholar 

  16. Nzingoula S. L’Hospital et la drepanocytose. In Galacteros F, Drepanocytose et sante publique. Colloque. Paris: Inserm ed, 1991; 161–171.

    Google Scholar 

  17. Laleman G, Magazani K, Perriens J et al. Prevention of blood-borne HIV transmission using a decentralised approach in Shaba, Zaire. AIDS 1992; 6: 1353–1358.

    Article  PubMed  CAS  Google Scholar 

  18. Aken-Ova YA, Olasode BJ, Ogunbiy JO et al. Hepatobiliary changes in Nigerians with sickle cell anaemia. Ann Trop Med Parasitol 1993; 87(6): 603–606.

    CAS  Google Scholar 

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Correspondence to L. M. Tshilolo.

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Tshilolo, L.M., Mukendi, R.K. & Wembonyama, S.O. Blood transfusion rate in congolese patients with sickle cell anemia. Indian J Pediatr 74, 735–738 (2007). https://doi.org/10.1007/s12098-007-0129-4

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  • DOI: https://doi.org/10.1007/s12098-007-0129-4

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