Lalloo Umesh G, Amod Farida C
Int'l Clinical Trials Unit, Adult AIDS Clinical Trials Group, Doris Duke Medical Research Institute, Nelson R. Mandela School of Medicine, Dept. of Medicine, University of KwaZulu Natal, 719 Umbilo Road, Durban 4001, South Africa.
Curr HIV/AIDS Rep. 2005 Aug;2(3):116-21. doi: 10.1007/s11904-005-0003-9.
Tuberculosis (TB) and cryptococcosis are common infectious complications in HIV in resource-limited settings and contribute substantial morbidity and mortality. The increasing access to highly active antiretroviral treatment (HAART) has invited numerous challenges such as timing of HAART, cotreatment (drug dosages and interaction), immune reconstitution syndromes, and withdrawal of chemoprophylaxis. Numerous small studies propose the feasibility of concomitant TB/HIV treatment that needs to be confirmed in large, randomized trials. Treatment of acute cryptococcocal meningo-encephalitis with amphoterecin B is fraught with logistic problems in resource-limited settings. An effective safe dose of fluconazole as monotherapy needs to be determined in phase II studies. Current management guidelines extrapolated from developed countries may not necessarily apply and need validation in resource-limited settings.