TY - JOUR
T1 - Cutaneous adverse events in chronic hepatitis c patients treated with new direct-Acting antivirals
T2 - A systematic review and meta-Analysis
AU - Patel, Parth
AU - Malik, Kunal
AU - Krishnamurthy, Karthik
N1 - Publisher Copyright:
© 2015 The Author(s).
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Background: Direct-Acting antivirals (DAAs) are known to present with additional dermatological events over pegylatedinterferon/ ribavirin (Peg-IFN/RBV). Objective: A systematic review and meta-Analysis was conducted to assess the incidence/risk of cutaneous adverse events (AEs) for simeprevir, sofosbuvir, ABT450/r-ombitasvir, dasabuvir, ledipasvir, daclatasvir, and asunaprevir. Methods: The databases searched included PubMed, Clinicaltrials.gov, and Clinicaloptions.com. Data on telaprevir and boceprevir were obtained from a previous study. Results: The incidences of cutaneous AEs were 34.3% (95% CI 18.4%-54.8%) for the old DAAs + Peg-IFN/RBV, 22.0% (95% CI 17.9%-26.8%) for the new DAAs + Peg-IFN/RBV, 9.8% (95% CI 8.6%-11.2%) for the DAAs + RBV, and 3.8% (95% CI 2.4%-6.1%) for DAAs only. Simeprevir + Peg-IFN/RBV was associated with an increased relative risk over Peg-IFN/RBV; RR = 1.319 (95% CI 1.026-1.697). Conclusion: Dermatological events are still an important issue for many of the new DAAs. Appropriate monitoring, management, and patient education are needed to minimize AEs and achieve HCV cure.
AB - Background: Direct-Acting antivirals (DAAs) are known to present with additional dermatological events over pegylatedinterferon/ ribavirin (Peg-IFN/RBV). Objective: A systematic review and meta-Analysis was conducted to assess the incidence/risk of cutaneous adverse events (AEs) for simeprevir, sofosbuvir, ABT450/r-ombitasvir, dasabuvir, ledipasvir, daclatasvir, and asunaprevir. Methods: The databases searched included PubMed, Clinicaltrials.gov, and Clinicaloptions.com. Data on telaprevir and boceprevir were obtained from a previous study. Results: The incidences of cutaneous AEs were 34.3% (95% CI 18.4%-54.8%) for the old DAAs + Peg-IFN/RBV, 22.0% (95% CI 17.9%-26.8%) for the new DAAs + Peg-IFN/RBV, 9.8% (95% CI 8.6%-11.2%) for the DAAs + RBV, and 3.8% (95% CI 2.4%-6.1%) for DAAs only. Simeprevir + Peg-IFN/RBV was associated with an increased relative risk over Peg-IFN/RBV; RR = 1.319 (95% CI 1.026-1.697). Conclusion: Dermatological events are still an important issue for many of the new DAAs. Appropriate monitoring, management, and patient education are needed to minimize AEs and achieve HCV cure.
KW - Dermatitis
KW - Dermatology
KW - Immunology
KW - Infectious Disease
UR - https://www.scopus.com/pages/publications/84959386286
U2 - 10.1177/1203475415595775
DO - 10.1177/1203475415595775
M3 - Review article
C2 - 26162860
AN - SCOPUS:84959386286
SN - 1203-4754
VL - 20
SP - 58
EP - 66
JO - Journal of Cutaneous Medicine and Surgery
JF - Journal of Cutaneous Medicine and Surgery
IS - 1
ER -