<front xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.0/xsd/JATS-journalpublishing1.xsd">
	<journal-meta>
		<journal-id journal-id-type="publisher-id">CJIDMM</journal-id>
		<journal-title-group>
			<journal-title>Canadian Journal of Infectious Diseases and Medical Microbiology</journal-title>
		</journal-title-group>
		<issn pub-type="ppub">1712-9532</issn>
		<publisher>
			<publisher-name>Pulsus Group Inc</publisher-name>
		</publisher>
	</journal-meta>
	<article-meta>
		<article-id pub-id-type="publisher-id">201516</article-id>
		<article-id pub-id-type="doi">10.1155/2013/201516</article-id>
		<article-categories>
			<subj-group>
				<subject>Original Article</subject>
			</subj-group>
		</article-categories>
		<title-group>
			<article-title>Evaluation of MRSA<italic>Select</italic>
				<sup>&#x2122;</sup> Chromogenic Medium for the Early Detection of Methicillin-Resistant <italic>Staphylococcus aureus</italic> from Blood Cultures</article-title>
		</title-group>
		<contrib-group>
			<contrib contrib-type="author" id="U52935620">
				<name>
					<surname>Manickam</surname>
					<given-names>Kanchana</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U67017245">
				<name>
					<surname>Walkty</surname>
					<given-names>Andrew</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
				<xref ref-type="aff" rid="I3">
					<sup>3</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U24762147">
				<name>
					<surname>Lagac&#xe9;-Wiens</surname>
					<given-names>Philippe RS</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" corresp="yes" id="U25960501">
				<name>
					<surname>Adam</surname>
					<given-names>Heather</given-names>
				</name>
				<email>hadam@dsmanitoba.ca</email>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U31580816">
				<name>
					<surname>Swan</surname>
					<given-names>Barbara</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U32742641">
				<name>
					<surname>McAdam</surname>
					<given-names>Brenda</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U32479769">
				<name>
					<surname>Pieroni</surname>
					<given-names>Peter</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U12523436">
				<name>
					<surname>Alfa</surname>
					<given-names>Michelle</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
			</contrib>
			<contrib contrib-type="author" id="U52928057">
				<name>
					<surname>Karlowsky</surname>
					<given-names>James A</given-names>
				</name>
				<xref ref-type="aff" rid="I1">
					<sup>1</sup>
				</xref>
				<xref ref-type="aff" rid="I2">
					<sup>2</sup>
				</xref>
			</contrib>
		</contrib-group>
		<aff id="I1">
			<sup>1</sup>
			<addr-line>Microbiology</addr-line>
			<addr-line>Diagnostic Services of Manitoba</addr-line>
			<country>Canada</country>
			<ext-link ext-link-type="domain-name">dsmanitoba.ca</ext-link>
		</aff>
		<aff id="I2">
			<sup>2</sup>
			<addr-line>Department of Medical Microbiology</addr-line>
			<addr-line>Faculty of Medicine</addr-line>
			<addr-line>University of Manitoba</addr-line>
			<country>Canada</country>
			<ext-link ext-link-type="domain-name">umanitoba.ca</ext-link>
		</aff>
		<aff id="I3">
			<sup>3</sup>
			<addr-line>Department of Medicine</addr-line>
			<addr-line>Health Sciences Centre</addr-line>
			<addr-line>Winnipeg</addr-line>
			<addr-line>Manitoba</addr-line>
			<country>Canada</country>
			<ext-link ext-link-type="domain-name">hsc.mb.ca</ext-link>
		</aff>
		<pub-date pub-type="publication-year">
			<year>2013</year>
		</pub-date>
		<volume>24</volume>
		<issue>4</issue>
		<fpage>e113</fpage>
		<lpage>e116</lpage>
		<permissions>
			<copyright-year>2013</copyright-year>
			<copyright-holder>Copyright &#x00A9; 2013 Hindawi Publishing Corporation.</copyright-holder>
			<license license-type="open-access">
				<license-p>This is an open access article distributed under the <ext-link xlink:href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
			</license>
		</permissions>
		<abstract>
			<p>INTRODUCTION: <italic>Staphylococcus aureus</italic> bacteremia is associated with considerable morbidity and mortality. In theory, reducing the turnaround time in reporting of methicillin-resistant <italic>S aureus</italic> (MRSA) among patients with bactermia could assist with the rapid optimization of antimicrobial therapy.</p>
			<p>OBJECTIVE: To evaluate the sensitivity and specificity of MRSA<italic>Select</italic> (Bio-Rad Laboratories, USA), a chromogenic medium, in the early detection of MRSA from blood cultures growing Gram-positive cocci in clusters, and to confirm that routine use of this medium would, in fact, reduce turnaround time for MRSA identification.</p>
			<p>METHODS: The present study was conducted at three microbiology laboratories in Manitoba. Between April 2010 and May 2011, positive blood cultures with Gram-positive cocci in clusters visualized on Gram stain were subcultured to both MRSA<italic>Select</italic> and routine media. MRSA isolates were identified using conventional microbiological methods from routine media and using growth with the typical colony morphology (pink colony) on MRSA<italic>Select</italic> medium.</p>
			<p>RESULTS: A total of 490 blood cultures demonstrating Gram-positive cocci in clusters on Gram stain were evaluated. <italic>S aureus</italic> was recovered from 274 blood cultures, with 51 <italic>S aureus</italic> isolates (51 of 274 [18.6&#x25;]) identified as MRSA. MRSA<italic>Select</italic> medium had a sensitivity of 98&#x25;, a specificity of 100&#x25;, a positive predictive value of 100&#x25; and a negative predictive value of 99.8&#x25; for the recovery and identification of MRSA directly from positive blood culture bottles. In addition, use of MRSA<italic>Select</italic> medium was found to improve turnaround time in the detection of MRSA by almost 24 h relative to conventional methods.</p>
			<p>DISCUSSION: These data support the utility of MRSA<italic>Select</italic> medium for the rapid identification of MRSA from positive blood cultures. Further clinical studies are warranted to determine whether the improvement in turnaround time will result in a measurable reduction in suboptimal antimicrobial therapy and/or improvement in patient outcome.</p>
		</abstract>
		<kwd-group>
			<kwd>Blood cultures</kwd>
			<kwd>Chromogenic agar</kwd>
			<kwd>MRSA</kwd>
			<kwd>
				<italic>Staphylococcus aureus</italic>
			</kwd>
		</kwd-group>
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			<ref-count count="23"/>
			<page-count count="4"/>
		</counts>
	</article-meta>
</front>
