29 results on '"TAZOBACTAM"'
Search Results
2. Cost-effectiveness of ceftolozane/tazobactam for the treatment of complicated intraabdominal and urinary tract infections in Colombia
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Fabián Hernández
- Subjects
ceftolozane ,tazobactam ,cost-effectiveness ,urinary tract infections ,intraabdominal infections ,Therapeutics. Pharmacology ,RM1-950 ,Infectious and parasitic diseases ,RC109-216 - Abstract
Objective: To evaluate the cost-effectiveness of ceftolozane/tazobactam + metronidazole (C/T+M) and ceftolozane/tazobactam (C/T) compared with 8 alternatives used in the treatment of complicated intraabdominal infection (cIAI) and complicated urinary tract infection (cUTI) respectively. Methods: A Monte Carlo simulation decision model was used for the estimation and comparison of treatment-related costs, and quality adjusted life years for patients with cIAI treated with C/T+M in comparison with cefepime + metronidazole, ciprofloxacin + metronidazole, doripenem, levofloxacin + metronidazole, meropenem, piperacillin/tazobactam, ceftazidime + metronidazole or imipenem/cilastatin and patients with cUTI treated with C/T in comparison with cefepime, ciprofloxacin, doripenem, levofloxacin, meropenem, piperacillin/tazobactam, ceftazidime or imipenem/cilastatin. Local costs were estimated using base cases identified by experts and consulting local databases. Sensitivity values of the PACTS (Program to Assess Ceftolozane/Tazobactam Susceptibility) study in Latin America were used in the model. Results: C/T+M and C/T obtained incremental cost-effectiveness ratios (ICER) that were below the Colombian cost-effectiveness threshold (3 GDP per capita) in most comparisons, and were dominated by meropenem, considering only gram-negative microorganisms. Sensitivity assessments were also carried out, in which only the population with P. aeruginosa infections was considered, showing positive results for C/T+M and C/T (cost-effective or dominant with regards to all comparators). Conclusions: C/T+M and C/T could be cost-effective alternatives in the treatment of CIAI and CUTI in Colombia, when there is an adequate and rational use of antibiotics. The results of the sensitivity analyses showed dominance and cost-effectiveness with regards to every comparator in patients infected with P. aeruginosa
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- 2020
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- View/download PDF
3. Esclerosis múltiple: por primera vez la OMS incluye fármacos en la lista de medicamentos esenciales
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- 2023
4. La OMS publica listas modelo de medicamentos esenciales
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- 2023
5. Huánuco: deficient storage of medicines at Hermilio Valdizan Hospital reported
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- 2023
6. Las superbacterias avanzan entre las trincheras de la guerra de Ucrania
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- 2023
7. Update of antimicrobial resistance in level III and IV health institutions in Colombia between January 2018 and December 2021
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De La Cadena E, Pallares CJ, García-Betancur JC, Porras JA, and Villegas MV
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- Colombia epidemiology, Piperacillin, Tazobactam, Hospitals, Pandemics
- Abstract
Introduction: Antimicrobial resistance surveillance is a fundamental tool for the development, improvement, and adjustment of antimicrobial stewardship programs, therapeutic guidelines, and universal precautions to limit the cross-transmission of resistant bacteria between patients. Since the beginning of 2020, the SARS-CoV-2 pandemic profoundly challenged the health system and, according to some reports, increased the rates of antimicrobial resistance., Objective: To describe the behavior of antimicrobial resistance of the most frequent bacterial pathogens in twenty Colombian hospitals from January 2018 to December 2021., Materials and Methods: We conducted a descriptive study based on the microbiological information recorded from January 2018 to December 2021 in twenty levels III and IV health institutions in twelve Colombian cities. We identified the species of the ten most frequent bacteria along with their resistance profile to the antibiotic markers after analyzing the data through WHONET., Results: We found no statistically significant changes in most pathogens’ resistance profiles from January 2018 to December 2021. Only Pseudomonas aeruginosa had a statistically significant increase in its resistance profile, particularly to piperacillin/tazobactam and carbapenems., Conclusions: The changes in antimicrobial resistance in these four years were not statistically significant except for P. aeruginosa to piperacillin/tazobactam and carbapenems.
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- 2023
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8. El insólito caso clínico del hombre que eyaculó semen por el ano durante 2 años
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- 2022
9. Comparación del esquema antibiótico entre la Piperacilina-Tazobactam y Amikacina vs Metronidazol y Gentamicina en el tratamiento de la apendicitis complicada en niños
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José Rodrigo Sandoval and Héctor Santos Luna
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apendicectomía ,metronidazol ,gentamicina ,piperacilina ,tazobactam ,amikacina ,Medicine (General) ,R5-920 - Abstract
Introducción. Los pacientes que tuvieron complicaciones infecciosas post cirugía de apendicitis siguen usualmente un esquema de tratamiento establecido de antibióticos en el Hospital San Juan de Dios (HSJD). Se realizó un análisis retrospectivo de 60 pacientes pediátricos con apendicitis complicada a quienes se les efectuó una apendicectomía abierta y se utilizó el esquema antibiótico de metronidazol y gentamicina. Objetivo. Evaluar la eficacia del esquema de antibióticos usados. Metodología. El estudio se efectuó en la Unidad de Cirugía Pediátrica del HGSJD en el período de tiempo de enero a diciembre de 2013. Se evaluaron las complicaciones infecciosas en los pacientes que requirieron la omisión de los antibióticos mencionados y el inicio de la combinación de piperacilina tazobactam – amikacina. Resultados. Hubo 56 (93%) pacientes en quienes el esquema inicial de metronidazol – gentamicina fue el único empleado sin que presentaran complicación infecciosa alguna, mientras que 4 (7%) pacientes presentaron colecciones abdominales que requirieron el cambio a piperacilina tazobactam-amikacina con lo que resolvieron la sepsis abdominal. Conclusiones. La utilización de la combinación antibiótica de metronidazol-gentamicina continúa siendo eficiente en la población pediátrica con apendicitis aguda complicada que consulta a nuestro hospital dejando el empleo de la piperacilina tazobactam y amikacina como una alternativa terapéutica útil.
