Spotswood L. Spruance, MD; Andrew T. Pavia, MD; Dolores Peterson, MD; Allison Berry, MD; Richard Pollard, MD; Thomas F. Patterson, MD; Ian Frank, MD; Scot C. Remick, MD; Melanie Thompson, MD; Rodger D. MacArthur, MD; G. E. Morey, MD; Carlos H. Ramirez-Ronda, MD; Barry M. Bernstein, MD; Donna E. Sweet, MD; Lawrence Crane, MD; Eskild A. Peterson, MD; Constance T. Pachucki, MD; Stephen L. Green, MD; Jerry Brand, MD, MPH; Adan Rios, MD; Lisa M. Dunkle, MD; Anne Cross, PhD; Michael J. Brown, PhD; Peter Ingraham, PhD; Ronald Gugliotti, MPH; Andrew H. Schindzielorz, MD; Laurie Smaldone, MD
Spruance SL, Pavia AT, Peterson D, Berry A, Pollard R, Patterson TF, et al. Didanosine Compared with Continuation of Zidovudine in HIV-infected Patients with Signs of Clinical Deterioration While Receiving Zidovudine: A Randomized, Double-Blind Clinical Trial. Ann Intern Med. 1994;120:360-368. doi: 10.7326/0003-4819-120-5-199403010-00002
Download citation file:
Published: Ann Intern Med. 1994;120(5):360-368.
To determine the benefits of switching to didanosine compared with continuing zidovudine among patients infected with human immunodeficiency virus (HIV) who have previously used zidovudine and have signs of clinical deterioration.
Randomized, double-blind, two-armed, parallel, comparative clinical trial with a blinded, compassionate crossover provision at 12 weeks.
Outpatient clinics at 19 tertiary care medical centers.
312 patients infected with HIV who had received zidovudine for 6 months or more, had CD4 cell counts of 300/mm3 or less, and had signs of clinical deterioration within 12 weeks before study entry.
Peroral didanosine tablets (600 mg/d adjusted for weight, “high dose”) or zidovudine capsules (600 mg/d).
Primary study end points were death, a new acquired immunodeficiency syndrome (AIDS)-defining event, or the combination of two new or recurrent HIV-related diagnoses with a 50% decrease in CD4 cells.
Switching to didanosine was associated with fewer end points than continuing zidovudine (relative risk [RR] for zidovudine:didanosine = 1.5; 95% CI, 1.1 to 2.0). This benefit was consistent across subgroups of patients with either AIDS-related complex or AIDS and was most apparent among those with a CD4 count at entry of 100/mm3 or more (RR = 2.2; CI, 1.1 to 4.4).
This study shows a positive treatment effect for switching from zidovudine to didanosine among patients with either AIDS-related complex or AIDS and validates the common practice of using clinical signs or a decrease in the CD4 count as an indication for changing therapy.
*For members of the Study Group, see the appendix.
Learn more about subscription options.
Register Now for a free account.
HIV, Infectious Disease.
Results provided by:
Copyright © 2017 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use
This PDF is available to Subscribers Only