Browsing by Author "Rees, D.C."

Now showing 1 - 2 of 2

Age-related changes in adaptation to severe anemia in childhood in developing countries
(National Academy of Sciences, 2007) O Donnell, A.; Premawardhena, A.; Arambepola, M.; Allen, S.J.; Peto, T.E.; Fisher, C.A.; Rees, D.C.; Olivieri, N.F.; Weatherall, D.J.
Severe forms of anemia in children in the developing countries may be characterized by different clinical manifestations at particular stages of development. Whether this reflects developmental changes in adaptation to anemia or other mechanisms is not clear. The pattern of adaptation to anemia has been assessed in 110 individuals with hemoglobin (Hb) E beta-thalassemia, one of the commonest forms of inherited anemia in Asia. It has been found that age and Hb levels are independent variables with respect to erythropoietin response and that there is a decline in the latter at a similar degree of anemia during development. To determine whether this finding is applicable to anemia due to other causes, a similar study has been carried out on 279 children with severe anemia due to Plasmodium falciparum malaria; the results were similar to those in the patients with thalassemia. These observations may have important implications both for the better understanding of the pathophysiology of profound anemia in early life and for its more logical and cost-effective management.
Global Burden of Haemoglobin Disorders
(Faculty of Medicine, University of Kelaniya, Sri Lanka, 2016) Rees, D.C.
OBJECTIVES: 1. To describe the world distribution of haemoglobin disorders 2. To describe the health burden of haemoglobin disorders Haemoglobin disorders are the commonest, severe inherited disorders in the world, particularly prevalent in low- and middle-income countries. The two main conditions caused by mutations in globin genes are sickle cell disease (SCD), and thalassaemias. Approximately 300 000 children are born each year with sickle cell disease, with estimates suggesting this will reach 400 000 per year by 2050. The largest numbers of SCD births are estimated to occur in Nigeria (90 000 births/year), Democratic Republic of Congo (39 700 births/year) and India (44 000 births/year). Worldwide there are approximately 30 000 most of these occurring in Asia and the Middle East. The relative importance of haemoglobin disorders is increasing in many countries as deaths from infectious diseases decrease, and both thalassaemia and SCD are recognised as global health problems by the World Health Organisation. Antenatal and neonatal screening programmes are important in managing haemoglobinopathies and are established in some high-income countries, including UK, USA and parts of the Middle East. However there are very few national screening programmes in lower-income countries in which these conditions are most prevalent. Local screening programmes are established in areas of many countries and are revealing important information about the microdistribution of these conditions. In SCD, relatively simple measures, such as vaccination, penicillin prophylaxis, antimalarial measures and treatment of infections are thought to significantly reduce the otherwise very high childhood mortality, although these are not available in many areas. Hydroxyurea is relatively cheap, and has been shown to alter the natural history of SCD, although its role in Africa and India is yet to be established. The treatment of severe thalassaemia relies largely on the availability of safe blood transfusions and iron chelation, which are available in relatively few Asian countries unless a patient is able to pay. Stem-cell based treatments are becoming increasingly important, and although expensive may be cost-effective in some settings. Overall haemoglobin disorders cause significant morbidity and mortality across the world. More research is needed to define the prevalence and natural history of these conditions in different countries, and to develop clinical trials and interventions appropriate to low- and middle-income settings.