ESCMID* guideline for the diagnosis and management of Candida diseases 2012: prevention and management of invasive infections in neonates and children caused by Candida spp.

Details

Serval ID
serval:BIB_0F6632F32AC3
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
ESCMID* guideline for the diagnosis and management of Candida diseases 2012: prevention and management of invasive infections in neonates and children caused by Candida spp.
Journal
Clinical Microbiology and Infection
Author(s)
Hope W.W., Castagnola E., Groll A.H., Roilides E., Akova M., Arendrup M.C., Arikan-Akdagli S., Bassetti M., Bille J., Cornely O.A., Cuenca-Estrella M., Donnelly J.P., Garbino J., Herbrecht R., Jensen H.E., Kullberg B.J., Lass-Flörl C., Lortholary O., Meersseman W., Petrikkos G., Richardson M.D., Verweij P.E., Viscoli C., Ullmann A.J.
Working group(s)
ESCMID Fungal Infection Study Group
ISSN
1469-0691 (Electronic)
ISSN-L
1198-743X
Publication state
Published
Issued date
2012
Volume
18
Number
Suppl. 7
Pages
38-52
Language
english
Notes
Publication types: Journal Article ; Practice Guideline ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Abstract
Invasive candidiasis (IC) is a relatively common syndrome in neonates and children and is associated with significant morbidity and mortality. These guidelines provide recommendations for the prevention and treatment of IC in neonates and children. Appropriate agents for the prevention of IC in neonates at high risk include fluconazole (A-I), nystatin (B-II) or lactoferrin ± Lactobacillus (B-II). The treatment of IC in neonates is complicated by the high likelihood of disseminated disease, including the possibility of infection within the central nervous system. Amphotericin B deoxycholate (B-II), liposomal amphotericin B (B-II), amphotericin B lipid complex (ABLC) (C-II), fluconazole (B-II), micafungin (B-II) and caspofungin (C-II) can all be potentially used. Recommendations for the prevention of IC in children are largely extrapolated from studies performed in adults with concomitant pharmacokinetic data and models in children. For allogeneic HSCT recipients, fluconazole (A-I), voriconazole (A-I), micafungin (A-I), itraconazole (B-II) and posaconazole (B-II) can all be used. Similar recommendations are made for the prevention of IC in children in other risk groups. With several exceptions, recommendations for the treatment of IC in children are extrapolated from adult studies, with concomitant pharmacokinetic studies. Amphotericin B deoxycholate (C-I), liposomal amphotericin B (A-I), ABLC (B-II), micafungin (A-I), caspofungin (A-I), anidulafungin (B-II), fluconazole (B-I) and voriconazole (B-I) can all be used.
Keywords
Adolescent, Antifungal Agents/therapeutic use, Candida/drug effects, Candida/isolation & purification, Candidiasis, Invasive/drug therapy, Candidiasis, Invasive/microbiology, Child, Child, Preschool, Humans, Infant, Infant, Newborn, Pediatrics
Pubmed
Web of science
Open Access
Yes
Create date
27/04/2013 11:53
Last modification date
20/08/2019 13:36
Usage data