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{\u0022basePath\u0022:\u0022\\\/\u0022,\u0022pathPrefix\u0022:\u0022\u0022,\u0022highwire\u0022:{\u0022markup\u0022:[{\u0022requested\u0022:\u0022full-text\u0022,\u0022variant\u0022:\u0022full-text\u0022,\u0022view\u0022:\u0022full\u0022,\u0022pisa\u0022:\u0022spmdc;14\\\/28\\\/26\u0022},{\u0022requested\u0022:\u0022long\u0022,\u0022variant\u0022:\u0022full-text\u0022,\u0022view\u0022:\u0022full\u0022,\u0022pisa\u0022:\u0022spmdc;14\\\/28\\\/26\u0022}],\u0022ac\u0022:{\u0022spmdc;14\\\/28\\\/26\u0022:{\u0022access\u0022:{\u0022reprint\u0022:true,\u0022full\u0022:true},\u0022pisa_id\u0022:\u0022spmdc;14\\\/28\\\/26\u0022,\u0022atom_uri\u0022:\u0022\u0022,\u0022jcode\u0022:\u0022spmdc\u0022}}},\u0022googleanalytics\u0022:{\u0022trackOutbound\u0022:1,\u0022trackMailto\u0022:1,\u0022trackDownload\u0022:1,\u0022trackDownloadExtensions\u0022:\u00227z|aac|arc|arj|asf|asx|avi|bin|csv|doc(x|m)?|dot(x|m)?|exe|flv|gif|gz|gzip|hqx|jar|jpe?g|js|mp(2|3|4|e?g)|mov(ie)?|msi|msp|pdf|phps|png|ppt(x|m)?|pot(x|m)?|pps(x|m)?|ppam|sld(x|m)?|thmx|qtm?|ra(m|r)?|sea|sit|tar|tgz|torrent|txt|wav|wma|wmv|wpd|xls(x|m|b)?|xlt(x|m)|xlam|xml|z|zip\u0022,\u0022trackUrlFragments\u0022:1},\u0022ajaxPageState\u0022:{\u0022js\u0022:{\u0022sites\\\/all\\\/libraries\\\/cluetip\\\/jquery.cluetip.js\u0022:1,\u0022sites\\\/all\\\/libraries\\\/cluetip\\\/lib\\\/jquery.hoverIntent.js\u0022:1,\u0022sites\\\/all\\\/libraries\\\/cluetip\\\/lib\\\/jquery.bgiframe.min.js\u0022:1,\u0022sites\\\/all\\\/modules\\\/highwire\\\/highwire\\\/plugins\\\/highwire_markup_process\\\/js\\\/highwire_at_symbol.js\u0022:1,\u0022sites\\\/all\\\/modules\\\/highwire\\\/highwire\\\/plugins\\\/highwire_markup_process\\\/js\\\/highwire_article_reference_popup.js\u0022:1,\u0022sites\\\/all\\\/modules\\\/contrib\\\/google_analytics\\\/googleanalytics.js\u0022:1,\u00220\u0022:1}}});\n\/\/--\u003E\u003C!]]\u003E\n\u003C\/script\u003E\n\u003Clink type=\u0022text\/css\u0022 rel=\u0022stylesheet\u0022 href=\u0022\/\/d282kpwvnogo5m.cloudfront.net\/sites\/default\/files\/cdn\/css\/http\/css_Xg7z6oCTVgud_Q0huYz9x9iiD5H_2YPSJ5z2ZViSWdY.css\u0022 media=\u0022all\u0022 \/\u003E\n\u003Clink rel=\u0027stylesheet\u0027 type=\u0027text\/css\u0027 href=\u0027\/sites\/all\/modules\/contrib\/panels\/plugins\/layouts\/onecol\/onecol.css\u0027 \/\u003E\u003C\/head\u003E\u003Cbody\u003E\u003Cdiv class=\u0022panels-ajax-tab-panel panels-ajax-tab-panel-sageoa-tab-art\u0022\u003E\u003Cdiv class=\u0022panel-display panel-1col clearfix\u0022 \u003E\n  \u003Cdiv class=\u0022panel-panel panel-col\u0022\u003E\n    \u003Cdiv\u003E\u003Cdiv class=\u0022panel-pane pane-highwire-markup\u0022 \u003E\n  \n      \n  \n  \u003Cdiv class=\u0022pane-content\u0022\u003E\n    \u003Cdiv class=\u0022highwire-markup\u0022\u003E\u003Cdiv xmlns=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022 id=\u0022content-block-markup\u0022 xmlns:xhtml=\u0022http:\/\/www.w3.org\/1999\/xhtml\u0022\u003E\u003Cdiv class=\u0022article fulltext-view \u0022\u003E\u003Cspan class=\u0022highwire-journal-article-marker-start\u0022\u003E\u003C\/span\u003E\u003Cdiv class=\u0022section abstract\u0022 id=\u0022abstract-1\u0022\u003E\u003Ch2\u003ESummary\u003C\/h2\u003E\n            \u003Cp id=\u0022p-1\u0022\u003EInvasive fungal disease warrants special considerations in special populations, such as children, patients being cared for in the intensive care unit (ICU), and patients who have undergone transplantation. This article discusses issues in pediatric candidiasis, fungal infections in the intensive care unit, as well as how to effectively use the clinical microbiology laboratory to address fungal infections in solid organ and bone marrow transplant patients.