Open Access Library Journal

Volume 9, Issue 9 (September 2022)

ISSN Print: 2333-9705   ISSN Online: 2333-9721

Google-based Impact Factor: 0.73  Citations  

Reasons for Consultation of Sickle Cell Patients at the Center for Mixed Medicine and SS Anemia

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DOI: 10.4236/oalib.1109132    36 Downloads   429 Views  

ABSTRACT

Background: Sickle cell disease is an autosomal recessive genetic disease characterized by a point mutation. In the Democratic Republic of Congo, approximately 40,000 newborns are born with sickle cell disease. Objective: The objective of the study is to determine the predominant reasons for consultation of sickle cell patients at the Center of Mixed Medicine and SS Anemia (CMMASS) in Kinshasa. Methods: This study was conducted at CMMASS. It is a retrospective study carried out on the files of elderly sickle cell patients who came for consultation in the period from January 1, 2018 to December 31, 2020. Any well-kept file of sickle cell patients over the age of 18 with a documented electrophoresis result having consulted during the study period was considered for work. The parameters of interest in this work were the different reasons for consultation. Results: 2463 SS homozygous sickle cell patients had been seen in consultation at the CMMASS. 1350 patients (54.8%) were women; thus giving a sex ratio of 1.21 in favor of women. The most represented age group is that of 18 to 25 years with 1148 patients (46.6%). The most common reasons for consultation in the series were osteoarticular pain (61.75%), fever (24.48%), pallor (12.59%), headache (7.8%), and cough (2.56%). Conclusion: Bone and joint pain was the most dominant reason for consultation among homozygous sickle cell patients at the CMMASS during the period from January 1, 2018 to December 31, 2020.

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Mulowayi, P., Bongenya, B., Bulanda, B., Kateba, E., Kodondi, S., Vangu, C., Nkolomoni, B. and Kamangu, E.N. (2022) Reasons for Consultation of Sickle Cell Patients at the Center for Mixed Medicine and SS Anemia. Open Access Library Journal, 9, 1-7. doi: 10.4236/oalibj.2022.99132.

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