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Risk of ruling out severe acute respiratory syndrome by ruling in another diagnosis: variable incidence of atypical bacteria coinfection based on diagnostic assays.

Identifieur interne : 002348 ( PubMed/Corpus ); précédent : 002347; suivant : 002349

Risk of ruling out severe acute respiratory syndrome by ruling in another diagnosis: variable incidence of atypical bacteria coinfection based on diagnostic assays.

Auteurs : George Zahariadis ; Ted A. Gooley ; Phyllis Ryall ; Christine Hutchinson ; Mary I. Latchford ; Margaret A. Fearon ; Frances B. Jamieson ; Susan Richardson ; Theodore Kuschak ; Barbara Mederski

Source :

RBID : pubmed:16470249

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) caused the first epidemic of the 21st century and continues to threaten the global community.

DOI: 10.1155/2006/862797
PubMed: 16470249

Links to Exploration step

pubmed:16470249

Le document en format XML

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<name sortKey="Gooley, Ted A" sort="Gooley, Ted A" uniqKey="Gooley T" first="Ted A" last="Gooley">Ted A. Gooley</name>
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Chlamydophila Infections (complications)</term>
<term>Chlamydophila Infections (diagnosis)</term>
<term>Chlamydophila pneumoniae (isolation & purification)</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mycoplasma pneumoniae (isolation & purification)</term>
<term>Pneumonia, Bacterial (complications)</term>
<term>Pneumonia, Bacterial (diagnosis)</term>
<term>Pneumonia, Bacterial (epidemiology)</term>
<term>Pneumonia, Mycoplasma (complications)</term>
<term>Pneumonia, Mycoplasma (diagnosis)</term>
<term>Retrospective Studies</term>
<term>SARS Virus (isolation & purification)</term>
<term>Severe Acute Respiratory Syndrome (complications)</term>
<term>Severe Acute Respiratory Syndrome (diagnosis)</term>
<term>Severe Acute Respiratory Syndrome (epidemiology)</term>
</keywords>
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<term>Chlamydophila Infections</term>
<term>Pneumonia, Bacterial</term>
<term>Pneumonia, Mycoplasma</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Chlamydophila Infections</term>
<term>Pneumonia, Bacterial</term>
<term>Pneumonia, Mycoplasma</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Pneumonia, Bacterial</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en">
<term>Chlamydophila pneumoniae</term>
<term>Mycoplasma pneumoniae</term>
<term>SARS Virus</term>
</keywords>
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<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Retrospective Studies</term>
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<front>
<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) caused the first epidemic of the 21st century and continues to threaten the global community.</div>
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<PMID Version="1">16470249</PMID>
<DateCompleted>
<Year>2006</Year>
<Month>08</Month>
<Day>29</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Print">1198-2241</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>13</Volume>
<Issue>1</Issue>
<PubDate>
<MedlineDate>2006 Jan-Feb</MedlineDate>
</PubDate>
</JournalIssue>
<Title>Canadian respiratory journal</Title>
<ISOAbbreviation>Can. Respir. J.</ISOAbbreviation>
</Journal>
<ArticleTitle>Risk of ruling out severe acute respiratory syndrome by ruling in another diagnosis: variable incidence of atypical bacteria coinfection based on diagnostic assays.</ArticleTitle>
<Pagination>
<MedlinePgn>17-22</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Severe acute respiratory syndrome (SARS) caused the first epidemic of the 21st century and continues to threaten the global community.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To assess the incidence of coinfection in patients confirmed to have SARS-associated coronavirus (SARS-CoV) infection, and thus, to determine the risk of ruling out SARS by ruling in another diagnosis.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The present report is a retrospective study evaluating the incidence and impact of laboratory-confirmed SARS-CoV and other pulmonary pathogens in 117 patients. These patients were evaluated in a Toronto, Ontario, community hospital identified as the epicentre for the second SARS outbreak.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Coinfection with other pulmonary pathogens occurred in patients with SARS. Seventy-three per cent of the patient population evaluated had laboratory-confirmed SARS-CoV infection. Serology showing acute or recent Chlamydophila pneumoniae or Mycoplasma pneumoniae infection revealed an incidence of 30% and 9%, respectively, in those with SARS. These rates are similar to previously published studies on coinfection in pneumonia. All nucleic acid diagnostic assays were negative for C pneumoniae and M pneumoniae in respiratory samples from patients with SARS having serological evidence for these atypical pathogens.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Diagnostic assays for well-recognized pulmonary pathogens have limitations, and ruling out SARS-CoV by ruling in another pulmonary pathogen carries significant risk. Despite positive serology for atypical pathogens, in a setting where clinical suspicion for SARS is high, specific tests for SARS should be performed to confirm or exclude a diagnosis.</AbstractText>
</Abstract>
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<LastName>Zahariadis</LastName>
<ForeName>George</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>University of Alberta, Edmonton, Canada. georgez@ualberta.ca</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gooley</LastName>
<ForeName>Ted A</ForeName>
<Initials>TA</Initials>
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<Author ValidYN="Y">
<LastName>Ryall</LastName>
<ForeName>Phyllis</ForeName>
<Initials>P</Initials>
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<LastName>Hutchinson</LastName>
<ForeName>Christine</ForeName>
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<ForeName>Mary I</ForeName>
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<ForeName>Margaret A</ForeName>
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<Language>eng</Language>
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<GrantID>P30 CA015704</GrantID>
<Acronym>CA</Acronym>
<Agency>NCI NIH HHS</Agency>
<Country>United States</Country>
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