\u003C\/p\u003E\n         \u003C\/div\u003E\u003Cul class=\u0022kwd-group\u0022\u003E\u003Cli class=\u0022kwd\u0022\u003EFungal Infections\u003C\/li\u003E\u003C\/ul\u003E\u003Cul class=\u0022kwd-group clinical-trial\u0022\u003E\u003Cli class=\u0022kwd\u0022\u003EInfectious Disease\u003C\/li\u003E\u003Cli class=\u0022kwd\u0022\u003EFungal Infections\u003C\/li\u003E\u003C\/ul\u003E\u003Cp id=\u0022p-2\u0022\u003EInvasive fungal disease warrants special considerations in special populations, such as children, patients being cared for in the intensive care unit (ICU), and patients who have undergone transplantation. William J. Steinbach, MD, Duke University School of Medicine, Durham, North Carolina, USA, discussed issues in pediatric candidiasis.\u003C\/p\u003E\u003Cp id=\u0022p-3\u0022\u003EIn pediatric patients, \u003Cem\u003ECandida glabrata\u003C\/em\u003E resistance to echinocandins and fluconazole is rising. The SENTRY global surveillance study conducted between 2006 and 2010 demonstrated fluconazole resistance in 9.7% of isolates; 98.8% of those were not susceptible to voriconazole, and 11.1% were also resistant to \u2265 1 echinocandin [Pfaller MA et al. \u003Cem\u003EJ Clin Microbiol\u003C\/em\u003E. 2012]. In contrast, echinocandin resistance was not detected between 2001 and 2004 in 110 \u003Cem\u003EC. glabrata\u003C\/em\u003E isolates that were resistant to fluconazole. In a study conducted at Duke, among 293 cases of \u003Cem\u003EC. glabrata\u003C\/em\u003E candidemia in adults between 2001 and 2010, echinocandin and fluconazole resistance increased by 7.4% and 12.1%, respectively (\u003Ca id=\u0022xref-fig-1-1\u0022 class=\u0022xref-fig\u0022 href=\u0022#F1\u0022\u003EFigure 1\u003C\/a\u003E) [Alexander BD et al. \u003Cem\u003EClin Infect Dis.\u003C\/em\u003E 2013]. In a retrospective study of 344 pediatric cases of candidemia, independent risk factors for pediatric \u003Cem\u003EC. glabrata\u003C\/em\u003E or \u003Cem\u003ECandida krusei\u003C\/em\u003E infection were age \u0026gt; 2 years, exposure to fluconazole in the past 15 days, or recent surgery in the past 15 days [Prasad PA et al. \u003Cem\u003EJ Pediatric Infect Dis Soc.\u003C\/em\u003E 2013].\u003C\/p\u003E\u003Cdiv id=\u0022F1\u0022 class=\u0022fig pos-float  odd\u0022\u003E\u003Cdiv class=\u0022highwire-figure\u0022\u003E\u003Cdiv class=\u0022fig-inline-img-wrapper\u0022\u003E\u003Cdiv class=\u0022fig-inline-img\u0022\u003E\u003Ca href=\u0022http:\/\/d282kpwvnogo5m.cloudfront.net\/content\/spmdc\/14\/28\/26\/F1.large.jpg?width=800\u0026amp;height=600\u0026amp;carousel=1\u0022 title=\u0022Resistance rates of Candida glabrata to echinocandins and fluconazole\u0022 class=\u0022fragment-images colorbox-load\u0022 rel=\u0022gallery-fragment-images-1336275638\u0022 data-figure-caption=\u0022\u0026amp;lt;div xmlns=\u0026amp;quot;http:\/\/www.w3.org\/1999\/xhtml\u0026amp;quot;\u0026amp;gt;Resistance rates of \u0026amp;lt;em\u0026amp;gt;Candida glabrata\u0026amp;lt;\/em\u0026amp;gt; to echinocandins and fluconazole\u0026amp;lt;\/div\u0026amp;gt;\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003E\u003Cimg class=\u0022fragment-image\u0022 alt=\u0022Figure 1.\u0022 src=\u0022http:\/\/d282kpwvnogo5m.cloudfront.net\/content\/spmdc\/14\/28\/26\/F1.medium.gif\u0022\/\u003E\u003C\/a\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cul class=\u0022highwire-figure-links inline\u0022\u003E\u003Cli class=\u00220 first\u0022\u003E\u003Ca href=\u0022http:\/\/d282kpwvnogo5m.cloudfront.net\/content\/spmdc\/14\/28\/26\/F1.large.jpg?download=true\u0022 class=\u0022highwire-figure-link highwire-figure-link-download\u0022 title=\u0022Download Figure 1.