Abstract

BackgroundIn recent years, there has been a significant increase in the incidence of fungal infections attributed to Candida species worldwide, with a major shift toward non-albicans Candida (NAC). In this study, we have described the distribution of Candida species among different hospital departments and calculated the antifungal consumption in our facility. We also correlated the consumption of certain antifungals and the prevalence of specific Candida species.MethodsThis was a retrospective review of all the Candida isolates recovered from the computerised microbiology laboratory database of Makassed General Hospital, a tertiary care centre in Beirut, Lebanon, between January 2010 and December 2015. Data on antifungal consumption between January 2008 and December 2015 were extracted from the hospital pharmacy electronic database. We used Spearman’s coefficient to find a correlation between Candida species distribution and antifungal consumption.ResultsBetween 2008 and 2015, we observed that the highest antifungal consumption was in the haematology/oncology department (days of therapy/1000 patient days = 348.12 ± 85.41), and the lowest was in the obstetrics/gynaecology department (1.36 ± 0.47). In general, the difference in antifungal consumption among various departments was statistically significant (P < 0.0001). Overall, azoles were the most common first-line antifungals in our hospital. Echinocandins and amphotericin B were mostly prescribed in the haematology/oncology department. As for Candida species distribution, a total of 1377 non-duplicate isolates were identified between 2010 and 2015. A non-homologous distribution of albicans vs. non-albicans was noted among the different departments (P = 0.02). The most commonly isolated NAC was Candida glabrata, representing 14% of total Candida species and 59% of NAC. Candida famata (9% of NAC), Candida parapsilosis (3.6% of NAC) and Candida krusei (3% of NAC) were recovered unequally from the different departments. The total antifungal consumption correlated positively with the emergence of NAC. The use of azoles correlated positively with Candida glabrata, while amphotericin B formulations correlated negatively with it. None of these correlations reached statistical significance.ConclusionDifferent Candida species were unequally distributed among different hospital departments, and this correlated with consumption of antifungals in respective departments, highlighting the need for antifungal stewardship.

Highlights

  • In recent years, there has been a significant increase in the incidence of fungal infections attributed to Candida species worldwide, with a major shift toward non-albicans Candida (NAC)

  • Antifungal consumption The rate of antifungal consumption in Days of therapy (DOT)/1000 Patient days (PD) and Defined daily dose (DDD)/1000 PD are shown in Tables 1 and 2, respectively

  • Correlation between antifungal consumption and the isolation of specific Candida species Using Spearman’s coefficient, we observed that none of the correlations reached a statistical significance due to the limited number of hospital departments involved (N = 5); these results indicated some trends and showed clinical significance (Table 5)

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Summary

Introduction

There has been a significant increase in the incidence of fungal infections attributed to Candida species worldwide, with a major shift toward non-albicans Candida (NAC). We have described the distribution of Candida species among different hospital departments and calculated the antifungal consumption in our facility. The world has witnessed a significant increase in the incidence of fungal infections due to Candida species [1], with Candida albicans (CA) being the most common causative organism [2]. Recent studies have documented a change in this aetiology shifting toward non-albicans Candida (NAC) [3]. This shift has been linked to the selective pressure caused by the extensive use of broad spectrum antibiotics and antifungals [4]. Two studies demonstrated an increase in the incidence of Candida parapsilosis associated with the use of caspofungin [12, 13]

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