| Literature DB >> 33991279 |
Salma Aldossary1, Anand Shah2,3.
Abstract
INTRODUCTION: Fungal infection and sensitization are common in chronic respiratory patient populations such as bronchiectasis, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF) and are often associated with prolonged antifungal therapy (Hohmann et al. in Clin Infect Dis 15:939-940, 2010; Vissichelli et al. in Infect Prev Pract 1:100029, 2019), morbidity, and mortality. Although the use of antifungal stewardship (AFS) is increasing within an invasive fungal disease setting, its use and impact within a chronic respiratory setting have not been defined.Entities:
Keywords: Antifungal; Antifungal resistance; Aspergillus fumigatus; Chronic; Respiratory disease; Stewardship
Mesh:
Substances:
Year: 2021 PMID: 33991279 PMCID: PMC8536614 DOI: 10.1007/s11046-021-00547-z
Source DB: PubMed Journal: Mycopathologia ISSN: 0301-486X Impact factor: 2.574
Fig. 1PRISMA flow diagram of search and selection process
Included study characteristics
| Study author, year | Study design | Type of fungal species | Intervention | Duration of intervention | Patient population, Settings | Presence of chronic respiratory patients | Outcomes after Stewardship | GRADE |
|---|---|---|---|---|---|---|---|---|
| Shah et al. [ | Retrospective | Invasive tests | 48 h–24 days | Immunocompetent adult patients treated in the medical and surgical intensive care units | Yes | Fungal testing of respiratory tract specimens does not add diagnostic value | Low | |
| Mondain et al. [ | Prospective observational | Invasive aspergillosis and candidaemia | Multifaceted antifungal stewardship discussion | 48 h–2 weeks | French teaching tertiary-care hospital | Yes | Antifungal stewardship programme was feasible, sustainable, and well accepted | Low |
| López-Medrano et al. [ | Intervention | Non-randomized uncontrolled before–after antimicrobial stewardship | 1–2 years | The University Hospital 12 de Octubre. A 1300-bed hospital | Yes | Primary outcome of the study was a reduction in antifungal expenditure | Low | |
| Alfandari et al. [ | Retrospective | Multidisciplinary collaborative use of antifungals in haematology | 4–5 days | Allograft and acute leukemia induction chemotherapy patients. The Lille Regional Teaching Hospital | No | Decreased antifungal consumption, stabilized invasive fungal infections (IFI), and decreased IFI-related mortality | Low | |
| Muñoz et al. [ | Retrospective | Educational and bedside intervention | 2 years | Hospitalized patients with cases of invasive candidiasis and invasive aspergillosis | Yes | Reduced consumption of DDDs and reduced expenditure on antifungals | Low | |
| Vissichelli et al. [ | Retrospective | Review of bronchoalveolar lavage results | 2 years | Autologous haematopoietic stem-cell transplant recipients | Yes | Antifungals were more likely to be escalated or changed | Low | |
| Whitney et al. [ | Retrospective | Antifungal susceptibility testing | 5–6 days | Adult in patients receiving amphotericin B, echinocandins, intravenous fluconazole, flucytosine, or voriconazole. St. George’s tertiary referral hospital | Yes | Antifungal expenditure initially reduced then increased to 20% above baseline over a 5-year period | Low | |
| Hamada et al. [ | Retrospective | N/A | Voriconazole trough concentration | 4 days | Hospitalized patients on voriconazole, at five hospitals in Japan | No | Reduced incidence of hepatotoxicity | Low |
| Shah et al. [ | Retrospective | Administration of fluconazole or an echinocandin | 5 + or − 2 days | Hospitalized patients with candidaemia | No | Less than 40% of echinocandin-treated patients with fluconazole-susceptible organisms were de-escalated to fluconazole | Low | |
| Gurram et al. [ | Retrospective | Bronchoalveolar lavage | 6–12 months | Adult immunocompromised patients who underwent bronchoscopy with Immunocompromised Host (ICH) Protocol | Yes | Patients with | Low | |
| Rautemaa-Richardson et al. [ | Retrospective | Antifungal therapy | 4 months | Patients prescribed micafungin for suspected or proven invasive candidosis. UK tertiary referral teaching hospital | Yes | Number of patients treated for invasive candidiasis decreased | Low | |
| Mondain et al. [ | Prospective observational | Systematic evaluation | 2–5 days | Teaching tertiary-care hospital | No | Improved quality of care and stable antifungal use and cost in the hospital | Very low | |
