2018
DOI: 10.1093/jac/dky047
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T2Candida MR as a predictor of outcome in patients with suspected invasive candidiasis starting empirical antifungal treatment: a prospective pilot study

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Cited by 49 publications
(32 citation statements)
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“…Of interest, in the present report, the overall 30-day mortality rate in patients with septic shock attributable to candidemia was 34.3%, which is significantly lower than that observed in two previous studies performed in Europe and St. Louis, where mortality rate remained around 50-60% [4,5]. The difference in septic shock definitions [9], improvements in fungal diagnosis [33,34], and the widespread implementation of sepsis bundle in recent years [38][39][40] may explain the lower incidence of mortality observed in this study.…”
Section: Discussioncontrasting
confidence: 46%
See 1 more Smart Citation
“…Of interest, in the present report, the overall 30-day mortality rate in patients with septic shock attributable to candidemia was 34.3%, which is significantly lower than that observed in two previous studies performed in Europe and St. Louis, where mortality rate remained around 50-60% [4,5]. The difference in septic shock definitions [9], improvements in fungal diagnosis [33,34], and the widespread implementation of sepsis bundle in recent years [38][39][40] may explain the lower incidence of mortality observed in this study.…”
Section: Discussioncontrasting
confidence: 46%
“…The fact that patients with other source of the infection (i.e., CVC or urinary tract) received a similar rate of adequate source control of candidemia (43.4% vs 40.5%, p = 0.86) and even a lower rate of adequate antifungal treatment (38.1% vs 61.5%, p = 0.008) is further consistent with this intriguing explanation. Although we do not have clear answer regarding to the best approach for reducing the incidence of septic shock in candidemic patients, we believe that new diagnostic strategies investigating the role of serological biomarkers such as β-D-glucan or T2MR [32][33][34][35] should be applied in order to early identify patients at risk of intra-abdominal candidiasis. Future studies addressing risk factors for developing intra-abdominal candidiasis are also needed to better clarify the best empiric or pre-emptive therapeutic approach.…”
Section: Discussionmentioning
confidence: 97%
“…153 Of note, some authors have also suggested that a positive T2Candida test could be a potential marker of poor outcome in patients receiving empirical antifungal therapy for suspected IC. 154 In the future, it is likely that cumulative evidence from different real-life experiences will allow to precisely delineate the positioning of the T2Candida panel within diagnostic algorithms, and to maximize its cost-effectiveness (also considering the local prevalence or Candida species not included in the panel). [155][156][157]…”
Section: Rapid Tests Based On Polymerase Chain Reactionmentioning
confidence: 99%
“…Despite these results, the fact is that the empirical approach remains a common practice both inside and outside ICU 154 and its role in high-risk patients still remains to be determined. In our opinion, further studies aimed to specify criteria for early initiation of antifungal therapy in critically ill patients are needed.…”
Section: Empirical Approachmentioning
confidence: 99%
“…Although a mortality benefit was not observed, possibly because of a small sample size, previous studies associate mortality benefits with expedited time to effective therapy among candidemia patients (30,31). A recent study evaluated the diagnostic value of T2Candida, Candida albicans germ tube antibodies (CAGT), and β-D-glucan (BDG) in predicting poor outcomes (i.e., diagnosis of invasive candidiasis defined as candidemia and deep-seated candidiasis, and/or death within the first 7 days of initiating antifungal therapy) for patients on definitive antifungal therapy (32). Although difference between good vs poor outcome was not differentiated by CAGT or BDG, a positive T2Candida was more commonly present in poor outcomes [5 of 14 (35.7%) vs 0 of 35 (0%); P = 0.0001].…”
Section: Direct Specimen Testingmentioning
confidence: 99%