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1.
Rev Argent Microbiol ; 40(4): 208-10, 2008.
Article in Spanish | MEDLINE | ID: mdl-19213242

ABSTRACT

Human infections by Pasteurella multocida are usually associated with bites or scratches from dogs and cats. Many of them are accompanied by other oropharyngeal microorganisms of these animals. We herein present a case of bacteremic meningitis by P. multocida in an 86-year-old woman who was living with seven cats. Even though no skin or soft tissue infection was recorded, it is possible that a mild infection had gone undetected and a subsequent bacteremia had impacted on the meninges, or that meningitis could have occurred after nasopharyngeal colonization (not demonstrated). The isolates obtained from blood cultures and cerebrospinal fluid were identified as P. multocida by API 20NE, API 20E, and Vitek 1. In agreement with findings in the literature, this strain was susceptible to penicillin, cefotaxime, levofloxacin and tetracyclines.


Subject(s)
Bacteremia/microbiology , Meningitis, Bacterial/microbiology , Pasteurella Infections/microbiology , Pasteurella multocida/isolation & purification , Aged, 80 and over , Ampicillin/therapeutic use , Animals , Anti-Bacterial Agents/therapeutic use , Cat Diseases/microbiology , Cats/microbiology , Ceftriaxone/therapeutic use , Dexamethasone/therapeutic use , Drug Therapy, Combination , Female , Humans , Pasteurella Infections/transmission , Pasteurella Infections/veterinary , Pasteurella multocida/drug effects
2.
Rev Argent Microbiol ; 37(1): 57-66, 2005.
Article in Spanish | MEDLINE | ID: mdl-15991480

ABSTRACT

Taking into account previous recommendations from the National Committee for Clinical Laboratory Standards (NCCLS), the Antimicrobial Committee, Sociedad Argentina de Bacteriología Clínica (SADEBAC), Asociación Argentina de Microbiología (AAM), and the experience from its members and some invited microbiologists, a consensus was obtained for antimicrobial susceptibility testing and interpretation in most frequent enterobacterial species isolated from clinical samples in our region. This document describes the natural antimicrobial resistance of some Enterobacteriaceae family members, including the resistance profiles due to their own chromosomal encoded beta-lactamases. A list of the antimicrobial agents that should be tested, their position on the agar plates, in order to detect the most frequent antimicrobial resistance mechanisms, and considerations on which antimicrobial agents should be reported regarding to the infection site and patient characteristics are included. Also, a description on appropriate phenotypic screening and confirmatory test for detection of prevalent extended spectrum beta-lactamases in our region are presented. Finally, a summary on frequent antimicrobial susceptibility profiles and their probably associated resistance mechanisms, and some infrequent antimicrobial resistance profiles that deserve confirmation are outlined.


Subject(s)
Anti-Bacterial Agents/pharmacology , Enterobacteriaceae/drug effects , Microbial Sensitivity Tests , Anti-Bacterial Agents/therapeutic use , Bacterial Proteins/analysis , Drug Resistance , Drug Resistance, Multiple, Bacterial , Enterobacteriaceae/enzymology , Enterobacteriaceae/isolation & purification , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae Infections/microbiology , Humans , Microbial Sensitivity Tests/economics , Microbial Sensitivity Tests/methods , Microbial Sensitivity Tests/standards , Phenotype , Quality Control , beta-Lactamases/analysis
3.
Rev. argent. microbiol ; 37(1): 57-66, ene.-mar. 2005. ilus, tab
Article in Spanish | LILACS | ID: lil-634489

ABSTRACT

En este documento se elaboraron una serie de recomendaciones para el ensayo, lectura, interpretación e informe de las pruebas de sensibilidad a los antimicrobianos para las enterobacterias aisladas con mayor frecuencia de especímenes clínicos. Se adoptaron como base las recomendaciones del National Committee for Clinical Laboratory Standards (NCCLS) de los EEUU, los de la subcomisión de Antimicrobianos, de la Sociedad Argentina de Bacteriología Clínica (SADEBAC), división de la Asociación Argentina de Microbiología (AAM) y de un grupo de expertos invitados. En él se indican las resistencias naturales de los diferentes miembros que integran la familia Enterobacteriaceae y se analiza la actividad de las diferentes beta-lactamasas cromosómicas, propias de cada especie, sobre las penicilinas, cefalosporinas y carbapenemes. Se recomiendan los antimicrobianos que se deberían ensayar, ubicados estratégicamente, para detectar los mecanismos de resistencia más frecuentes y cuales se deberían informar de acuerdo a la especie aislada, el sitio de infección y el origen de la cepa (intra o extrahospitalario). Se detallan los métodos de "screening" y de confirmación fenotipíca para detectar beta-lactamasas de espectro extendido (BLEE) que son más adecuados a nuestra realidad. Por último, se mencionan patrones infrecuentes de sensibilidad/resistencia que deberían verificarse y los perfiles de sensibilidad que pueden hallarse en las distintas enterobacterias en relación con los probables mecanismos de resistencia. Se debe resaltar que el contenido de este documento debe ser considerado como recomendaciones realizadas por expertos argentinos basadas en una revisión de la literatura y datos personales.


