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研究护士在资源有限环境中使用口服包封两性霉素B治疗隐球菌性脑膜炎的经验。

Experience of research nurses with oral encochleated amphotericin B for treatment of cryptococcal meningitis in a resource-limited setting.

作者信息

Ahimbisibwe Cynthia, Kwizera Richard, Ndyetukira Jane Frances, Namujju Olivie Carolyne, Sadiq Alisat, Atukunda Mucunguzi, Skipper Caleb P, Boulware David R, Meya David B

机构信息

Infectious Diseases Institute, College of Health Sciences, Makerere University, Kampala, Uganda.

Department of Research, Infectious Diseases Institute, College of Health Sciences, Makerere University, P.O.BOX 22418, Kampala, Uganda.

出版信息

BMC Infect Dis. 2025 Jul 15;25(1):920. doi: 10.1186/s12879-025-11319-1.

Abstract

BACKGROUND

Besides the commonly used intravenous formulations of amphotericin B, an oral nanocrystal amphotericin B (MAT2203) formulation is being evaluated for efficacy to treat invasive fungal infections. This new experimental oral formulation has not been used before.

METHODS

Herein, we describe our experiences with using oral amphotericin B for management of patients with HIV-associated cryptococcal meningitis in Uganda from a research nurse perspective.

RESULTS

We found oral amphotericin B a better alternative to intravenous amphotericin B deoxycholate due to less toxicity, mostly limited to gastrointestinal-related toxicities only. We clinically observed no drug reactions like rigors, phlebitis, and less vomiting among patients on oral amphotericin B as compared to those on intravenous amphotericin B deoxycholate. Subjectively, meningitis symptoms of patients on oral amphotericin B seemed to overall clinically improve more rapidly compared to those receiving intravenous amphotericin B deoxycholate. Few adverse events were observed. A novel challenge with oral amphotericin was difficulty in monitoring adherence for the night doses in the absence of the healthcare providers.

CONCLUSIONS

Oral amphotericin B was generally safe and well tolerated. However, it requires some training for the nurse, patient and care takers for better administration, adherence and treatment outcomes.

TRIAL REGISTRATION

This was observational sub-study that was nested under the EnACT trial. The EnACT trial was registered prospectively. ClincalTrials.gov: NCT04031833; Registration date: July 24, 2019; Last verified: March 31, 2023.

摘要

背景

除了常用的两性霉素B静脉制剂外,一种口服纳米晶体两性霉素B(MAT2203)制剂正在接受治疗侵袭性真菌感染疗效的评估。这种新型实验性口服制剂此前尚未使用过。

方法

在此,我们从研究护士的角度描述了在乌干达使用口服两性霉素B治疗HIV相关隐球菌性脑膜炎患者的经验。

结果

我们发现口服两性霉素B是比静脉注射脱氧胆酸两性霉素B更好的选择,因为其毒性较小,主要局限于胃肠道相关毒性。我们临床观察到,与接受静脉注射脱氧胆酸两性霉素B的患者相比,口服两性霉素B的患者没有出现寒战、静脉炎等药物反应,呕吐也较少。主观上,与接受静脉注射脱氧胆酸两性霉素B的患者相比,口服两性霉素B的患者的脑膜炎症状在临床上似乎总体改善得更快。观察到的不良事件很少。口服两性霉素B面临的一个新挑战是,在没有医护人员的情况下,难以监测夜间剂量的依从性。

结论

口服两性霉素B总体上安全且耐受性良好。然而,需要对护士、患者和护理人员进行一些培训,以实现更好的给药、依从性和治疗效果。

试验注册

这是一项嵌套在EnACT试验中的观察性子研究。EnACT试验已进行前瞻性注册。ClinicalTrials.gov:NCT04031833;注册日期:2019年7月24日;最后核实日期:2023年3月31日。

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