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- 2016
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10. Eficacia y seguridad del tratamiento empírico con piperacilina/tazobactan como monoterapia en episodios de neutropenia y fiebre en niños con cáncer: revisión sistemática y meta-análisis
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María Teresa Rosanova, Roberto Lede, and Leticia Cuellar-Pompa
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Gynecology ,medicine.medical_specialty ,business.industry ,Public Health, Environmental and Occupational Health ,medicine.disease ,neutropenia febril ,Tazobactam ,riesgo de fracaso terapéutico ,Infectious Diseases ,medicine ,polycyclic compounds ,piperacilina ,business ,tazobactan ,Febrile neutropenia ,Piperacillin ,medicine.drug - Abstract
Resumen Introducción: La neutropenia febril en niños con patología oncohematològica requiere un tratamiento empírico precoz y adecuado. Esta revisión sistemática se realizó para evaluar si piperacilina/tazobactam (PTZ) monoterapia es más efectiva y segura que los comparadores, en niños con episodios de neutropenia febril de causa oncológica. Material y Métodos: Se realizó una búsqueda bibliográfica en Embase, MEDLINE utilizando los términos de búsqueda ((‘febrile neutropenia’ OR hemato oncology OR haemato oncology OR ‘immunocompromised host’ OR ‘immunocompromised patient’ OR ‘chemotherapy-induced febrile neutropenia’) AND (piperacillin OR tazobactam OR ‘piperacillin plus tazobactam’ OR ‘piperacillin/tazobactam’ OR ‘piperacillin-tazobactam’ OR tazocin OR ‘piperacillin-tazobactam drug combination’)). El criterio de valoración de eficacia fue la incidencia de fracaso terapéutico. El punto final de seguridad fue la ausencia de cualquier efecto adverso (EA). Resultados: Se identificaron 1.388 estudios, de los cuales se incluyeron 11 que cumplían los criterios de elegibilidad. Los estudios presentaron notable homogeneidad ( I 2 0%) y no se detectó sesgo de publicación (p 0,36). El riesgo de fracaso terapéutico de PTZ no fue mayor que en los comparadores (RR global: 0,94; IC95% 0,83 a 1,07) como tampoco lo fue, la incidencia de EA. Conclusiones: El riesgo de fracaso terapéutico no fue superior para la PTZ como monoterapia frente a los comparadores
- Published
- 2021
11. Resistencia antimicrobiana de uropatógenos en adultos mayores de una clínica privada de Lima, Perú
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Joseph A. Pinto, Fabrizio Ramirez, Jacqueline Miranda, Margot Faustino, and Billy Joel Sanchez-Jacinto
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perú ,Klebsiella pneumoniae ,geriatría ,lcsh:Medicine ,Drug resistance ,medicine.disease_cause ,Tazobactam ,Enterococcus faecalis ,Microbiology ,Farmacorresistencia Bacteriana ,Infecciones bacterianas ,Geriatría ,Perú ,farmacorresistencia bacteriana ,polycyclic compounds ,medicine ,Escherichia coli ,lcsh:R5-920 ,biology ,lcsh:R ,Public Health, Environmental and Occupational Health ,General Medicine ,biochemical phenomena, metabolism, and nutrition ,biology.organism_classification ,Proteus mirabilis ,Amikacin ,infecciones bacterianas ,bacteria ,lcsh:Medicine (General) ,medicine.drug ,Piperacillin - Abstract
Se describen los principales mecanismos de resistencia antimicrobiana mediante el sistema Vitek® 2 en uropatógenos aislados en adultos mayores de una clínica privada en Lima. Estudio descriptivo realizado entre enero de 2014 y octubre de 2016. Escherichia coli, Klebsiella pneumoniae y Proteus mirabilis obtuvieron una sensibilidad mayor a 80% frente a piperacilina/tazobactam, amikacina y carbapenems. Asimismo, 83,6% de Escherichia coli fueron cepas sensibles a nitrofurantoina. El 41,7% de Escherichia coli, 50,9% de Klebsiella pneumoniae y 50% de Proteus mirabilis fueron productoras de betalactamasas de espectro extendido. De igual modo, 60% de Pseudomonas aeruginosa fueron productoras de carbapenemasas. La modificación de sitio activo (PBP) y la inactivación enzimática por penicilinasas se presentaron en el 7,8% de Enterococcus faecalis. La resistencia a aminoglicósidos se presentó en Escherichia coli (27,1%), Klebsiella pneumoniae (46,7%) y Proteus mirabilis (84,6%) por la producción de enzimas modificadoras. Existe un incremento de la resistencia bacteriana en relación a la edad. La inactivación enzimática de betalactámicos y aminoglicósidos es el mecanismo de resistencia más frecuente.