Taking into account previous recommendations from the National Committee for Clinical Laboratory Standards (NCCLS), the Antimicrobial Committee, Sociedad Argentina de Bacteriología Clínica (SADEBAC), Asociación Argentina de Microbiología (AAM), and the experience from its members and some invited microbiologists, a consensus was obtained for antimicrobial susceptibility testing and interpretation in most frequent enterobacterial species isolated from clinical samples in our region. This document describes the natural antimicrobial resistance of some Enterobacteriaceae family members, including the resistance profiles due to their own chromosomal encoded beta-lactamases. A list of the antimicrobial agents that should be tested, their position on the agar plates, in order to detect the most frequent antimicrobial resistance mechanisms, and considerations on which antimicrobial agents should be reported regarding to the infection site and patient characteristics are included. Also, a description on appropriate phenotypic screening and confirmatory test for detection of prevalent extended spectrum beta-lactamases in our region are presented. Finally, a summary on frequent antimicrobial susceptibility profiles and their probably associated resistance mechanisms, and some infrequent antimicrobial resistance profiles that deserve confirmation are outlined.


Subject(s)
Humans , Anti-Bacterial Agents/pharmacology , Enterobacteriaceae/drug effects , Microbial Sensitivity Tests , Anti-Bacterial Agents/therapeutic use , Bacterial Proteins/analysis , Drug Resistance , Drug Resistance, Multiple, Bacterial , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae Infections/microbiology , Enterobacteriaceae/enzymology , Enterobacteriaceae/isolation & purification , Microbial Sensitivity Tests/economics , Microbial Sensitivity Tests/methods , Microbial Sensitivity Tests/standards , Phenotype , Quality Control , beta-Lactamases/analysis
4.
Rev. argent. microbiol ; 37(1): 57-66, 2005 Jan-Mar.
Article in Spanish | BINACIS | ID: bin-38420

ABSTRACT

Taking into account previous recommendations from the National Committee for Clinical Laboratory Standards (NCCLS), the Antimicrobial Committee, Sociedad Argentina de Bacteriología Clínica (SADEBAC), Asociación Argentina de Microbiología (AAM), and the experience from its members and some invited microbiologists, a consensus was obtained for antimicrobial susceptibility testing and interpretation in most frequent enterobacterial species isolated from clinical samples in our region. This document describes the natural antimicrobial resistance of some Enterobacteriaceae family members, including the resistance profiles due to their own chromosomal encoded beta-lactamases. A list of the antimicrobial agents that should be tested, their position on the agar plates, in order to detect the most frequent antimicrobial resistance mechanisms, and considerations on which antimicrobial agents should be reported regarding to the infection site and patient characteristics are included. Also, a description on appropriate phenotypic screening and confirmatory test for detection of prevalent extended spectrum beta-lactamases in our region are presented. Finally, a summary on frequent antimicrobial susceptibility profiles and their probably associated resistance mechanisms, and some infrequent antimicrobial resistance profiles that deserve confirmation are outlined.

5.
Diagn Microbiol Infect Dis ; 50(3): 223-5, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15541610

ABSTRACT

The "Slidex MRSA Detection" test (Denka Seiken, Japan) is a latex agglutination assay able to detect PBP2a. We evaluated its ability to differentiate mecA-positive from mecA-negative coagulase-negative staphylococci. We included 100 coagulase-negative staphylococci clinical isolates belonging to 9 species, 54 mecA positive and 46 mecA negative, as characterized by PCR. The specificity achieved using the manufacturer's instructions was 100%, but the sensitivity was only 57%. To increase sensitivity, we introduced modifications into the standard protocol. Using either large inocula or oxacillin induction before test performance, we achieved 100% sensitivity.