\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload figure\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00221\u0022\u003E\u003Ca href=\u0022http:\/\/d282kpwvnogo5m.cloudfront.net\/content\/spmdc\/14\/28\/26\/F1.large.jpg\u0022 class=\u0022highwire-figure-link highwire-figure-link-newtab\u0022 target=\u0022_blank\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EOpen in new tab\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00222 last\u0022\u003E\u003Ca href=\u0022\/highwire\/powerpoint\/11846\u0022 class=\u0022highwire-figure-link highwire-figure-link-ppt\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload powerpoint\u003C\/a\u003E\u003C\/li\u003E\u003C\/ul\u003E\u003C\/div\u003E\u003Cdiv class=\u0022fig-caption attrib\u0022\u003E\u003Cspan class=\u0022fig-label\u0022\u003EFigure 1.\u003C\/span\u003E \n            \u003Cp id=\u0022p-4\u0022 class=\u0022first-child\u0022\u003EResistance rates of \u003Cem\u003ECandida glabrata\u003C\/em\u003E to echinocandins and fluconazole\u003C\/p\u003E\n         \u003Cq class=\u0022attrib\u0022 id=\u0022attrib-1\u0022\u003EReproduced from \u003Cem\u003EClin Infect Dis\u003C\/em\u003E, Alexander BD, Increasing Echinocandin Resistance in \u003Cem\u003ECandida glabrata\u003C\/em\u003E: Clinical Failure Correlates With Presence of FKS Mutations and Elevated Minimum Inhibitory Concentrations, 2014;56:1724\u20131732, Copyright 2014, with permission from Infectious Diseases Society of America.\u003C\/q\u003E\u003Cdiv class=\u0022sb-div caption-clear\u0022\u003E\u003C\/div\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cp id=\u0022p-5\u0022\u003EAnother issue is that there are no pediatric-specific diagnostic recommendations for invasive candidiasis (IC) in the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) guideline [Hope WW et al. \u003Cem\u003EClin Microbiol Infect\u003C\/em\u003E. 2012]. In adults, 3 daily blood cultures for a total of 40 to 60 mL are recommended [Cuenca-Estrella M et al. \u003Cem\u003EClin Microbiol Infect\u003C\/em\u003E. 2012]; however, this guideline cannot be followed for pediatric patients due to lower blood volume. In addition, the diagnostic sensitivity of blood cultures is not high; for example, the sensitivity for all candidiasis is estimated to be 50% in adults, and the sensitivity is unknown in children [Clancy CJ et al. \u003Cem\u003EClin Infect Dis\u003C\/em\u003E 2013]. Dr Steinbach suggested that the sensitivity is likely lower because of the lower blood volume in children. In addition, there are few studies of molecular diagnostics for \u003Cem\u003ECandida\u003C\/em\u003E in children. Only case reports or case series have been published using the Fungitell (1\u21923)-\u03b2-glucan assay; there are no published reports for use of the Platelia Candida mannan antigen and anti-mannan antibody assay, polymerase chain reaction (PCR) for \u003Cem\u003ECandida\u003C\/em\u003E, and the T2Candida test in children. In a meta-analysis of the Fungitell (1\u21923)-\u03b2-glucan assay in adults, the sensitivity for 2 consecutive tests was 49.6% (95% CI, 34 to 65.3), and the specificity was 98.9% (95% CI, 97.4 to 99.5) [Lamoth F et al. \u003Cem\u003EClin Infect Dis.\u003C\/em\u003E 2012]. The positive predictive value was 83.5%, and the negative predictive value was 94.6%. In a study of 120 nonimmunocompromised pediatric patients with a mean age of 9.2 years, the mean value of beta-glucan was higher (68 pg\/mL) than what was previously reported for adults (48 pg\/mL) [Smith PB et al. \u003Cem\u003EClin Vaccine Immunol\u003C\/em\u003E. 2007]. Several other small studies or case reports have been published; 1 study of 61 neonates found that the optimal cutoff value was 125 pg\/mL [Goudjil S et al. \u003Cem\u003EJ Matern Fetal Neonatal Med.