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- 2019
12. Evaluación de la sensibilidad de cepas de Pseudomonas aeruginosa multi-resistentes frente a ceftolozano/tazobactam
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Manuel Antonio Rodríguez-Iglesias, Sofía García-Martín, Carolina Freyre-Carrillo, César Del Prado-Montoro, J. Ruiz-Aragón, and Carmen Martínez Rubio
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Pseudomonas aeruginosa ,business.industry ,Public Health, Environmental and Occupational Health ,infecciones ,multi-resistencia ,medicine.disease_cause ,Tazobactam ,Molecular biology ,ceftolozano/tazobactam ,Infectious Diseases ,Reference values ,medicine ,Sensibilidad ,business ,medicine.drug - Abstract
Introduccion: Pseudomonas aeruginosa es un patogeno oportunista asociado a alta morbi-mortalidad. Para cepas multirresistentes (MDR), Ceftolozano/Tazobactam (CTZ) se ha autorizado por la Agencia Europea del Medicamento (EMA) para infecciones del tracto urinario complicadas, pielonefritis aguda e infecciones intraabdominales complicadas. El objetivo del estudio ha sido determinar la sensibilidad a CTZ de P. aeruginosa MDR en muestras clinicas aisladas en el Hospital Universitario Puerto Real. Material y Metodos: Se estudio la sensibilidad segun criterios EUCAST a CTZ de cepas de P. aeruginosa MDR, entre enero de 2015 y agosto de 2017. Los criterios de multirresistencia fueron definidos por el Centers for Disease Control and Prevention. La sensibilidad antibiotica se obtuvo mediante sistema MicroScan ® (Beckman Coulter). La sensibilidad a CTZ se determino mediante tiras de gradiente (Liofilchem®, Werfen). Resultados: De 1253 cepas, el 7% fueron MDR. Se estudio la sensibilidad de 78 cepas de P. aeruginosa MDR, de las cuales 5 (6,4%) resultaron resistentes a CTZ segun criterios EUCAST. Conclusiones: En nuestro medio la resistencia in-vitro a CTZ en cepas de P. aeruginosa MDR es aproximadamente un 6%. CTZ es una opcion de tratamiento de infecciones por cepas de P. aeruginosa MDR cuando no exista otra alternativa y se haya comprobado su sensibilidad in-vitro .
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- 2019
13. Evaluación de la sensibilidad de cepas de Pseudomonas aeruginosa multi-resistentes frente a ceftolozano/tazobactam
- Author
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Prado-Montoro, César Del, Ruiz-Aragón, Jesús, Martínez Rubio, Carmen, García-Martín, Sofía, Freyre-Carrillo, Carolina, and Rodríguez-Iglesias, Manuel Antonio
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Tazobactam ,ceftolozane/tazobactam ,Reproducibility of Results ,infecciones ,Microbial Sensitivity Tests ,multi-resistencia ,Real-Time Polymerase Chain Reaction ,multidrug-resistance ,Mass Spectrometry ,ceftolozano/tazobactam ,Anti-Bacterial Agents ,Cephalosporins ,Reference Values ,Susceptibility ,Drug Resistance, Multiple, Bacterial ,Pseudomonas aeruginosa ,Sensibilidad ,infections - Abstract
Resumen Introducción: Pseudomonas aeruginosa es un patógeno oportunista asociado a alta morbi-mortalidad. Para cepas multi-resistentes (MDR), ceftolozano/tazobactam (CTZ) se ha autorizado por la Agencia Europea del Medicamento (EMA) para infecciones del tracto urinario complicadas, pielonefritis aguda e infecciones intra-abdominales complicadas. Objetivo: Determinar la sensibilidad a CTZ de P. aeruginosa MDR en muestras clínicas aisladas en el Hospital Universitario Puerto Real. Material y Métodos: Se estudió la sensibilidad según criterios EUCAST a CTZ de cepas de P. aeruginosa MDR, entre enero de 2015 y agosto de 2017. Los criterios de multi-resistencia fueron definidos por el Centers for Disease Control and Prevention. La sensibilidad antimicrobiana se obtuvo mediante sistema MicroScan® (Beckman Coulter). La sensibilidad a CTZ se determinó mediante tiras de gradiente (Liofilchem®, Werfen). Resultados: De 1253 cepas, 7% fueron MDR. Se estudió la sensibilidad de 78 cepas de P. aeruginosa MDR, de las cuales cinco (6,4%) resultaron resistentes a CTZ según criterios EUCAST. Conclusiones: En nuestro medio la resistencia in vitro a CTZ en cepas de P. aeruginosa MDR es aproximadamente 6%; CTZ es una opción de tratamiento de infecciones por cepas de P. aeruginosa MDR cuando no exista otra alternativa y se haya comprobado su sensibilidad in vitro. Background: Pseudomonas aeruginosa is an opportunistic pathogen associated with high morbidity and mortality. For multidrug-resistant strains (MDR), ceftolozane/tazobactam (CTZ) has been authorized by the European Medicines Agency (EMA) for complicated urinary tract infections, acute pyelonephritis, and complicated intraabdominal infections. Aim: To determine the susceptibility to CTZ of P. aeruginosa MDR in isolated clinical samples at the University Hospital Puerto Real. Methods: The susceptibility according to the EUCAST to CTZ criteria of strains of P. aeruginosa MDR, between January 2015 and August 2017 has been studied. The multiresistance criteria were those defined by the Centers for Disease Control and Prevention. The antibiotic susceptibility was obtained by automated MicroScan® system (Beckman Coulter). Susceptibility to CTZ was determined using gradient strips (Liofilchem®, Werfen). Results: Of 1253 strains isolated, 7% presented MDR. We studied the susceptibility of a total of 78 strains of MDR P. aeruginosa, of which 5 (6.4%) were resistant to CTZ according to the EUCAST criteria. Conclusions: In our environment, the in vitro resistance to CTZ in MDR P. aeruginosa strains is approximately 6%. CTZ is an option for the treatment of infections by MDR P. aeruginosa when there is no other alternative and its in-vitro susceptibility has been proven.