| Antworth et al. [ | Single-centre, quasi-experimental | Comprehensive candidemia care bundle | 3 days | Patients with candidemia. A 930-bed academic hospital | No | Improved management of patients with candidemia | Low | |
| Menichetti et al. [ | Retrospective | Infectious disease consultation | 30 days | Patients with documented candidemia cared for in Pisa tertiary care, University hospital | No | A lower 30-day in-hospital mortality rate for candidemia patients treated with infectious diseases consultation (IDC) with respect to those treated without | Moderate | |
| Swoboda et al. [ | Retrospective | Standardized practice of antifungal therapy | 45 days | Patients with an intensive care unit (ICU) stay of 1–24 h and either recovery of fungi from any site and/or application of systemic antifungals | No | Significant decrease in the use of antifungal agents as well as costs | Moderate | |
| Browne et al. [ | Retrospective | Complex lung infection multidisciplinary meeting | 6–12 months | Hospitalized patients with suspected fungal lung disease | Yes | Allowed a refinement in diagnosis of | Very Low | |
| Reed et al. [ | Quasi-experimental | ASP pharmacist's intervention | 1–2 years | The Ohio state Wexner Medical Centre, a 1229-bed teaching hospital | Yes | Timely notification from microbiology to the ASP PharmD in conjunction with ASP PharmD interventions resulted in more patients with candidemia receiving timely effective antifungal therapy | Moderate | |
| Veringa et al. [ | Retrospective | Therapeutic drug monitoring (TDM) of anti-infective drugs | 1–2 days | In-patients | No | TDM plays an important role in the optimization of treatment with anti-infective drugs | Low | |
| Morris et al. [ | Phased, multisite cohort | Antimicrobial stewardship | 3–5 days | Patients admitted to each ICU at the academic ICUs in Toronto, Canada | Yes | Sustained improvements in antimicrobial consumption and cost | Low | |
| Pfaller and Castan Heira [ | Prospective | Rapid diagnostic testing and antifungal stewardship | 24 h, 7 days | Hospitalized individuals | No | Improved care by increasing the awareness of candidiasis. Improve diagnostic efforts | Low | |
| Märtson et al. [ | Retrospective | Therapeutic drug monitoring of posaconazole | 1–3 years | Patients with haematological malignancies. The University Medical Center Groningen, the Netherlands | No | 64% was the adequate posaconazole exposure; in the longitudinal analysis from all the confounders, only dose had a significant effect on posaconazole concentrations | Low | |
| Kawaguchi et al. [ | Single-centre, observational | Antifungal stewardship programs (AFSPs) | 1–3 years | Patients who received systemic antifungals at the Osaka City University Hospital (980-bed, tertiary-care teaching hospital) | Yes | As the appropriate selection of antifungals increases, a decrease in antifungal usage and cost reduction also occurs. This trend leads to improved prognoses of patients with candidemia | Low | |
| Ito-Takeichi et al. [ | Single-institutional prospective cohort | 1‐3, | 1–2 days | In patients receiving intravenous antifungals at the 614-bed Gifu University Hospital | No | Parental antifungal use was significantly reduced | Low | |
| Cavalieri et al. [ | Retrospective | MALDI-TOF mass spectrometry / Vitek 2 | 1–2 days | Hospitalized patients | Yes | An average 18 h faster microbial ID and antimicrobial susceptibility test results | Low | |
| Steuber et al. [ | Single-centre, retrospective, observational | T2 Candida Panel (T2CP) | 3 years | Patients with positive or negative T2CP at a 971-bed community hospital | No | Antifungal optimization occurred in 54% of patients who had antifungal orders at the time of T2CP test | Low | |
| Hashemi et al. [ | Retrospective | Disc diffusion and micro-dilution | N/A | Clinical isolates of | No | The | Very low | |
| Chabavizadeh et al. [ | Retrospective | Ganoderma lucidum (alcoholic extract) | N/A | Patients with candidemia admitted to some specialized hospitals in Tehran | No | Very low | ||
| Nwankwo et al. [ | Prospective | Antifungal stewardship team impact assessment | 18 months | Chronic lung disease in patients and out-patients with fungal infections | Yes | The commonest infection was CPA, reduction in monthly antifungal expenditure as well as antifungal use after implementing AFS without increase in mortality/morbidity | Low |