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Similar
Adherence Rates Favor Different Virologic Outcomes for Patients
Treated with Non Nucleoside Analogues or Protease Inhibitors
This prospective study
verified the effect of adherence on the risk of virologic
failure. At enrollment in the study, a total of
543 patients who were following a steady (duration, >or=6 months)
and effective (viral load, <50 human immunodeficiency virus [HIV]
RNA copies/mL) regimen of highly active antiretroviral therapy (HAART)
completed a self-reported questionnaire derived from the Adult AIDS
Clinical Trials Group Adherence Follow-up Questionnaire.
Patients
were followed up for the subsequent 6 months to document virologic
failure, which was defined as 2 consecutive viral load measurements
of >500 HIV RNA copies/mL.
Results
Only
the type of treatment and the adherence rate at baseline were significantly
associated with the virologic end point.
Among
patients who reported an adherence rate of <or=75%, the rate
of virologic failure was 17.4%; this rate decreased to 12.2% for
patients whose adherence rate was 76%-85%, to 4.3% for patients
whose adherence rate was 86%-95%, and to 2.4% for patients whose
adherence rate was >95%.
When
analysis was adjusted according to the type of regimen received,
patients who were receiving protease
inhibitor (PI)-based HAART
and who had an adherence rate of up to 85% had a virologic failure
rate of >20%, whereas, only for patients who were receiving non
nucleoside reverse-transcriptase inhibitor (NNRTI)-based HAART
and who had an adherence rate of <or=75%, the virologic failure
rate was >10%.
For
the comparison of NNRTI-treated patients and PI-treated patients
with an adherence rate of 75%-95%, the odds ratio was 0.157 (95%
confidence interval, 0.029-0.852).
The
number of pills and daily doses received correlated with the reported
adherence rate.
Conclusions
The
authors conclude:
- Patients receiving NNRTIs report
a higher rate of adherence than do patients receiving PIs;
- Adherence is significantly influenced
by the number of pills and daily doses received;
- Low adherence is a major determinant
of virologic failure;
- However, different therapies have
different cutoff values for adherence that determine a significant
increment of risk.
Division of Infectious
Diseases, Unit of Antiviral Therapy, Ospedali Riuniti, Bergamo,
Italy.
01/10/05
Reference
F
Maggiolo and others. Similar adherence rates favor different virologic
outcomes for patients treated with non nucleoside analogues or protease
inhibitors. Clinical Infectious Diseases 40(1):158-63. January
1, 2005. [Epub December 6, 2004].
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