\u003C\/em\u003E 2013].\u003C\/p\u003E\u003Cp id=\u0022p-6\u0022\u003EThe 2012 ESCMID guideline for the diagnosis and treatment of \u003Cem\u003ECandida\u003C\/em\u003E diseases includes a discussion on the treatment of IC in children [Hope WW et al. \u003Cem\u003EClin Microbiol Infect\u003C\/em\u003E. 2012]. In nonneutropenic adults, an echinocandin is recommended for patients who have moderate to severe disease or had recent exposure to an azole agent, whereas fluconazole is recommended for patients who are less critically ill and had no recent azole exposure. Dr Steinbach highlighted that treatment of \u003Cem\u003ECandida\u003C\/em\u003E in children generally follows this recommendation, but there is a lack of evidence to support its use. Dr Steinbach outlined what he does in practice. For a fluconazole loading dose, he administers 25 mg\/kg on day 1, followed by 12 mg\/kg\/d. In children on extracorporeal membrane oxygenation, he administers a 35 mg\/kg loading dose, followed by 12 mg\/kg\/d.\u003C\/p\u003E\u003Cp id=\u0022p-7\u0022\u003EThere are dosing issues in children. For caspofungin, a body surface area dosing scheme is used; for micafungin, age is important to consider because the drug\u0027s clearance increases substantially in younger patients, particularly neonates; and there has been only 1 pharmacokinetic study in children for anidulafungin. In this study, anidulafungin was cleared more quickly in children according to a nonlinear association with weight; therefore, higher doses are likely needed as weight decreases to achieve equivalent drug exposure [Hope WW et al. \u003Cem\u003EAntimicrob Agents Chemother\u003C\/em\u003E. 2007]. Voriconazole pharmacokinetics also differs in children. The adult bioavailability is 96%, whereas the pediatric bioavailability is 44.6% [Karisson MO et al. \u003Cem\u003EAntimicrob Agents Chemother\u003C\/em\u003E. 2009]. For oral voriconazole, lower peak concentrations were observed in children ages 2 to 5 years compared to children 6 to 11 years; 1 cohort received 4 mg\/kg IV q12h, then 6 mg\/kg IV q12h, and then 4 mg\/kg orally q12h, and the other cohort received 6 mg\/kg IV q12h, then 8 mg\/kg IV q12h, and then 6 mg\/kg orally q12h [Walsh TJ et al. \u003Cem\u003EAntimicrob Agents Chemother\u003C\/em\u003E. 2010]. In a study of pediatric patients in Japan, children age \u0026lt; 3 years needed a greater oral dose compared with children \u2265 3 years [Shima H et al. \u003Cem\u003EPediatr Blood Cancer\u003C\/em\u003E. 2010]. Based on the available data, the optimal dosing of IV and oral voriconazole is dependent on age (\u003Ca id=\u0022xref-table-wrap-1-1\u0022 class=\u0022xref-table\u0022 href=\u0022#T1\u0022\u003ETable 1\u003C\/a\u003E).\u003C\/p\u003E\u003Cdiv id=\u0022T1\u0022 class=\u0022table pos-float\u0022\u003E\u003Cdiv class=\u0022table-inline\u0022\u003E\u003Cdiv class=\u0022callout\u0022\u003E\u003Cspan\u003EView this table:\u003C\/span\u003E\u003Cul class=\u0022callout-links\u0022\u003E\u003Cli class=\u00220 first\u0022\u003E\u003Ca href=\u0022\/\u0022 class=\u0022table-expand-inline\u0022 data-table-url=\u0022\/highwire\/markup\/11847\/expansion?postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media%2Chighwire_embed\u0026amp;table-expand-inline=1\u0022 html=\u00221\u0022 fragment=\u0022#\u0022 external=\u00221\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView inline\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00221\u0022\u003E\u003Ca href=\u0022\/highwire\/markup\/11847\/expansion?width=1000\u0026amp;height=500\u0026amp;iframe=true\u0026amp;postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media\u0022 class=\u0022colorbox