Division of Infectious Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan; Division of Infectious Diseases, Chang Gung University, Kwei-Shan, Taoyuan, Taiwan.
Department of General Surgery, Chang Gung Memorial Hospital, Kwei-Shan, Taoyuan, Taiwan.
J Microbiol Immunol Infect. 2014 Jun;47(3):245-53. doi: 10.1016/j.jmii.2013.09.006. Epub 2013 Nov 15.
Although echinocandins have high in vitro antifungal efficacy according to prior reports, comparative studies on the clinical cure rates of anidulafungin, caspofungin, and micafungin in systemic candida infections have not yet been reported.
Interpretation of clinical and microbiological responses to anidulafungin, caspofungin, and micafungin in 109 cases of candidemia was done according to the published criteria. The clinical cure rates between patients treated with echinocandins and patients treated with fluconazole were also compared. The minimal inhibitory concentrations (MICs) of anidulafungin, caspofungin, micafungin, and fluconazole for these 109 blood isolates of candida were determined with the Clinical and Laboratory Standards Institute M27-A reference microdilution method. Logistic regression with forward selection was used to determine the important factors of prognosis with variables such as age, underlying diseases, acute physiology and chronic health evaluation (APACHE) III score, persistent candidemia, and antimicrobial therapy.
Among the 109 cases of candidemia, 70 were treated with echinocandins, azoles, or amphotericin B for ≥7 days. The clinical cure rate of cases treated with antifungal agents adequately (≥7 days) and inadequately (<7 days) were 44/70 (62.9%) and 4/39 (10.2%), respectively, with significant difference (p < 0.0001). Clinical cure rates of anidulafungin, caspofungin, micafungin, and fluconazole were 18/30 (60.0%), 8/9 (88.9%), 5/7 (71.4%), and 9/18 (50%), respectively. The difference in APACHE III score between treatment success and failure cases was significant. The MIC50/MIC90 of anidulafungin, caspofungin, and micafungin for all Candida spp. were 0.03/1 μg/mL, 0.06/0.5 μg/mL, and 0.008/1 μg/mL, respectively.
Adequate antifungal therapy and APACHE III score are both independent factors affecting the clinical outcome. The clinical cure rate of the echinocandins group was higher than that of the fluconazole group without significant difference. Although caspofungin had the best clinical cure rate in this study, there was no significant difference between the clinical cure rates among these three echinocandins. All Candida spp. were susceptible in vitro to these three echinocandins.
尽管棘白菌素类药物在体外具有很高的抗真菌疗效,但目前尚未有关于棘白菌素类药物(安尼芬净、卡泊芬净和米卡芬净)在系统性念珠菌感染中的临床治愈率的对照研究报道。
根据已发表的标准,对 109 例念珠菌血症患者应用安尼芬净、卡泊芬净和米卡芬净的临床和微生物学反应进行解读。同时,还比较了应用棘白菌素类药物和氟康唑治疗的患者之间的临床治愈率。采用美国临床和实验室标准协会(CLSI)M27-A 参考微量稀释法,确定 109 株念珠菌血液分离株的安尼芬净、卡泊芬净、米卡芬净和氟康唑的最小抑菌浓度(MIC)。采用向前选择的逻辑回归,结合年龄、基础疾病、急性生理学和慢性健康评估(APACHE)III 评分、持续性念珠菌血症和抗菌治疗等变量,确定预后的重要因素。
在 109 例念珠菌血症中,70 例患者接受了棘白菌素类、唑类或两性霉素 B 治疗≥7 天。接受抗真菌药物治疗(≥7 天)和治疗不充分(<7 天)的患者的临床治愈率分别为 44/70(62.9%)和 4/39(10.2%),差异具有统计学意义(p<0.0001)。安尼芬净、卡泊芬净、米卡芬净和氟康唑的临床治愈率分别为 18/30(60.0%)、8/9(88.9%)、5/7(71.4%)和 9/18(50%)。治疗成功与失败病例之间的 APACHE III 评分差异具有统计学意义。所有念珠菌属对安尼芬净、卡泊芬净和米卡芬净的 MIC50/MIC90 分别为 0.03/1μg/mL、0.06/0.5μg/mL 和 0.008/1μg/mL。
充分的抗真菌治疗和 APACHE III 评分均是影响临床结局的独立因素。棘白菌素类药物组的临床治愈率高于氟康唑组,但差异无统计学意义。虽然本研究中卡泊芬净的临床治愈率最高,但三种棘白菌素类药物之间的临床治愈率无显著差异。所有念珠菌属在体外均对这三种棘白菌素类药物敏感。