Assessment of Renal Function in Egyptian HCV Patients Treated with Combination Therapy of Sofosbuvir and Daclatasvir

Authors

  • Hala Abd El Maguid Department of Gastroenterology and Infectious Diseases, Ahmed Maher Teaching Hospital, Cairo, Egypt
  • Ahmed Heiba Department of Gastroenterology and Infectious Diseases, Ahmed Maher Teaching Hospital, Cairo, Egypt; Department of Internal Medicine, National Research Centre, El-Buhouth St., Dokki, Cairo, Egypt
  • Enass El Sayed Department of Nephrology, Ahmed Maher Teaching Hospital, Cairo, Egypt
  • Hazem El-Hariri Department of Community Medicine, National Research Centre, El-Buhouth St., Dokki, Cairo, Egypt https://orcid.org/0000-0001-9886-2087
  • Haythem Tolba Department of Nephrology, National Institute of Nephrology and Urology, Cairo, Egypt
  • Muhammad Abdel Ghaffar Department of Gastroenterology and Infectious Diseases, Ahmed Maher Teaching Hospital, Cairo, Egypt https://orcid.org/0000-0003-2768-3465

DOI:

https://doi.org/10.3889/oamjms.2022.7529

Keywords:

Hepatitis C virus, Glomerular filtration rate, Sofosbuvir, Daclatasvir

Abstract

BACKGROUND: According to the most recent Egyptian demographic health census, the estimated Hepatitis C virus (HCV) prevalence in the 15–59 age range was 14.7%. Globally, the incidence of renal impairment in HCV-positive individuals is 40% higher than in HCV-negative patients. HCV-induced renal impairment can range from mild-to-severe, and it frequently complicates the treatment outcome of HCV infection.

AIM: This study aimed to explore the changes in renal function in Egyptian HCV patients treated with a combination of Sofosbuvir (SOF) and Daclatasvir (DCV).

METHODOLOGY: Six hundred and eleven chronic HCV patients treated with SOF-DCV were enrolled. Patients were classified into three groups according to their baseline renal function: unimpaired group (estimated glomerular filtration rate [eGFR] ≥ 90 ml/min/1.73 m2), mildly impaired group (eGFR of ≥60–89 ml/min/1.73 m2), and moderately impaired group (eGFR of ≥30–59 ml/min/1.73 m2). Every month during treatment and at 24 weeks after treatment (sustained virological response 24), the eGFR level was evaluated.

RESULTS: Our findings indicated that the eGFR level was significantly increased (p < 0.001) in all groups during the treatment but subsequent decline (p < 0.001) in all groups was documented after 6 months of treatment. Multivariate analysis identified baseline renal impairment (<90 ml/min/1.73 m2, p < 0.001) and baseline anemia (p < 0.001) as independent risk factors for renal function deterioration at the end of treatment.

CONCLUSION: Clinical physicians should closely monitor renal function in patients treated with SOF-DCV. Furthermore, anemia therapy prior to SOF-DCV treatment should be recommended.

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References

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Published

2022-01-02

How to Cite

1.
El Maguid HA, Heiba A, El Sayed E, El-Hariri H, Tolba H, Abdel Ghaffar M. Assessment of Renal Function in Egyptian HCV Patients Treated with Combination Therapy of Sofosbuvir and Daclatasvir. Open Access Maced J Med Sci [Internet]. 2022 Jan. 2 [cited 2024 Nov. 22];10(B):82-6. Available from: https://oamjms.eu/index.php/mjms/article/view/7529

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Infective Diseases

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