Liposomal amphotericin B as an antifungal prophylaxis in bilateral lung transplantation: a safety analysis.

IF 2.7 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Annalisa Boscolo, Nicolò Sella, Sabrina Congedi, Irene Paiusco, Elisa Pistollato, Alessia Zanaga, Francesca Chiapperini, Francesco Zarantonello, Giulia Mormando, Giulia Pagliarini, Alessandro De Cassai, Tommaso Pettenuzzo, Andrea Dell'Amore, Paolo Navalesi
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引用次数: 0

Abstract

Background: Lung transplantation (LT) is the definitive treatment for end-stage chronic respiratory failure. Despite improvements in surgical and perioperative care, fungal infections remain a major complication in LT recipients, and antifungal prophylaxis with liposomal amphotericin B (L-AmB) is commonly used. However, evidence on the safety of L-AmB administration in LT recipients remains limited. This retrospective observational study aimed to assess the profile of renal, hepatic and hematologic safety, and the incidence of hypersensitivity adverse events following prophylactic L-AmB use in LT recipients.

Methods: A retrospective, single-center observational study of adult patients (≥ 18 years) who underwent their first bilateral LT at the University Hospital of Padua (Italy), between January 2020 and March 2025. All patients received intravenous L-AmB (3 mg/kg/day for 5 days) as postoperative antifungal prophylaxis. Adverse effects were assessed based on acute kidney injury (AKI), liver toxicity, hematotoxicity, and infusion reactions. Laboratory values were collected at baseline, on days 1, 2, 3, 7, and 14 post-L-AmB initiation.

Results: 189 LT recipients were screened and 140 enrolled. Concerning safety profile, AKI occurred in 55 (39%) patients, with serum creatinine peaking at 48 h (p = 0.025), as compared to baseline. Mild transaminase elevations occurred in 86% of patients within the first 48 h, and bilirubin increased in 10%, with no episodes of acute liver failure. Anemia (85%) and transient thrombocytopenia (9%) were observed. Hypokalemia was found in 28%. Renal replacement therapy was needed in 2%. No infusion-related or allergic reactions to L-AmB were observed. According to the institutional fungal surveillance protocol, no proven, probable, or possible invasive fungal infections were documented during the observation period. However, the present study was not designed to assess the prophylactic efficacy of L-AmB.

Conclusions: In this cohort of bilateral LT recipients receiving standardized L-AmB prophylaxis, no discontinuation, dose adjustment, infusion reaction, or proven fungal infection was documented. Renal, hepatic, hematologic, and electrolyte abnormalities were frequent; but cannot be specifically attributed to L-AmB in the absence of a comparator group, given the multifactorial pathophysiology of the early post-transplant period. These findings underscore the importance of vigilant monitoring of organ function during L-AmB administration in this vulnerable population.

两性霉素B脂质体在双侧肺移植中的抗真菌预防作用:安全性分析。
背景:肺移植(LT)是终末期慢性呼吸衰竭的最终治疗方法。尽管手术和围手术期护理有所改善,真菌感染仍然是肝移植受者的主要并发症,通常使用脂质体两性霉素B (L-AmB)进行抗真菌预防。然而,关于左肾移植受者使用L-AmB的安全性的证据仍然有限。这项回顾性观察性研究旨在评估肝移植受体预防性使用L-AmB后肾、肝和血液学安全性的概况,以及过敏不良事件的发生率。方法:对2020年1月至2025年3月期间在意大利帕多瓦大学医院接受首次双侧肝移植的成年患者(≥18岁)进行回顾性、单中心观察研究。所有患者术后均静脉注射L-AmB (3mg /kg/天,连续5天)作为抗真菌预防。根据急性肾损伤(AKI)、肝毒性、血液毒性和输液反应评估不良反应。在l - amb启动后的第1、2、3、7和14天收集基线时的实验室值。结果:筛选了189名肝移植受者,140名入组。在安全性方面,55例(39%)患者发生AKI,与基线相比,血清肌酐在48小时达到峰值(p = 0.025)。86%的患者在治疗前48小时内出现轻度转氨酶升高,10%的患者胆红素升高,无急性肝衰竭发作。观察到贫血(85%)和短暂性血小板减少(9%)。28%的患者出现低钾血症。2%的患者需要肾脏替代治疗。未观察到L-AmB输注相关反应或过敏反应。根据机构真菌监测方案,在观察期间没有证实的、可能的或可能的侵袭性真菌感染记录。然而,本研究的目的不是评估L-AmB的预防作用。结论:在这组接受标准化L-AmB预防治疗的双侧肝移植患者中,没有停药、剂量调整、输液反应或证实的真菌感染的记录。肾、肝、血液学和电解质异常频繁;但考虑到移植后早期的多因素病理生理,在没有比较组的情况下,不能特别归因于L-AmB。这些发现强调了在这些易感人群中使用L-AmB期间警惕监测器官功能的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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