947 
Low Rates of HCV Therapy among Treatment-eligible Injection Drug Users with and without HIV Co-infection
M Sulkowski, S Mehta, R Moore, Ruben Montes de Oca*, and D Thomas
Johns Hopkins Univ, Baltimore, MD, US
Background: Most HCV+
injection drug users (IDU) do not receive hepatitis C virus (HCV) treatment. The
objective of this study was to determine the proportion of HIV+ and HIV–
IDU (former and active) who are eligible for and initiate HCV therapy with pegylated interferon (pegINF) + ribavirin (RBV) in the absence of geographic and financial
barriers.
Methods: Between March 2004
and March 2006, HCV+ IDU were enrolled sequentially from the Johns
Hopkins Program for Alcoholism and Other Drug Dependencies and the Johns
Hopkins University HIV clinic. Each IDU underwent a comprehensive
evaluation: medical, psychiatric, and
drug/alcohol use history, depression screening, physical exam, and laboratory
testing. Subjects were deemed ineligible for pegINF+RBV
therapy if any of the following criteria were met: HCV RNA not detected; pregnant or not willing
to use birth control; life
expectancy <2 years (eg, advanced AIDS or cancer);
active depression with suicidal ideation; allergic reaction to pegINF+RBV; severe hematologic
abnormality (eg, hemoglobin <10.5 g/dL, ANC <1000/mm3, platelet count <50,000/mm3); renal insufficiency (creatinine
>2.5). All treatment-eligible subjects were given the opportunity to take pegINF+RBV, available on-site at no cost.
Result: We enrolled 332 subjects (172 HIV/HCV
co-infected; 158 HCV mono-infected). HIV-co-infected IDU were younger (41 to
<44 years) and were more likely to be African American (90% to >74%),
have a monthly income >$500 (52% to >23%) than those with HCV alone. No
difference was observed in the prevalence of mental illness (~64%), alcohol
abuse (~20%), or interest in receiving HCV treatment (~93%). HIV-co-infected
IDU were more likely to have detectable HCV RNA (20 of 172 HIV/HCV co-infected,
11%; 29 of 143 of HCV mono-infected, 20%; p
<0.001) and less likely to be eligible for HCV treatment (75 of 152 of HIV/HCV,
49%; 78 of 114 HCV, 68%; p = 0.002). Reasons for ineligibility were: severe depression (HIV/HCV 12%; HCV 30%); life
expectancy <2 years (HIV/HCV 40%; HCV 30%); hematologic
abnormality (HIV/HCV 49%; HCV 22%); renal insufficiency (HIV/HCV 10%; HCV 8%). Of
the treatment-eligible IDU, ~40% initiated HCV therapy, defined as at least pegINF injection (31 of 75 HIV/HCV, 41%; 27 of 80 HCV,
36%).
Conclusions: While ~50% of HIV/HCV-co-infected IDU were
ineligible for HCV treatment, most (~80%) of HCV-mono-infected IDU were
treatment-eligible. Despite the removal of financial and geographic barriers,
only ~40% of treatment-eligible IDU initiated HCV treatment. Strategies are
needed to increase HCV treatment uptake among IDU.
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