Meta-analysis of two randomized controlled trials comparing combined zidovudine and didanosine therapy with combined zidovudine, didanosine, and nevirapine therapy in patients with HIV
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作者:
Raboud, JM
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Raboud, JM
Rae, S
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Rae, S
Vella, S
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Vella, S
Harrigan, PR
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Harrigan, PR
Bucciardini, R
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Bucciardini, R
Fragola, V
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Fragola, V
Ricciardulli, D
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Ricciardulli, D
Montaner, JSG
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机构:Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
Montaner, JSG
机构:
[1] Canadian HIV Trials Network, Vancouver, BC V6Z 1Y6, Canada
[2] Univ British Columbia, Dept Hlth Care & Epidemiol, Vancouver, BC V6T 1W5, Canada
[3] Ist Super Sanita, I-00161 Rome, Italy
[4] St Pauls Hosp, Ctr Excellence HIV AIDS, Vancouver, BC V6Z 1Y6, Canada
Objectives: To extend the range of CD4 counts in which a plasma viral load nadir (pVL) <20 copies/ml was known to be predictive of the duration of virologic response. To determine whether baseline pVL is predictive of virologic response during the study periods. Methods: A meta-analysis was conducted of the original individual patient data from two randomized controlled trials comparing zidovudine (ZDV)/didanosine (ddI) with ZDV/ddI/nevirapine (NVP). Results: In total, 87 patients received ZDV/ddI and 83 received ZDV/ddI/NVP. Study subjects on triple therapy with baseline gVL <100,000 copies/ml were more likely to achieve a pVL <300 copies/ml (odds ratio [OR] = 2.49; p = .02) and <20 copies/ml (OR = 4.76; p = .001) during the trial than those with baseline pVL >100,000 copies/ml. Among triple therapy patients, the relative risk of virologic failure was higher for patients with higher baseline pVL (rate ratio [RR] = 2.51/log(10) copies/ml, p = .01), after controlling for compliance and pVL nadir. The relative risks of virologic failure associated with pVL nadir <20 copies/ml and between 21 and 400 copies/ml were .04 (p = .0001) and .56 (p = .26), respectively, compared with patients with a pVL nadir >400 copies/ml. Conclusions: We have extended our earlier results that achieving a pVL nadir <20 copies/ml is important for maintaining virologic suppression. In particular, we have demonstrated that a pVL nadir <20 copies/ml is at least fivefold more protective against virologic failure than achieving a pVL nadir between 20 and 400 copies/ml. Baseline pVL is significantly associated with the probability of achieving and sustaining virologic suppression.
机构:
Univ Calif San Diego, San Diego Vet Affairs Med Ctr, San Diego, CA 92161 USAUniv Calif San Diego, San Diego Vet Affairs Med Ctr, San Diego, CA 92161 USA
Haubrich, R
Richman, D
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机构:
Univ Calif San Diego, San Diego Vet Affairs Med Ctr, San Diego, CA 92161 USAUniv Calif San Diego, San Diego Vet Affairs Med Ctr, San Diego, CA 92161 USA
Richman, D
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION,
1999,
281
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