Evolving Landscape of Sickle Cell Anemia Management in Africa: A Critical Review

被引:0
作者
Musuka, Hazel W. [1 ]
Iradukunda, Patrick Gad [2 ]
Mano, Oscar [3 ]
Saramba, Eric [4 ]
Gashema, Pierre [4 ]
Moyo, Enos [5 ]
Dzinamarira, Tafadzwa [6 ,7 ]
机构
[1] Univ Aberdeen, Sch Med Med Sci & Nutr, Aberdeen AB25 2ZR, Scotland
[2] Rwanda Food & Drug Author, Kigali 3243, Rwanda
[3] Univ Zimbabwe, Dept Med Lab Sci, Harare 263, Zimbabwe
[4] Univ Rwanda, Coll Med & Hlth Sci, Kigali 3286, Rwanda
[5] Univ KwaZulu Natal, Fac Med & Hlth Sci, Sch Nursing & Publ Hlth, ZA-4000 Durban, South Africa
[6] Univ Pretoria, Sch Hlth Syst & Publ Hlth, ZA-0028 Pretoria, South Africa
[7] ICAP Zimbabwe, Harare 263, Zimbabwe
关键词
sickle cell disease; Africa; disease management; DISEASE;
D O I
10.3390/tropicalmed9120292
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Sickle cell disease (SCD) is a prevalent inherited blood disorder, particularly affecting populations in Africa. This review examined the disease's burden, its diverse clinical presentations, and the challenges associated with its management in African settings. Africa bears a significant burden of SCD, with prevalence varying across countries and age groups. Newborn screening programs have highlighted the high prevalence of SCD at birth, emphasizing the need for early diagnosis and intervention. The clinical manifestations of SCD in Africa are multifaceted, encompassing acute complications like vaso-occlusive crises, acute chest syndrome, and stroke, as well as chronic complications such as organ damage and leg ulcers. Biological factors, including fetal hemoglobin levels, and demographic factors, like age and sex, influence disease severity and outcomes. The management of SCD in Africa faces numerous challenges. Limited access to resources, including diagnostic tools, medications, and trained healthcare professionals, hinders optimal care. The high cost of advanced therapies further restricts patient access. Cultural stigma and a lack of awareness create additional barriers to effective management. To address these challenges, early diagnosis through newborn screening programs and point-of-care testing is crucial. Comprehensive care models, including hydroxyurea therapy, pain management, and patient education, are essential for improving outcomes. Collaboration with international networks and leveraging local resources can enhance the sustainability of SCD programs. In conclusion, SCD significantly impacts African populations. Overcoming the challenges associated with its management requires addressing resource limitations, affordability issues, and cultural barriers. Early diagnosis, comprehensive care models, and ongoing research focused on affordability and accessibility are crucial for improving the lives of individuals living with SCD in Africa.
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页数:20
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共 67 条
  • [1] Prevalence of sickle cell disease and sickle cell trait among children admitted to Al Fashir Teaching Hospital North Darfur State, Sudan
    Adam, Mudathir A.
    Adam, Nassreldeen K.
    Mohamed, Babiker A.
    [J]. BMC RESEARCH NOTES, 2019, 12 (01)
  • [2] Renin as a Biomarker of Acute Kidney Injury and Mortality in Children With Severe Malaria or Sickle Cell Disease
    Adan Jr, Daniel
    Batte, Anthony
    Namazzi, Ruth
    Mufumba, Ivan
    Kazinga, Caroline
    Mellencamp, Kagan A.
    Bond, Caitlin
    Opoka, Robert O.
    John, Chandy C.
    Conroy, Andrea L.
    [J]. CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (09)
  • [3] Clinical and genetic factors are associated with kidney complications in African children with sickle cell anaemia
    Adebayo, Oyindamola Christiana
    Betukumesu, DieuMerci Kabasele
    Nkoy, Agathe Bikupe
    Adesoji, Oluyomi Modupe
    Ekulu, Pepe Mfutu
    Van den Heuvel, Lambertus P.
    Levtchenko, Elena N.
    Labarque, Veerle
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2022, 196 (01) : 204 - 214
  • [4] A Critical Review of Sickle Cell Disease Burden and Challenges in Sub-Saharan Africa
    Adigwe, Obi Peter
    Onoja, Solomon Oloche
    Onavbavba, Godspower
    [J]. JOURNAL OF BLOOD MEDICINE, 2023, 4 : 367 - 376
  • [5] Aim A.K., 2024, Eur. J. Med. Health Res, V2, P138, DOI [10.59324/ejmhr.2024.2(1).23, DOI 10.59324/EJMHR.2024.2(1).23]
  • [6] Akinsete A., 2022, J. Glob. Med, V2, DOI [10.51496/jogm.v2.79, DOI 10.51496/JOGM.V2.79]
  • [7] Cerebral revascularization surgery reduces cerebrovascular events in children with sickle cell disease and moyamoya syndrome: Results of the stroke in sickle cell revascularization surgery retrospective study
    Aldana, Philipp R.
    Hanel, Ricardo A.
    Piatt, Joseph
    Han, Sabrina H.
    Bansal, Manisha M.
    Schultz, Corinna
    Gauger, Cynthia
    Pederson, John M.
    Wellons III, John C.
    Hulbert, Monica L.
    Jordan, Lori C.
    Qureshi, Adnan
    Garrity, Kelsey
    Robert, Adam P.
    Hatem, Asmaa
    Stein, Jennifer
    Beydler, Emily
    Adelson, P. David
    Greene, Stephanie
    Grabb, Paul
    Johnston, James
    Lang, Shih-Shan
    Leonard, Jeffrey
    Magge, Suresh N.
    Scott, Alex
    Shah, Sanjay
    Smith, Edward R.
    Smith, Jodi
    Strahle, Jennifer
    Vadivelu, Sudhakar
    Webb, Jennifer
    Wrubel, David
    [J]. PEDIATRIC BLOOD & CANCER, 2023, 70 (07)
  • [8] Ally M., 2023, Current Challenges and New Approaches to Implementing Optimal Management of Sickle Cell Disease in Sub-Saharan Africa Seminars in Hematology
  • [9] Ally M., 2023, Stud. J. Health Res. Afr, V4, P7
  • [10] Ambrose E.E., 2020, Surveillance for Sickle Cell Disease