AIDSWEEKLY Plus; Monday, March 1, 1999
Daniel J. DeNoon, Senior Editor
Clinicians face this question for each patient responding to highly active antiretroviral therapy (HAART). When can such a patient cease taking medicines that prevent opportunistic infections (OIs)? And when should OI prophylaxis be reinstated? The answer must be based on data that only now is beginning to emerge from longitudinal studies.
"We can see that with discontinuation of prophylaxis risk seems to be diminishingly small for many opportunistic infections," said Constance Benson of the University of Colorado. "The challenge for clinicians is to identify those patients who can safely stop primary and secondary prophylaxis."
Benson spoke in a symposium on immune reconstitution at the 6th Conference on Retroviruses and Opportunistic Infections, held January 31-February 4, 1999, in Chicago, Illinois.
Benson noted that from 1996 to 1997 there was a 15 percent decrease in AIDS-defining events in the U.S.
"This is due to the decline in incidence of every opportunistic infection associated with AIDS," she said.
Benson, a noted AIDS clinical researcher since the beginning of the epidemic, said it is clear that the natural history of OIs in HIV disease has been altered by the use of HAART. But exactly how much HAART reduces the risk of an OI - and whether risk is decreased for a specific CD4 threshold - remains unknown.
However, some indications are emerging. The incidence of OIs in patients on HAART is associated with the degree of CD4 count increase. And regardless of a patient's viral load, the higher a patient's CD4 count the lower the risk of an OI.
Benson said the Spectrum of Disease Study undertaken by the U.S. Centers for Disease Control and Prevention (CDC) found that Pneumocystis carinii pneumonia (PCP) and disseminated Mycobacterium avium complex (MAC) infection occur at the same low CD4 counts for HAART patients as for untreated patients. Two independent predictors of OIs are a 0.5 log[10] decrease in viral load or no increase in CD4 after HAART initiation. Finally, patients whose viral loads are less than 5,000 copies/mL are at a low risk of progression.
"Those of us in clinical practice, however, have to deal with the exceptions," Benson warned.
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