Clinical Study

Impact of Pentoxifylline and Vitamin E on Ribavirin-Induced Haemolytic Anaemia in Chronic Hepatitis C Patients: An Egyptian Survey

Table 1

Guidelines for dose modification and discontinuation of PEG-Intron or PEG-Intron/Rebetol for Hematologic toxicity [16].

Laboratory values PEGPEG-IntronRebetol

Hb*
 <10.0 g/dLDecrease by 200 mg/day
 <8.5 g/dLPermanently discontinuePermanently discontinue
WBC
 <1.5 × 109/LReduce dose by 50%
 <1.0 × 109/LPermanently discontinuePermanently discontinue
Neutrophil
 <0.75 × 109/LReduce dose by 50%
 <0.5 × 109/LPermanently discontinuePermanently discontinue
Platelets
 <80 × 109/LReduce dose by 50%
 <50 × 109/LPermanently discontinuePermanently discontinue

*For patients with a history of stable cardiac disease receiving PEG-Intron in combination with ribavirin, the PEG-Intron dose should be reduced by half and the ribavirin dose by 200 mg/day if a >2 g/dL decrease in haemoglobin is observed during any 4-week period. Both PEG-Intron and ribavirin should be permanently discontinued if patients have haemoglobin levels <12 g/dL after this ribavirin dose reduction.
Hb: haemoglobin
WBC: White blood cell.