ORAL AZTREONAM, A POORLY ABSORBED YET EFFECTIVE THERAPY FOR BACTERIALDIARRHEA IN UNITED-STATES TRAVELERS TO MEXICO

Objective. - To evaluate a poorly absorbed antimicrobial with in vitro activity against all major bacterial enteropathogens in oral therapy for bacterial diarrhea. Design. - One hundred ninety-one US students w ith diarrhea acquired in Mexico received 100 mg of aztreonam or matchi ng placebo three times a day for 5 days. Stools were cultured for bact erial enteropathogens before and after therapy. Setting. - We studied US students who acquired diarrhea in Mexico (travelers' diarrhea) in v iew of the high frequency of bacterial agents in this setting. Main Ou tcome Measure. - We examined time of clinical recovery, treatment fail ures, adverse experiences, and microbiologic eradication from stool of the etiologic agent in subjects randomized to receive aztreonam or pl acebo. Results. - Aztreonam reduced the average duration of diarrhea c ompared with the placebo: for all cases, by 40 hours (P << .01); for t hose with enterotoxigenic Escherichia coli diarrhea, by 50 hours (P < .01); for those with shigellosis, by 90 hours (P, not significant [sma ll sample size]); for all bacterial agents, by 57 hours (P << .01). Cl inical failures during the 5 days of therapy were seen in six patients (6%) receiving aztreonam and 25 (27%) receiving placebo (P < .01). Pa thogen eradication occurred in 95% of those receiving aztreonam and in 70% of those receiving the placebo (P < .01). All bacterial enteropat hogens were susceptible in vitro to aztreonam. The drug was well toler ated. Conclusions. - Oral aztreonam, which is poorly absorbed, was wel l tolerated and was an effective therapy for bacterial diarrhea in US adults in Mexico.