Subject(s)
Latex Fixation Tests/methods , Oxacillin/pharmacology , Penicillin Resistance , Penicillin-Binding Proteins/analysis , Staphylococcus/drug effects , Penicillin Resistance/genetics , Reagent Kits, Diagnostic/microbiology , Sensitivity and Specificity , Species Specificity , Staphylococcus/classification , Staphylococcus/genetics
6.
Rev Argent Microbiol ; 36(2): 81-4, 2004.
Article in Spanish | MEDLINE | ID: mdl-15470867

ABSTRACT

Brucella canis and other species of the genus Brucella can cause human disease. However, this species infrequently cause human disease, including in countries where dogs population is highly infected. A 15 years old male was admitted to the hospital with 15 days history of fever without visible focus. Physical examination revealed pain at liver palpation and axillar, cervical and inguinal lymphoadenomegalies. Abdominal ultrasonography showed spleenomegally, the chest Rx and the trans thoracic echocardiogram were normal. Five blood samples were obtained and cultured in 2 standards bottles (time of positivization 72 - 64.8 hours), and 3 pediatric FAN bottles (time of positivization 74.5; 72 and 67.2 hours) (Bact-Alert system, Biomerieux, Marcy, l'Etolie, France). The microorganism was presuntive identified as B. canis, and then was confirmed in the National Reference Center Instituto ANLIS "Carlos G. Malbran". After 14 days of initiating ceftriaxone treatment the patient was afebrile. When the confirmation of Brucella was made, he was discharged and ambulatory was prescribed with doxycycline and rifampin for 21 days. Bones were not compromised and the outcome was good with complete resolution of his illness.


Subject(s)
Bacteremia/microbiology , Brucella canis/isolation & purification , Brucellosis/diagnosis , Adolescent , Bacteremia/diagnosis , Bacteriological Techniques , Humans , Male
7.
Rev Argent Microbiol ; 36(1): 24-7, 2004.
Article in Spanish | MEDLINE | ID: mdl-15174746

ABSTRACT

Bact-Alert automatized system for blood cultures: 5 vs 7 days of incubation. First Argentine multicentre study. Between January and December 2001, we analyzed 80,141 blood cultures by the Bact-Alert system (14,960 FAN aerobics, 3,855 FAN anaerobic, 11,114 standards aerobics, 11,367 standards anaerobic, 12,054 pediatrics and 26,791 FAN pediatrics bottles) and 44.235 series from 27.615 patients at eight hospitals of Buenos Aires city, one of La Plata city and three of the Buenos Aires province. A total of 13,657 blood cultures yielded a positive result. Only 181 of them had been detected as positive between the 5th and 7th day of incubation and only 26 (0.19%) had clinical significance (Staphylococcus aureus 3; coagulase negative staphylococci 2; Enterococcus faecalis 1; Streptococcus pneumoniae 2; Campylobacter spp 1; Escherichia coli 1; Enterobacter cloacae 1; Enterobacteraerogenes 1; Citrobacter freundii 1; Klebsiella pneumoniae 1; Proteus mirabilis 1; Serratia marcescens 4; yeasts 7, including one strain of Cryptococcus neoformans). Of the total of contaminants, 38% were isolated by the anaerobic standard (65% were Propionibacterium spp and 29% coagulase negative staphylococci), 31.2% by the FAN aerobic (33.3% difphteroids and 28.9% Bacillus spp), 11.8% by the pediatric, 9% by FAN pediatric, 8.33% by aerobic standard and 1.4% by FAN anaerobic bottle. Our results show that the prolonged incubation of blood cultures for more than 5 days using the Bact-Alert system is unnecessary.


Subject(s)
Bacteremia/microbiology , Bacteria, Aerobic/isolation & purification , Bacteria, Anaerobic/isolation & purification , Bacteriological Techniques , Blood/microbiology , Argentina/epidemiology , Automation , Bacteremia/epidemiology , Bacteria, Aerobic/growth & development , Bacteria, Anaerobic/growth & development , Humans , Laboratories, Hospital/statistics & numerical data , Time Factors
8.
Rev Argent Microbiol ; 36(1): 36-40, 2004.
Article in Spanish | MEDLINE | ID: mdl-15174748

ABSTRACT

Methicillin-resistant Staphylococcus aureus (MRSA) is a significant pathogen that has emerged over the last four decades, causing both nosocomial and community-acquired infections. Rapid and accurate detection of methicillin resistance in S. aureus is important for the use of appropriate antimicrobial therapy and for the control of nosocomial spread of MRSA strains. We evaluated the efficiency of conventional methods for detection of methicillin resistance such as the disk diffusion, agar dilution, oxacillin agar screen test, and the latex agglutination test MRSA-Screen latex, in 100 isolates of S. aureus, 79 mecA positive and 21 mecA negative. The MRSA-Screen latex (Denka Seiken, Niigata, Japón), is a latex agglutination method that detects the presence of PLP-2a, product of mecA gene in S. aureus. The PCR of the mecA gene was used as the "gold standard" for the evaluation of the different methods tested. The percentages of sensitivity and specificity were as follows: disk difusión 97 and 100%, agar dilution 97 and 95%, oxacillin agar screen test 100 and 100%, and MRSA-Screen latex, 100 and 100 %. All methods presented high sensitivity and specificity, but MRSA-Screen latex had the advantage of giving a reliable result, equivalent to PCR, in only 15 minutes.


