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Colonization Density of the Upper Respiratory Tract as a Predictor of Pneumonia-Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus, and Pneumocystis jirovecii.
Park, Daniel E; Baggett, Henry C; Howie, Stephen R C; Shi, Qiyuan; Watson, Nora L; Brooks, W Abdullah; Deloria Knoll, Maria; Hammitt, Laura L; Kotloff, Karen L; Levine, Orin S; Madhi, Shabir A; Murdoch, David R; O'Brien, Katherine L; Scott, J Anthony G; Thea, Donald M; Ahmed, Dilruba; Antonio, Martin; Baillie, Vicky L; DeLuca, Andrea N; Driscoll, Amanda J; Fu, Wei; Gitahi, Caroline W; Olutunde, Emmanuel; Higdon, Melissa M; Hossain, Lokman; Karron, Ruth A; Maiga, Abdoul Aziz; Maloney, Susan A; Moore, David P; Morpeth, Susan C; Mwaba, John; Mwenechanya, Musaku; Prosperi, Christine; Sylla, Mamadou; Thamthitiwat, Somsak; Zeger, Scott L; Feikin, Daniel R.
Afiliación
  • Park DE; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Baggett HC; Milken Institute School of Public Health, Department of Epidemiology and Biostatistics, George Washington University, Washington, District of Columbia.
  • Howie SRC; Global Disease Detection Center, Thailand Ministry of Public Health-US Centers for Disease Control and Prevention Collaboration, Nonthaburi.
  • Shi Q; Division of Global Health Protection, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Watson NL; Medical Research Council Unit, Basse, The Gambia.
  • Brooks WA; Department of Paediatrics, University of Auckland, and.
  • Deloria Knoll M; Centre for International Health, University of Otago, Dunedin, New Zealand.
  • Hammitt LL; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Kotloff KL; Emmes Corporation, Rockville, Maryland.
  • Levine OS; Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Madhi SA; International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka and Matlab.
  • Murdoch DR; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • O'Brien KL; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Scott JAG; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi.
  • Thea DM; Division of Infectious Disease and Tropical Pediatrics, Department of Pediatrics, Center for Vaccine Development, Institute of Global Health, University of Maryland School of Medicine, Baltimore.
  • Ahmed D; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Antonio M; Bill & Melinda Gates Foundation, Seattle, Washington.
  • Baillie VL; Medical Research Council, Respiratory and Meningeal Pathogens Research Unit, and.
  • DeLuca AN; Department of Science and Technology/National Research Foundation, Vaccine Preventable Diseases Unit, University of the Witwatersrand, Johannesburg, South Africa.
  • Driscoll AJ; Department of Pathology, University of Otago, and.
  • Fu W; Microbiology Unit, Canterbury Health Laboratories, Christchurch, New Zealand.
  • Gitahi CW; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Olutunde E; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi.
  • Higdon MM; Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, United Kingdom.
  • Hossain L; Center for Global Health and Development, Boston University School of Public Health, Massachusetts.
  • Karron RA; International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka and Matlab.
  • Maiga AA; Medical Research Council Unit, Basse, The Gambia.
  • Maloney SA; Department of Pathogen Molecular Biology, London School of Hygiene & Tropical Medicine, and.
  • Moore DP; Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Coventry, United Kingdom.
  • Morpeth SC; Medical Research Council, Respiratory and Meningeal Pathogens Research Unit, and.
  • Mwaba J; Department of Science and Technology/National Research Foundation, Vaccine Preventable Diseases Unit, University of the Witwatersrand, Johannesburg, South Africa.
  • Mwenechanya M; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Prosperi C; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health.
  • Sylla M; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Thamthitiwat S; Department of International Health, International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Zeger SL; Department of Rheumatology, Johns Hopkins School of Medicine, and.
  • Feikin DR; Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi.
Clin Infect Dis ; 64(suppl_3): S328-S336, 2017 Jun 15.
Article en En | MEDLINE | ID: mdl-28575367
ABSTRACT
BACKGROUND. There is limited information on the association between colonization density of upper respiratory tract colonizers and pathogen-specific pneumonia. We assessed this association for Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus, and Pneumocystis jirovecii. METHODS. In 7 low- and middle-income countries, nasopharyngeal/oropharyngeal swabs from children with severe pneumonia and age-frequency matched community controls were tested using quantitative polymerase chain reaction (PCR). Differences in median colonization density were evaluated using the Wilcoxon rank-sum test. Density cutoffs were determined using receiver operating characteristic curves. Cases with a pathogen identified from lung aspirate culture or PCR, pleural fluid culture or PCR, blood culture, and immunofluorescence for P. jirovecii defined microbiologically confirmed cases for the given pathogens. RESULTS. Higher densities of H. influenzae were observed in both microbiologically confirmed cases and chest radiograph (CXR)-positive cases compared to controls. Staphylococcus aureus and P. jirovecii had higher densities in CXR-positive cases vs controls. A 5.9 log10 copies/mL density cutoff for H. influenzae yielded 86% sensitivity and 77% specificity for detecting microbiologically confirmed cases; however, densities overlapped between cases and controls and positive predictive values were poor (<3%). Informative density cutoffs were not found for S. aureus and M. catarrhalis, and a lack of confirmed case data limited the cutoff identification for P. jirovecii. CONCLUSIONS. There is evidence for an association between H. influenzae colonization density and H. influenzae-confirmed pneumonia in children; the association may be particularly informative in epidemiologic studies. Colonization densities of M. catarrhalis, S. aureus, and P. jirovecii are unlikely to be of diagnostic value in clinical settings.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonía por Pneumocystis / Infecciones del Sistema Respiratorio / Staphylococcus aureus / Haemophilus influenzae / Moraxella catarrhalis / Neumonía Bacteriana / Pneumocystis carinii Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neumonía por Pneumocystis / Infecciones del Sistema Respiratorio / Staphylococcus aureus / Haemophilus influenzae / Moraxella catarrhalis / Neumonía Bacteriana / Pneumocystis carinii Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2017 Tipo del documento: Article