ABSTRACT
OBJECTIVE: Gastrostomy tube is the best option for long-term enteral nutrition. Among its limitations, infections represent the most frequent minor complication. Our aim is the knowledge of the number and type of gastrostomy tubes and its main indication in our hospital. In addition, prevalence of infectious complications was studied paying attention to the main etiologic agents and their antibiotic susceptibility. METHODS: Observational retrospective study from January 2010 to July 2015 through the electronic clinical history and the clinical microbiology laboratory software. Identification and antibiotic susceptibility of clinically significant isolates from patients with suspicion of gastrostomy tube infection have been analysed. RESULTS: Percutaneous endoscopic gastrostomy was performed in 203 patients (70.5%) and surgical gastrostomy in 85 (29.5%). The main reason identified for starting enteral nutrition through gastrostomy tube was malignant neoplasy, above all, lip, oral cavity and pharynx cancer (11.8%) and that from digestive organs (8.7%). Global prevalence of gastrostomy tube infection was 16.6%. The most common bacterial pathogens isolated were Staphylococcus aureus (21.3%), Pseudomonas aeruginosa (13.1%), and Escherichia coli (9.8%). The percentage of multi resistant isolates was 3.1%. CONCLUSIONS: Gastrostomy tube indications and type, and also, prevalence and microorganisms isolated from culture in infectious complications are similar to those described previously in the literature. The study allows the adaptation of the antibiotic prophylaxis and empirical antibiotic treatment thanks to the knowledge of the etiologic agents and their antibiotic susceptibility.
Subject(s)
Catheter-Related Infections/epidemiology , Gastrostomy/adverse effects , Gastrostomy/instrumentation , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents , Catheter-Related Infections/microbiology , Drug Resistance, Microbial , Drug Resistance, Multiple, Bacterial , Enteral Nutrition , Female , Gastrointestinal Neoplasms/complications , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Prevalence , Retrospective Studies , Surgical Wound Infection/prevention & control , Tertiary Care CentersABSTRACT
No disponible
Subject(s)
Humans , Female , Child, Preschool , Pseudomonas/pathogenicity , Pseudomonas Infections/complications , Meningitis, Bacterial/diagnosis , Multiple Trauma/complications , Subdural Effusion/complicationsABSTRACT
The activity of seven macrolides, clindamycin and telithromycin against clinical isolates of Corynebacterium spp. was studied. Of these, 36 isolates were identified as C. jeikeium and 57 as C. amycolatum. The frequency of resistance to erythromycin and other macrolides as well as clindamycin was high, with CMI(90) >256 microg/ml. Telithromycin showed the best activity, with 52.3% of C. amycolatum and 70% of C. jeikeium erythromycin-resistant strains susceptible to this ketolide. All strains had the MLSb constitutive phenotype. The ermX gene was present in all erythromycin-resistant strains, and in C. amycolatum was 100% homologous with that of C. striatum and C. diphtheriae.
Subject(s)
Anti-Bacterial Agents/pharmacology , Bacterial Proteins/genetics , Corynebacterium/drug effects , Corynebacterium/genetics , Drug Resistance, Bacterial/genetics , Ketolides/pharmacology , Macrolides/pharmacology , Humans , Microbial Sensitivity TestsABSTRACT
Se ha estudiado la actividad de siete macrólidos, clindamicina y telitromicina frente a aislamientos clínicos del género Corynebacterium. Deéstos, 36 pertenecían a la especie C. jeikeium y 57 a C. amycolatum. Todos los macrólidos estudiados y la clindamicina presentaron escasaactividad, con CMI90 >256 mg/l. La telitromicina presentó mejor actividad, siendo sensibles un 52,3% de C. amycolatum y un 70% de C.jeikeium resistentes a la eritromicina. El fenotipo de resistencia fue de tipo MLSb constitutivo en todos los aislamientos. El gen ermX fue detectadoen el 100% de las cepas resistentes a eritromicina, presentando una homología, en el caso de C. amycolatum, de un 100% con elde C. striatum y C. diptheriae
The activity of seven macrolides, clindamycin and telithromycin against clinical isolates of Corynebacterium spp. was studied. Of these, 36isolates were identified as C. jeikeium and 57 as C. amycolatum. The frequency of resistance to erythromycin and other macrolides as wellas clindamycin was high, with CMI90 >256 ìg/ml. Telithromycin showed the best activity, with 52.3% of C. amycolatum and 70% of C. jeikeiumerythromycin-resistant strains susceptible to this ketolide. All strains had the MLSb constitutive phenotype. The ermX gene was presentin all erythromycin-resistant strains, and in C. amycolatum was 100% homologous with that of C. striatum and C. diphtheriae
Subject(s)
Humans , Macrolides/pharmacokinetics , Corynebacterium , Drug Resistance, Bacterial , Anti-Bacterial Agents/pharmacokinetics , Corynebacterium/pathogenicity , Clindamycin/pharmacokinetics , Erythromycin/pharmacokinetics , Genes, MDR , Microbial Sensitivity Tests/methodsABSTRACT
The in vitro activity of ciprofloxacin, erythromycin, telithromycin, teicoplanin, linezolid and quinupristin-dalfopristin was tested against human derived pathogenic corynebacteria. The MICs of these antibiotics were measured using the agar dilution method against 31 strains of Corynebacterium jeikeium, 58 Corynebacterium amycolatum (including 33 multidrug-resistant strains) and 64 Corynebacterium urealyticum clinical strains. A high resistance rate to ciprofloxacin and erythromycin was found in the three species. Telithromycin was much more active than erythromycin (MIC(90) of erythromycin >or=128 mg/l for all three species; MIC(90) of telithromycin: 4 mg/l for C. jeikeium, 64 mg/l for C. amycolatum and 1 mg/l for C. urealyticum). There were no teicoplanin-resistant (MIC(90) 1, 0.5 and 1 mg/l, respectively) or linezolid-resistant strains (MIC(90) 1, 0.2 and 0.5 mg/l, respectively). Quinupristin-dalfopristin was active against most strains with an activity similar to linezolid, but three C. jeikeium and one C. amycolatum showed MICs >or=4 mg/l. Telithromycin showed much better activity against corynebacteria than older macrolides. Synercid and linezolid were active against most isolates tested, including multidrug resistant strains.