Subject(s)
Latex Fixation Tests , Methicillin Resistance , Microbial Sensitivity Tests/methods , Staphylococcus aureus/drug effects , Bacterial Proteins/analysis , Bacterial Proteins/genetics , Carrier Proteins/analysis , DNA, Bacterial/genetics , Hexosyltransferases/analysis , Methicillin Resistance/genetics , Muramoylpentapeptide Carboxypeptidase/analysis , Penicillin-Binding Proteins , Peptidyl Transferases/analysis , Polymerase Chain Reaction , Sensitivity and Specificity , Staphylococcus aureus/genetics
9.
Rev. argent. microbiol ; 36(2): 81-4, abr.-jun. 2004.
Article in Spanish | LILACS-Express | LILACS, BINACIS | ID: biblio-1171745

ABSTRACT

Brucella canis and other species of the genus Brucella can cause human disease. However, this species infrequently cause human disease, including in countries where dogs population is highly infected. A 15 years old male was admitted to the hospital with 15 days history of fever without visible focus. Physical examination revealed pain at liver palpation and axillar, cervical and inguinal lymphoadenomegalies. Abdominal ultrasonography showed spleenomegally, the chest Rx and the trans thoracic echocardiogram were normal. Five blood samples were obtained and cultured in 2 standards bottles (time of positivization 72 - 64.8 hours), and 3 pediatric FAN bottles (time of positivization 74.5; 72 and 67.2 hours) (Bact-Alert system, Biomerieux, Marcy, l’Etolie, France). The microorganism was presuntive identified as B. canis, and then was confirmed in the National Reference Center Instituto ANLIS [quot ]Carlos G. Malbran[quot ]. After 14 days of initiating ceftriaxone treatment the patient was afebrile. When the confirmation of Brucella was made, he was discharged and ambulatory was prescribed with doxycycline and rifampin for 21 days. Bones were not compromised and the outcome was good with complete resolution of his illness.

10.
Rev. argent. microbiol ; 36(1): 36-40, Jan.-Mar. 2004. tab
Article in Spanish | LILACS | ID: lil-634456

ABSTRACT

Staphylococcus aureus meticilino-resistente (MRSA) es un patógeno que ha emergido en las últimas cuatro décadas causando tanto infecciones nosocomiales como de la comunidad. La rápida y precisa detección de MRSA es relevante para guiar una apropiada terapia antibiótica y evitar la diseminación nosocomial de MRSA.En este trabajo se evaluó la eficiencia de métodos convencionales para la detección de meticilino-resistencia como difusión por discos, CIM en medio sólido, screening de oxacilina, y el nuevo test de aglutinación MRSA-Screen latex sobre 100 aislamientos de S. aureus, 79 mecA positivos y 21 mecA negativos. El test de aglutinación MRSA-Screen latex (Denka Seiken, Niigata, Japón) detecta la presencia de la PLP-2a, producto del gen mecA en cepas de S. aureus. La detección del gen mecA por PCR se utilizó como gold standard para comparar los resultados de los diferentes métodos. La sensibilidad y especificidad fueron 97 y 100 % para el método de difusión, 97 y 95 % para la CIM en medio sólido, 100 y 100 % para el screening de oxacilina y 100 y 100 % para MRSA-Screen latex. Todos los métodos presentaron alta sensibilidad y especificidad, pero el “MRSA-Screen latex” mostró la ventaja de poder brindar un resultado confiable, equivalente a la PCR, en sólo 15 minutos.


Methicillin-resistant Staphylococcus aureus (MRSA) is a significant pathogen that has emerged over the last four decades, causing both nosocomial and community-acquired infections. Rapid and accurate detection of methicillin resistance in S. aureus is important for the use of appropriate antimicrobial therapy and for the control of nosocomial spread of MRSA strains. We evaluated the efficiency of conventional methods for detection of methicillin resistance such as the disk diffusion, agar dilution, oxacillin agar screen test, and the latex agglutination test MRSA-Screen latex, in 100 isolates of S. aureus, 79 mecA positive and 21 mecA negative. The MRSA-Screen latex (Denka Seiken, Niigata, Japón), is a latex agglutination method that detects the presence of PLP-2a, product of mecA gene in S. aureus. The PCR of the mecA gene was used as the “gold standard” for the evaluation of the different methods tested. The percentages of sensitivity and specificity were as follows: disk difusión 97 and 100 %, agar dilution 97 and 95 %, oxacillin agar screen test 100 and 100 %, and MRSA-Screen latex, 100 and 100 %. All methods presented high sensitivity and specificity, but MRSA-Screen latex had the advantage of giving a reliable result, equivalent to PCR, in only 15 minutes.


