Publication:
Candida infections in non-neutropenic children after the neonatal period

dc.contributor.buuauthorHacımustafaoğlu, Mustafa Kemal
dc.contributor.buuauthorÇelebi, Solmaz
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentPediatri ve Pediatri Enfeksiyon Hastalıkları Ana Bilim Dalı
dc.contributor.scopusid6602154166
dc.contributor.scopusid7006095295
dc.date.accessioned2022-01-06T11:32:02Z
dc.date.available2022-01-06T11:32:02Z
dc.date.issued2011-10
dc.description.abstractThere are a variety of diseases, from local mucous membrane infections to invasive systemic infections, that are caused by Candida species. As a causative agent, Candida albicans is the most common; however, the other Candida species can also cause the same clinical syndromes. Most invasive fungal infections in children occur in the hospital setting. Candidemia is a serious condition associated with high morbidity and mortality and increased healthcare costs in pediatric patients. Children at the highest risk are those with prolonged intensive care unit stays, reduced immune function, recent surgery, prior bacterial infection, prior use of antibiotics and/or corticosteroids and other immunosuppressive agents, as well as use of a central venous catheter, total parenteral nutrition, mechanical ventilation and dialysis. Positive blood culture is the gold standard of candidemia; it should not be accepted as contamination or colonization in children with an intravascular catheter. However, in oropharyngeal or vulvovaginal candidiasis, culture of lesions is rarely indicated unless the disease is recalcitrant or recurrent. Recovery of Candida from the sputum should usually be considered as colonization and should not be treated with antifungal therapy. Antigen and antibody detecting tests are evaluated in invasive Candida infections; however, there are no published results in children, and their roles in diagnosis are also unclear. For the therapy of invasive Candida infections in non-neutropenic patients, fluconazole or an echinocandin is usually recommended. Alternatively, amphotericin B deoxycholate or lipid formulations of amphotericin B can also be used. The recommended therapy of Candida meningitis is amphotericin B combined with flucytosine. The combination therapy for Candida infections is usually not indicated. Prophylaxis in non-neonatal, immunocompetent children is not recommended.
dc.identifier.citationHacımustafaoğlu, M. ve Çelebi, S. (2011). "Candida infections in non-neutropenic children after the neonatal period". Expert Review of Anti-Infective Therapy, 9(10), 923-940.
dc.identifier.endpage940
dc.identifier.issn1478-7210
dc.identifier.issn1744-8336
dc.identifier.issue10
dc.identifier.pubmed21973304
dc.identifier.scopus2-s2.0-80053630376
dc.identifier.startpage923
dc.identifier.urihttps://doi.org/10.1586/eri.11.104
dc.identifier.urihttps://www.tandfonline.com/doi/abs/10.1586/eri.11.104
dc.identifier.urihttp://hdl.handle.net/11452/23905
dc.identifier.volume9
dc.identifier.wos000297299600018
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherTaylor & Francis
dc.relation.journalExpert Review of Anti-Infective Therapy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectInfectious diseases
dc.subjectMicrobiology
dc.subjectPharmacology & pharmacy
dc.subject.emtreeAmphotericin B
dc.subject.emtreeAnidulafungin
dc.subject.emtreeAntifungal agent
dc.subject.emtreeButaconazole
dc.subject.emtreeCaspofungin
dc.subject.emtreeClotrimazole
dc.subject.emtreeEchinocandin
dc.subject.emtreeFluconazole
dc.subject.emtreeFlucytosine
dc.subject.emtreeItraconazole
dc.subject.emtreeKetoconazole
dc.subject.emtreeMicafungin
dc.subject.emtreeMiconazole
dc.subject.emtreeNystatin
dc.subject.emtreePyrrole
dc.subject.emtreeTerconazole
dc.subject.emtreeTioconazole
dc.subject.emtreeTriazole
dc.subject.emtreeUnclassified drug
dc.subject.emtreeVoriconazole
dc.subject.emtreeAntibody detection
dc.subject.emtreeAntigen detection
dc.subject.emtreeAsymptomatic infection
dc.subject.emtreeCandida albicans
dc.subject.emtreeCandidemia
dc.subject.emtreeCandidiasis
dc.subject.emtreeCandiduria
dc.subject.emtreeCardiac candidiasis
dc.subject.emtreeCentral nervous system candidiasis
dc.subject.emtreeChild
dc.subject.emtreeChildhood disease
dc.subject.emtreeClinical feature
dc.subject.emtreeDrug bioavailability
dc.subject.emtreeDrug dosage form comparison
dc.subject.emtreeDrug dose comparison
dc.subject.emtreeDrug dose reduction
dc.subject.emtreeEsophagus candidiasis
dc.subject.emtreeFungal colonization
dc.subject.emtreeFungal detection
dc.subject.emtreeFungal virulence
dc.subject.emtreeFungus growth
dc.subject.emtreeFungus transmission
dc.subject.emtreeGastrointestinal candidiasis
dc.subject.emtreeGram staining
dc.subject.emtreeHigh risk infant
dc.subject.emtreeHistopathology
dc.subject.emtreeHuman
dc.subject.emtreeInfection risk
dc.subject.emtreeLaboratory test
dc.subject.emtreeLoading drug dose
dc.subject.emtreeMolecular pathology
dc.subject.emtreeMortality
dc.subject.emtreeMucocutaneous candidiasis
dc.subject.emtreeMusculoskeletal candidiasis
dc.subject.emtreeMycosis
dc.subject.emtreeNeutropenia
dc.subject.emtreeNewborn
dc.subject.emtreeNewborn period
dc.subject.emtreeNonhuman
dc.subject.emtreeOcular candidiasis
dc.subject.emtreeOropharynx candidiasis
dc.subject.emtreePeritoneal candidiasis
dc.subject.emtreePolymerase chain reaction
dc.subject.emtreePrevalence
dc.subject.emtreePyelonephritis
dc.subject.emtreeRadiodiagnosis
dc.subject.emtreeRespiratory tract candidiasis
dc.subject.emtreeReview
dc.subject.emtreeRisk assessment
dc.subject.emtreeRisk factor
dc.subject.emtreeSkin candidiasis
dc.subject.emtreeUrinary tract candidiasis
dc.subject.emtreeVagina candidiasis
dc.subject.meshAmphotericin B
dc.subject.meshAntifungal agents
dc.subject.meshCandida
dc.subject.meshCandidemia
dc.subject.meshCatheter-related infections
dc.subject.meshChild
dc.subject.meshCross infection
dc.subject.meshDeoxycholic acid
dc.subject.meshDrug combinations
dc.subject.meshEchinocandins
dc.subject.meshFluconazole
dc.subject.meshFlucytosine
dc.subject.meshHumans
dc.subject.meshInfant, newborn
dc.subject.meshIntensive care units
dc.subject.meshLeukocyte count
dc.subject.meshMycological typing techniques
dc.subject.meshNeutrophils
dc.subject.meshSurvival rate
dc.subject.meshUnited states
dc.subject.scopusCandidemia; Invasive Candidiasis; Candida Parapsilosis
dc.subject.wosInfectious diseases
dc.subject.wosMicrobiology
dc.subject.wosPharmacology & pharmacy
dc.titleCandida infections in non-neutropenic children after the neonatal period
dc.typeReview
dc.wos.quartileQ1
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Pediatri ve Pediatri Enfeksiyon Hastalıkları Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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