Table 2.
Three studies which assessed but do not separately report missed doses of interferon and ribavirin
| Study | No. of subjects |
% HIV-co -infected |
Type of study /HCV treatment |
Method of adherence assessment |
80/80/80 Adherence | Adherence - virological outcome relationship |
|---|---|---|---|---|---|---|
| McHutchison et al. 200228 |
1521 | 0 | 3 clinical trials combined – interferon or PEG-IFN + RBV |
Pill counts (RBV) and subject diaries |
62% took at least 80% of prescribed interferon and at least 80% of prescribed ribavirin for at least 80% of the recommended duration of treatment and were considered ‘adherent’ |
80/80/80 adherence was associated with SVR in genotype 1 but not genotype 2/3 subjects |
| Sola et al. 200629 | 157 | 50.3 | Prospective-interferon + RBV |
Pill counts (RBV) and self-report questionnaire |
76% took at least 80% of prescribed interferon and at least 80% of prescribed ribavirin for at least 80% of the recommended duration of treatment and were considered ‘adherent’ |
80/80/80 adherence was associated with SVR |
| Sylvestre and Clements 200727 |
71 | 1.4 | Prospective-interferon + RBV |
Return of empty vials (IFN); pill counts (RBV); self-report questionnaire |
68% took at least 80% of prescribed interferon and at least 80% of prescribed ribavirin for at least 80% of the recommended duration of treatment and were considered ‘adherent’ |
80/80/80 adherence was associated with SVR |