Pharmacokinetics and Antifungal Activity of Echinocandins in Ascites Fluid of Critically Ill Patients

被引:8
|
作者
Welte, Rene [1 ]
Oberacher, Herbert [2 ]
Gasperetti, Tiziana [1 ]
Pfisterer, Hartwig [3 ]
Griesmacher, Andrea [3 ]
Santner, Tobias [3 ]
Lass-Floerl, Cornelia [4 ]
Hoertnagl, Caroline [4 ]
Leitner-Rupprich, Sandra [4 ]
Aigner, Maria [4 ,13 ]
Lorenz, Ingo [5 ]
Schmid, Stefan [6 ,7 ]
Edlinger, Michael [8 ]
Eller, Philipp [9 ]
Dankl, Daniel [10 ,11 ]
Joannidis, Michael [12 ]
Bellmann, Romuald [1 ,12 ]
机构
[1] Med Univ Innsbruck, Dept Internal Med 1, Div Med Intens Care & Emergency Med, Clin Pharmacokinet Unit, Innsbruck, Austria
[2] Med Univ Innsbruck, Inst Legal Med & Core Facil Metabol, Innsbruck, Austria
[3] Innsbruck Gen Hosp, Cent Inst Med & Chem Lab Diagnost, Innsbruck, Austria
[4] Med Univ Innsbruck, Dept Hyg & Med Microbiol, Innsbruck, Austria
[5] Med Univ Innsbruck, Ctr Operat Med, Dept Gen & Surg Intens Care Med, Gen & Surg ICU, Innsbruck, Austria
[6] Innsbruck Gen Hosp, Ctr Operat Med, Dept Gen & Surg Intens Care Med, Traumatol ICU, Innsbruck, Austria
[7] Med Univ Innsbruck, Innsbruck, Austria
[8] Med Univ Innsbruck, Dept Med Stat Informat & Hlth Econ, Div Med Stat & Informat, Innsbruck, Austria
[9] Med Univ Graz, Dept Internal Med, Graz, Austria
[10] Salzburg Gen Hosp, Salzburg, Austria
[11] Paracelsus Private Med Univ, Salzburg, Austria
[12] Med Univ Innsbruck, Dept Internal Med 1, Div Med Intens Care & Emergency Med, Innsbruck, Austria
[13] INNPATH GmbH, Tirol Kliniken, Innsbruck, Austria
基金
奥地利科学基金会;
关键词
antifungals; invasive candidiasis; fungal peritonitis; target-site pharmacokinetics; antifungal pharmacodynamics; FUNGAL PERITONITIS; LIVER-CIRRHOSIS; AMPHOTERICIN-B; CASPOFUNGIN; FLUCONAZOLE; CANDIDIASIS; INFECTIONS; MICAFUNGIN; MANAGEMENT; UPDATE;
D O I
10.1128/AAC.02565-20
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The pharmacokinetics and antifungal activity of the echinocandins anidulafungin (AFG), micafungin (MFG), and caspofungin (CAS) were assessed in ascites fluid and plasma of critically ill adults treated for suspected or proven invasive candidiasis. Ascites fluid was obtained from ascites drains or during paracentesis. The antifungal activity of the echinocandins in ascites fluid was assessed by incubation of Candida albicans and Candida glabrata at concentrations of 0.03 to 16.00 mu g/ml. In addition, ascites fluid samples obtained from our study patients were inoculated with the same isolates and evaluated for fungal growth. These patient samples had to be spiked with echinocandins to restore the original concentrations because echinocandins had been lost during sterile filtration. In ascites fluid specimens of 29 patients, echinocandin concentrations were below the simultaneous plasma levels. Serial sampling in 20 patients revealed a slower rise and decline of echinocandin concentrations in ascites fluid than in plasma. Proliferation of C. albicans in ascites fluid was slower than in culture medium and growth of C. glabrata was lacking, even in the absence of antifungals. In CAS-spiked ascites fluid samples, fungal CFU counts moderately declined, whereas spiking with AFG or MFG had no relevant effect. In ascites fluid of our study patients, echinocandin concentrations achieved by therapeutic doses did not result in a consistent eradication of C. albicans or C. glabrata. Thus, therapeutic doses of AFG, MFG, or CAS may result in ascites fluid concentrations preventing relevant proliferation of C. albicans and C. glabrata, but do not warrant reliable eradication.
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页数:9
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