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- 2019
14. Evaluación de susceptibilidad y respuesta al tratamiento con piperacilina/tazobactam en pacientes con infecciones por Escherichia coli productoras de β-lactamasas de espectro extendido (BLEE) CTX-M
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Álvaro Rojas, Paulina Meza, Camila Carvajal, Piero Guggiana, Patricia García, Javier Revello, Jaime Labarca, and Jorge Alvarez
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medicine.medical_specialty ,medicine.disease_cause ,Tazobactam ,Gastroenterology ,Minimum inhibitory concentration ,Internal medicine ,polycyclic compounds ,medicine ,In patient ,CTX-M ,Escherichia coli ,β-lactamasas de espectro extendido ,business.industry ,concentración inhibitoria mínima ,Public Health, Environmental and Occupational Health ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,University hospital ,medicine.disease ,piperacilina/tazobactam ,female genital diseases and pregnancy complications ,Infectious Diseases ,Bacteremia ,Piperacillin/tazobactam ,business ,medicine.drug ,Piperacillin - Abstract
Resumen Introducción: En las infecciones por enterobacterias productoras de β-lactamasas de espectro extendido (BLEE), los β-lactámicos preferidos para tratamiento son los carbapenémicos. Sin embargo, estudios clínicos muestran eficacia de piperacilina/tazobactam en ciertas infecciones por Escherichia coli productoras de BLEE. Objetivo: Determinar la cura clínica y microbiológica con piperacilina/tazobactam en pacientes con infecciones por E. coli productoras de BLEE, tipo CTX-M. Materiales/Métodos: Estudio descriptivo, retrospectivo, con adultos internados en un hospital universitario. Incluimos infecciones del tracto urinario (ITU), intra-abdominales (IIA) e infecciones de tejidos blandos (ITB). Resultados: Estudiamos 40 pacientes, donde 65% correspondían a ITU, 25% IIA y 10 % ITB. La cura clínica global se logró en 89,4%, con mejores resultados en las ITU (100%), seguidas de ITB (80%) e IIA (70%). El 85% de las cepas tenía concentraciones inhibitorias mínimas (CIM) ≤ 8 μg/mL y 70% con CIM ≤ 4 μg/mL. La tasa de fracaso fue mayor en las infecciones con inóculos altos intraabdominales. La BLEE del tipo CTX-M-15 se encontró en 62,5%. Conclusiones: Piperacilina/tazobactam logró cura clínica y microbiológica, en pacientes con infecciones por E. coli productoras de BLEE susceptibles, especialmente en ITU e IPB y en menor medida en IIA.
- Published
- 2018
15. Piperacillin/tazobactam plus amikacin vs. piperacilin/tazobactam: treatment for children with febrile neutropenia
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Pacheco-Rosas DO, Peregrino-Bejarano L, López-Aguilar JE, Juan-Shum L, and Miranda-Novales MG
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- Adolescent, Child, Child, Preschool, Female, Hematologic Neoplasms complications, Humans, Infant, Intention to Treat Analysis, Logistic Models, Male, Neoplasms complications, Amikacin therapeutic use, Anti-Bacterial Agents therapeutic use, Febrile Neutropenia drug therapy, Piperacillin, Tazobactam Drug Combination therapeutic use
- Abstract
Background: Pediatric patients with febrile neutropenia usually receive a combination of broad spectrum antimicrobials. Treatment without aminoglycoside seems to have advantages., Objective: To compare the efficacy of piperacillin/tazobactam plus amikacin versus piperacillin/tazobactam., Methods: Randomized, open label, controlled clinical trial. Sample size for an efficacy of 55%, and delta of 25%; 80 episodes were required for each group. Selection criteria were patients with febrile neutropenia, candidates to receive parenteral antimicrobial treatment; they were randomized to one of two groups, piperacillin/tazobactam plus amikacin (Group A), or piperacillin/tazobactam (Group B). The outcomes were failure, adverse events and death. Mantel-Haenszel chi squaretest and exact Fisher test were used. Reduction of relative and absolute risk (RRR and ARR), 95% confidence intervals (CI 95%) and number needed to treat (NNT) were calculated., Results: 88 Episodes were analyzed in group A and 76 in group B. There was no statistical difference in general characteristics of patients or type of infections. There was not significant statistical difference in: failure 31.8% group A, 30.2% group B (RR 1.05, CI 95% 0.66-1.66, p = 0.86), or adverse events (one in each group). The RRR was 1.5%, and ARR 2%, with a NNT of 67., Conclusion: Piperacillin/tazobactam without amikacin was as effective as combination therapy in pediatric patients with febrile neutropenia.
- Published
- 2019
16. Epidemiología molecular de infección nosocomial por Klebsiella pneumoniae productora de betalactamasas de espectro extendido
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Aura Lucía Leal, Paula Andrea Espinal, Celia Alpuche, Carlos Saavedra, Emilia María Valenzuela, and José Ramón Mantilla
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SHV-5 ,Imipenem ,medicine.medical_specialty ,lcsh:Arctic medicine. Tropical medicine ,lcsh:RC955-962 ,Klebsiella pneumoniae ,Medicina ,Cefepime ,lcsh:Medicine ,Tazobactam ,General Biochemistry, Genetics and Molecular Biology ,Microbiology ,Intensive care ,medicine ,biology ,lcsh:R ,bacterial resistance ,biochemical phenomena, metabolism, and nutrition ,bacterial infections and mycoses ,biology.organism_classification ,Trimethoprim ,Surgery ,ESBL ,genotyping ,Amikacin ,nosocomial infection ,medicine.drug ,Piperacillin - Abstract
La epidemiología molecular aplicada al estudio de las infecciones nosocomiales ha sido fundamental para la formulación y la evaluación de las medidas de control; con este fin, se caracterizaron microbiológica y molecularmente aislamientos de Klebsiella pneumoniae productores de beta-lactamasas de espectro extendido (BLEE) obtenidos de pacientes en un hospital de tercer nivel de Bogotá, D.C., Colombia. Se tipificaron quince aislamientos por electroforesis en gel de campo pulsado (PFGE) y por amplificación de secuencias de ADN repetidas (REP-PCR). La susceptibilidad antimicrobiana y la producción de BLEE se determinaron de acuerdo con las normas de NCCLS. Las beta-lactamasas se evaluaron por isoelectroenfoque y PCR. El 80% de estos aislamientos se asociaron con infección nosocomial y de éstos, el 91,7% provenía de unidades de cuidado intensivo. La susceptibilidad antibiótica mostró 13 patrones de resistencia; 87% de los aislamientos presentó corresistencia a amikacina, 53% a gentamicina, 33,3% a ciprofloxacina, 40% a cefepime, 66,7% a piperacilina/tazobactam, 60% trimetoprim/sulfametoxazol y 46,7% a cloranfenicol. Todos fueron sensibles a imipenem. En la mayoría de los aislamientos se detectó producción simultánea de beta-lactamasas del tipo TEM y SHV y el 93,3% produjo ceftazidimasa de pI 8.2 del tipo SHV-5. Los 15 aislamientos fueron agrupados por PFGE y REP-PCR en 11 y 12 patrones electroforéticos, respectivamente. Esta variabilidad genética está relacionada con infecciones nosocomiales de origen endógeno más que por infecciones cruzadas.