Subject(s)
Anti-Bacterial Agents/pharmacology , Corynebacterium/drug effects , Ketolides , Macrolides/pharmacology , Acetamides/pharmacology , Corynebacterium/classification , Drug Resistance, Bacterial , In Vitro Techniques , Linezolid , Microbial Sensitivity Tests , Oxazolidinones/pharmacologyABSTRACT
The in vitro activity of levofloxacin, moxifloxacin, gatifloxacin, erythromycin, telithromycin, linezolid, synercid and vancomycin was measured against 36 genetically defined, gyrA/grlA double mutant MRSA clinical strains with an MIC to ciprofloxacin > or = 8 mg/l. The three newer fluoroquinolones tested were more active than ciprofloxacin. Resistance rates for levofloxacin and gatifloxacin were high (44.5 and 36.1%, respectively). All the strains were moxifloxacin-susceptible, though most of them had MICs close to the break point. All the strains were intermediate or resistant to erythromycin and most were also resistant to telithromycin. No strains were resistant to linezolid, synercid or vancomycin (MIC(90): 2, 1 and 2 mg/l, respectively).
Subject(s)
Anti-Bacterial Agents/pharmacology , Ketolides , Macrolides , Methicillin Resistance , Staphylococcus aureus/drug effects , Acetamides/pharmacology , Drug Resistance, Bacterial , Drug Resistance, Multiple , In Vitro Techniques , Linezolid , Microbial Sensitivity Tests , Oxazolidinones/pharmacology , Staphylococcus aureus/genetics , Staphylococcus aureus/isolation & purification , Vancomycin/pharmacology , Virginiamycin/pharmacologyABSTRACT
The activity of six quinolones (ciprofloxacin, levofloxacin, trovafloxacin, moxifloxacin, clinafloxacin and grepafloxacin) against 86 clinical isolates of Corynebacterium spp. obtained from different clinical sources was studied. Of these, 30 isolates were identified as C. jeikeium, 30 as C. urealyticum and 26 as C. amycolatum. C. amycolatum was the most resistant species, with 85.5% of the strains analyzed resistant to all the quinolones studied. Clinafloxacin showed the best activity against these species with a concentration range between <0.01 and 8 mg/l, and MIC50 and MIC90 64 and 32 times lower, respectively, than the MICs of ciprofloxacin. The majority of the isolates (90%) of C. jeikeium and C. urealyticum were susceptible to all the quinolones studied. Only 9.9% of the C. jeikeium strains and 13.2% of the C. urealyticum strains were resistant to ciprofloxacin, which showed the lowest activity of the antimicrobial agents evaluated. Clinafloxacin, grepafloxacin and moxifloxacin were the most active quinolones against these two multiresistant species.
Subject(s)
Anti-Infective Agents/pharmacology , Corynebacterium/drug effects , Anti-Infective Agents/therapeutic use , Corynebacterium Infections/microbiology , Drug Resistance, Microbial , Fluoroquinolones , Humans , Microbial Sensitivity TestsABSTRACT
The aim of this study was to determine the in vitro activity of five quinolones against clinical strains of methicillin-susceptible and -resistant Staphylococcus aureus clinical isolates characterized at the molecular level with respect to the presence of mutations in genes coding for resistance to quinolones (grlA, gyrA and gyrB). The relationship between the mutations found and the activities of these quinolones was also analyzed. Trovafloxacin was the most active against methicillin-susceptible S. aureus and showed good activity against methicillin-resistant S. aureus, with a MIC90 of 2 mg/l. The grlA-gyrA double mutation was the most frequent (55% of the strains). Single mutation in grlA was detected only in 5% of strains; 39% of strains showed a wild-type genotype. The grlA-gyrA double mutants presented a high level of resistance against the fluoroquinolones tested except for trovafloxacin, with the MIC ranging between 0.5 and 4 mg/l. Wild-type strains were susceptible to all the fluoroquinolones tested and the single grlA mutants had a low level of quinolone resistance but were still below the breakpoint for resistance. Trovafloxacin and sparfloxacin were less affected by this mutation.
