Invasive fungal infections in hemato-oncology

被引:1
作者
Oberoi, Jaswinder Kaur [1 ]
Sheoran, Lata [2 ]
Sagar, Tanu [2 ]
Saxena, Sonal [2 ]
机构
[1] Sir Ganga Ram Hosp, Inst Clin Microbiol & Immunol, New Delhi 110060, India
[2] Maulana Anad Med Coll, Dept Microbiol, New Delhi 110002, India
关键词
Diagnosis; Hemato-oncology; Invasive fungal infection; ANTIFUNGAL TREATMENT STRATEGIES; LINKED-IMMUNOSORBENT-ASSAY; REAL-TIME PCR; PULMONARY ASPERGILLOSIS; BRONCHOALVEOLAR LAVAGE; CLINICAL-EVALUATION; ACUTE-LEUKEMIA; DIAGNOSIS; GALACTOMANNAN; CHEMOTHERAPY;
D O I
10.1016/j.ijmmb.2023.01.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Patients with hematologic malignancies (HM) carries a significant risk of developing invasive fungal infection (IFI) and are associated with a high risk of attributable morbidity and mortality. Objectives: This review has highlighted the importance of diagnosis and management of invasive fungal infections in highly immunocompromised Hemato-Oncology patients.Content: IFI continues to be a therapeutic issue in immunocompromised HM patients despite of many advancements in the field of fungal diagnosis and therapies. Non-specific and often overlapping signs and symptoms render fungal infections clinically undifferentiated from bacterial infections. Definite diagnosis requires microbiological diagnostic procedures in addition to imaging techniques. Many international committees have formulated definitions to aid in the diagnosis of IFI in immunocompromised patients and assigned 3 levels of probability to the diagnosis "proven," "probable," and "possible" IFI. Early specific risk-based antifungal strategies such as prophylaxis, pre-emptive and empirical therapies, are common practices in HM patients. For low-risk patients, fluconazole is recommended as primary prophylaxis, while, posaconazole and voriconazole are recommended for high-risk patients. Emerging antifungal-resistant IFIs and breakthrough fungal infections are the new threat to these heavily immunosuppressed patients. Antifungal agents such as azoles have variable pharmacokinetics leading to uncertainty in the drug dose-exposure relationship, especially in the initiation phase. TDM (therapeutic drug monitoring) of voriconazole is strongly recommended.
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