- Published
- 2004
17. Effect of ß-lactamases inhibitors on the evolution of resistance to ß-lactams in Gram-negatives bacilli
- Author
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Martín, N.G., Carmona, O., and Guzmán Blanco, M.
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sulbactam ,tazobactam ,ß-lactamasas ,bacilos Gram-negativos ,resistencia bacteriana ,ß-lactámicos ,inhibidores de ß-lactamasas - Abstract
Los ß-lactámicos, primeros antibióticos introducidos para uso en clínica, siguen siendo los más usados. También es frecuente el desarrollo de resistencia a ellos, la cual fue identificada inmediatamente después de la introducción de la penicilina. El mecanismo de resistencia más frecuente en bacilos Gram-negativos a los ß-lactámicos es la producción de ß-lactamasas, y su forma de transmisión es a través de plásmidos y cromosomas. Los bacilos Gram-negativos aeróbicos son los principales responsables de infección nosocomial. Hemos publicado los valores de resistencia de éstos ante ß-lactámicos, haciendo un diagnóstico de la situación a nivel nacional. Además de seguir su evolución durante la década 1988-1998, estudiamos los cambios producidos sobre la evolución de la resistencia, en presencia de inhibidores de ß-lactamasas. Desde 1988, el Grupo Venezolano de Vigilancia de la Resistencia Bacteriana, cuyos miembros pertenecen a 29 instituciones de salud de siete estados, está a cargo de analizar y publicar resultados de resistencia bacteriana a antimicrobianos de bacterias aisladas de pacientes con infecciones hospitalarias y de la comunidad. Se usó el método de difusión de disco, de acuerdo a las normas de la NCCLS. Se siguió el programa software WHONET (World Health Organization Net). Las diferencias de sensibilidad entre el ß-lactámico y el ß-lactámico más el inhibidor de ß-lactamasas son: 1. Piperacilina versus piperacilina/tazobactam: entre el 10 y el 30% para la mayoría de los gérmenes estudiados, excepto para E. coli (45%) y Serratia sp. (60%). 2. Ampicilina versus ampicilina/sulbactam: entre el 10 y el 30%. 3. Cefoperazona versus cefoperazona/sulbactam: entre el 5 y el 25%. Como era de esperar, la resistencia de bacilos Gram-negativos aeróbicos a betalactámicos en presencia del inhibidor de ß-lactamasas es menor que ante el ß-lactámico solo; además, esta diferencia se hace mayor con el tiempo. Las diferencias entre las dos series durante el primer año (1988) son menores que las encontradas entre las series durante el último año (1998) en muchas de las bacterias estudias. Estos resultados son relevantes especialmente si recordamos el mecanismo de inductores de betalactamasas que se les ha atribuido. The ß-lactams antimicrobial were the first to be used, and today they still are the most frequently used. Among the bacteria responsible of high resistance to ß-lactams are gramnegative rods; the most frequent mechanism is the production of ß-lactamase We follow the trends of resistance of Gram-negative rods to ß-lactams alone and with ß-lactamase-inhibitors during the decade 1988-1998. Since 1988, The Venezuelan Group of Vigilance of the Bacterial Resistance, with 29 health institution in the country; they identify, analyze and publish data on bacteria resistance of isolates from patients with bacterial infection coming from hospitals and the community. It was used diffusion disk, according NCCLS. The software program WHONET (World Health Organization Net) was used. The difference in sensitivity among ß-lactam and ß-lactam/ß-lactamase-inhibitor are: 1. Piperacillin versus piperacillin/tazobactam: between 10 and 30% of resistance for most isolated, except for E. coli (45%) and Serratia sp. (60%). 2. Ampicillin versus ampicillin/sulbactam: between 10 and 30%. 3. Cefoperazone versus Cefoperazone/sulbactam: between 5 and 25%. How is expected gramnegative rods resistance to ß-lactams with a betalactamase-inhibitor (ß-L-I), is lower than the ß-lactam alone; furthermore the difference between them, grows higher with time. This results are relevant, since ß-L-I are described as ß-lactamase inductors.
- Published
- 2002
18. [Inhibitory activity of dihydroxy-phenyl-propenone on betalactamase of Enterobacter cloacae : preliminary study for drug development to overcome bacterial resistance. ].
- Author
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Mora CL, Castaño J, and Jaramillo MC
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- Ampicillin pharmacology, Bacterial Proteins isolation & purification, Bacterial Proteins metabolism, Chalcones chemical synthesis, Chalcones chemistry, Chromatography, Affinity, Colony Count, Microbial, Colorimetry, Drug Evaluation, Preclinical, Drug Synergism, Enterobacter cloacae enzymology, Enterobacteriaceae Infections microbiology, Humans, Microbial Sensitivity Tests, Molecular Structure, Penicillanic Acid analogs & derivatives, Penicillanic Acid antagonists & inhibitors, Penicillinase isolation & purification, Tazobactam, beta-Lactamase Inhibitors chemical synthesis, beta-Lactamase Inhibitors chemistry, Bacterial Proteins antagonists & inhibitors, Chalcones pharmacology, Enterobacter cloacae drug effects, Penicillinase metabolism, beta-Lactam Resistance drug effects, beta-Lactamase Inhibitors pharmacology
- Abstract
Introduction: Enterobacter cloacae is a pathogenic microorganism with the ability to produce betalactamase enzymes, which makes them resistant to betalactamic antibiotics. Additionally, the limited activity of enzymatic inhibitors has been identified, and, therefore, the design of new drugs and the promotion of their rational use are the only possibilities to overcome this problem., Objective: The aim of this research was to evaluate the effect of dihydroxy-phenyl-propenone on a clinical isolate of E. cloacae , as well as its activity on a betalactamase isolated from this resistant microorganism in order to contribute to the search for new betalactamase inhibitors., Materials and Methods: Dihydroxy-phenyl-propenone chalcone was synthesized and evaluated on a clinical isolate of E. cloacae to determine the minimum inhibitory concentration by broth microdilution; once the betalactamase enzyme was purified by affinity chromatography, a spectrophotometric analysis was done to evaluate its kinetic activity., Results: The minimum inhibitory concentration value of dihydroxy-phenyl-propenone on E. cloacae was 35 µg/ml; the recovery percentage of the betalactamase from the microorganism was 31.75% and the kinetic parameters were V max =1.7 x 10 -3 µM/min and K M = 2330 µM, which show an important inhibitory activity., Conclusion: Dihydroxy-phenyl-propenone has shown inhibitory activity on betalactamase enzymes and the ability to protect the chemical integrity of betalactamic antibiotics; this synergistic effect turns it into a promising compound in the search for new alternatives to overcome bacterial resistance.
