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2.
Braz. j. infect. dis ; 10(3): 179-184, June 2006. tab
Article in English | LILACS | ID: lil-435283

ABSTRACT

OBJECTIVE: Determine the prevalence of Vancomycin-resistant enterococci (VRE) colonizing the intestinal tract of hospitalized patients and define risk factors. MATERIAL AND METHODS: A point prevalence survey of VRE fecal carriage was carried out among patients who stayed at a 600-bed teaching hospital for at least two days. Resistance to vancomycin was detected by the E-test method. Epidemiological data was recorded for all patients included in the study and was used for the risk factor analysis. RESULTS: A total of 128 patients hospitalized for at least two days were enrolled in this investigation. Thirty-nine patients (30.5 percent) were colonized with vancomycin-resistant enterococci. Twenty-three of the 39 strains were identified as Enterococcus faecium, 13 were identified as Enterococcus gallinarum and three strains as Enterococcus casseliflavus. The risk factors that were significantly associated with VRE colonization included length of hospital stay (13.2 days vs. 8.6 days), age (60.7 years vs. 47.7 years) and the presence of underlying malignancies (28.2 percent vs. 11.2 percent). An association was found between VRE colonization and the use of antimicrobials with anaerobic activity, such as metronidazole, piperacillin/tazobactam and imipenem. The use of vancomycin was associated with VRE colonization in the intensive care unit. CONCLUSIONS: VRE colonization must be monitored, and risk factors should be determined, because they are useful for screening hospitalized patients for VRE colonization in order to establish prevention and control measures.


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Infant, Newborn , Male , Middle Aged , Anti-Bacterial Agents/therapeutic use , Cross Infection/microbiology , Enterococcus/drug effects , Feces/microbiology , Vancomycin Resistance , Anti-Bacterial Agents/pharmacology , Cross Infection/prevention & control , Enterococcus/isolation & purification , Greece , Hospitals, University , Microbial Sensitivity Tests , Prevalence , Risk Factors
3.
Article in English | IMSEAR | ID: sea-65535

ABSTRACT

AIM: To evaluate the efficacy and safety of three hypolipidemic agents in patients with non-alcoholic fatty liver disease associated with hyperlipidemia. METHODS: Patients with dyslipidemia (Fredrickson type IIb), asymptomatic persistent transaminasemia lasting 24 weeks, and evidence of hepatic fat infiltration on ultrasonography and liver biopsy were studied. Those with predominant hypertriglyceridemia received omega-3 fatty acids (5 mL thrice daily) (Group A), those with predominant hypercholesterolemia received atorvastatin 20 mg/daily (Group B), and overweight patients received orlistat 120 mg thrice daily before meals (Group C). After 24 weeks of treatment, serum transaminase and lipid levels and liver ultrasonography were repeated. RESULTS: Serum transaminase levels decreased significantly (p< 0.001) in all groups but the decrease was more marked in Group C (AST 75 [16] to 31 [7] IU/L; ALT 120 [38] to 41 [10] IU/L) than in Group A (AST 70 [14] to 41 [6]; ALT 110 [20] to 68 [12]) or Group B (AST 68 [13] to 46 [9]; ALT 115 [22] to 76.6 [13]). After treatment, ultrasonography showed resolution of fatty liver in 35% of patients in Group A, 61% in Group B, and in 86% in Group C (p< 0.001, Group C vs. A). CONCLUSIONS: A decline in transaminase levels and normalization of ultrasonographic evidence of fatty liver were observed on treatment with omega-3 fatty acids in patients with hypertriglyceridemia, with atorvastatin in those with hypercholesterolemia, and orlistat in overweight patients with hyperlipidemia.


Subject(s)
Adult , Aged , Chi-Square Distribution , Dose-Response Relationship, Drug , Drug Administration Schedule , Fatty Acids, Omega-3/administration & dosage , Fatty Liver/complications , Female , Follow-Up Studies , Heptanoic Acids/administration & dosage , Humans , Hyperlipidemias/complications , Lactones/administration & dosage , Male , Middle Aged , Prospective Studies , Pyrroles/administration & dosage , Risk Assessment , Severity of Illness Index , Treatment Outcome
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