A multisite evaluation of antifungal use in critical care: implications for antifungal stewardship

Author:

Logan C12ORCID,Hemsley C3,Fife A4,Edgeworth J35,Mazzella A12,Wade P36,Goodman A357ORCID,Hopkins P8,Wyncoll D9,Ball J10,Planche T12,Schelenz S4,Bicanic T12ORCID

Affiliation:

1. Clinical Infection Group, St George’s University Hospitals NHS Foundation Trust , London , UK

2. Institute of Infection & Immunity, St George’s University of London , London , UK

3. Department of Infectious Diseases, Guy’s & St Thomas’ NHS Foundation Trust , London , UK

4. Infection Sciences, King’s College Hospital NHS Foundation Trust , London , UK

5. Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, King’s College London Guy’s & St Thomas’ NHS Foundation Trust , London , UK

6. Directorate of Pharmacy & Medicines Optimisation, Guy’s & St Thomas’s NHS Foundation Trust , London , UK

7. MRC Clinical Trials Unit at University College London , London , UK

8. Department of Critical Care, King’s College Hospital NHS Foundation Trust , London , UK

9. Department of Critical Care, Guy’s & St Thomas’ NHS Foundation Trust , London , UK

10. Department of Critical Care, St George’s University Hospitals NHS Foundation Trust , London , UK

Abstract

Abstract Background ICUs are settings of high antifungal consumption. There are few data on prescribing practices in ICUs to guide antifungal stewardship implementation in this setting. Methods An antifungal therapy (AFT) service evaluation (15 May–19 November 2019) across ICUs at three London hospitals, evaluating consumption, prescribing rationale, post-prescription review, de-escalation and final invasive fungal infection (IFI) diagnostic classification. Results Overall, 6.4% of ICU admissions (305/4781) received AFT, accounting for 11.41 days of therapy/100 occupied bed days (DOT/100 OBD). The dominant prescribing mode was empirical (41% of consumption), followed by targeted (22%), prophylaxis (18%), pre-emptive (12%) and non-invasive (7%). Echinocandins were the most commonly prescribed drug class (4.59 DOT/100 OBD). In total, 217 patients received AFT for suspected or confirmed IFI; 12%, 10% and 23% were classified as possible, probable or proven IFI, respectively. Hence, in 55%, IFI was unlikely. Proven IFI (n = 50) was mostly invasive candidiasis (92%), of which 48% had been initiated on AFT empirically before yeast identification. Where on-site (1 → 3)-β-d-glucan (BDG) testing was available (1 day turnaround), in those with suspected but unproven invasive candidiasis, median (IQR) AFT duration was 10 (7–15) days with a positive BDG (≥80 pg/mL) versus 8 (5–9) days with a negative BDG (<80 pg/mL). Post-prescription review occurred in 79% of prescribing episodes (median time to review 1 [0–3] day). Where suspected IFI was not confirmed, 38% episodes were stopped and 4% de-escalated within 5 days. Conclusions Achieving a better balance between promptly treating IFI patients and avoiding inappropriate antifungal prescribing in the ICU requires timely post-prescription review by specialist multidisciplinary teams and improved, evidence-based-risk prescribing strategies incorporating rapid diagnostics to guide AFT start and stop decisions.

Funder

Gilead UK & Ireland Fellowship in Invasive Fungal Disease

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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