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1.
J Clin Oncol ; 19(14): 3415-21, 2001 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-11454890

RESUMO

PURPOSE: To identify clinical and laboratory parameters present at the time of a first evaluation that could help predict which children with cancer, fever, and neutropenia were at high risk or low risk for an invasive bacterial infection. PATIENTS AND METHODS: Over a 17-month period, all children with cancer, fever, and neutropenia admitted to five hospitals in Santiago, Chile, were enrolled onto a prospective protocol. Associations between admission parameters and risk for invasive bacterial infection were assessed by univariate and logistic regression analyses. RESULTS: A total of 447 febrile neutropenic episodes occurred in 257 children. Five parameters were statistically independent risk factors for an invasive bacterial infection. Ranked by order of significance, they were as follows: C-reactive protein levels of 90 mg/L or higher (relative risk [RR], 4.2; 95% confidence interval [CI], 3.6 to 4.8); presence of hypotension (RR, 2.7; 95% CI, 2.3 to 3.2); relapse of leukemia as cancer type (RR, 1.8, 95% CI, 1.7 to 2.3); platelet count less than or equal to 50,000/mm(3) (RR, 1.7; 95% CI, 1.4 to 2.2); and recent (< or = 7 days) chemotherapy (RR, 1.3; 95% CI, 1.1 to 1.6). Other previously postulated risk factors (magnitude of fever, monocyte count) were not independent risk factors in this study population. CONCLUSION: In a large population of children, common clinical and laboratory admission parameters were identified that can help predict the risk for an invasive bacterial infection. These results encourage the possibility of a more selective management strategy for these children.


Assuntos
Infecções Bacterianas/etiologia , Infecções Bacterianas/prevenção & controle , Febre/complicações , Neoplasias/complicações , Neutropenia/complicações , Síndrome de Resposta Inflamatória Sistêmica/etiologia , Síndrome de Resposta Inflamatória Sistêmica/prevenção & controle , Adolescente , Antibacterianos/uso terapêutico , Antineoplásicos/uso terapêutico , Infecções Bacterianas/epidemiologia , Proteína C-Reativa/metabolismo , Criança , Pré-Escolar , Feminino , Febre/imunologia , Febre/terapia , Humanos , Hipotensão/complicações , Lactente , Modelos Logísticos , Masculino , Neoplasias/tratamento farmacológico , Neoplasias/imunologia , Neutropenia/imunologia , Neutropenia/terapia , Estudos Prospectivos , Fatores de Risco , Síndrome de Resposta Inflamatória Sistêmica/epidemiologia
2.
Rev Med Chil ; 128(7): 758-65, 2000 Jul.
Artigo em Espanhol | MEDLINE | ID: mdl-11050837

RESUMO

BACKGROUND: Chlamydia trachomatis is one of the most common identifiable infectious agents in neonatal conjunctivitis. It also causes pneumonitis, that is preceded by conjunctivitis in one third of cases. AIM: To asses the prevalence of Chlamydia trachomatis in newborns with conjunctivitis. PATIENTS AND METHODS: In 162 newborns, coming from 14 Primary Health Centers from Santiago de Chile, C. trachomatis was detected by indirect fluorescence and two polymerase chain reaction (PCR 1 and 2), which amplified different sequences from the common endogenous plasmid. Those patients with positive indirect fluorescence and PCR 2 were defined as infected: RESULTS: The prevalence of C. trachomatis was 8%, and the distribution of the positive cases was similar in the different Health Centers. Other isolates were: S. aureus (9.8%), S. pneumoniae (8%), S. viridans (6.2%) y H. influenzae (5.5%). CONCLUSIONS: The prevalence of C. trachomatis in neonatal conjunctivitis in Chile is similar to that of developed countries. Therefore, C. trachomatis should be considered in the election of antimicrobials for the treatment of neonatal conjunctivitis, to avoid ocular and respiratory complications.


Assuntos
Chlamydia trachomatis/isolamento & purificação , Conjuntivite de Inclusão/microbiologia , Chile/epidemiologia , Chlamydia trachomatis/genética , Conjuntivite de Inclusão/diagnóstico , Conjuntivite de Inclusão/epidemiologia , DNA Bacteriano/análise , Ensaio de Imunoadsorção Enzimática , Feminino , Imunofluorescência , Amplificação de Genes , Humanos , Recém-Nascido , Masculino , Reação em Cadeia da Polimerase , Prevalência , Fatores de Risco , Sensibilidade e Especificidade
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