- Published
- 2014
- Full Text
- View/download PDF
19. [Fournier's gangrene caused by Streptococcus agalactiae in a non-pregnant woman].
- Author
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Batista N, Fernández MP, Gambra ML, and Rodríguez L
- Subjects
- Adult, Anti-Bacterial Agents administration & dosage, Anti-Bacterial Agents therapeutic use, Clindamycin administration & dosage, Clindamycin therapeutic use, Combined Modality Therapy, Debridement, Diabetes Mellitus, Type 1 complications, Disease Susceptibility, Drug Therapy, Combination, Female, Fournier Gangrene drug therapy, Fournier Gangrene surgery, Humans, Metronidazole administration & dosage, Metronidazole therapeutic use, Obesity complications, Penicillanic Acid administration & dosage, Penicillanic Acid analogs & derivatives, Penicillanic Acid therapeutic use, Perineum, Piperacillin administration & dosage, Piperacillin therapeutic use, Reoperation, Streptococcal Infections drug therapy, Streptococcal Infections surgery, Tazobactam, Fournier Gangrene microbiology, Streptococcal Infections microbiology, Streptococcus agalactiae isolation & purification
- Published
- 2009
- Full Text
- View/download PDF
20. [Hepatic abscess due to Klebsiella pneumoniae in an Asian immigrant].
- Author
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García-Morillo JS, de la Cruz-Vicente F, López-Ruiz T, and Bernabeu-Wittel M
- Subjects
- Adult, Anti-Bacterial Agents therapeutic use, Bacteremia complications, Bacteremia drug therapy, Bacteremia microbiology, Biliary Fistula etiology, China ethnology, Cholangiopancreatography, Endoscopic Retrograde, Cholangitis drug therapy, Combined Modality Therapy, Diagnosis, Differential, Drainage, Duodenal Diseases etiology, Hepatitis drug therapy, Hepatitis microbiology, Humans, Intestinal Fistula etiology, Jaundice, Obstructive diagnostic imaging, Jaundice, Obstructive etiology, Klebsiella Infections complications, Klebsiella Infections diagnostic imaging, Klebsiella Infections drug therapy, Liver Abscess complications, Liver Abscess diagnostic imaging, Liver Abscess drug therapy, Liver Abscess surgery, Male, Penicillanic Acid administration & dosage, Penicillanic Acid analogs & derivatives, Penicillanic Acid therapeutic use, Piperacillin administration & dosage, Piperacillin therapeutic use, Spain epidemiology, Sphincterotomy, Endoscopic, Tazobactam, Cholangitis etiology, Cholangitis microbiology, Emigration and Immigration, Hepatitis etiology, Klebsiella Infections microbiology, Klebsiella pneumoniae isolation & purification, Liver Abscess microbiology
- Published
- 2006
- Full Text
- View/download PDF
21. [New Beta-lactam agent in the treatment of intra-abdominal sepsis: double blind and randomized stage III study of ertapenem versus piperacillin/tazobactam].
- Author
-
Barboza E, Solomkin J, Goldstein EJ, del Castillo M, Alvarado R, Barboza A, and Teppler H
- Subjects
- Abdominal Abscess microbiology, Adult, Aged, Double-Blind Method, Ertapenem, Female, Humans, Male, Middle Aged, Prospective Studies, Sepsis drug therapy, Sepsis microbiology, Tazobactam, Treatment Outcome, Abdominal Abscess drug therapy, Anti-Bacterial Agents therapeutic use, Lactams, Penicillanic Acid analogs & derivatives, Penicillanic Acid therapeutic use, Piperacillin therapeutic use, beta-Lactams therapeutic use
- Abstract
The clinical and safety efficacy of a new wide spectrum beta-lactam agent for most pathogen intra-abdominal infection germs is evaluated herein. Its chemical name is Ertapenem (MK-0826). Its pharmacokinetic characteristics and the known antibacterial spectrum enable the potential use of one daily dose in the treatment of infections by aerobic and anaerobic bacteria. This is a sub-group of patients that have been treated within a multinational, prospective, randomized, controlled and double-blind study, to compare the safety and efficacy of ertapenem (100% vs 88%) with piperacillin/tazobactam in patients that have undergone surgery due to complicated intra-abdominal infection, from April 1998 to October 1999, pursuant to the IDSA/FDA standards. Twenty local patients were evaluated from a total of 623 patients in 17 countries. Acute perforated appendicitis was the most frequent pathology in both groups. The recovery ratio was slightly higher in the group, which was administered ertapenem, with no documented clinical failure. This study shows the efficacy of ertapenem in the treatment of intra-abdominal infections using a single 1-gr/day dose, equivalent to 3.375 gr of piperacillin/tazobactam every six hours. Tolerance and safety were similar in both groups. No side effects, or mortality cases were registered. The results of this study indicate that ertapenem might be the therapeutic option to discard the combination of antibiotics or the use of multiple doses in intra-abdominal infections.
