Hepatitis C: Epidemiological, Clinical and Therapeutic Aspects in Dakar (Senegal)
- 1 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
- 2 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
- 3 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
- 4 Cheikh Anta Diop University of Dakar, Hospital Idrissa Pouye, Dakar, Senegal
- 5 Assane Seck University of Ziguinchor, Hospital de la Paix, Ziguinchor, Senegal
- 6 Cheikh Anta Diop University of Dakar, Hospital Idrissa Pouye, Dakar, Senegal
- 7 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
- 8 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
- 9 Cheikh Anta Diop University of Dakar, Hospital Aristide Le Dantec, Dakar, Senegal
Abstract
Viral hepatitis C is a major public health problem. The aim of our work was to determine the epidemiological, diagnostic and treatment profiles of patients with HCV in Dakar (Senegal). We conducted a retrospective, descriptive, multicentre study between January 1, 2010, and December 31, 2019. We included 26 patients. The mean age of the patients was 53.5 years [28 - 70 years] and 46.2% were males. Of the 26 patients included, 7 (26.9%) were Senegalese, and the majority were from other African countries. Risk factors for contamination found were surgery in 11 patients (42.3%) and blood transfusion in 1 patient (3.8%). The mean viral load was 6.47 log IU/ml [4.26 - 7.26 log IU/ml]. Ten patients were infected by genotype 4. No patients were co-infected with HIV or HBV. Six patients (23.1% of patients) had significant fibrosis, of which five (19.2% of patients) were in the stage of cirrhosis. Twelve patients (46.2%) started treatment. Eleven were treatment-na ï ve and 1 did not respond to ribavirin-pegylated interferon-based therapy after 48 weeks. Ten cases of antiviral therapy were based on DAA and ribavirin-pegylate d interferon in 2 patients. For the patients treated with peginterferon and ribavirin, a rapid virologic response was observed at 12 weeks in one patient, and the other patient was lost to follow-up. Among DAA-treated patients, 7 had sustained virologic responses at 12 weeks, 2 persisted, and 1 was lost to follow-up. Moderate thrombocytopenia and weight loss were observed in one patient receiving peginterferon and ribavirin. In our study, no patient died on treatment and no patients developed de novo HCC during or after DAA therapy. Conclusion: Viral hepatitis C is rare in Senegal. Despite the progress made in the therapeutic management of viral hepatitis C, it remains a challenge in Senegal. Indeed, DAAs are expensive and are not marketed, which makes them inaccessible to most patients.
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