Chronic complications and quality of life of patients living with sickle cell disease and receiving care in three hospitals in Cameroon: a cross-sectional study

Author:

Andong Anne M.,Ngouadjeu Eveline D. T.,Bekolo Cavin E.,Verla Vincent S.,Nebongo Daniel,Mboue-Djieka Yannick,Choukem Simeon-Pierre

Publisher

Springer Science and Business Media LLC

Subject

Hematology,Molecular Biology

Reference22 articles.

1. Ballas SK, Kesen MR, Goldberg MF, Lutty GA, Dampier C, Osunkwo I, et al. Beyond the Definitions of the Phenotypic Complications of Sickle Cell Disease: An Update on Management. Sci World J. 2012;2012:949535.

2. Asnani MR, Reid ME, Ali SB, Lipps G, Williams-Green P. Quality of life in patients with sickle cell disease in Jamaica: rural–urban differences. Rural Remote Health. 2008;8:890.

3. World Health Organization. Sickle-cell disease and other haemoglobin disorders: Fact sheet N°308. 2011. http://www.who.int/mediacentre/factsheets/fs308/en/ . Accessed 4 Sept 2016.

4. Makani J, Cox SE, Soka D, Komba AN, Oruo J, Mwamtemi H, et al. Mortality in Sickle Cell Anemia in Africa: A Prospective Cohort Study in Tanzania. PLoS One. 2011;6:e14699.

5. Akinyanju OO, Otaigbe AI, Ibidapo MOO. Outcome of holistic care in Nigerian patients with sickle cell anaemia. Clin Lab Haematol. 2005;27:195–9.

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