Subject(s)
Latex Fixation Tests , Methicillin Resistance , Microbial Sensitivity Tests/methods , Staphylococcus aureus/drug effects , Bacterial Proteins/analysis , Bacterial Proteins/genetics , Carrier Proteins/analysis , DNA, Bacterial/genetics , Hexosyltransferases/analysis , Methicillin Resistance/genetics , Muramoylpentapeptide Carboxypeptidase/analysis , Penicillin-Binding Proteins , Polymerase Chain Reaction , Peptidyl Transferases/analysis , Sensitivity and Specificity , Staphylococcus aureus/genetics
11.
Rev. argent. microbiol ; 36(1): 24-7, Jan.-Mar. 2004.
Article in Spanish | LILACS-Express | LILACS, BINACIS | ID: biblio-1171741

ABSTRACT

Bact-Alert automatized system for blood cultures: 5 vs 7 days of incubation. First Argentine multicentre study. Between January and December 2001, we analyzed 80,141 blood cultures by the Bact-Alert system (14,960 FAN aerobics, 3,855 FAN anaerobic, 11,114 standards aerobics, 11,367 standards anaerobic, 12,054 pediatrics and 26,791 FAN pediatrics bottles) and 44.235 series from 27.615 patients at eight hospitals of Buenos Aires city, one of La Plata city and three of the Buenos Aires province. A total of 13,657 blood cultures yielded a positive result. Only 181 of them had been detected as positive between the 5th and 7th day of incubation and only 26 (0.19


) had clinical significance (Staphylococcus aureus 3; coagulase negative staphylococci 2; Enterococcus faecalis 1; Streptococcus pneumoniae 2; Campylobacter spp 1; Escherichia coli 1; Enterobacter cloacae 1; Enterobacteraerogenes 1; Citrobacter freundii 1; Klebsiella pneumoniae 1; Proteus mirabilis 1; Serratia marcescens 4; yeasts 7, including one strain of Cryptococcus neoformans). Of the total of contaminants, 38


were isolated by the anaerobic standard (65


were Propionibacterium spp and 29


by the FAN aerobic (33.3


difphteroids and 28.9


by the pediatric, 9


by aerobic standard and 1.4


by FAN anaerobic bottle. Our results show that the prolonged incubation of blood cultures for more than 5 days using the Bact-Alert system is unnecessary.

12.
Rev. argent. microbiol ; 36(1): 24-7, 2004 Jan-Mar.
Article in Spanish | BINACIS | ID: bin-38707

ABSTRACT

Bact-Alert automatized system for blood cultures: 5 vs 7 days of incubation. First Argentine multicentre study. Between January and December 2001, we analyzed 80,141 blood cultures by the Bact-Alert system (14,960 FAN aerobics, 3,855 FAN anaerobic, 11,114 standards aerobics, 11,367 standards anaerobic, 12,054 pediatrics and 26,791 FAN pediatrics bottles) and 44.235 series from 27.615 patients at eight hospitals of Buenos Aires city, one of La Plata city and three of the Buenos Aires province. A total of 13,657 blood cultures yielded a positive result. Only 181 of them had been detected as positive between the 5th and 7th day of incubation and only 26 (0.19


) had clinical significance (Staphylococcus aureus 3; coagulase negative staphylococci 2; Enterococcus faecalis 1; Streptococcus pneumoniae 2; Campylobacter spp 1; Escherichia coli 1; Enterobacter cloacae 1; Enterobacteraerogenes 1; Citrobacter freundii 1; Klebsiella pneumoniae 1; Proteus mirabilis 1; Serratia marcescens 4; yeasts 7, including one strain of Cryptococcus neoformans). Of the total of contaminants, 38


were isolated by the anaerobic standard (65


were Propionibacterium spp and 29


coagulase negative staphylococci), 31.2


by the FAN aerobic (33.3


difphteroids and 28.9


Bacillus spp), 11.8


by the pediatric, 9


by FAN pediatric, 8.33


by aerobic standard and 1.4


by FAN anaerobic bottle. Our results show that the prolonged incubation of blood cultures for more than 5 days using the Bact-Alert system is unnecessary.

