全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Cost of Managing a Painful Vaso-Occlusive Crisis at National Center for Research and Care for Sickle Cell Patients of Lomé in 2024

DOI: 10.4236/ojbd.2025.151003, PP. 25-35

Keywords: Sickle Cell Disease, Cost, Vaso-Occlusive Crisis, Togo

Full-Text   Cite this paper   Add to My Lib

Abstract:

Introduction: Despite reduced fees, many patients struggle to access care at the National Center for Research and Care for Sickle Cell Patients (CNRSD). This prompted an evaluation of the costs associated with managing a painful vaso-occlusive crisis (VOC), the most common reason for hospitalization among individuals with sickle cell disease. Methods: This was a cross-sectional study which was conducted among patients admitted to the CNRSD for painful VOC. Costs were calculated in CFA francs (XOF), encompassing consultation fees, medication expenses, laboratory test costs, and hospitalization charges. The total cost per patient was derived by summing these components. Results: The study included 300 patients with a median age of 16.5 years. Most were children and adolescents (61.33% were under 20 years of age) with an SS genotype (64%). The average length of hospital stay was 3.1 days, with variations based on genotype. The median cost of managing a VOC episode was 64,130 XOF (€97.77), with 66.5% of this expenditure attributable to medications and consumables. Costs were influenced by age and genotype but were not associated with the presence of comorbidities. Notably, 67.33% of patients reported no fixed monthly income, significantly hindering their ability to afford care. Conclusion: The cost of managing a painful VOC episode is relatively high, exceeding the minimum wage in Togo. The lack of universal health insurance coverage exacerbates the difficulty for individuals with chronic conditions, such as sickle cell disease, to access quality care.

References

[1]  Inusa, B., Hsu, L., Kohli, N., Patel, A., Ominu-Evbota, K., Anie, K., et al. (2019) Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment. International Journal of Neonatal Screening, 5, Article No. 20.
https://doi.org/10.3390/ijns5020020
[2]  Mattioni, S., Stojanovic, K.S., Girot, R. and Lionnet, F. (2016) La drépanocytose en France. Revue Francophone des Laboratoires, 2016, 61-66.
https://doi.org/10.1016/s1773-035x(16)30129-0
[3]  Fiawoo, M., Douti, N.K., Agbeko, F., Guédenon, K.M., Takassi, O.E., Akolly, D.A.E., et al. (2020) Acute Complications of Sickle Cell Disease in Hospitalized Children in Togo. Journal of Scientific Research at University of Lomé (Togo), 22, 683-690.
[4]  Mbassi, A.H.D., Dongmo, F., Ngo, U.S., Mafo, F.V., Alima, Y.A., Njom, N.A.E., et al. (2017) Epidemiological, Clinical and Therapeutic Aspects Related to the Occurrence of Vaso-Occlusive Crises in Homozygous Sickle Cell Children in Three Hospitals of Yaoundé. Health Sciences and Diseases, 18, 89-97.
[5]  Hunt, S. and Alisky, J. (2013) Inpatient Management of Sickle Cell Disease. Hospital Medicine Clinics, 2, e247-e262.
https://doi.org/10.1016/j.ehmc.2012.11.001
[6]  Kafando, E., Ayeréoue, J., Nikiéma, M., Toé, E., Obiri-Yeboah, D., Kam, L., et al. (2017) Assessment of the Direct Cost Associated with the Management of Major Sickle Cell Syndromes in the Pediatric Department of the Yalgado Ouédraogo University Hospital. International Journal of Current Advanced Research, 6, 1502-1512.
[7]  Ngolet, L.O., Ntsiba, H. and Elira, D.A. (2013) The Cost of Hospital Treatment for Sickle Cell Crises. Annals of Marien NGOUABI University, 14, 14-19.
[8]  Amarachukwu, C.N., Okoronkwo, I.L., Nweke, M.C. and Ukwuoma, M.K. (2022) Economic Burden and Catastrophic Cost among People Living with Sickle Cell Disease, Attending a Tertiary Health Institution in South-East Zone, Nigeria. PLOS ONE, 17, e0272491.
https://doi.org/10.1371/journal.pone.0272491
[9]  Republic of Togo. Decree No. 2015-078/PR of October 28, 2015, Establishing the Creation and Operation of the National Center for Research and Care for Sickle Cell Patients.
[10]  Gbadoe, A.D., Kampatibe, N., Bakonde, B., Assimadi, J.K. and Kessie, K. (1998) Therapeutic Attitude in Times of Crisis and Non-Crisis of Sickle Cell Patients in Togo. Médecine dAfrique Noire, 45, 154-160.
[11]  Délicat-Loembet, L.M., Orango Bourdette, J.O., Rotimbo Mbourou, D.R., Bisvigou, U., Omengue, D.F., N’Tchoreret, O.A., Mabiala Nno, A.D., Ngombi Pemba, L.P., Nieguitsila, A. and Avoune, E. (2023) Sickle Cell Disease in Southeast Zone of Gabon a Central African Country: A Socio-Economic Study. International Journal of Advanced Multidisciplinary Research and Studies, 3, 942-949.
[12]  Ngolet, L.O., Moyen Engoba, M., Kocko, I., Elira Dokekias, A., Mombouli, J. and Moyen, G.M. (2016) Sickle-Cell Disease Healthcare Cost in Africa: Experience of the Congo. Anemia, 2016, Article ID: 2046535.
https://doi.org/10.1155/2016/2046535
[13]  Galacteros, F. (2001) Pathophysiological Bases of Sickle Cell Disease, Management and Therapeutic News. Bulletin of the Society of Exotic Pathology, 94, 77-79.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133