Limited Exchange Transfusion Can Be Very Beneficial in Sickle Cell Anemia with Acute Chest Syndrome: A Case Report from Tanzania

Author:

Chamba Clara1ORCID,Iddy Hamisa1,Tebuka Erius2,Tluway Furahini1ORCID,Osati Elisha3,Budodi Neema3,Meda Collins3,Yonazi Mbonea3,Schuh Anna4,Luzzatto Lucio1,Makani Julie1

Affiliation:

1. Sickle Cell Programme, Department of Hematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania

2. Department of Pathology, Catholic University of Health and Allied Sciences, Mwanza, Tanzania

3. Haematology Unit, Department of Internal Medicine, Muhimbili National Hospital, Dar es Salaam, Tanzania

4. Department of Oncology, University of Oxford, Oxford, UK

Abstract

Acute chest syndrome (ACS) is a life-threatening complication of sickle cell disease (SCD) with blood transfusion an integral part in its management. Red cell exchange (RCE) transfusion is usually regarded as preferable to top-up transfusion, because it reduces the proportion of Hemoglobin (Hb) S while at the same time avoiding circulatory overload. Despite its obvious benefits, RCE is underutilized, particularly in low-resource settings which may be due to scarcity of blood products and of expertise in carrying out exchange transfusion. We report on a young woman with SCD with severe ACS who responded promptly and dramatically to a RCE of only 0.95 L (instead of the recommended 1.4 L) and had in the end an HbS level of 48% (instead of the recommended level below 30%). Limited RCE resulted in significant clinical improvement. We suggest that limited RCE may be of benefit than no RCE in SCD patients with ACS, particularly in settings where RCE is not available.

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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