13.
Rev. argent. microbiol ; 36(1): 36-40, 2004 Jan-Mar.
Article in Spanish | BINACIS | ID: bin-38704

ABSTRACT

Methicillin-resistant Staphylococcus aureus (MRSA) is a significant pathogen that has emerged over the last four decades, causing both nosocomial and community-acquired infections. Rapid and accurate detection of methicillin resistance in S. aureus is important for the use of appropriate antimicrobial therapy and for the control of nosocomial spread of MRSA strains. We evaluated the efficiency of conventional methods for detection of methicillin resistance such as the disk diffusion, agar dilution, oxacillin agar screen test, and the latex agglutination test MRSA-Screen latex, in 100 isolates of S. aureus, 79 mecA positive and 21 mecA negative. The MRSA-Screen latex (Denka Seiken, Niigata, Japón), is a latex agglutination method that detects the presence of PLP-2a, product of mecA gene in S. aureus. The PCR of the mecA gene was used as the [quot ]gold standard[quot ] for the evaluation of the different methods tested. The percentages of sensitivity and specificity were as follows: disk difusión 97 and 100


, agar dilution 97 and 95


, oxacillin agar screen test 100 and 100


, and MRSA-Screen latex, 100 and 100


. All methods presented high sensitivity and specificity, but MRSA-Screen latex had the advantage of giving a reliable result, equivalent to PCR, in only 15 minutes.

14.
Rev. argent. microbiol ; 36(2): 81-4, 2004 Apr-Jun.
Article in Spanish | BINACIS | ID: bin-38614

ABSTRACT

Brucella canis and other species of the genus Brucella can cause human disease. However, this species infrequently cause human disease, including in countries where dogs population is highly infected. A 15 years old male was admitted to the hospital with 15 days history of fever without visible focus. Physical examination revealed pain at liver palpation and axillar, cervical and inguinal lymphoadenomegalies. Abdominal ultrasonography showed spleenomegally, the chest Rx and the trans thoracic echocardiogram were normal. Five blood samples were obtained and cultured in 2 standards bottles (time of positivization 72 - 64.8 hours), and 3 pediatric FAN bottles (time of positivization 74.5; 72 and 67.2 hours) (Bact-Alert system, Biomerieux, Marcy, lEtolie, France). The microorganism was presuntive identified as B. canis, and then was confirmed in the National Reference Center Instituto ANLIS [quot ]Carlos G. Malbran[quot ]. After 14 days of initiating ceftriaxone treatment the patient was afebrile. When the confirmation of Brucella was made, he was discharged and ambulatory was prescribed with doxycycline and rifampin for 21 days. Bones were not compromised and the outcome was good with complete resolution of his illness.

15.
Rev Argent Microbiol ; 35(2): 91-5, 2003.
Article in Spanish | MEDLINE | ID: mdl-12920990

ABSTRACT

In Instituto de Cardiología y Cirugía Cardiovascular, Fundación Favaloro, between January 1996 and October 1999, 10,793 blood cultures and 942 episodes of bacteremia, corresponding to 1883 positive blood cultures, were studied by means of the Bact-Alert System (Organon Teknika), 94% being monomicrobial episodes. Gram positive bacteria were isolated in 45%, Gram negative in 52% and fungi in 3% of episodes. Associated foci of infection were: catheters 36.5%, mediastinitis 9%, pneumonia 6%, endocarditis 6%, abdominal 6%, urinary tract infections 9%, prosthesis 2.6%, empyema 0.2%, arthritis 0.1%, skin and soft tissue 2.5%, diarrhea 0.1%, aortic aneurysm 0.2%, meningitis 0.2%, pericarditis 0.3%, endarteritis 0.1%, infusion fluids 0.2% and unknown 21%. Median time (in hours) for positivization of blood cultures according to different foci were: catheters 16.4, mediastinitis 19.2, pneumonia 14.2, endocarditis 14.5, abdominal infections 11.8, urinary tract infections 13.0 and unknown origin 19.0. As for contaminating microorganisms, the value was 30.5. Seventy two percent of blood cultures became positive within 24 h, and 87% within 48 h; only 1% became positive between 5th and 7th day. There were no important differences in time to detect positive cultures according to different foci. It was not useful to incubate blood cultures more than five days, except for special circumstances, because it does not improve recovery of clinically significant microorganisms.


Subject(s)
Bacteremia/epidemiology , Bacteria/isolation & purification , Bacteriological Techniques , Cardiology Service, Hospital/statistics & numerical data , Cross Infection/epidemiology , Argentina/epidemiology , Bacteremia/diagnosis , Bacteremia/microbiology , Cross Infection/diagnosis , Cross Infection/microbiology , Female , Fungemia/diagnosis , Fungemia/epidemiology , Fungemia/microbiology , Fungi/isolation & purification , Humans , Male , Specimen Handling/statistics & numerical data , Time Factors
16.
Rev Argent Microbiol ; 35(1): 29-40, 2003.
Article in Spanish | MEDLINE | ID: mdl-12833678

ABSTRACT

Antimicrobial susceptibility testing is mainly performed in Argentina by disk diffusion method, following National Committee for Clinical Laboratory Standards (NCCLS) recommendations. We worked out new recommendations for the reporting and interpretation of this test when dealing with gram-positive cocci, in accordance to local trends and epidemiology. General considerations for performing the diffusion assay, quality control, and an update on susceptibility testing for gram-positive cocci are reported in this first document. The present update should be considered as a group of recommendations summarized by Argentinean experts and as the result of a consensus meeting coordinated by the Subcomisión de Antimicrobianos of the Sociedad Argentina de Bacteriología Clínica (Asociación Argentina de Microbiología). Experts in antimicrobial agents were convened in order to prepare this final document. These recommendations take into account local needs, affordability and availability to be used in current practice, tending to contribute to the correct antimicrobial treatment election, according to the particular microorganism and the infection sites.