Subject(s)
Anti-Infective Agents/pharmacology , DNA Topoisomerases, Type II/drug effects , DNA Topoisomerases, Type II/genetics , Staphylococcus aureus/drug effects , Staphylococcus aureus/genetics , DNA Gyrase , DNA Topoisomerase IV , DNA, Bacterial/drug effects , DNA, Bacterial/genetics , Fluoroquinolones , Microbial Sensitivity Tests , Mutation , Polymorphism, Single-Stranded Conformational , Reverse Transcriptase Polymerase Chain ReactionABSTRACT
Se ha estudiado la actividad de seis quinolonas (ciprofloxacino, levofloxacino, trovafloxacino, moxifloxacino, clinafloxacino y grepafloxacino) frente a 86 aislamientos clínicos de Corynebacterium spp. procedentes de diferentes muestras clínicas. De éstos, 30 pertenecían a la especie C. jeikeium, 30 a C. urealyticum y 26 a C. amycolatum. La especie más resistente fue C. amycolatum, de la cual el 85,5 por ciento de las cepas estudiadas fueron resistentes a todas las quinolonas probadas, siendo clinafloxacino la que presentó una mejor actividad, con un rango de concentración entre <0,01 y 8 mg/l y CMI50 y CMI90 64 y 32 veces inferiores a las de ciprofloxacino, respectivamente. Más del 90 por ciento de las cepas de C. jeikeium y C. urealyticum fueron sensibles a todas las quinolonas, siendo ciprofloxacino la de peor actividad, con un porcentaje de cepas resistentes del 9,9 por ciento en el caso de C. jeikeium y un 13,2 por ciento para C. urealyticum. Clinafloxacino, grepafloxacino y moxifloxacino fueron las nuevas quinolonas más activas frente a estas dos especies de corinebacterias multirresistentes (AU)
Subject(s)
Humans , Fluoroquinolones , Anti-Infective Agents , Corynebacterium Infections , Corynebacterium , Drug Resistance, Microbial , Microbial Sensitivity TestsABSTRACT
Se ha estudiado la actividad in vitro de cinco fluoroquinolonas frente a cepas clínicas de Staphylococcus aureus, sensibles y resistentes a la meticilina, caracterizadas desde el punto de vista genético respecto a la existencia de mutaciones en los genes causantes de la resistencia a las quinolonas (grlA, gyrA y gyrB). También se comprobó el efecto de estas mutaciones en la actividad de las quinolonas. El trovafloxacino apareció como el más activo de los antimicrobianos estudiados frente a S. aureus sensibles a la meticilina (SASM), presentando también una buena actividad frente a los resistentes a ésta (SARM), con una CMI90 de 2 mg/l. El patrón más frecuente fue la doble mutación gyrA y grlA (55 por ciento de las cepas), siendo mucho menos frecuente la mutación únicamente en grlA (5 por ciento). El 39 por ciento de las cepas presentaron un genotipo silvestre. Las cepas con doble mutación presentaron altos grados de resistencia a todas las fluoroquinolonas probadas excepto a trovafloxacino, con un rango de CMI de 0,5-4 mg/l. Las cepas silvestres fueron sensibles a todas las quinolonas ensayadas; en las cinco cepas con mutación en grlA se observó un ligero aumento de las CMI para todos los antimicrobianos, aunque siempre por debajo del punto de corte que determina resistencia. Las quinolonas menos afectadas por esta mutación fueron trovafloxacino y esparfloxacino (AU)
Subject(s)
Staphylococcus aureus , Polymorphism, Single-Stranded Conformational , Mutation , Fluoroquinolones , DNA Gyrase , Reverse Transcriptase Polymerase Chain Reaction , DNA Topoisomerase IV , Anti-Infective Agents , DNA, Bacterial , Microbial Sensitivity TestsABSTRACT
The in vitro activities of 13 fluoroquinolones (FQs) were tested against 90 Staphylococcus aureus clinical isolates: 30 wild type for gyrA, gyrB, grlA and norA and 60 with mutations in these genes. Clinafloxacin (CI-960), sparfloxacin, and grepafloxacin were the most active FQs against wild-type isolates (MICs at which 90% of isolates were inhibited, 0.06 to 0.1 microgram/ml). Mutations in grlA did not affect the MICs of newer FQs. grlA-gyrA double mutations led to higher MICs for all the FQs tested. Efflux mechanisms affected the newer FQs to a much lesser extent than the less recently developed FQs.
