Use of Intrathecal Amphotericin for Coccidioidal Meningitis

鞘内注射两性霉素治疗球孢子菌性脑膜炎

阅读:1

Abstract

BACKGROUND: Cases of coccidioidomycosis are increasing dramatically in the United States. The utility of intrathecal (IT) amphotericin in treating coccidioidal meningitis (CM) in the era of azole therapy is unknown. We sought to understand how IT therapy is associated with mortality. METHODS: We conducted a retrospective chart review of adult patients with laboratory-proven CM seen at Stanford Healthcare by an infectious diseases physician from 2008 to 2023. RESULTS: Fifty-seven patients met inclusion criteria. All patients received azole therapy. Twenty-seven of those patients (47.4%) additionally received IT amphotericin. Patients receiving IT therapy had a higher median initial cerebrospinal fluid white blood cell count at diagnosis (462.5 vs 188 cells/μL, P = .05), higher rates of intravenous liposomal amphotericin use (88.9% vs 56.7%, P = .02) and corticosteroid use (51.9% vs 26.7%, P = .09), and higher median therapeutic switches per year (0.84 vs 0.44, P = .01). An unadjusted Kaplan-Meier curve demonstrated a 5-year mortality rate of 26.7% in the IT amphotericin group, compared to 6.7% in the nonreceiver group (P = .28). A Cox regression revealed that older age at diagnosis (hazard ratio [HR], 1.07 [95% confidence interval {CI}, 1.03-1.11]), receipt of IT amphotericin (HR, 13.9 [95% CI, 1.92-100.48]), and corticosteroid use (HR, 8.3 [95% CI, 1.92-35.4]) were significantly associated with mortality, with a significant interaction between IT amphotericin and corticosteroids (interaction HR, 0.14 [95% CI, .02-.97]). CONCLUSIONS: Patients who received IT amphotericin had higher mortality rates than those who did not, likely reflecting disease refractory to treatment. More therapies are needed for those who have disease progression on azole therapy.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。