Subject(s)
Anti-Bacterial Agents/pharmacology , Gram-Positive Cocci/drug effects , Microbial Sensitivity Tests , Algorithms , Drug Resistance , Drug Resistance, Multiple, Bacterial , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/microbiology , Gram-Positive Cocci/isolation & purification , Humans , Microbial Sensitivity Tests/economics , Microbial Sensitivity Tests/methods , Microbial Sensitivity Tests/standards , Phenotype , Quality Control
17.
Rev. argent. microbiol ; 35(2): 91-95, abr.-jun. 2003.
Article in Spanish | LILACS | ID: lil-356636

ABSTRACT

Entre enero de 1996 y octubre de 1999, se estudiaron en el Instituto Cardiovascular, Fundación Favaloro, 10.793 hemocultivos y 942 episodios de bacteriemia. Utilizando el Sistema Bact-Alert (Organon Teknika) estos cultivos fueron positivos en 1.883 casos. 94 por ciento de los episodios fueron monomicrobianos. Del total de espisodios se aislaron 45 por ciento de bacterias gram positivas, 52 por ciento de gram negativas y 3 por ciento de hongos. Los focos de infección asociados fueron: 36,5 por ciento infecciones asociadas a catéteres, 9 por ciento mediastinitis, 9 por ciento infecciones urinarias, 6 por ciento neumonías, 6 por ciento endocarditis, 6 por ciento infecciones intraabdominales, 2,6 por ciento infecciones de prótesis, 2,5 por ciento infecciones de piel y partes blandas, 0,3 por ciento pericarditis, 0,2 por ciento meningitis, 2 por ciento empiemas, 0,2 por ciento aneurismas de aorta, 0,2 por ciento infecciones por líquido de infusión contaminado, 0,1 por ciento artritis, 0,1 por ciento endarteritis, 0,1 por ciento diarreas, y foco desconocido en 21 por ciento de los casos. La mediana en horas para positivización de los hemocultivos acorde a los distinto focos fue: 16,4 para infecciones asociadas a catéteres, 19,2 mediastinitis, 14,2 neumonías, 14,5 endocarditis, 11,8 infecciones intraabdominales, 13 infecciones urinarias y 19 para bacteremias de origen desconocido. El valor fue de 30,5 h para las contaminaciones. El 72 por ciento de los hemocultivos positivos con un microorganismo considerado como clínicamente significativo se detectó a las 24 h, 87 por ciento dentro de las 48 h y sólo 1 por ciento entre el 5§ y 7§ día. No hubo diferencias importantes en el tiempo de detección de hemocultivos positivos acorde a distintos focos. Tampoco resultó de utilidad la incubación de las botellas más allá del 5§ día, excepto para circunstancias especiales, puesto que no mejoró la recuperación de microorganismos clínicamente significativos.


Subject(s)
Humans , Argentina , Bacteremia , Environmental Monitoring
18.
Rev. argent. microbiol ; 35(2): 91-95, abr.-jun. 2003.
Article in Spanish | BINACIS | ID: bin-4851

ABSTRACT

Entre enero de 1996 y octubre de 1999, se estudiaron en el Instituto Cardiovascular, Fundación Favaloro, 10.793 hemocultivos y 942 episodios de bacteriemia. Utilizando el Sistema Bact-Alert (Organon Teknika) estos cultivos fueron positivos en 1.883 casos. 94 por ciento de los episodios fueron monomicrobianos. Del total de espisodios se aislaron 45 por ciento de bacterias gram positivas, 52 por ciento de gram negativas y 3 por ciento de hongos. Los focos de infección asociados fueron: 36,5 por ciento infecciones asociadas a catéteres, 9 por ciento mediastinitis, 9 por ciento infecciones urinarias, 6 por ciento neumonías, 6 por ciento endocarditis, 6 por ciento infecciones intraabdominales, 2,6 por ciento infecciones de prótesis, 2,5 por ciento infecciones de piel y partes blandas, 0,3 por ciento pericarditis, 0,2 por ciento meningitis, 2 por ciento empiemas, 0,2 por ciento aneurismas de aorta, 0,2 por ciento infecciones por líquido de infusión contaminado, 0,1 por ciento artritis, 0,1 por ciento endarteritis, 0,1 por ciento diarreas, y foco desconocido en 21 por ciento de los casos. La mediana en horas para positivización de los hemocultivos acorde a los distinto focos fue: 16,4 para infecciones asociadas a catéteres, 19,2 mediastinitis, 14,2 neumonías, 14,5 endocarditis, 11,8 infecciones intraabdominales, 13 infecciones urinarias y 19 para bacteremias de origen desconocido. El valor fue de 30,5 h para las contaminaciones. El 72 por ciento de los hemocultivos positivos con un microorganismo considerado como clínicamente significativo se detectó a las 24 h, 87 por ciento dentro de las 48 h y sólo 1 por ciento entre el 5º y 7º día. No hubo diferencias importantes en el tiempo de detección de hemocultivos positivos acorde a distintos focos. Tampoco resultó de utilidad la incubación de las botellas más allá del 5º día, excepto para circunstancias especiales, puesto que no m


