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米卡芬净与其他棘白菌素类和唑类药物在已有Child-Pugh B级或C级肝病患者中的安全性和耐受性比较:一项病例对照回顾性研究。

Comparison of the Safety and Tolerance Profile of Micafungin with that of Other Echinocandins and Azoles in Patients with Pre-existing Child-Pugh B or C Liver Disease: A Case-Control Retrospective Study.

作者信息

Vena Antonio, Bouza Emilio, Bassetti Matteo, Menichetti Francesco, Merelli Maria, Grau Santiago, Fortun Jesús, Sánchez María Isabel, Aguado José María, Merino Paloma, Bonache Francisco, Muñoz Patricia

机构信息

Clinical Microbiology and Infectious Diseases, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Instituto de Investigación Sanitaria Hospital Gregorio Marañón, Madrid, Spain.

出版信息

Infect Dis Ther. 2020 Mar;9(1):151-163. doi: 10.1007/s40121-020-00282-w. Epub 2020 Feb 21.

Abstract

INTRODUCTION

To assess the association between exposure to micafungin, other echinocandins, or azoles and the development of short-term liver injury (STLI) or long-term liver injury (LTLI) in patients with Child-Pugh B or C liver disease.

METHODS

Multicenter case-control study of patients with Child-Pugh B or C liver disease who received antifungals (AF) for ≥ 72 h (May 2009-May 2015) in six Spanish and Italian hospitals. All micafungin patients were randomly matched with one patient who received another echinocandin and with one patient who received azole treatment. Primary outcome was development of STLI or LTLI (development of any type of liver tumor during the follow-up period).

RESULTS

Of 2335 patients with chronic liver disease admitted to the six centers, 20 (0.85%) were found to have Child-Pugh B or C liver disease and received micafungin for ≥ 72 h. During AF treatment, the frequency of STLI was 10% in each group. Most cases of STLI were asymptomatic, and AFs had to be switched to another class of AF in only two patients (one micafungin and one azole). No patients developed acute liver insufficiency, were admitted to the ICU, or had to undergo transplantation. Follow-up data (median of 1.3 years) were available for 30 patients. LTLI was observed in only one patient, who had previously received treatment with azoles.

CONCLUSIONS

Our study suggests that the administration of micafungin to patients with end-stage liver disease does not imply a higher risk of developing STLI or LTLI.

摘要

引言

评估接受米卡芬净、其他棘白菌素类药物或唑类药物治疗与Child-Pugh B或C级肝病患者发生短期肝损伤(STLI)或长期肝损伤(LTLI)之间的关联。

方法

对2009年5月至2015年5月期间在西班牙和意大利的6家医院接受抗真菌药物(AF)治疗≥72小时的Child-Pugh B或C级肝病患者进行多中心病例对照研究。所有米卡芬净治疗的患者均随机与一名接受其他棘白菌素类药物治疗的患者以及一名接受唑类治疗的患者进行匹配。主要结局是STLI或LTLI的发生(随访期间出现任何类型的肝肿瘤)。

结果

在6个中心收治的2335例慢性肝病患者中,有20例(0.85%)被发现患有Child-Pugh B或C级肝病并接受米卡芬净治疗≥72小时。在AF治疗期间,每组STLI的发生率均为10%。大多数STLI病例无症状,仅2例患者(1例米卡芬净治疗患者和1例唑类治疗患者)需要将AF换成另一类AF。没有患者发生急性肝衰竭、入住重症监护病房或必须接受肝移植。30例患者有随访数据(中位随访时间为1.3年)。仅1例患者发生LTLI,该患者之前接受过唑类治疗。

结论

我们的研究表明,对终末期肝病患者使用米卡芬净并不意味着发生STLI或LTLI的风险更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb3/7054556/f168997a710f/40121_2020_282_Fig1_HTML.jpg

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