Epidemiological profile of the death of afro-descendant individuals with Sickle Cell Anemia
DOI:
https://doi.org/10.6008/CBPC2236-9600.2023.003.0006Keywords:
Afro-descendants, Sickle Cell Anemia, EpidemiologyAbstract
Sickle Cell Anemia (SCA), in Brazil, is the most frequent single-gene hereditary disease, with a total estimate of 3,000 births per year; in addition, it affects 0.1 to 0.3% of the Afro-descendant population. This anomaly has a genetic origin from the regions of West Africa, Greece and the southern Mediterranean, in addition to southern India. In view of this, the survey of the epidemiological profile of Afro-descendants with SCA can help public health actions and the creation of new epidemiological surveillance strategies to improve the quality of life of this population. Thus, the present work is a descriptive epidemiological study, based on data made available by the Department of Informatics of the Unified Health System (DATASUS) about deaths from PA in blacks and browns, in addition to a literature review on the VHL platforms. and PUBMED. From the information obtained, it was found that brown individuals represent 47% of deaths, and black individuals, 25%. The Southeast and Northeast regions stood out due to the intense slave trade from the 16th century onwards. There was no significant difference in deaths for males and females. Regarding the place of occurrence of deaths of Afro-descendants, approximately 73% occurred in a hospital environment. Finally, in relation to the age group, patients aged 20 to 29 years stood out.
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