Incidence of discontinuation of highly active antiretroviral combination therapy (HAART) and its determinants
To determine the incidence and determinants for discontinuation of initial highly active antiretroviral therapy (HAART). In this retrospective follow-up study from hospital files and pharmacy dispensing data, a standard dataset was collected including patient characteristics, therapy characteristics...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes and human retrovirology 1999-03, Vol.20 (3), p.290-294 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To determine the incidence and determinants for discontinuation of initial highly active antiretroviral therapy (HAART).
In this retrospective follow-up study from hospital files and pharmacy dispensing data, a standard dataset was collected including patient characteristics, therapy characteristics, and HIV-monitoring parameters (e.g., CD4+ lymphocyte counts, viral load determinations). Kaplan-Meier estimates of the cumulative probability of discontinuation of initial HAART were calculated. Cox proportional hazard analysis was used to identify determinants for discontinuation of initial HAART.
All patients starting HAART (n = 99) during June 1996 to February 1997 at our regional AIDS center.
Incidence and determinants for discontinuation of HAART.
During the mean follow-up of 450+/-10 days, 27 patients switched initial HAART, 3 patients stopped any antiretroviral therapy. Reasons for switching were increasing viral load (18x), insufficient decrease of viral load (3x), and adverse events (6x). Nonnaivete for antiretroviral therapy and a lower CD4+ lymphocyte count at start were identified as determinants for discontinuation of initial HAART.
The overall incidence density for discontinuation of initial HAART was 25 per 100 patients/year. The main reason for switching was an increasing viral load. CD4+ lymphocyte counts at start and nonnaivete for antiretroviral therapy were identified as determinants for discontinuation. |
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ISSN: | 1077-9450 2331-6993 |
DOI: | 10.1097/00042560-199903010-00012 |