colorbox-load table-expand-popup\u0022 rel=\u0022gallery-fragment-tables\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView popup\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00222 last\u0022\u003E\u003Ca href=\u0022\/highwire\/powerpoint\/11847\u0022 class=\u0022highwire-figure-link highwire-figure-link-ppt\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload powerpoint\u003C\/a\u003E\u003C\/li\u003E\u003C\/ul\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cdiv class=\u0022table-caption\u0022\u003E\u003Cspan class=\u0022table-label\u0022\u003ETable 1.\u003C\/span\u003E \n            \u003Cp id=\u0022p-8\u0022 class=\u0022first-child\u0022\u003EDosing of Voriconazole for Pediatric Patients\u003C\/p\u003E\n         \u003Cdiv class=\u0022sb-div caption-clear\u0022\u003E\u003C\/div\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cp id=\u0022p-10\u0022\u003ELuis Ostrosky-Zeichner, MD, University of Texas Health Science Center, Houston, Texas, USA, discussed fungal infections in the intensive care unit (ICU). According to the EPIC II survey, 17% of infections in the ICU population are \u003Cem\u003ECandida\u003C\/em\u003E, and 1.4% are \u003Cem\u003EAspergillus\u003C\/em\u003E [Vincent JL et al. \u003Cem\u003EJAMA\u003C\/em\u003E. 2009].\u003C\/p\u003E\u003Cp id=\u0022p-11\u0022\u003EA major problem related to fungal infections in the ICU is diagnostic capabilities. Traditional diagnostic techniques such as blood cultures are not reliable, because 50% of patients with \u003Cem\u003ECandida\u003C\/em\u003E will have a negative blood culture for \u003Cem\u003ECandida\u003C\/em\u003E, and most blood cultures will test negative for \u003Cem\u003EAspergillus\u003C\/em\u003E and \u003Cem\u003EMucor\u003C\/em\u003E in patients with invasive fungal infections (IFIs) [Ostrosky-Zeichner L. \u003Cem\u003EAm J Med.\u003C\/em\u003E 2012]. Tissue biopsies and other types of cultures are not always feasible, and contamination can be a problem. To maximize the sensitivity of blood culturing, it is important to use the latest, most advanced techniques, including those that are automated.\u003C\/p\u003E\u003Cp id=\u0022p-12\u0022\u003EMarkers such as \u003Cem\u003ECandida\u003C\/em\u003E-specific antigens, including mannan antigen and anti-mannan antibody, are primarily used in Europe, but they have been shown to have 75% to 100% specificity and 52% to 83% sensitivity for candidemia [Arendrup MC et al. \u003Cem\u003EClin Microbiol Infect\u003C\/em\u003E. 2010]. \u003Cem\u003ECandida\u003C\/em\u003E PCR is a promising methodology, and a meta-analysis of \u003Cem\u003ECandida\u003C\/em\u003E PCR concluded that the more stringent the criteria for the positive and negative controls, the better the results of this technique to diagnose IC [Avni T et al. \u003Cem\u003EJ Clin Microbiol\u003C\/em\u003E. 2011]. Another molecular-based diagnostic assay uses the T2 detection technology, which has been reported to have extremely high sensitivity and specificity for several \u003Cem\u003ECandida\u003C\/em\u003E species to diagnose candidemia [Beyda ND et al. \u003Cem\u003EDiag Microbiol Infect Dis.\u003C\/em\u003E 2013]. A large, multicenter validation study evaluating the T2 detection technology is expected to be published in late 2014 or early 2015. A meta-analysis showed that the \u03b2-D-glucan marker was a good marker for IFI, with sensitivity and specificity rates of 76.8% and 85.3%, respectively, to distinguish proven or probable IFI vs no IFI [Karageorgopoulos DE et al. \u003Cem\u003EClin Infect Dis.\u003C\/em\u003E 2011].