The prevalence of phenotypic drug resistance was assessed in 60 patients wi
th a viral rebound after they received a protease inhibitor (PI)- or nonnuc
leoside reverse transcriptase inhibitor (NNRTI)-containing regimen (baselin
e), Resistance testing was done within 36 weeks of viral rebound; no resist
ance testing was available at baseline, All patients had previously receive
d zidovudine; 86.0% had received lamivudine, In total, 45.1% of the patient
s had strains resistant to the PI that they started and 88.9% given nevirap
ine had strains with reduced susceptibility to that drug. Overall, 46 patie
nts (76.7%) harbored a strain resistant to greater than or equal to 1 drug
of their initial PI- or NNRTI-containing regimen. Of 53 patients who remain
ed on treatment at the time of the study (40 had switched to a different co
mbination from that at baseline), 6 harbored isolates susceptible to all dr
ugs they had ever received. Thus, patients with viral rebound while on pote
nt antiretroviral therapy usually have reduced susceptibility to greater th
an or equal to 1 drug. Viral rebound also occurs in persons in whom resista
nt strains could not be detected by the assay used.