Clinical and pharmacoeconomic evaluation of antifungal prophylaxis with continuous micafungin in patients undergoing allogeneic stem cell transplantation: A six-year cohort analysis

被引:2
|
作者
Wingen-Heimann, Sebastian M. [1 ,2 ]
Cornely, Oliver A. [1 ,3 ,4 ,5 ]
Vehreschild, Maria J. G. T. [1 ,3 ,6 ]
Wisplinghoff, Hilmar [7 ,8 ,9 ]
Franke, Bernd [1 ]
Schons, Max [1 ]
von Bergwelt-Baildon, Michael [1 ,10 ]
Scheid, Christof [1 ]
Vehreschild, Joerg Janne [1 ,3 ]
机构
[1] Univ Hosp Cologne, Ctr Integrated Oncol Aachen Bonn Cologne Duesseld, Dept Internal Med 1, Cologne, Germany
[2] FOM Univ Appl Sci, Cologne, Germany
[3] German Ctr Infect Res DZIF, Partner Site Bonn Cologne, Cologne, Germany
[4] Univ Hosp Cologne, Cologne Excellence Cluster Cellular Stress Respon, Cologne, Germany
[5] Univ Hosp Cologne, Clin Trials Ctr Cologne ZKS, Cologne, Germany
[6] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Dept Internal Med, Infect Dis, Frankfurt, Germany
[7] Univ Hosp Cologne, Inst Med Microbiol Immunol & Hyg, Cologne, Germany
[8] Wisplinghoff Labs, Cologne, Germany
[9] WittenHerdecke Univ, Inst Virol & Microbiologa, Witten, Germany
[10] Ludwig Maximilians Univ LMU, Univ Hosp Munich, Dept Internal Med Hematol & Oncol 3, Munich, Germany
关键词
allogeneic stem cell transplantation; antifungal prophylaxis; cost savings; micafungin; pharmacoeconomic evaluation; posaconazole; INVASIVE FUNGAL-INFECTIONS; HIGH-RISK PATIENTS; ACUTE MYELOGENOUS LEUKEMIA; EPIDEMIOLOGY; VORICONAZOLE; FLUCONAZOLE; COMBINATION; RECIPIENTS; DISEASES; THERAPY;
D O I
10.1111/myc.13232
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Patients undergoing allogeneic stem cell transplantation (aSCT) are at high risk to develop an invasive fungal disease (IFD). Optimisation of antifungal prophylaxis strategies may improve patient outcomes and reduce treatment costs. Objectives To analyse the clinical and economical impact of using continuous micafungin as antifungal prophylaxis. Patients/Methods We performed a single-centre evaluation comparing patients who received either oral posaconazole with micafungin as intravenous bridging as required (POS-MIC) to patients who received only micafungin (MIC) as antifungal prophylaxis after aSCT. Epidemiological, clinical and direct treatment cost data extracted from the Cologne Cohort of Neutropenic Patients (CoCoNut) were analysed. Results Three hundred and thirteen patients (97 and 216 patients in the POS-MIC and MIC groups, respectively) were included into the analysis. In the POS-MIC and MIC groups, median overall length of stay was 42 days (IQR: 35-52 days) vs 40 days (IQR: 35-49 days; p = .296), resulting in median overall costs of euro42,964 (IQR: euro35,040-euro56,348) vs euro43,291 (IQR: euro37,281 vs euro51,848; p = .993), respectively. Probable/proven IFD in the POS-MIC and MIC groups occurred in 5 patients (5%) vs 3 patients (1%; p = .051), respectively. The Kaplan-Meier analysis showed improved outcome of patients in the MIC group at day 100 (p = .037) and day 365 (p < .001) following aSCT. Conclusions Our study results demonstrate improved outcomes in the MIC group compared with the POS-MIC group, which can in part be explained by a tendency towards less probable/proven IFD. Higher drug acquisition costs of micafungin did not translate into higher overall costs.
引用
收藏
页码:437 / 444
页数:8
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