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<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" article-type="abstract"><?properties open_access?><front><journal-meta><journal-id journal-id-type="nlm-ta">Open Forum Infect Dis</journal-id><journal-id journal-id-type="iso-abbrev">Open Forum Infect Dis</journal-id><journal-id journal-id-type="publisher-id">ofid</journal-id><journal-title-group><journal-title>Open Forum Infectious Diseases</journal-title></journal-title-group><issn pub-type="epub">2328-8957</issn><publisher><publisher-name>Oxford University Press</publisher-name><publisher-loc>US</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmc">6252520</article-id><article-id pub-id-type="doi">10.1093/ofid/ofy210.1386</article-id><article-id pub-id-type="publisher-id">ofy210.1386</article-id><article-categories><subj-group subj-group-type="heading"><subject>Abstracts</subject><subj-group subj-group-type="category-toc-heading"><subject>Poster Abstracts</subject></subj-group></subj-group></article-categories><title-group><article-title>1558. Commensal <italic>Neisseria</italic> Species as a Cause of Disease in Patients Taking Eculizumab</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Crew</surname><given-names>Page</given-names></name><degrees>PharmD, MPH</degrees><xref ref-type="aff" rid="AF0001">1</xref></contrib><contrib contrib-type="author"><name><surname>McNamara</surname><given-names>Lucy</given-names></name><degrees>PhD, MS</degrees><xref ref-type="aff" rid="AF0002">2</xref></contrib><contrib contrib-type="author"><name><surname>Waldron</surname><given-names>Peter</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="AF0001">1</xref></contrib><contrib contrib-type="author"><name><surname>McCulley</surname><given-names>Lynda</given-names></name><degrees>PharmD</degrees><xref ref-type="aff" rid="AF0001">1</xref></contrib><contrib contrib-type="author"><name><surname>Jones</surname><given-names>S Christopher</given-names></name><degrees>PharmD, MS, MPH</degrees><xref ref-type="aff" rid="AF0001">1</xref></contrib><contrib contrib-type="author"><name><surname>Bersoff-Matcha</surname><given-names>Susan</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="AF0001">1</xref></contrib></contrib-group><aff id="AF0001"><label>1</label>Division of Pharmacovigilance, Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland</aff><aff id="AF0002"><label>2</label>National Center for Immunization and Respiratory Diseases, CDC, Atlanta, Georgia</aff><pub-date pub-type="collection"><month>11</month><year>2018</year></pub-date><pub-date pub-type="epub" iso-8601-date="2018-11-26"><day>26</day><month>11</month><year>2018</year></pub-date><pub-date pub-type="pmc-release"><day>26</day><month>11</month><year>2018</year></pub-date><!-- PMC Release delay is 0 months and 0 days and was based on the <pub-date pub-type="epub"/>. --><volume>5</volume><issue>Suppl 1</issue><issue-title>ID Week 2018 Abstracts</issue-title><fpage>S484</fpage><lpage>S485</lpage><permissions><copyright-statement>&#x000a9; The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</copyright-statement><copyright-year>2018</copyright-year><license license-type="cc-by-nc-nd" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/">http://creativecommons.org/licenses/by-nc-nd/4.0/</ext-link>), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com</license-p></license></permissions><self-uri xlink:href="ofy210.1386.pdf"/><abstract><title>Abstract</title><sec id="s1"><title>Background</title><p>Non-meningococcal and nongonococcal <italic>Neisseria</italic> spp. are usually commensal and rarely cause invasive disease in humans. Eculizumab, a terminal complement inhibitor, increases susceptibility to meningococcal disease, but data on atypical <italic>Neisseria</italic> spp. disease in persons receiving eculizumab are lacking. This case series describes postmarketing reports of disease by commensal <italic>Neisseria</italic> spp. in patients receiving eculizumab.</p></sec><sec id="s2"><title>Methods</title><p>The FDA Adverse Event Reporting System (FAERS) database and the medical literature were searched for cases of disease by any nonmeningococcal and nongonococcal <italic>Neisseria</italic> spp. in patients receiving eculizumab. Included cases had a diagnosis of disease by any atypical <italic>Neisseria</italic> spp. with onset on or before January 31, 2018 and &#x02265;1 dose of eculizumab in the 3 months prior to disease.</p></sec><sec id="s3"><title>Results</title><p>The search identified seven FAERS cases, including one case also reported in the literature. Patient ages ranged from 4 to 38 years. Five patients had positive blood cultures, of which three had an indwelling catheter for vascular access (<italic>n</italic> = 2, <italic>N. sicca/subflava</italic>) or hemodialysis (<italic>n</italic> = 1, <italic>N. cinerea</italic>). Two patients with bacteremia had <italic>N. cinerea</italic> septic shock with possible cholecystitis, and <italic>N. mucosa</italic> sepsis with concurrent <italic>Streptococcus</italic> bacteremia after gastroenteritis. The remaining two cases in the series included one with <italic>N. sicca</italic> bacterial peritonitis associated with a peritoneal dialysis catheter (negative blood cultures, other cultures not specified), and one with a diagnosis of <italic>N. flavescens</italic> sepsis while neutropenic (specimen source not specified). All seven patients were hospitalized and three had sepsis or septic shock. All cases resolved with antibiotics and supportive care.</p></sec><sec id="s4"><title>Conclusion</title><p>We identified seven cases of serious disease caused by atypical <italic>Neisseria</italic> spp. among eculizumab recipients. Since these organisms are typical inhabitants of the oropharynx and urogenital tract and are not skin flora, the source of disease was unclear. Our data suggest that eculizumab may confer increased risk for disease by usually commensal <italic>Neisseria</italic> spp. Healthcare professionals are encouraged to treat all <italic>Neisseria</italic> spp. isolated from sterile sites as pathogenic, and not as contaminants, in patients receiving eculizumab.</p><p>
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</p></sec><sec id="s5"><title>Disclosures</title><p>
<bold>All authors:</bold> No reported disclosures.</p></sec></abstract><counts><page-count count="2"/></counts></article-meta></front><back><notes id="n1"><p>
<bold>Session:</bold> 151. Viruses and Bacteria in Immunocompromised Patients</p><p>
<italic>Friday, October 5, 2018: 12:30 PM</italic>
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