Aspergillus fumigatus-a systematic review to inform the World Health Organization priority list of fungal pathogens

被引:5
|
作者
Morrissey, C. Orla [1 ,2 ]
Kim, Hannah Y. [3 ,4 ,5 ]
Duong, Tra-My N. [3 ]
Moran, Eric [6 ]
Alastruey-Izquierdo, Ana [7 ]
Denning, David W. [8 ,9 ]
Perfect, John R. [10 ]
Nucci, Marcio [11 ,12 ]
Chakrabarti, Arunaloke [13 ]
Rickerts, Volker [14 ]
Chiller, Tom M. [15 ]
Wahyuningsih, Retno [16 ,17 ]
Hamers, Raph L. [18 ,19 ]
Cassini, Alessandro [20 ,21 ,24 ]
Gigante, Valeria [22 ]
Sati, Hatim [22 ]
Alffenaar, Jan-Willem [3 ,4 ,5 ]
Beardsley, Justin [3 ,23 ]
机构
[1] Alfred Hlth, Dept Infect Dis, Level 2,Burnet Bldg,85 Commercial Rd, Melbourne, Vic, Australia
[2] Monash Univ, Level 2,Burnet Bldg,85 Commercial Rd, Melbourne, Vic, Australia
[3] Univ Sydney, Infect Dis Inst Sydney ID, Sydney, NSW, Australia
[4] Univ Sydney, Fac Med & Hlth, Sch Pharm, Sydney, NSW, Australia
[5] Westmead Hosp, Westmead, NSW, Australia
[6] Sinclair Dermatol, East Melbourne, Vic, Australia
[7] Inst Salud Carlos III, Mycol Reference Lab, Natl Ctr Microbiol, Majadahonda, Madrid, Spain
[8] Global Act Fungal Infect, Geneva, Switzerland
[9] Univ Manchester, Fac Biol Med & Hlth, Manchester Acad Hlth Sci Ctr, Manchester, England
[10] Duke Univ, Sch Med, Div Infect Dis & Int Hlth, Durham, NC USA
[11] Univ Fed Rio de Janeiro, Rio De Janeiro, RJ, Brazil
[12] Grp Oncoclin, Rio De Janeiro, RJ, Brazil
[13] Doodhadhari Burfani Hosp & Res Inst, Haridwar, India
[14] Robert Koch Inst Berlin, FG16,Seestr 10, D-13353 Berlin, Germany
[15] CDCP, Mycot Dis Branch, Atlanta, GA USA
[16] Univ Indonesia, Fac Med, Dept Parasitol, Jakarta, Indonesia
[17] Univ Kristen, Fac Med, Dept Parasitol, Jakarta, Indonesia
[18] Univ Indonesia, Oxford Univ Clin Res Unit Indonesia, Fac Med, Jakarta, Indonesia
[19] Univ Oxford, Ctr Trop Med & Global Hlth, Nuffield Dept Med, Oxford, England
[20] Lausanne Univ Hosp, Infect Dis Serv, Lausanne, Switzerland
[21] Canton Vaud, Publ Hlth Dept, Lausanne, Switzerland
[22] WHO, AMR Div, Geneva, Switzerland
[23] Westmead Inst Med Res, Westmead, NSW, Australia
[24] WHO, Geneva, Switzerland
关键词
Aspergillus fumigatus; invasive aspergillosis; invasive fungal disease; mortality; susceptibility; risk factors; incidence; epidemiology; INVASIVE PULMONARY ASPERGILLOSIS; PATHONOSTICS ASPERGENIUS ASSAY; AZOLE ANTIFUNGAL DRUGS; PCR-BASED DETECTION; REAL-TIME PCR; TRIAZOLE RESISTANCE; BRONCHOALVEOLAR LAVAGE; CLINICAL-EVALUATION; ACUTE-LEUKEMIA; DISEASE;
D O I
10.1093/mmy/myad129
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Recognizing the growing global burden of fungal infections, the World Health Organization established a process to develop a priority list of fungal pathogens (FPPL). In this systematic review, we aimed to evaluate the epidemiology and impact of invasive infections caused by Aspergillus fumigatus to inform the first FPPL. The pre-specified criteria of mortality, inpatient care, complications and sequelae, antifungal susceptibility, risk factors, preventability, annual incidence, global distribution, and emergence were used to search for relevant articles between 1 January 2016 and 10 June 2021. Overall, 49 studies were eligible for inclusion. Azole antifungal susceptibility varied according to geographical regions. Voriconazole susceptibility rates of 22.2% were reported from the Netherlands, whereas in Brazil, Korea, India, China, and the UK, voriconazole susceptibility rates were 76%, 94.7%, 96.9%, 98.6%, and 99.7%, respectively. Cross-resistance was common with 85%, 92.8%, and 100% of voriconazole-resistant A. fumigatus isolates also resistant to itraconazole, posaconazole, and isavuconazole, respectively. The incidence of invasive aspergillosis (IA) in patients with acute leukemia was estimated at 5.84/100 patients. Six-week mortality rates in IA cases ranged from 31% to 36%. Azole resistance and hematological malignancy were poor prognostic factors. Twelve-week mortality rates were significantly higher in voriconazole-resistant than in voriconazole-susceptible IA cases (12/22 [54.5%] vs. 27/88 [30.7%]; P = .035), and hematology patients with IA had significantly higher mortality rates compared with solid-malignancy cases who had IA (65/217 [30%] vs. 14/78 [18%]; P = .04). Carefully designed surveillance studies linking laboratory and clinical data are required to better inform future FPPL.
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