Subject(s)
Humans , Bacteremia/microbiology , Bacteremia/epidemiology , Bacteremia/etiology , Environmental Monitoring , Argentina
19.
Rev. argent. microbiol ; 35(1): 29-40, ene.-mar. 2003.
Article in Spanish | LILACS | ID: lil-356646

ABSTRACT

El antibiograma por difusión en agar con discos se encuentra ampliamente difundido en nuestro medio y se basa primariamente en las recomendaciones del National Committee for Clinical Laboratory Standards (NCCLS). En este documento se elaboraron una serie de recomendaciones para el ensayo, lectura, interpretación e informe de las pruebas de sensibilidad a los antimicrobianos en cocos gram-positivos, adaptadas a la realidad argentina. En esta primera etapa se redactaron las consideraciones generales para la realización de la prueba por difusión, los controles de calidad internos para todos los microorganismos y una actualización sobre las pruebas de sensibilidad en cocos gram-positivos. Se debe resaltar que el contenido de este documento debe ser considerado como recomendaciones realizadas por expertos argentinos y que son el resultado de reuniones de consenso organizadas por la Subcomisión de Antimicrobianos de la Sociedad Argentina de Bacteriología Clínica, división de la Asociación Argentina de Microbiología. Se formó un equipo de trabajo integrado por expertos en antimicrobianos y a partir de una propuesta inicial, basada en una revisión de la literatura se fueron elaborando diversos documentos de trabajo que fueron mejorados después de ser debatidos por los miembros del grupo de trabajo hasta llegar al documento final. El criterio general fue elaborar recomendaciones acordes a las necesidades de nuestro país que puedan utilizarse en la práctica diaria con el objeto de colaborar en la adecuada elección del tratamiento antibiótico según la especie bacteriana aislada y la localización de la infección.


Subject(s)
Argentina , Enterococcus , Gram-Positive Cocci , Microbial Sensitivity Tests , Staphylococcus , Streptococcus
20.
Rev. argent. microbiol ; 35(1): 29-40, ene.-mar. 2003.
Article in Spanish | BINACIS | ID: bin-4841

ABSTRACT

El antibiograma por difusión en agar con discos se encuentra ampliamente difundido en nuestro medio y se basa primariamente en las recomendaciones del National Committee for Clinical Laboratory Standards (NCCLS). En este documento se elaboraron una serie de recomendaciones para el ensayo, lectura, interpretación e informe de las pruebas de sensibilidad a los antimicrobianos en cocos gram-positivos, adaptadas a la realidad argentina. En esta primera etapa se redactaron las consideraciones generales para la realización de la prueba por difusión, los controles de calidad internos para todos los microorganismos y una actualización sobre las pruebas de sensibilidad en cocos gram-positivos. Se debe resaltar que el contenido de este documento debe ser considerado como recomendaciones realizadas por expertos argentinos y que son el resultado de reuniones de consenso organizadas por la Subcomisión de Antimicrobianos de la Sociedad Argentina de Bacteriología Clínica, división de la Asociación Argentina de Microbiología. Se formó un equipo de trabajo integrado por expertos en antimicrobianos y a partir de una propuesta inicial, basada en una revisión de la literatura se fueron elaborando diversos documentos de trabajo que fueron mejorados después de ser debatidos por los miembros del grupo de trabajo hasta llegar al documento final. El criterio general fue elaborar recomendaciones acordes a las necesidades de nuestro país que puedan utilizarse en la práctica diaria con el objeto de colaborar en la adecuada elección del tratamiento antibiótico según la especie bacteriana aislada y la localización de la infección. (AU)


Subject(s)
Microbial Sensitivity Tests/standards , Gram-Positive Cocci/drug effects , Staphylococcus/drug effects , Enterococcus/drug effects , Streptococcus/drug effects , Argentina
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