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1.
Antimicrob Agents Chemother ; 40(4): 895-8, 1996 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8849247

RESUMO

In June 1993, the National Committee for Clinical Laboratory Standards (NCCLS) recommended stringent new interpretive guidelines for antibiotics indicated for Streptococcus pneumoniae meningitis. To assess the predictive values of the recommended breakpoints, retrospective data were collected from patients who had S. pneumoniae infections and were treated with cefotaxime monotherapy. Susceptibilities based on the NCCLS interpretative categories were compared with clinical and bacteriologic outcomes. In 76 evaluable patients, the most common infections were bacteremia-septicemia (n = 49), meningitis (n = 37), and lower respiratory tract infection (n = 14). Under the NCCLS breakpoints proposed in 1993, 55 isolates would have been classed as susceptible to cefotaxime (MIC, < or = 0.25 microgram/ml), 18 would have been classed as intermediate (MIC, 0.5 to 1.0 microgram/ml), and 2 would have been classed as resistant (MIC, > or = 2 micrograms/ml). Of 75 cefotaxime-treated patients for whom cefotaxime MICs were recorded, 73 were clinically cured or improved (37 of 37 with meningitis and 36 of 38 with other infections). One case of bacteremia and one case of bone-and-joint infection were scored as therapeutic failures because initial monotherapy had to be modified because of an adverse drug reaction. Excluding these patients, there were 18 patients infected with S. pneumoniae that would have been classed as not fully susceptible (i.e., MICs > or = 0.5 microgram/ml); all of these patients were cured or improved. The results of this analysis demonstrate that successful treatment with cefotaxime did not correlate well with the guidelines for the susceptibility of pneumococcal isolates to either penicillin or cefotaxime established by the 1993 NCCLS breakpoint recommendations. Because of this study and other similar findings, the NCCLS adopted more clinically relevant guidelines in 1994.


Assuntos
Bacteriemia/tratamento farmacológico , Cefotaxima/uso terapêutico , Cefalosporinas/uso terapêutico , Meningite Pneumocócica/tratamento farmacológico , Streptococcus pneumoniae/efeitos dos fármacos , Idoso , Cefotaxima/farmacologia , Resistência às Cefalosporinas , Cefalosporinas/farmacologia , Feminino , Humanos , Lactente , Masculino , Testes de Sensibilidade Microbiana , Guias de Prática Clínica como Assunto
2.
Diagn Microbiol Infect Dis ; 22(1-2): 105-10, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7587022

RESUMO

Cefotaxime has been used extensively in many pediatric centers in the United States for the past 10 or more years. Its main usage has been for the treatment of various serious bacterial infections in pediatric patients, primarily meningitis and sepsis. It has also been used to treat intraabdominal, urinary tract, soft tissue, bone, and joint infections. Although there has been a marked reduction in the incidence of invasive Haemophilus influenzae type b infections following the introduction of effective vaccines, cefotaxime remains very useful against the other common pathogens causing serious infections in pediatric patients. The increasing number of pneumococci resistant to penicillin and third-generation cephalosporins has created a new challenge for the management of serious pneumococcal infections. In many institutions, cephalosporins in general have been overused and abused, resulting in the emergence of resistant organisms and an increasing burden on resources. The judicious use of cefotaxime and other cephalosporins should be emphasized.


Assuntos
Infecções Bacterianas/tratamento farmacológico , Cefotaxima/uso terapêutico , Cefalosporinas/uso terapêutico , Meningite por Haemophilus/tratamento farmacológico , Meningite Pneumocócica/tratamento farmacológico , Infecções Bacterianas/microbiologia , Cefotaxima/administração & dosagem , Cefotaxima/farmacologia , Cefalosporinas/administração & dosagem , Cefalosporinas/farmacologia , Ensaios Clínicos como Assunto , Resistência Microbiana a Medicamentos , Humanos , Lactente , Testes de Sensibilidade Microbiana
4.
Pediatr Infect Dis J ; 12(4): 275-9, 1993 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-8483620

RESUMO

This multicenter, randomized, parallel treatment, observer-blinded study was designed to evaluate the safety and efficacy of cefpodoxime proxetil (5 mg/kg twice daily for 10 days) compared with penicillin V (13.4 mg/kg three times daily for 10 days) for treatment of Group A streptococcal pharyngitis and tonsillitis in pediatric patients. Clinical and microbiologic results were evaluated before therapy, during therapy (Study Days 3 to 5), at the end of therapy (Study Days 14 to 18) and at long term follow-up (Study Days 30 to 32). Both drugs were well-tolerated in 578 patients evaluable for safety. Mild gastrointestinal complaints were noted in 6.7% of 386 cefpodoxime-treated patients and in 5.2% of 192 penicillin-treated patients. In 413 patients evaluable for efficacy, both treatment regimens resulted in comparably favorable clinical outcome; cure rates were 83.8% for 275 cefpodoxime-treated patients and 77.5% for 138 penicillin-treated patients. However, eradication of S. pyogenes at end of therapy was significantly higher with cefpodoxime (93.1%) than with penicillin (81.2%) (P < 0.01). Cefpodoxime proxetil provides an effective alternative to penicillin V for the treatment of streptococcal pharyngitis and tonsillitis.


Assuntos
Ceftizoxima/análogos & derivados , Penicilina V/uso terapêutico , Faringite/tratamento farmacológico , Infecções Estreptocócicas/tratamento farmacológico , Streptococcus pyogenes/efeitos dos fármacos , Tonsilite/tratamento farmacológico , Adolescente , Ceftizoxima/efeitos adversos , Ceftizoxima/uso terapêutico , Criança , Pré-Escolar , Esquema de Medicação , Avaliação de Medicamentos , Feminino , Humanos , Lactente , Masculino , Testes de Sensibilidade Microbiana , Penicilina V/efeitos adversos , Faringite/microbiologia , Método Simples-Cego , Estatística como Assunto , Tonsilite/microbiologia , Resultado do Tratamento , Cefpodoxima Proxetil
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