BACKGROUND: Poor adherence to Hepatitis C virus (HCV) treatment is an important cause of treatment failure. Traditional ribavirin 200 mg (RBV) treatment is associated with a significant daily pill burden. RibaPak (RBP), available as 400 mg and 600 mg ribavirin tablets, offers simplified dosing at two pills daily. AIM: To examine whether improved adherence was associated with RBP vs. RBV. METHODS: Accurate Dosing in Hepatitis C: Examining the RibaPak Experience (ADHERE) was a U.S., multi-centre, prospective registry capturing data on adherence with RBP vs. RBV in adults with HCV. Adherence was measured by the proportion of subjects remaining on treatment at weeks 4, 12 and 24; by pill counts; and by the proportion of subjects who took > or = 80% of their prescribed dose. RESULTS: A total of 503 patients (RBP = 346, RBV = 157) from 33 sites were included. A greater proportion of RBV vs. RBP subjects prematurely discontinued treatment. At 12 and 24 weeks, a greater proportion of RBP vs. RBV subjects took > or = 80% of their prescribed doses (P < 0.05). For patients who remained on treatment, the mean milligrams missed per day was significantly greater for RBV vs. RBP at 24 weeks. CONCLUSIONS: First line treatment with RBP may offer the best prospect for less discontinuation and improved treatment adherence.
BACKGROUND: Poor adherence to Hepatitis C virus (HCV) treatment is an important cause of treatment failure. Traditional ribavirin 200 mg (RBV) treatment is associated with a significant daily pill burden. RibaPak (RBP), available as 400 mg and 600 mg ribavirin tablets, offers simplified dosing at two pills daily. AIM: To examine whether improved adherence was associated with RBP vs. RBV. METHODS: Accurate Dosing in Hepatitis C: Examining the RibaPak Experience (ADHERE) was a U.S., multi-centre, prospective registry capturing data on adherence with RBP vs. RBV in adults with HCV. Adherence was measured by the proportion of subjects remaining on treatment at weeks 4, 12 and 24; by pill counts; and by the proportion of subjects who took > or = 80% of their prescribed dose. RESULTS: A total of 503 patients (RBP = 346, RBV = 157) from 33 sites were included. A greater proportion of RBV vs. RBP subjects prematurely discontinued treatment. At 12 and 24 weeks, a greater proportion of RBP vs. RBV subjects took > or = 80% of their prescribed doses (P < 0.05). For patients who remained on treatment, the mean milligrams missed per day was significantly greater for RBV vs. RBP at 24 weeks. CONCLUSIONS: First line treatment with RBP may offer the best prospect for less discontinuation and improved treatment adherence.
Authors: Donna M Evon; Carol E Golin; Jason E Bonner; Catherine Grodensky; Jennifer Velloza Journal: J Clin Gastroenterol Date: 2015 May-Jun Impact factor: 3.062
Authors: Jiska M Balk; Guido Rmm Haenen; Özgür M Koc; Ron Peters; Aalt Bast; Wim Jf van der Vijgh; Ger H Koek Journal: Pharmgenomics Pers Med Date: 2015-08-12
Authors: Louis S Matza; Sandhya J Sapra; John F Dillon; Anupama Kalsekar; Evan W Davies; Mary K Devine; Jessica B Jordan; Amanda S Landrian; David H Feeny Journal: Eur J Health Econ Date: 2014-12-07