Publication:
Predictors of choice of initial antifungal treatment in intraabdominal candidiasis.

dc.contributor.authorLagunes, L
dc.contributor.authorBorgatta, B
dc.contributor.authorMartín-Gomez, M T
dc.contributor.authorRey-Pérez, A
dc.contributor.authorAntonelli, M
dc.contributor.authorRighi, E
dc.contributor.authorMerelli, M
dc.contributor.authorBrugnaro, P
dc.contributor.authorDimopoulos, G
dc.contributor.authorGarnacho-Montero, J
dc.contributor.authorColombo, A L
dc.contributor.authorLuzzati, R
dc.contributor.authorMenichetti, F
dc.contributor.authorMuñoz, P
dc.contributor.authorNucci, M
dc.contributor.authorScotton, G
dc.contributor.authorViscoli, C
dc.contributor.authorTumbarello, M
dc.contributor.authorBassetti, M
dc.contributor.authorRello, J
dc.contributor.authorIAC Study Investigators
dc.date.accessioned2023-01-25T08:34:30Z
dc.date.available2023-01-25T08:34:30Z
dc.date.issued2016-07-16
dc.description.abstractIntraabdominal candidiasis (IAC) is the second most frequent form of invasive candidiasis, and is associated with high mortality rates. This study aims to identify current practices in initial antifungal treatment (IAT) in a real-world scenario and to define the predictors of the choice of echinocandins or azoles in IAC episodes. Secondary analysis was performed of a multinational retrospective cohort at 13 teaching hospitals in four countries (Italy, Greece, Spain and Brazil), over a 3-year period (2011-2013). IAC was identified in 481 patients, 323 of whom received antifungal therapy (classified as the treatment group). After excluding 13 patients given amphotericin B, the treatment group was further divided into the echinocandin group (209 patients; 64.7%) and the azole group (101 patients; 32.3%). Median APACHE II scores were significantly higher in the echinocandin group (p 0.013), but IAT did not differ significantly with regard to the Candida species involved. Logistic multivariate stepwise regression analysis, adjusted for centre effect, identified septic shock (adjusted OR (aOR) 1.54), APACHE II >15 (aOR 1.16) and presence in surgical ward at diagnosis (aOR 1.16) as the top three independent variables associated with an empirical echinocandin regimen. No differences in 30-day mortality were observed between groups. Echinocandin regimen was the first choice for IAT in patients with IAC. No statistical differences in mortality were observed between regimens, but echinocandins were administered to patients with more severe disease. Some disagreements were identified between current clinical guidelines and prescription of antifungals for IAC at the bedside, so further educational measures are required to optimize therapies.
dc.identifier.doi10.1016/j.cmi.2016.06.005
dc.identifier.essn1469-0691
dc.identifier.pmid27432766
dc.identifier.unpaywallURLhttp://www.clinicalmicrobiologyandinfection.com/article/S1198743X16301902/pdf
dc.identifier.urihttp://hdl.handle.net/10668/10284
dc.issue.number8
dc.journal.titleClinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
dc.journal.titleabbreviationClin Microbiol Infect
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen Macarena
dc.page.number719-24
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.rights.accessRightsopen access
dc.subjectAdequate treatment
dc.subjectAntifungal therapy
dc.subjectCandida
dc.subjectGuidelines
dc.subjectIntraabdominal candidiasis
dc.subjectInvasive fungal disease
dc.subjectSeptic shock
dc.subject.meshAged
dc.subject.meshAntifungal Agents
dc.subject.meshCandidiasis, Invasive
dc.subject.meshClinical Decision-Making
dc.subject.meshConsensus
dc.subject.meshDisease Management
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIntraabdominal Infections
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshRetrospective Studies
dc.titlePredictors of choice of initial antifungal treatment in intraabdominal candidiasis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number22
dspace.entity.typePublication

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