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. 2018 Apr 10;21(Suppl Suppl 2):e25076. doi: 10.1002/jia2.25076

Table 1.

Interpretation of pre‐treatment assessment in DAA candidates

Variable Test Interpretation
HCV genotype Commercial assay using the sequence of the 5′untranslated region plus a portion of another genomic region, generally the core‐coding or the NS5B‐coding regions Choose DAA regimen for specific HCV genotype following international guidelines
Disease stage Transient elastography
APRI:
[{AST (IU/L)/AST_ULN (IU/L)} × 100]/ platelet count (109/L)
FIB‐4: age (yr) × AST(IU/L)/platelet count (109/L × [ALT(IU/L)1/2]
Liver biopsy
Cirrhosis: Plan surveillance schedule and assess complete liver function.
Choose DAA regimen schedule based on fibrosis stage.
Liver function Child‐Pugh‐Turcotte Score (Albumin, INR, Bilirubin, Ascites, encephalopathy) CPT = A6 Prefer DAAs not including protease inhibitors.
CPT >A6 Protease inhibitors must be avoided
Kidney function Assess eGFR (Ckd‐Epi, Cockcroft‐Gault formula, MDRD) eGFR <30 ml/min/m2 avoid sofosbuvir‐based regimens.
Concomitant medications Assess comorbidities and concomitant medications (focus on immunosuppressant, cardiovascular and lipid‐lowering drugs).
Warnings for PPIs and HIV medications
Check international guidelines and http://www.hep-druginteractions.org
HBV status HBsAg, Anti‐HBs, Anti‐HBc.
If HBsAg + check HBV DNA, HBeAg and anti‐HBeAg
  1. HBsAg negative, anti‐HBc positive: Monitor and test for HBV reactivation in case of ALT elevation (check every 4 weeks).

  2. HbsAg‐positive patients fulfilling the standard criteria for HBV treatment should receive treatment following international guidelines.

  3. HBsAg‐positive patients not meeting HBV treatment criteria should be considered for concomitant nucleos(t)ide analogue prophylaxis until week 12 post DAA, and monitored closely.