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.

Journal: BMC hematology

Volume: 17

Issue: 

Year of Publication: 

Affiliated Institutions:  Department of Internal Medicine and Pediatrics, Faculty of Health Sciences, University of Buea, Buea, Cameroon. Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon. Ministry of Public Health, Centre Medical d'Arrondissement de Bare, Nkongsamba, Cameroon. Health and Human Development (HD) Research Network, P.O. Box , Douala, Cameroon.

Abstract summary 

Sickle Cell Disease (SCD) is associated with chronic multisystem complications that significantly influence the quality of life (QOL) of patients early in their life. Although sub-Saharan Africa bears 75% of the global burden of SCD, there is a paucity of data on these complications and their effects on the QOL. We aimed to record these chronic complications, to estimate the QOL, and to identify the corresponding risk factors in patients with SCD receiving care in three hospitals in Cameroon.In this cross-sectional study, a questionnaire was used to collect data from consecutive consenting patients. Information recorded included data on the yearly frequency of painful crisis, the types of SCD, and the occurrence of chronic complications. A 36-Item Short Form (SF-36) standard questionnaire that examines the level of physical and mental well-being, was administered to all eligible participants. Data were analyzed with STATA® software.Of 175 participants included, 93 (53.1%) were female and 111 (aged ≥14 years) were eligible for QOL assessment. The median (interquartile range, IQR) age at diagnosis was 4.0 (2.0-8.0) years and the median (IQR) number of yearly painful crisis was 3.0 (1.0-7.0). The most frequent chronic complications reported were: nocturnal enuresis, chronic leg ulcers, osteomyelitis and priapism (30.9%, 24.6%, 19.4%, and 18.3% respectively). The prevalence of stroke and avascular necrosis of the hip were 8.0% and 13.1% respectively. The median (IQR) physical and mental scores were 47.3 (43.9-58.5) and 41.0 (38.8-44.6) respectively. Age and chronic complications such as stroke and avascular necrosis were independently associated with poor QOL.In this population of patients living with SCD, chronic complications are frequent and their QOL is consequently poor. Our results highlight the need for national guidelines for SCD control, which should include new-born screening programs and strategies to prevent chronic complications.

Authors & Co-authors:  Andong Anne M AM Ngouadjeu Eveline D T EDT Bekolo Cavin E CE Verla Vincent S VS Nebongo Daniel D Mboue-Djieka Yannick Y Choukem Simeon-Pierre SP

Study Outcome 

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Citations :  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. doi: 10.1100/2012/949535.
Authors :  7
Identifiers
Doi : 7
SSN : 2052-1839
Study Population
Female
Mesh Terms
Other Terms
Cameroon;Chronic complications;Prevalence;Quality of life;Sickle cell disease
Study Design
Cross Sectional Study
Study Approach
Country of Study
Cameroon
Publication Country
England