© 1997 Canadian Medical Association
Postexposure assessment should take into account the nature of the exposure, the likelihood of HIV infection in the source patient and, in cases of known infection, the HIV titre and likelihood of drug resistance. Appropriate counselling for the exposed worker is crucial, and the risk of infection should be weighed against the potential toxicity of antiretroviral agents. When given, prophylaxis should be started within 1 or 2 hours after the exposure and continue for 4 weeks.
The advice of an expert in antiretroviral therapy should be sought when drug resistance is possible. Prophylactic AZT in the recommended dose is well tolerated, but higher doses may cause gastrointestinal symptoms, fatigue and headache. Given in the second or third trimester of pregnancy, it has been associated with mild reversible anemia in the infant but not with adverse effects in the mother. Its use in the first trimester has received only limited study.[3] The toxicity of prophylactic 3TC and IDV is uncertain, and the safety of these drugs for use during pregnancy has not been established.
The extrapolation of guidelines for postexposure prophylaxis to other situations such as sexual assault is being considered at some centres. Like the use of combination therapy advocated by the CDC, such extensions are based on sound science but are difficult to test objectively. It is likely that well-crafted guidelines will reduce the risk of HIV infection among health care workers and others. Such guidelines must be applied intelligently to avoid waste, needless side effects and the diversion of the drug supply away from more clearly beneficial applications. Physicians should remain alert to recommendations as they evolve and ensure that the necessary drugs are at hand.
David M. Patrick, MD
British Columbia Centre for Disease Control
Vancouver, BC