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Session 5
Oral Abstract Session
Epidemiology and Infection Control Session Time: Monday, 10 am - 12:30 pm Room 6C |
Background: Optimal timing of
antiretroviral therapy (ART) initiation for HIV-infected patients is of great
clinical and public health importance, yet remains unclear. Clinicians variably advocate earlier (higher
CD4+ cell count [CD4]) vs later (lower CD4) ART
initiation, but sparse data exist to support either strategy. Methods: Patients well-characterized
by CD4 and ART use history from January 1996 to March 2001 at 8 Results: Data from
126 patients with CD4 501-750 cells/mm3, 315 with CD4 351-500, and
377 with CD4 201-350 were analyzed. ART
initiators vs delayers within each stratum had many
similar demographics. In each of the 3 CD4 strata, more than two-thirds of
delayers started ART in the next lower stratum.
Median years of follow-up for initiators and delayers were,
respectively, 5.9 and 5.3 for those with CD4 501-750; 3.7 and 3.4 for CD4
351-500; and 3.0 and 3.3 for CD4 201-350 cells/mm3 (p>0.3 for
each). For those with CD4 501-750, 7.5
deaths/1000 person-years occurred in 54 initiators and 3.0/1000 person-years in
72 delayers (rate ratio [RR]=2.52; 95% CI: 0.23, 27.8;
p>0.4), but only 3 deaths occurred in this stratum, none apparently
HIV-related. For those with CD4 between
351-500, 229 initiated and 86 delayed ART, with 10.7 and 18.2 deaths/1000
person years, respectively (RR= 0.59; 95% CI: 0.21, 1.65; p>0.3). For those
with CD4 201-350, 325 initiated and 52 delayed ART, with 20.8 and 70.6
deaths/1000 person years, respectively (RR= 0.29; 95% CI: 0.15, 0.58;
p<.001).
Conclusions: These preliminary data suggest that
initiation of ART for patients with CD4 201-350 cells/mm3, and
possibly those with CD4 351-500, is associated with reduction in mortality in
comparison with those for whom such therapy is delayed. Such survival benefits should be considered
when evaluating the optimal timing of ART initiation. |
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©2002 9th Conference on Retroviruses and Opportunistic Infections |