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以半乳甘露聚糖为指导的抢先与经验性抗真菌治疗在持续发热中性粒细胞减少患者中的前瞻性随机研究。

Galactomannan-guided preemptive vs. empirical antifungals in the persistently febrile neutropenic patient: a prospective randomized study.

机构信息

Department of Infectious Diseases, Singapore General Hospital, Singapore 169608.

出版信息

Int J Infect Dis. 2011 May;15(5):e350-6. doi: 10.1016/j.ijid.2011.01.011. Epub 2011 Mar 11.

Abstract

BACKGROUND

Patients with neutropenic fever after 4-7 days of broad-spectrum antibiotics are given antifungals empirically. This strategy may lead to over-treatment.

METHODS

Patients with hematological malignancies undergoing intensive chemotherapy or hematopoietic stem cell transplantation were randomized to two arms. Patients in the 'preemptive' arm had regular galactomannan (GM) assays, and received caspofungin, amphotericin or voriconazole (CAV) for persistent febrile neutropenia if they had two positive GM results, or a positive GM result and a computed tomography (CT) of the thorax suggestive of invasive pulmonary aspergillosis (IPA). Patients in the 'empirical' arm received CAV in accordance with established guidelines.

RESULTS

Of 27 episodes in the preemptive arm, two cases of IPA were picked up by monitoring. In six episodes, CAV was started despite persistently negative GM readings. One additional patient received CAV for a false-positive GM. Of 25 episodes in the empirical arm, CAV was started empirically in 10, one of whom had CT features of IPA. By intent-to-treat and evaluable-episode analyses, respectively, the preemptive approach saved 11% and 14% of patients from empirical antifungals. Twelve-week survival was 85.2% in the preemptive arm and 84% in the empirical arm.

CONCLUSIONS

A preemptive approach may reduce empirical antifungal use without compromising survival in persistently febrile neutropenic patients.

摘要

背景

在接受广谱抗生素治疗 4-7 天后出现中性粒细胞减少性发热的患者,经验性给予抗真菌药物。这种策略可能会导致过度治疗。

方法

正在接受强化化疗或造血干细胞移植的血液系统恶性肿瘤患者被随机分为两组。“抢先”组的患者定期进行半乳甘露聚糖(GM)检测,如果连续两次 GM 检测结果阳性,或 GM 检测阳性且胸部 CT 提示侵袭性肺曲霉病(IPA),则给予卡泊芬净、两性霉素或伏立康唑(CAV)治疗持续发热性中性粒细胞减少症。“经验性”组的患者根据既定指南接受 CAV 治疗。

结果

抢先组 27 个病例中,通过监测发现两例 IPA。6 个病例尽管 GM 检测持续阴性,但仍开始 CAV 治疗。另外一名患者因 GM 假阳性而接受 CAV 治疗。经验性组 25 个病例中,10 例经验性使用 CAV,其中 1 例有 IPA 的 CT 特征。意向治疗和可评估病例分析分别显示,抢先治疗方法使 11%和 14%的患者免于接受经验性抗真菌药物治疗。抢先组的 12 周生存率为 85.2%,经验性组为 84%。

结论

抢先治疗方法可能会减少经验性抗真菌药物的使用,而不会影响持续发热性中性粒细胞减少症患者的生存。

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