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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: J Viral Hepat. 2017 Sep 21;25(2):187–197. doi: 10.1111/jvh.12784

TABLE 5.

Characteristics of 6 patients with >4 log increases in HBV DNA during treatment or after treatment with direct-acting antivirals

Age Cirrhosis Alcohol misusea Baseline HBsAg+ Pre-DAA treatment baseline HBV DNA (IU/mL) Max HBV DNA increase (IU/mL) Max ALT increase (IU/L) Max total bili increase (μg/dL) Time between start of DAA therapy and HBV DNA flare (d) Time between start of DAA therapy and HBV treatment initiation (d) HBV therapy Outcome
58 No No No 0 10 902 15 0.1 28 38 TDF HBV DNA cleared
64 Yes No Yes Unknown 18 900 3 0.4 45 45 TDF Unknown
53 No No Yes 27 900 254 304 9 1.1 316 Started concomitant with DAA FTC/TDF+ETV HBV DNA dropped by 3-log
60 Yes No Yes 0 1 559 851 241 0.2 194 195 ETV HBV DNA dropped by 6-log
53 No No Yes 0b 2 885 983 24 0 168 Started concomitant with DAA TDF HBV DNA cleared
56 Yes No Yes 2361 >22 000 000 1467 17.3 57 67 FTC/TDF HBV DNA cleared

DAA, direct-acting antiviral; HCV, hepatitis C virus; TDF, tenofovir; FTC, emtricitabine; ETV, entecavir; bili, bilirubin; ALT, alanine aminotransferase.

a

Alcohol misuse was identified with the alcohol use disorder identification test, score ≥4 for males and ≥3 for females indicates hazardous drinking.

b

HBV DNA was available within 1.5 y of DAA start date.