- Published
- 2003
22. [Candida parapsilosis endocarditis after prolonged antibiotic therapy].
- Author
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Castillo Caparrós A and Montijano Cabrera AM
- Subjects
- Candida classification, Candidiasis etiology, Cardiac Tamponade etiology, Cefazolin administration & dosage, Disease Susceptibility, Endocarditis etiology, Fatal Outcome, Humans, Ischemia etiology, Leg blood supply, Male, Middle Aged, Opportunistic Infections etiology, Penicillanic Acid administration & dosage, Piperacillin administration & dosage, Postoperative Complications etiology, Tazobactam, Candida isolation & purification, Candidiasis microbiology, Cefazolin adverse effects, Drug Therapy, Combination adverse effects, Endocarditis microbiology, Opportunistic Infections microbiology, Penicillanic Acid adverse effects, Penicillanic Acid analogs & derivatives, Piperacillin adverse effects, Postoperative Complications microbiology, Superinfection
- Abstract
Infective endocarditis is still a very serious disease whose prognosis has improved in recent years, even though advanced technologies have brought a greater number of cases attributable to increased growth of fungi in more virulent forms. We describe a case of endocarditis caused by Candida parapsilosis on a previously healthy aortic valve in a man who had received prolonged intravenous antibiotic treatment a few months earlier. The initial presentation included acute arterial ischaemia of the lower limbs. The diagnosis of endocarditis was then confirmed by echocardiography and microbiology. Specific antifungal therapy was started, and embolectomy and valve replacement were performed; however, the infection could not be controlled and the patient died a few days later.
- Published
- 2002
23. [Cost of antibiotic therapy in neutropenic patients undergoing peripheral blood stem cell transplantation for breast cancer].
- Author
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Palau J, Picón I, Aznar E, Climent MA, and Máiquez J
- Subjects
- Amikacin administration & dosage, Amikacin economics, Antineoplastic Agents adverse effects, Breast Neoplasms complications, Breast Neoplasms drug therapy, Breast Neoplasms economics, Drug Therapy, Combination therapeutic use, Female, Fever etiology, Gram-Negative Bacterial Infections drug therapy, Gram-Negative Bacterial Infections economics, Gram-Negative Bacterial Infections etiology, Gram-Positive Bacterial Infections drug therapy, Gram-Positive Bacterial Infections economics, Gram-Positive Bacterial Infections etiology, Hospital Costs, Humans, Neutropenia chemically induced, Neutropenia economics, Penicillanic Acid administration & dosage, Penicillanic Acid analogs & derivatives, Penicillanic Acid economics, Piperacillin administration & dosage, Piperacillin economics, Spain, Tazobactam, Teicoplanin administration & dosage, Teicoplanin economics, Transplantation Conditioning adverse effects, Treatment Failure, Treatment Outcome, Vancomycin administration & dosage, Vancomycin economics, Breast Neoplasms therapy, Drug Costs, Drug Therapy, Combination economics, Hematopoietic Stem Cell Transplantation economics, Neutropenia complications
- Abstract
The increase in pharmaceutical costs, especially for expensive procedures such as bone marrow transplants, has led to the study of the economic impact of febrile neutropenia in peripheral blood stem cell transplantation (PBSCT). We analyzed 89 consecutive patients with breast cancer who underwent PBSCT. All patients developed febrile neutropenia and were administered an empirical intravenous regimen based on the combination of piperacillin-tazobactam and amikacin. We analyzed the direct costs of this treatment and grouped them into drug acquisition cost, administration costs (cost of the additional material), and preparation costs (time employed for the preparation and administration of the drug). We found that the overall cost was $1,110, 65% of which corresponded to the initial therapy and the rest (35%) to the use of additional antibiotics. This higher cost was especially related to the use of vancomycin or teicoplanin (50%). The acquisition costs accounted for 90% of the overall treatment costs. Thirty-six patients (40%) did not need additional antibiotics and the cost in this group was less ($663). We concluded that knowledge of the costs of pharmacological therapy for infection in PBSCT is indispensable for the appropriate development of treatment units, especially in terms of optimizing resources and comparing different therapeutic or prophylactic approaches.
- Published
- 2000
24. [Activity of betalactamase inhibitors against Acinetobacter baumannii].
- Author
-
Cuenca FF
- Subjects
- Acinetobacter enzymology, Animals, Humans, Penicillanic Acid pharmacology, Penicillanic Acid therapeutic use, Tazobactam, Acinetobacter drug effects, Acinetobacter Infections drug therapy, Anti-Bacterial Agents pharmacology, Anti-Bacterial Agents therapeutic use, Penicillanic Acid analogs & derivatives, Sulbactam pharmacology, Sulbactam therapeutic use, beta-Lactamase Inhibitors
- Published
- 2000
25. [A national multicenter study of the in-vitro activity of piperacillin-tazobactam. The Spanish Piperacillin-Tazobactam Group].
