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BACKGROUND Staphylococcus aureus is a frequent cause of hospital-acquired bacteremia in paediatrics patients. Vancomycin is the drug of choice for the treatment of methicillin-resistant strains, although treatment failure is frequently observed. Area under the curve (AUC) of plasma concentrations over the minimum inhibitory concentration (MIC) has been proposed as the best index to predict treatment response, although information about its clinical impact on paediatric patients is scarce. The objective of this study is to determine if early recovery of an AUC/MIC>400 mg*h/L for vancomycin in paediatric patients with S. aureus bacteremia is associated with clinical and microbiological treatment response. METHODS Retrospective observational study. Paediatric patients younger than 3 years with vancomycin-treated S. aureus bacteremia were included. The pharmacokinetic parameters were calculated from the vancomycin value obtained in the first 72 hours of treatment, assuming a bicompartmental model. A multivariate analysis was performed to analyze factors associated with early clinical response, treatment failure, microbiological response and 30-day mortality. RESULTS 51 patients with S. aureus bacteremia were included in the study. In 18 patients (35.3%), strains with a MIC higher than 1.0 mg/L were isolated, being in eight (15.7%) greater than 1.5 mg/L. 22 (43.1%) patients did not reach an estimated AUC/MIC>400 during the first 72 hours. A significant association was observed between attainment of an AUC/MIC>400 and early clinical response [OR:3.23(95%CI:1.07-12.03)]. No significant association was found between an AUC/MIC>400 and microbiological response or mortality. CONCLUSIONS An AUC/MIC>400 is associated with early response to vancomycin in paediatric patients with S. aureus bacteremia.

This double masked study demonstrates the ability of prostaglandin F2-alpha (PG F2α) tromethamine to partially prevent the development of postoperative intraocular hypertension in extracapsular surgery with intraocular lens (IOL) implantation. Topical application of 100 wgr of PG F2α 4 hours prior to surgery and 6 and 18 hours postsurgery resulted in a biphasic curve with relative increase of preoperative intraocular pressure (IOP) and postoperative decrease in a 48-hour follow-up in 21 patients, when compared with 21 controls receiving one drop of BSS. Eighty percent of patients receiving PG F2α complained of a burning sensation, while only 14% did so in the control group. We conclude that PG F2α or analogues could be useful for postoperative IOP control.