{"title":"基于药代动力学/药效学分析的热复宁抗念珠菌给药方案优化","authors":"Jiuli Hu, Junhui Hu","doi":"10.4236/pp.2020.116008","DOIUrl":null,"url":null,"abstract":"Invasive candidiasis was the most common nosocomial fungal infection with \nhigh morbidity and mortality, which is mainly occurring in immunodeficiency and \ncritical patients. Echinocandins were recommended as first-line drugs for the \ntreatment and prevention of invasive candidiasis. In our study, we aimed to optimize \nthe dosage of Rezafungin against Candida spp. based on \npharmacokinetic/pharmacodynamics (PK/PD) analysis. We collected the published \ndata about pharmacokinetic parameters of rezafungin and the MIC distribution of Candida spp. on rezafungin. Monte Carlo simulation was used to calculate \nprobability of target attainment and a cumulative fraction of response to \nassess the best dosing regimen. The optimal dosage regimen for C. albicans and C. glabrata was 50 mg \nIV, and the optimal dosage regimen for C. parapsilosis was \n100 mg IV. Lastly, rezafungin has an excellent antifungal effect on C. albicans, C. glabrata and C. parapsilosis.","PeriodicalId":20031,"journal":{"name":"Pharmacology & Pharmacy","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimization of Dosage Regimen of Rezafungin against Candida spp. Based on Pharmacokinetic/Pharmacodynamic Analysis\",\"authors\":\"Jiuli Hu, Junhui Hu\",\"doi\":\"10.4236/pp.2020.116008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Invasive candidiasis was the most common nosocomial fungal infection with \\nhigh morbidity and mortality, which is mainly occurring in immunodeficiency and \\ncritical patients. Echinocandins were recommended as first-line drugs for the \\ntreatment and prevention of invasive candidiasis. In our study, we aimed to optimize \\nthe dosage of Rezafungin against Candida spp. based on \\npharmacokinetic/pharmacodynamics (PK/PD) analysis. We collected the published \\ndata about pharmacokinetic parameters of rezafungin and the MIC distribution of Candida spp. on rezafungin. Monte Carlo simulation was used to calculate \\nprobability of target attainment and a cumulative fraction of response to \\nassess the best dosing regimen. The optimal dosage regimen for C. albicans and C. glabrata was 50 mg \\nIV, and the optimal dosage regimen for C. parapsilosis was \\n100 mg IV. Lastly, rezafungin has an excellent antifungal effect on C. albicans, C. glabrata and C. parapsilosis.\",\"PeriodicalId\":20031,\"journal\":{\"name\":\"Pharmacology & Pharmacy\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-06-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacology & Pharmacy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4236/pp.2020.116008\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/pp.2020.116008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Optimization of Dosage Regimen of Rezafungin against Candida spp. Based on Pharmacokinetic/Pharmacodynamic Analysis
Invasive candidiasis was the most common nosocomial fungal infection with
high morbidity and mortality, which is mainly occurring in immunodeficiency and
critical patients. Echinocandins were recommended as first-line drugs for the
treatment and prevention of invasive candidiasis. In our study, we aimed to optimize
the dosage of Rezafungin against Candida spp. based on
pharmacokinetic/pharmacodynamics (PK/PD) analysis. We collected the published
data about pharmacokinetic parameters of rezafungin and the MIC distribution of Candida spp. on rezafungin. Monte Carlo simulation was used to calculate
probability of target attainment and a cumulative fraction of response to
assess the best dosing regimen. The optimal dosage regimen for C. albicans and C. glabrata was 50 mg
IV, and the optimal dosage regimen for C. parapsilosis was
100 mg IV. Lastly, rezafungin has an excellent antifungal effect on C. albicans, C. glabrata and C. parapsilosis.