- Author
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Gobernado M, Bouza E, Perea E, Alvarez-Bravo J, and García Rodríguez JA
- Subjects
- Bacteria drug effects, Bacteria isolation & purification, Chi-Square Distribution, Drug Combinations, Humans, Microbial Sensitivity Tests methods, Microbial Sensitivity Tests statistics & numerical data, Penicillanic Acid pharmacology, Prospective Studies, Spain, Tazobactam, Enzyme Inhibitors pharmacology, Penicillanic Acid analogs & derivatives, Penicillins pharmacology, Piperacillin pharmacology, beta-Lactamase Inhibitors
- Abstract
The action of piperacillin-tazobactam on 4,137 of the 4,364 strains collected in a Spanish multicenter study involving 46 participating hospitals was studied. The samples were from the following: 41% urine, 18% exuded from wound abscesses, 13% respiratory, 9% blood, 3% peritoneal liquid, and the remainder from other various sources. The gram-negative bacteria included 2,778 strains from 13 genera: Escherichia (1,289), Pseudomonas (451), Proteus (230), Klebsiella (203), Haemophilus (172), Enterobacter (145), Acinetobacter (88), Salmonella (60), Bacteroides (57), Morganella (53), Serratia (46), Citrobacter (46), Stenotrophonomas (23) and Moraxella (21). The gram-positive bacteria were S. aureus (316), E. faecalis (239), S. epidermis (130), S. pneumoniae (115) and Clostridium spp. (12). The global susceptibility of the gram-negatives to piperacillin-tazobactam was 94%: E. coli 98%, P. aeruginosa 92%, and P. mirabilis, Morganella, K. pneumoniae, Serratia and Salmonella spp. all greater than 94%. The susceptibility of other bacteria was as follows: 91% Citrobacter, 77% E. cloacae, 42% A. baumannii, 61% S. maltophilia, 97% E. faecalis, 93% S. epidermidis, 100% M. catarrhalis, 99% H. influenzae and 100% anaerobic bacteria. The action on S. pneumoniae and S. aureus varied according to the susceptibility or lack there of to penicillin or methicillin. In comparison to other antibiotics (piperacillin, cefoxitin, cefotaxime, ceftazidime, cefepime, imipenem and ciprofloxacin), piperacillin-tazobactam was far better than piperacillin alone and better or similar to the others.
- Published
- 1998
26. [Comparison of the therapeutic efficacy of the piperacillin/tazobactame combination vs. ampicillin and gentamycin in in the management of post-cesarean endometritis].
- Author
-
Figueroa-Damian R, Villagrana-Zesati R, San Martín-Herrasti JM, and Arredondo-Garcia JL
- Subjects
- Adolescent, Adult, Age Factors, Drug Therapy, Combination, Endometritis drug therapy, Female, Humans, Parity, Penicillanic Acid therapeutic use, Pregnancy, Tazobactam, Ampicillin therapeutic use, Anti-Bacterial Agents therapeutic use, Cesarean Section adverse effects, Endometritis etiology, Enzyme Inhibitors therapeutic use, Gentamicins therapeutic use, Penicillanic Acid analogs & derivatives, Penicillins therapeutic use, Piperacillin therapeutic use
- Abstract
Traditionally obstetric infections have been treated with combination antimicrobial agents that provide coverage against aerobic and anaerobic bacteria commonly found in these infections. New antibiotics may be a monotherapy alternative for this type of infections. The objective of the study was to compare the efficacy of the agent piperacillin/tazobactam against ampicillin plus gentamicin in the treatment of postcesarean endometritis. By randomized way 14 patients were enrolled in the piperacillin/tazobactam group and 42 in the ampicillin-gentamicin group. A favorable clinical response occurred in 78.6% of piperacillin/tazobactam patients and 88.1% of ampicillin and gentamicin patients (p = NS). There was no statistically significant difference in the times to recovery and days of hospitalization between the two groups. The combination piperacillin/tazobactam did not show advantage towards the standard treatment, so combination antimicrobial agent continue been the optimal approach to the management of obstetric infection.
- Published
- 1996
27. [Drugs: piperacillin/tazobactam].
- Subjects
- Bacterial Infections drug therapy, Drug Combinations, Humans, Penicillanic Acid administration & dosage, Penicillanic Acid economics, Penicillanic Acid pharmacology, Piperacillin economics, Piperacillin pharmacology, Tazobactam, beta-Lactamase Inhibitors, Penicillanic Acid analogs & derivatives, Piperacillin administration & dosage
- Published
- 1995
28. [Bacteremia by Escherichia coli resistant to amoxycillin/clavulanic acid, ampicillin/sulbactam and piperacillin/tazobactam].
- Author
-
Alós JI, Gómez-Garcés JL, and Mateos MV
- Subjects
- Aged, Ampicillin therapeutic use, Clavulanic Acid, Clavulanic Acids therapeutic use, Drug Resistance, Microbial, Female, Humans, Penicillanic Acid analogs & derivatives, Penicillanic Acid therapeutic use, Sulbactam therapeutic use, Tazobactam, Drug Therapy, Combination therapeutic use, Escherichia coli drug effects, Escherichia coli Infections drug therapy
- Published
- 1994
29. [Efficiency of tazobactam as inhibitor of beta-lactamases, combined with piperacillin, against resistant strains to this penicillin].
- Author
-
Roy C, Tirado M, Teruel D, Reig R, and Ràfols M
- Subjects
- Amoxicillin pharmacology, Chemical Phenomena, Chemistry, Clavulanic Acids pharmacology, Drug Evaluation, Drug Therapy, Combination pharmacology, Female, Microbial Sensitivity Tests, Penicillin Resistance, Tazobactam, Enterobacteriaceae drug effects, Penicillanic Acid pharmacology, Piperacillin pharmacology, beta-Lactamases pharmacology
- Abstract
We studied the efficacy of tazobactam (YTR 830), a new beta-lactamase inhibitor in combination with piperacillin (P) against 198 Enterobacteriaceae strains. A comparative study of susceptibility (MIC determined on Mueller Hinton agar; inoculum 10(4) cfu) was made with the combination amoxicillin (A) + clavulanic acid (CA). Of 181 strains resistant to P, 79.56% were susceptible to it in the presence of tazobactam (TZ). The characteristics of the beta-lactamases of 37 strains resistant to P + TZ (MIC greater than 40 micrograms/ml) were studied; 11 were hyperproducers of chromosomic beta-lactamase and 7 produced two types of plasmidic beta-lactamase. The MICs of TZ alone were uniform and high (64-128 micrograms/ml), independently of the characteristics of the strains beta-lactamase. Of 17 strains susceptible to P, the efficacy of P + TZ was significant among carriers of plasmidic beta-lactamase; there was practically no change in the P susceptibility among the non carriers. The efficacy of P + TZ was similar to that of A + AC against E. coli strains; it was higher against strains of Enterobacter, Citrobacter and Serratia.
- Published
- 1989
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