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Downloaded from http://journals.lww.com/co-hivandaids by BhDMf5ePHKbH4TTImqenVA5KvPVPZ0P5BEgU+IUTEfzO/GUWifn2IfwcEVVH9SSn on 06/05/2020 REVIEW URRENT Assessing liver disease in HIV–HCV PINION coinfected patients a b Emmanuel A. Tsochatzis and Laurent Castera Purpose of review It is estimated that up to 10% of patients with HIV have chronic hepatitis C (HCV)–HIV coinfection in the Western world. Assessment of liver disease is essential in such patients in order to diagnose cirrhosis at an early stage, prioritize for anti-HCV treatment but also assess fibrosis regression after sustained viral response (SVR). In this review, we present a critical appraisal of liver disease assessment in patients with HIV–HCV co-infection. Recent findings Liver biopsy has largely been replaced by noninvasive fibrosis assessment in most coinfected patients, although it is still of value if there are concerns of additional diagnoses. Noninvasive assessment includes serum markers and liver stiffness measurement using elastography-based techniques. Certain serum markers, such as FIB-4, SHASTA index, and Fibrometer HIVC have been specifically developed in patients with HIV–HCV coinfection. Transient elastography has advantages over serum markers, as it is not influenced by concomitant antiretroviral medication, HIV replication, CD4 cell count, or nonliver inflammatory processes. Summary Noninvasive markers are increasingly used for clinical decision-making and predicting clinical outcomes in HIV–HCV
Current Opinion in HIV & AIDS – Wolters Kluwer Health
Published: Sep 1, 2015
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