\u003C\/p\u003E\u003Cp id=\u0022p-13\u0022\u003EA diagnostic marker for \u003Cem\u003EAspergillus\u003C\/em\u003E is galactomannan, which has been demonstrated to have a sensitivity rate of 85% in patients with proven fungal disease and a specificity of 70% [Marr KA et al. \u003Cem\u003EClin Infect Dis.\u003C\/em\u003E 2005]. For \u003Cem\u003EAspergillus\u003C\/em\u003E PCR, a recent meta-analysis demonstrated that it has a sensitivity of about 90% and specificity in the 80% range for invasive aspergillosis [Arvanitis M et al. \u003Cem\u003EJ Clin Microbiol\u003C\/em\u003E. 2014]. High-resolution computed tomography (CT) can have good sensitivity as well, and classic signs of invasive \u003Cem\u003EAspergillus\u003C\/em\u003E infection include the presence of a \u201chalo,\u201d crescent, nodules, ground glass, and cavitation [Gotway MB et al. \u003Cem\u003EJ Comput Assist Tomogr\u003C\/em\u003E. 2002]. Dr Ostrosky-Zeichner stated that we need to move away from treating full-blown disease and move toward preventing fungal infection and engaging in preemptive treatment of early disease.\u003C\/p\u003E\u003Cp id=\u0022p-14\u0022\u003EKimberly E. Hanson, MD, MHS, University of Utah, Salt Lake City, Utah, USA, used case studies to illustrate how to effectively use the clinical microbiology laboratory to address fungal infections in solid organ and bone marrow transplant patients. In 1 case, a 29-year-old man with aplastic anemia presented with painful skin lesions and sinusitis. Histopathologic analysis of skin biopsies taken from the lesions showed invasive fungal elements and septated fungal hyphae. Dr Hanson pointed out that, microscopically, it is impossible to distinguish between different fungal genera, because septated hyphae with acute angle branching are a common characteristic of many species. Panfungal PCR followed by DNA sequencing of tissue samples can be used to differentiate among species. In terms of growing cultures, clues for clinical significance include fungal elements on direct staining, a site of isolation from the host, the same fungus is isolated from multiple specimens, and multiple colonies grow from the same specimen.\u003C\/p\u003E\u003Cp id=\u0022p-15\u0022\u003ETo identify the species, DNA sequencing can be used; however, the regions most commonly used in sequencing are highly conserved in \u003Cem\u003EFusaria\u003C\/em\u003E, and therefore dedicated PCR targets are needed. It is important to identify the specific species because the susceptibility profile can be different. One study found that the minimum inhibitory concentration (MIC) at 50% ranged between 2 and 4 \u03bcg\/mL for amphotericin, and between 4 and 8 \u03bcg\/mL for voriconazole, and it was \u0026gt; 16 \u03bcg\/mL for posaconazole (\u003Ca id=\u0022xref-table-wrap-2-1\u0022 class=\u0022xref-table\u0022 href=\u0022#T2\u0022\u003ETable 2\u003C\/a\u003E) [Espinel-Ingroff A et al. \u003Cem\u003EJ Clin Microbiol\u003C\/em\u003E. 2007]. Antifungal susceptibility testing is important to determine treatment options, to rule out secondary resistance after prolonged exposure to the drug, and to rule out resistance when the infection is refractory to treatment.\u003C\/p\u003E\u003Cdiv id=\u0022T2\u0022 class=\u0022table pos-float\u0022\u003E\u003Cdiv class=\u0022table-inline\u0022\u003E\u003Cdiv class=\u0022callout\u0022\u003E\u003Cspan\u003EView this table:\u003C\/span\u003E\u003Cul class=\u0022callout-links\u0022\u003E\u003Cli class=\u00220 first\u0022\u003E\u003Ca href=\u0022\/\u0022 class=\u0022table-expand-inline\u0022 data-table-url=\u0022\/highwire\/markup\/11848\/expansion?postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media%2Chighwire_embed\u0026amp;table-expand-inline=1\u0022 html=\u00221\u0022 fragment=\u0022#\u0022 external=\u00221\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView inline\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00221\u0022\u003E\u003Ca href=\u0022\/highwire\/markup\/11848\/expansion?width=1000\u0026amp;height=500\u0026amp;iframe=true\u0026amp;postprocessors=highwire_figures%2Chighwire_math%2Chighwire_inline_linked_media\u0022 class=\u0022colorbox colorbox-load table-expand-popup\u0022 rel=\u0022gallery-fragment-tables\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView popup\u003C\/a\u003E\u003C\/li\u003E\u003Cli class=\u00222 last\u0022\u003E\u003Ca href=\u0022\/highwire\/powerpoint\/11848\u0022 class=\u0022highwire-figure-link highwire-figure-link-ppt\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EDownload powerpoint\u003C\/a\u003E\u003C\/li\u003E\u003C\/ul\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cdiv class=\u0022table-caption\u0022\u003E\u003Cspan class=\u0022table-label\u0022\u003ETable 2.\u003C\/span\u003E \n            \u003Cp id=\u0022p-16\u0022 class=\u0022first-child\u0022\u003EAntifungal Susceptibility Profile for \u003Cem\u003EFusarium\u003C\/em\u003E spp\u003C\/p\u003E\n         \u003Cdiv class=\u0022sb-div caption-clear\u0022\u003E\u003C\/div\u003E\u003C\/div\u003E\u003C\/div\u003E\u003Cp id=\u0022p-19\u0022\u003EIn patients who have undergone solid organ transplants, the most common \u003Cem\u003ECandida\u003C\/em\u003E species that cause infection are \u003Cem\u003ECandida albicans\u003C\/em\u003E (46%) and \u003Cem\u003EC. glabrata\u003C\/em\u003E (25%) [Lockhart SR et al. \u003Cem\u003EJ Clin Microbiol\u003C\/em\u003E. 2011]. Fluconazole resistance is common in \u003Cem\u003EC. glabrata\u003C\/em\u003E (23%) and \u003Cem\u003EC. krusei\u003C\/em\u003E (100%), whereas about 1% of \u003Cem\u003EC. albicans\u003C\/em\u003E is resistant. Methods for rapid identification of \u003Cem\u003ECandida\u003C\/em\u003E include peptide nucleic acid fluorescent in situ hybridization, multiplex reverse transcription-PCR, and matrix-assisted laser desorption ionization-time-of-flight mass spectrometry. Rapid identification can decrease the time to optimal therapy and, in some cases, decrease overall costs.\u003C\/p\u003E\u003Cp id=\u0022p-20\u0022\u003EIn conclusion, rapid and early identification of fungal species is important to improve treatment decisions and to administer optimal therapy to patients with invasive fungal disease. Although there are limitations to many of the current diagnostic techniques, newer techniques have demonstrated promising sensitivity and specificity.\u003C\/p\u003E\u003Cul class=\u0022copyright-statement\u0022\u003E\u003Cli class=\u0022fn\u0022 id=\u0022copyright-statement-1\u0022\u003E\u00a9 2014 MD Conference Express\u00ae\u003C\/li\u003E\u003C\/ul\u003E\u003Cspan class=\u0022highwire-journal-article-marker-end\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Cspan id=\u0022related-urls\u0022\u003E\u003C\/span\u003E\u003C\/div\u003E\u003Ca href=\u0022http:\/\/mdc.sagepub.com\/content\/14\/28\/26.abstract\u0022 class=\u0022hw-link hw-link-article-abstract\u0022 data-icon-position=\u0022\u0022 data-hide-link-title=\u00220\u0022\u003EView Summary\u003C\/a\u003E\u003C\/div\u003E  \u003C\/div\u003E\n\n  \n  \u003C\/div\u003E\n\u003C\/div\u003E\n  \u003C\/div\u003E\n\u003C\/div\u003E\n\u003C\/div\u003E\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_figures.js?nzm17d\u0022\u003E\u003C\/script\u003E\n\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_openurl.js?nzm17d\u0022\u003E\u003C\/script\u003E\n\u003Cscript type=\u0022text\/javascript\u0022 src=\u0022http:\/\/mdc.sagepub.com\/sites\/all\/modules\/highwire\/highwire\/plugins\/highwire_markup_process\/js\/highwire_tables.js?nzm17d\u0022\u003E\u003C\/script\u003E\n\u003C\/body\u003E\u003C\/html\u003E"}